Index of Molecular Images
To facilitate comparison of similar structures, the images are listed by clan and family.
Clan | MEROPS ID | Peptidase | Comment | PDB Entry |
---|---|---|---|---|
AA | A01.003 | gastricsin | activation intermediate 2 | 1AVF |
AA | A01.003 | gastricsin | precursor | 1HTR |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | protease domain; complex with Glu-Val-Asn-leucinol-2-methyl-propionyl-Ala-Glu-Phe inhibitor | 1FKN_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor OM00-3 | 1M4H |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | unbound catalytic domain | 1SGZ |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 1TQF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | 1W50 | |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 3-[((1S,2R)-1-benzyl-2-hydroxy-3-[(3-methoxybenzyl)amino]propylamino)(hydroxy)methyl]-N,N-dipropylbenzamide | 1W51 |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-aur200 | 1YM2_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-amk640 | 1YM4_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2B8L_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with l- l000430,469 | 2B8V_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with axq093, a macrocyclic inhibitor | 2F3E_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bdf488, a macrocyclic inhibitor | 2F3F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2HIZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2IRZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2IS0_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2NTR_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2OAH_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with isophthalamide s2 hydroxyethylamine inhibitor | 2P83_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2P8H_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2PH6_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 2PH8_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 1 | 2Q11_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 3a | 2Q15_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 1 | 2QU2_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 2 | 2QU3_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with i21 | 2QZK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with ixs | 2QZL_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with n-((1s,2r)-1-benzyl-2-hydroxy-3-((1,1,5- trimethylhexyl)amino)propyl)-3-(ethylamino)-5-(2-oxopyrrolidin-1-yl) benzamide | 2VIE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 3-(1,1-dioxidotetrahydro-2h-1,2-thiazin- 2-yl)-5-(ethylamino)-n-((1s,2r)-2-hydroxy-1-(phenylmethyl)-3-(1,2,3, 4- tetrahydro-1-naphthalenylamino)propyl)benzamide | 2VIJ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with n-((1s,2r)-3-(((1s)-2-(cyclohexylamino)- 1-methyl-2-oxoethyl)amino)-2-hydroxy-1-(phenylmethyl)propyl)-3- (pentylsulfonyl)benzamide | 2VIY_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with n-((1s,2r)-3-(((1s)-2-(cyclohexylamino)- 1-methyl-2-oxoethyl)amino)-2-hydroxy-1-(phenylmethyl)propyl)-3-(2- oxo- 1-pyrrolidinyl)-5-(propyloxy)benzamide | 2VIZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with n-((1s,2r)-3-(((1s)-2-(cyclohexylamino)- 1-methyl-2-oxoethyl)amino)-2-hydroxy-1-(phenylmethyl)propyl)-3- (ethylamino)-5-(2-oxo-1-pyrrolidinyl)benzamide | 2VJ6_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 3-(ethylamino)-n-((1s,2r)-2-hydroxy-1- (phenylmethyl)-3-(((3-(trifluoromethyl)phenyl)methyl)amino)propyl)-5-(2-oxo-1-pyrrolidinyl)benzamide | 2VJ7_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with n-((1s,2r)-3-(cyclohexylamino)-2-hydroxy-1-(phenylmethyl)propyl)-3-(ethylamino)-5-(2-oxo-1-pyrrolidinyl) benzamide | 2VJ9_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 3-(1,1-dioxidotetrahydro-2h-1,2-thiazin- 2-yl)-5-(ethylamino)-n-((1s,2r)-2-hydroxy-1-(phenylmethyl)-3-(((3- (trifluoromethyl)phenyl)methyl)amino)propyl)benzamide | 2VNM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 7-ethyl-n-((1s,2r)-2-hydroxy-1- (phenylmethyl)-3-(((3-(trifluoromethyl)phenyl)methyl)amino)propyl)-1-methyl-3,4-dihydro-1h-(1,2,5)thiadiazepino(3,4,5-hi)indole-9- carboxamide 2,2-dioxide | 2VNN_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 1-ethyl-n-((1s,2r)-2-hydroxy-3-(((3- (methyloxy)phenyl)methyl)amino)-1-(phenylmethyl)propyl)-4-(2-oxo-1- pyrrolidinyl)-1h-indole-6-carboxamide | 2WEZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 4-ethyl-n-((1s,2r)-2-hydroxy-1- (phenylmethyl)-3-(((3-(trifluoromethyl)phenyl)methyl)amino)propyl)-8-(2-oxo-1-pyrrolidinyl)-6-quinolinecarboxamide | 2WF0_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 7-ethyl-n-((1s,2r)-2-hydroxy-3-(((3- (methyloxy)phenyl(methyl)amino)-1-(phenylmethyl)propyl)-1-methyl-3,4-dihydro-1h-(1,2,5)thiadiazepino(3,4,5-hi)indole-9-carboxamide 2,2- dioxide | 2WF1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 8-ethyl-n-((1s,2r)-2-hydroxy-3-(((3- (methyloxy)phenyl)methyl)amino)-1-(phenylmethyl)propyl)-1-methyl-3,4,7, 8-tetrahydro-1h,6h-(1,2,5)thiadiazepino(5,4,3-de)quinoxaline-10- carboxamide 2,2-dioxide | 2WF2_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 6-(ethylamino)-n-((1s,2r)-2-hydroxy-3- (((3-(methyloxy)phenyl)methyl)amino)-1-(phenylmethyl)propyl)-1- methyl-1, 3,4,5-tetrahydro-2,1-benzothiazepine-8-carboxamide 2,2- dioxide | 2WF3_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with 6-ethyl-1-methyl-n-((1s)-2-oxo-1- (phenylmethyl)-3-(tetrahydro-2h-pyran-4-ylamino)propyl)-1,3,4,6- tetrahydro(1,2)thiazepino(5,4,3-cd)indole-8-carboxamide 2,2-dioxide | 2WF4_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with n-((1s,2r)-3-(((1s)-2-(cyclohexylamino)- 1-methyl-2-oxoethyl)amino)-2-hydroxy-1-(phenylmethyl)propyl)-3- ((methylsulfonyl)(phenyl)amino)benzamide | 2XFI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with n-((1s,2r)-3-(((1s)-2-(cyclohexylamino)- 1-methyl-2-oxoethyl)amino)-2-hydroxy-1-(phenylmethyl)propyl)-3- (ethylamino)-5-(2-oxo-1-pyrrolidinyl)benzamide | 2XFJ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 in complex with n-((1s,2r)-3-(((1s)-2-(cyclohexylamino)- 1-methyl-2-oxoethyl)amino)-2-hydroxy-1-(phenylmethyl)propyl)-3- (ethylamino)-5-((methylsulfonyl)(phenyl)amino)benzamide | 2XFK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 3.b.10 | 2ZDZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 6g | 2ZE1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor OM99-2 at pH 5.0 | 2ZHR |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | at pH 4.0 | 2ZHS |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | at pH 4.5 | 2ZHT |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | at pH 5.0 | 2ZHU |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | at pH 7.0 | 2ZHV |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | catalytic domain; complex with 4-(4-fluoro-benzyl)-piperazine-2-carboxylic acid(3-mercapto-propyl)-amide | 2ZJK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | catalytic domain; complex with n-[1-(5-chloro-2-isopropoxy-3-methoxy-benzyl)- piperidin-4-yl]-2-(4-sulfamoyl-phenoxy)-acetamide | 2ZJM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | catalytic domain; complex with n-[1-(5-chloro-2-isopropoxy-3-methoxy-benzyl)- piperidin-4-yl]-2-(2-methyl-4-sulfamoyl-phenoxy)-acetamide | 2ZJN_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 1 | 3BRA_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 2 | 3BUF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 3 | 3BUG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 4 | 3BUH_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with statine-based inhibitor | 3DM6_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-afj144 | 3DUY_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-arv999 | 3DV1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bav544 | 3DV5_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 3EXO_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with spiropiperdine iminohydantoin inhibitor | 3FKT_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | discovery of aminoheterocycles as a novel beta-secretase inhibitor class | 3H0B_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with ev0 | 3HVG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with ligand ev2 | 3HW1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | potent beta-secretase 1 hydroxyethylene inhibitor | 3I25_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 3 | 3IGB_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 30 | 3IN3_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 38 | 3IN4_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminohydantoin compound 29 | 3IND_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminohydantoin compound s-34 | 3INE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminohydantoin compound 37 | 3INF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminohydantoin compound r-58 | 3INH_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | potent beta-secretase 1 inhibitor | 3IXK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 complex with nb-216 | 3K5C_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with ahm178 | 3K5D_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 complex with ayh011 | 3K5F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | human bace-1 complex with bjc060 | 3K5G_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a norstatine type inhibitor | 3KYR_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminopyridine compound 44 | 3L38_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminopyridine compound 32 | 3L3A_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch589432 | 3L58_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch710413 | 3L59_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch713601 | 3L5B_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch723871 | 3L5C_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch723873 | 3L5D_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch736062 | 3L5E_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch736201 | 3L5F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminohydantoin compound 4g | 3LHG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch745132 | 3LPI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch743641 | 3LPJ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with sch747123 | 3LPK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 3MSJ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | fragment based discovery and optimisation of bace-1 inhibitors | 3MSK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | fragment based discovery and optimisation of bace-1 inhibitors | 3MSL_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bms-655295 aka n~3~-((1s,2r)-1- benzyl-2-hydroxy-3-((3- methoxybenzyl)amino)propyl)-n~1~, n~1~-dibutyl-1h-indole-1,3- dicarboxamide | 3OHF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bms-681889 aka n~1~-butyl-5-cyano- n~3~-((1s,2r)-1-(3,5- difluorobenzyl)-2-hydroxy-3-((3- methoxybenzyl)amino)propyl)-n~1~- methyl-1h-indole-1,3- dicarboxamide | 3OHH_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with the aminohydantoin compound 102 | 3OOZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bfg356 | 3PI5_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | structure based design, synthesis and sar of cyclic hydroxyethylamine (hea) bace-1 inhibitors | 3QBH_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of hydroxyethylamine (hea) bace-1 inhibitors: prime side chromane-containing inhibitors | 3QI1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bms-693391 aka (2s)-2-((3r)-3-acetamido-3-isobutyl-2-oxo-1- pyrrolidinyl)-n-((1s,2r)-1-(3,5-difluorobenzyl)-2-hydroxy-2-((2r,4r)-4-propoxy-2-pyrrolidinyl)ethyl)-4-phenylbutanamide | 3R2F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 3-(2- aminoquinolin-3-yl)-n-(cyclohexylmethyl)propanamide | 3RU1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-((2-amino-6-o- tolylquinolin-3-yl)methyl)-n-(cyclohexylmethyl)pentanamide | 3RVI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | fragment based discovery and optimisation of bace-1 inhibitors | 3S2O_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | pyrazolyl and thienyl aminohydantoins as potent bace1 inhibitors | 3S7L_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | pyrazolyl and thienyl aminohydantoins as potent bace1 inhibitors | 3S7M_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (2s)-2-((3s)-3-(acetylamino)-3-(butan-2-yl)-2-oxopyrrolidin-1- yl)-n-((2s,3r)-3-hydroxy-4-((3-methoxybenzyl)amino)-1-phenylbutan-2- yl)-4-phenylbutanamide | 3SKF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (2s)-2-((3r)-3-acetamido-3-isobutyl-2-oxo-1-pyrrolidinyl)-n- ((1s,2r)-1-(3,5-difluorobenzyl)-2-hydroxy-2-(1,2,3,4-tetrahydro-3- isoquinolinyl)ethyl)-4-phenylbutanamide | 3SKG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | apo form | 3TPJ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | apo form | 3TPL_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3TPP_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3TPR_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | rational design and synthesis of aminopiperazinones as beta secretase (bace) inhibitors | 3U6A_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3UQP_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3UQR_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3UQU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3UQW_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 3UQX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-avi326 | 3VEU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bqq711 | 3VF3_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bur436, derived from a soaking experiment | 3VG1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-amino-3-methyl-6-((1s, 2r)-2-phenylcyclopropyl)pyrimidin-4(3h)-one | 3VV6_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-amino-3,6- dimethyl-6-(2-phenylethyl)-3,4,5,6-tetrahydropyrimidin-4-one | 3WB4_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (6s)-2-amino-3,6- dimethyl-6-[(1r,2r)-2-phenylcyclopropyl]-3,4,5,6-tetrahydropyrimidin-4-one | 3WB5_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with chemical ligand | 3ZMG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with chemical ligand | 3ZOV_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 14 | 4ACU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 23 | 4ACX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of bace1 inhibitors with in vivo brain reduction of beta-amyloid peptides (compound 10) | 4AZY_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of bace1 inhibitors with in vivo brain reduction of beta-amyloid peptides (compound (r)-41) | 4B00_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with azd3839 | 4B05_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | new aminoimidazoles as bace-1 inhibitors: from rational design to ab- lowering in brain | 4B1C_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminoimidazoles as bace-1 inhibitors: from de novo design to ab-lowering in brain | 4B70_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminoimidazoles as bace-1 inhibitors: from de novo design to ab-lowering in brain | 4B72_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminoimidazoles as bace-1 inhibitors: from de novo design to ab-lowering in brain | 4B77_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminoimidazoles as bace-1 inhibitors: from de novo design to ab-lowering in brain | 4B78_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with chemical ligand | 4BEK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with chemical ligand | 4BFD_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bur436, derived from a co-crystallization experiment | 4D83_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bvi151 | 4D85_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bxq490 | 4D88_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bxd552, derived from a soaking experiment | 4D89_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with nvp-bxd552, derived from a co-crystallization experiment | 4D8C_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxyethylamine inhibitor37 | 4DI2_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-imino-3-methyl-5,5-diphenylimidazolidin- 4-one | 4DJU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-imino-3-methyl-5-phenyl-5-(3-(pyridin-3- yl)phenyl)imidazolidin-4-one | 4DJW_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-(3-(5-chloropyridin-3-yl)phenyl)-5- cyclopropyl-2-imino-3-methylimidazolidin-4-one | 4DJX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (r)-5-cyclopropyl-2-imino-3-methyl-5-(3-(5-(prop-1-yn-1-yl)pyridin-3-yl)phenyl)imidazolidin-4-one | 4DJY_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a hea-macrocyclic type inhibitor | 4DPF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hea-macrocyclic inhibitor, mv078512 | 4DPI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 4DV9_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 4DVF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of potent hydroxyethylamine (hea) bace-1 inhibitors | 4EWO_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of potent hydroxyethylamine (hea) bace-1 inhibitors | 4EXG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 4FCO_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 4FGX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 14g | 4FM7_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 12a | 4FM8_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with biarylspiro aminooxazoline 6 | 4FRI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with aminooxazoline xanthene 9l | 4FRJ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with aminooxazoline xanthene 11a | 4FRK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (s)-4-(3-chloro-5-(5-(prop-1-yn-1- yl)pyridin-3-yl)thiophen-2-yl)-1,4-dimethyl-6-oxotetrahydropyrimidin-2(1h)-iminium | 4FRS_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with n-(n-(4-amino-3,5- dichlorobenzyl)carbamimidoyl)-3-(4- methoxyphenyl)-5- methyl-4-isothiazolecarboxamide | 4FSE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | bace-db-mutant; complex with n-(n-(4- acetamido-3-chloro-5-methylbenzyl) carbamimidoyl)-3-(4- methoxyphenyl)-5-methyl-4-isothiazolecarboxamide | 4FSL_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 4GID_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hea-type macrocyclic inhibitor, mv078571 | 4GMI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-6-benzoyl-7a-(4-(3-cyanophenyl) thiophen-2-yl)-3-methyl-4-oxohexahydro-1h-pyrrolo[3,4-d]pyrimidin- 2(3h)-iminium | 4H1E_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 3-(5-((7ar)-2-imino-6-(6-methoxypyridin-2- yl)-3-methyl-4-oxooctahydro-1h-pyrrolo[3,4-d]pyrimidin-7a-yl) thiophen-3-yl)benzonitrile | 4H3F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-((7ar)-7a-(4-(3-cyanophenyl)thiophen-2- yl)-2-imino-3-methyl-4-oxohexahydro-1h-pyrrolo[3,4-d]pyrimidin-6(2h)-yl)nicotinonitrile | 4H3G_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 3-(5-((7ar)-2-imino-6-(3-methoxypyridin-2- yl)-3-methyl-4-oxooctahydro-1h-pyrrolo[3,4-d]pyrimidin-7a-yl) thiophen-3-yl)benzonitrile | 4H3I_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-fluoro-5-(5-(2-imino-3-methyl-4-oxo-6- phenyloctahydro-1h-pyrrolo[3,4-d]pyrimidin-7a-yl)thiophen-2-yl) benzonitrile | 4H3J_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (s)-3-(5-(2-imino-1,4-dimethyl-6- oxohexahydropyrimidin-4-yl)thiophen-3-yl)benzonitrile | 4HA5_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | structure-based design of novel dihydroisoquinoline bace-1 inhibitors that do not engage the catalytic aspartates | 4HZT_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors ***caveat 4i0d a his 423 ca has chirality not corresponding to the amino ***caveat 2 4i0d acid definition. some close contacts | 4I0D_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors ***caveat 4i0e several close contacts | 4I0E_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors | 4I0F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors ***caveat 4i0g few water molecules are involved in close contacts | 4I0G_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spr and structural analysis yield insight towards mechanism of inhibition of bace inhibitors. | 4I0H_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spr and structural analysis yield insight towards mechanism of inhibition of bace inhibitors | 4I0I_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spr and structural analysis yield insight towards mechanism of inhibition of bace inhibitors | 4I0J_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | structure-based design of novel dihydroisoquinoline bace-1 inhibitors that do not engage the catalytic aspartates | 4I0Z_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | structure-based design of novel dihydroisoquinoline bace-1 inhibitors that do not engage the catalytic aspartates | 4I10_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | structure-based design of novel dihydroisoquinoline bace-1 inhibitors that do not engage the catalytic aspartates. | 4I11_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors | 4I12_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | design and synthesis of thiophene dihydroisoquinolins as novel bace-1 inhibitors | 4I1C_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 4IVS_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with an inhibitor | 4IVT_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((s)-2-amino-4-methyl-5,6-dihydro-4h-[1,3]oxazin- 4-yl)-4-fluoro-phenyl]-amide | 4J0P_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-ethoxy-pyridine-2- carboxylic acid [3-((r)-2-amino-5,5-difluoro-4-methyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J0T_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4r,5r)-2-amino-5-fluoro-4-methyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J0V_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4r,5s)-2-amino-5-fluoro-4-methyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J0Y_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4s,5r)-2-amino-5-fluoro-4-fluoromethyl-5,6- dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J0Z_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((s)-2-amino-4-difluoromethyl-5,6-dihydro-4h-[1, 3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J17_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((s)-2-amino-5,5-difluoro-4-fluoromethyl-5,6- dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J1C_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4s,6s)-2-amino-4-fluoromethyl-6-trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J1E_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4s,6s)-2-amino-4-methyl-6-trifluoromethyl-5,6- dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J1F_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4s,6r)-2-amino-4-methyl-6-trifluoromethyl-5,6- dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]-amide | 4J1H_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4r,5r,6r)-2-amino-5-fluoro-4-methyl-6- trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]- amide | 4J1I_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-cyano-pyridine-2- carboxylic acid [3-((4r,5r,6s)-2-amino-5-fluoro-4-methyl-6- trifluoromethyl-5,6-dihydro-4h-[1,3]oxazin-4-yl)-4-fluoro-phenyl]- amide | 4J1K_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spirocyclic beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4JOO_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spirocyclic beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4JP9_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spirocyclic beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4JPC_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | spirocyclic beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4JPE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | hydroxyethylamine-based inhibitors of bace1: p1-p3 macrocyclization can improve potency, selectivity, and cell activity | 4K8S_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor | 4K9H_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxyethylamine- macrocyclic inhibitor 13 | 4KE0_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxyethylamine- macrocyclic inhibitor 19 | 4KE1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | diethylaminosulfur trifluoride-mediated intramolecular cyclization of 2-hydroxy-benzylureas to fused bicyclic aminooxazoline compounds and evaluation of their biochemical activity against beta-secretase-1 (bace1) | 4L7G_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | diethylaminosulfur trifluoride-mediated intramolecular cyclization of 2-hydroxy-benzylureas to fused bicyclic aminooxazoline compounds and evaluation of their biochemical activity against beta-secretase-1 (bace-1) | 4L7H_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | diethylaminosulfur trifluoride-mediated intramolecular cyclization of 2-hydroxy-benzylureas to fused bicyclic aminooxazoline compounds and evaluation of their biochemical activity against beta-secretase-1 (bace-1) | 4L7J_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminooxazoline inhibitor of bace-1 | 4LC7_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 11a | 4LXA_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 11d | 4LXK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 12a | 4LXM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | discovery of 7-thp chromans: bace1 inhibitors that reduce a-beta in the cns | 4N00_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | synthesis, characterization and pk/pd studies of a series of spirocyclic pyranochromene bace1 inhibitors | 4PZW_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | synthesis, characterization and pk/pd studies of a series of spirocyclic pyranochromene bace1 inhibitors | 4PZX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | 8-tetrahydropyran-2-yl chromans: highly selective beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4R5N_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (r)-4-(2-cyclohexylethyl)-4-(((r)-1-(2- cyclopentylacetyl)pyrrolidin-3-yl)methyl)-1-methyl-5-oxoimidazolidin-2-iminium | 4R8Y_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (r)-4-(2-cyclohexylethyl)-4-(((1s,3r)-3- (cyclopentylamino)cyclohexyl)methyl)-1-methyl-5-oxoimidazolidin-2- iminium | 4R91_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (r)-4-(2-cyclohexylethyl)-4-(((1s,3r)-3- (isonicotinamido)cyclohexyl)methyl)-1-methyl-5-oxoimidazolidin-2- iminium | 4R92_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (r)-4-(2-cyclohexylethyl)-1-methyl-5-oxo-4- (((1s,3r)-3-(3-phenylureido)cyclohexyl)methyl)imidazolidin-2-iminium | 4R93_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-(((1r,3s)-3-(((r)-4-(2-cyclohexylethyl)-2- iminio-1-methyl-5-oxoimidazolidin-4-yl)methyl)cyclohexyl)amino) quinolin-1-ium | 4R95_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a 2-aminooxazoline 4- azaxanthene inhibitor | 4RCD_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with aminooxazoline xanthene inhibitor 2 | 4RCE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-aminooxazoline 4- fluoroxanthene inhibitor 49 | 4RCF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | 8-tetrahydropyran-2-yl chromans: highly selective beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4RRN_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | 8-tetrahydropyran-2-yl chromans: highly selective beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4RRO_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | 8-tetrahydropyran-2-yl chromans: highly selective beta-site amyloid precursor protein cleaving enzyme 1 (bace1) inhibitors | 4RRS_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a syn-hea-type inhibitor | 4TRW_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a hea-type inhibitor | 4TRY_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-thiophenyl hea-type inhibitor | 4TRZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-aminooxazoline 3-aza-4- fluoro-xanthene inhibitor 22 | 4WTU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 24b | 4WY1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 36 | 4WY6_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 6 | 4X2L_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with amino thiazine inhibitor ly2886721 | 4X7I_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-aminooxazoline 3- azaxanthene inhibitor 28 | 4XKX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a pyrazole-substituted tetrahydropyranthioamidine | 4XXS_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with amino thiazine inhibitor ly2811376 | 4YBI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 4-(cyclohexylamino)-1-(3-fluorophenyl)-8-(3- isopropoxybenzyl)-1,3,8-triazaspiro[4.5]dec-3-en-2-one | 4ZPE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 8-(3-((1-aminopropan-2-yl)oxy)benzyl)-4- (cyclohexylamino)-1-(3-fluorophenyl)-1,3,8-triazaspiro[4.5]dec-3-en- 2-one | 4ZPF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 8-benzyl-4-(cyclohexylamino)-1-(3-fluorophenyl)-7-methyl-1,3,8-triazaspiro[4.5]dec-3-en-2-one | 4ZPG_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bicyclic aminothiazine fragment | 4ZSM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with bicyclic aminothiazine inhibitor | 4ZSP_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with tricyclic aminothiazine inhibitor | 4ZSQ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with tricyclic aminothiazine inhibitor | 4ZSR_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | 1,4-oxazine bace1 inhibitors | 5CLM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 0211 | 5DQC_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 18 | 5ENK_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 10 | 5ENM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (1r,2r)-2-[(r)-2-amino-4-(4-difluoromethoxy-phenyl)-4,5-dihydro-oxazol-4-yl]-cyclopropyl-(5- chloro-pyridin-3-yl)-methanone | 5EZX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (4s)-4-[3-(5-chloro-3- pyridyl)phenyl]-4-[4-(difluoromethoxy)-3-methyl-phenyl]-5h-oxazol-2- amine | 5EZZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 5-[3-[(3-chloro-8- quinolyl)amino]phenyl]-5-methyl-2,6-dihydro-1,4-oxazin-3-amine | 5F00_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (1sr,2sr)-2-((r)-2-amino- 5,5-difluoro-4-methyl-5,6-dihydro-4h-1,3-oxazin-4-yl)-n-(3- chloroquinolin-8-yl)cyclopropanecarboxamide | 5F01_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-7a-(4-(3-cyanophenyl)thiophen-2-yl)-6-(5-fluoropyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4- d]pyrimidin-2-iminium | 5HD0_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-7a-(4-(3-cyanophenyl)thiophen-2-yl)-6-(5- fluoro-4-methoxypyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium | 5HDU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(5-fluoro-4- methoxy-6-methylpyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3,4-d]pyrimidin-2-iminium | 5HDV_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(4-ethoxy-5- fluoro-6-methylpyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h-pyrrolo[3, 4-d]pyrimidin-2-iminium | 5HDX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(5-fluoro-4- methyl-6-(methylthio)pyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h- pyrrolo[3,4-d]pyrimidin-2-iminium | 5HDZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (4ar,7as)-7a-(2,6-difluorophenyl)-6-(5-fluoro- 4-methoxy-6-methylpyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h- pyrrolo[3,4-d]pyrimidin-2-iminium | 5HE4_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (7ar)-7a-(5-cyanothiophen-2-yl)-6-(5-fluoro-4- methyl-6-(methylamino)pyrimidin-2-yl)-3-methyl-4-oxooctahydro-2h- pyrrolo[3,4-d]pyrimidin-2-iminium | 5HE5_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (4ar,7as)-7a-(2,4-difluorophenyl)-6-(5-fluoro- 4-methoxy-6-methylpyrimidin-2-yl)-2-imino-3-methyloctahydro-4h- pyrrolo[3,4-d]pyrimidin-4-one | 5HE7_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (s)-5-(3-chloro-5-(5-(prop-1-yn-1-yl)pyridin-3- yl)thiophen-2-yl)-2,5-dimethyl-1,2,4-thiadiazinan-3-iminium 1,1- dioxide | 5HTZ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 4-(3-(furan-2-carboxamido)phenyl)-1-methyl-5- oxo-4-phenylimidazolidin-2-iminium | 5HU0_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (r)-n-(3-(3-amino-2,5-dimethyl-1,1-dioxido-5,6- dihydro-2h-1,2,4-thiadiazin-5-yl)-4-fluorophenyl)-5- fluoropicolinamide | 5HU1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with aminoquinoline compound 1 | 5I3V_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-aminooxazoline-3- azaxanthene inhibitor 2 | 5I3W_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with aminoquinoline inhibitor 6 | 5I3X_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with aminoquinoline inhibitor 9 | 5I3Y_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 3-(2-amino-6-(o-tolyl) quinolin-3-yl)-n-(3,3-dimethylbutyl)propanamide | 5IE1_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | (4~s,6~s)-4-[2,4-bis(fluoranyl)phenyl]-4-methyl-6-pyrimidin-5-yl- 5,6-dihydro-1,3-thiazin-2-amine (compound 12) bound to bace1 | 5KQF_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | (4~s,6~s)-4-[2,4-bis(fluoranyl)phenyl]-6-(3,5-dimethyl-1,2-oxazol-4-yl)-4-methyl-5,6-dihydro-1,3-thiazin-2-amine (compound 5) bound to bace1 | 5KR8_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with active site inhibitor GRL-8234 and exosite peptide | 5MCO_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with active site and exosite binding peptide inhibitor | 5MCQ_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with ligand 32397778 | 5MXD_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminomethyl-derived beta secretase (bace1) inhibitors: engaging gly230without an anilide functionality | 5T1U_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | aminomethyl-derived beta secretase (bace1) inhibitors: engaging gly230without an anilide functionality | 5T1W_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with n-(3-((4as,7as)-2-amino-4,4a,5,6-tetrahydro-7ah-furo[2,3-d][1, 3]thiazin-7a-yl)-4-fluorophenyl)-5-bromo-2-pyridinecarboxamide | 5TOL_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with 2-aminooxazoline-3- azaxanthene compound 12 | 5UYU_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with inhibitor 5g | 5V0N_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with n-(3-((4r,5r,6s)-2-amino-6-(1,1- difluoroethyl)-5-fluoro-4-methyl-5,6-dihydro-4h-1,3-oxazin-4-yl)-4- fluorophenyl)-5-(fluoromethoxy)pyrazine-2-carboxamide | 5YGX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with (s)-n-(3-(2-amino-6- (fluoromethyl)-4 -methyl-4h-1,3-oxazin-4-yl)-4-fluorophenyl)-5- cyanopicolinamide | 5YGY_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxy pyrrolidine inhibitor | 6BFD_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxy pyrrolidine inhibitor | 6BFE_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxy morpholine inhibitor | 6BFW_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with hydroxy pyrrolidine inhibitor | 6BFX_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with : n-(3-((1r,5s, 6r)-3-amino-5-methyl-2-oxa-4-azabicyclo[4.1.0]hept-3-en-5-yl)-4- fluorophenyl)-5-methoxypyrazine-2-carboxamide | 6C2I_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a bicyclic isoxazoline carboxamide as the p3 ligand | 6DHC_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with a multiconformer ligand 5t5 | 6DMI_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with compound 28 | 6EJ2_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with B7T ((1r,4r)-4-methoxy-6'-(5-methyl-3-pyridinyl)-3'H-dispiro[cyclohexane-1,2'-indene-1',4''-[1,3]oxazol]-2''-amine) | 6EJ3_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with cnp520 | 6EQM_A |
AA | A01.004 | BACE1 g.p. (Homo sapiens) | complex with amino-1,4-oxazine compound 4 | 6FGY_A |
AA | A01.006 | chymosin | recombinant | 1CMS |
AA | A01.006 | chymosin | complex with inhibitor CP-113972 | 1CZI |
AA | A01.006 | chymosin | Val111Phe mutant | 3CMS |
AA | A01.006 | chymosin | 4AA8 | |
AA | A01.006 | chymosin | complex with pepstatin | 4AUC |
AA | A01.006 | chymosin | 4CMS | |
AA | A01.006 | chymosin | camel chymosin at 1.6a resolution | 4AA9_A |
AA | A01.007 | renin | recombinant glycosylated form | 1BBS |
AA | A01.007 | renin | complex with butanediamide inhibitor BILA 1908 | 1BIL |
AA | A01.007 | renin | complex with butanediamide inhibitor BILA 2151 | 1BIM |
AA | A01.007 | renin | complex with polyhydroxymonoamide inhibitor BILA 980 | 1HRN |
AA | A01.007 | renin | complex with CGP 38,560 | 1RNE |
AA | A01.007 | renin | complex with PF00074777 | 2BKS_A |
AA | A01.007 | renin | complex with PF00257567 | 2BKT_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the c ring | 2FS4_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G1N_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G1O_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the c ring | 2G1R_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the c ring | 2G1S_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G1Y_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the c ring | 2G20_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G21_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G22_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G24_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G26_A |
AA | A01.007 | renin | ketopiperazine-based renin inhibitors: optimization of the "c" ring | 2G27_A |
AA | A01.007 | renin | complex with PF02342674 | 2I4Q_A |
AA | A01.007 | renin | complex with 5-4-[(3,5-difluorobenzyl)amino]phenyl-6-ethylpyrimidine-2,4-diamine | 2IKO_A |
AA | A01.007 | renin | complex with 6-ethyl-5-[(2S)-1-(3-methoxypropyl)-2-phenyl-1,2,3,4-tetrahydroquinolin-7-yl]pyrimidine-2,4-diamine | 2IKU_A |
AA | A01.007 | renin | complex with N-[2-(2-amino-6-ethyl-5-[4-(3-methoxypropyl)-2,2-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl]pyrimidin-4-ylamino)ethyl]naphthalene-2-sulfonamide | 2IL2_A |
AA | A01.007 | renin | recombinant | 2REN |
AA | A01.007 | renin | complex with inhibitor 10 (aliskiren) | 2V0Z_C |
AA | A01.007 | renin | complex with inhibitor 9 ((2R,4S,5S,7S)-5-amino-N-butyl-4-hydroxy-7-[4-methoxy-3-(3-methoxypropoxy)benzyl]-2,8-dimethylnonanamide) | 2V10_C |
AA | A01.007 | renin | complex with inhibitor 6 ((2S,4S,5R,7R)-4-amino-8-(butylamino)-5-hydroxy-2,7-dimethyl-8-oxooctyl 1-benzyl-1H-indole-3-carboxylate) | 2V11_C |
AA | A01.007 | renin | complex with inhibitor 8 (N-[(2S,4S,5S,7R)-4-amino-8-(butylamino)-5-hydroxy-7-methyl-2-(1-methylethyl)-8-oxooctyl]-2-(3-methoxypropoxy)benzamide) | 2V12_C |
AA | A01.007 | renin | complex with inhibitor 7 (N-[(2R,4S,5S,7R)-4-amino-8-(butylamino)-5-hydroxy-2,7-dimethyl-8-oxooctyl]-2-(3-methoxypropoxy)benzamide) | 2V13_A |
AA | A01.007 | renin | complex with inhibitor 3 | 2V16_A |
AA | A01.007 | renin | complex with inhibitor 3 | 2V16_C |
AA | A01.007 | renin | complex with human angiotensinogen | 2X0B_A |
AA | A01.007 | renin | complex with remikiren | 3D91 |
AA | A01.007 | renin | 3G6Z | |
AA | A01.007 | renin | 3G70 | |
AA | A01.007 | renin | 3G72 | |
AA | A01.007 | renin | 3GW5 | |
AA | A01.007 | renin | 3K1W | |
AA | A01.007 | renin | 3KM4 | |
AA | A01.007 | renin | 3O9L | |
AA | A01.007 | renin | 3OAD | |
AA | A01.007 | renin | complex with piperidine inhibitor | 3OAG |
AA | A01.007 | renin | 3OOT | |
AA | A01.007 | renin | 3OQF | |
AA | A01.007 | renin | 3OQK | |
AA | A01.007 | renin | 3OWN | |
AA | A01.007 | renin | 3Q3T | |
AA | A01.007 | renin | 3Q4B | |
AA | A01.007 | renin | 3Q5H | |
AA | A01.007 | renin | 3SFC | |
AA | A01.007 | renin | 3VCM | |
AA | A01.007 | renin | 3VSW | |
AA | A01.007 | renin | 3VSX | |
AA | A01.007 | renin | 3VUC | |
AA | A01.007 | renin | 3VYD | |
AA | A01.007 | renin | 3VYE | |
AA | A01.007 | renin | 3VYF | |
AA | A01.007 | renin | 4AMT | |
AA | A01.007 | renin | 4GJ5 | |
AA | A01.007 | renin | 4GJ6 | |
AA | A01.007 | renin | 4GJ7 | |
AA | A01.007 | renin | 4GJ8 | |
AA | A01.007 | renin | 4GJ9 | |
AA | A01.007 | renin | 4GJA | |
AA | A01.007 | renin | 4GJB | |
AA | A01.007 | renin | 4GJC | |
AA | A01.007 | renin | 4GJD | |
AA | A01.007 | renin | 4PYV | |
AA | A01.007 | renin | 4Q1N | |
AA | A01.007 | renin | 4RYC | |
AA | A01.007 | renin | 4RYG | |
AA | A01.007 | renin | 4RZ1 | |
AA | A01.007 | renin | 4S1G | |
AA | A01.007 | renin | 4XX3 | |
AA | A01.007 | renin | 4XX4 | |
AA | A01.007 | renin | discovery of tak-272: a novel, potent and orally active renin in- hibitor ***caveat 5koq nag b 401 has wrong chirality at atom c1 | 5KOQ_A |
AA | A01.007 | renin | discovery of tak-272: a novel, potent and orally active renin in- hibitor | 5KOS_A |
AA | A01.007 | renin | discovery of tak-272: a novel, potent and orally active renin in- hibitor | 5KOT_A |
AA | A01.007 | renin | structure-based design of a new series of n-piperidin-3-ylpyrimidine- 5-carboxamides as renin inhibitors | 5SXN_A |
AA | A01.007 | renin | structure-based design of a new series of n-piperidin-3-ylpyrimidine- 5-carboxamides as renin inhibitors | 5SY2_A |
AA | A01.007 | renin | structure-based design of a new series of n-piperidin-3-ylpyrimidine- 5-carboxamides as renin inhibitors | 5SY3_A |
AA | A01.007 | renin | structure-based design of a new series of n-piperidin-3-ylpyrimidine- 5-carboxamides as renin inhibitors | 5SZ9_A |
AA | A01.007 | renin | novel approach of fragment-based lead discovery applied to renin inhibitors | 5T4S_A |
AA | A01.007 | renin | optimization of 3,5-disubstitued piperidine: discovery of non-peptide mimetics as an orally active renin inhibitor | 5TMG_A |
AA | A01.007 | renin | optimization of 3,5-disubstitued piperidine: discovery of non-peptide mimetics as an orally active renin inhibitor | 5TMK_A |
AA | A01.007 | renin | complex with a biphenylpipderidinylcarbinol | 5V8V_A |
AA | A01.007 | renin | complex with a biphenylpipderidinylcarbinol | 5VPM_A |
AA | A01.007 | renin | complex with a biphenylpipderidinylcarbinol | 5VRP_A |
AA | A01.007 | renin | complex with human angiotensinogen | 6I3F_B |
AA | A01.008 | renin-2 | complex with inhibitor CH-66 | 1SMR_A |
AA | A01.008 | renin-2 | precursor | 5MLG_A |
AA | A01.009 | cathepsin D | 1LYA | |
AA | A01.009 | cathepsin D | complex with pepstatin | 1LYB |
AA | A01.009 | cathepsin D | pH 7.5 | 1LYW_A |
AA | A01.009 | cathepsin D | 4OBZ | |
AA | A01.009 | cathepsin D | 4OC6 | |
AA | A01.009 | cathepsin D | 4OD9 | |
AA | A01.010 | cathepsin E | theoretical model | 1LCG |
AA | A01.010 | cathepsin E | activation intermediate | 1TZS |
AA | A01.011 | penicillopepsin | complex with isoval-Val-Val-Lysta-O-Et | 1APT |
AA | A01.011 | penicillopepsin | complex with isoval-Val-Val-Sta-O-Et | 1APU |
AA | A01.011 | penicillopepsin | complex with isoval-Val-Val-hydrated difluorostatone-N-methylamide | 1APV |
AA | A01.011 | penicillopepsin | complex with isoval-Val-Val-difluorostatone-N-methylamide | 1APW |
AA | A01.011 | penicillopepsin | complex with ethyl cyclo[(2S)-2-[[(1R)-1-(N-(l-N-(3-methylbutanoyl)valyl-L-aspartyl)amino)-3-methylbutyl]hydroxyphosphinyloxy]-3-(3-aminomethyl)phenylpropanoate | 1BXO |
AA | A01.011 | penicillopepsin | complex with phosphonate inhibitor | 1BXQ |
AA | A01.011 | penicillopepsin | complex with isoval-Val-Val-Sta(P)-O-Et | 1PPK |
AA | A01.011 | penicillopepsin | complex with isoval-Val-Val-Leu(P)-O(Phe)-OME | 1PPL |
AA | A01.011 | penicillopepsin | complex with CBZ-Ala-Ala-Leu(P)-(O)Phe-OME | 1PPM |
AA | A01.011 | penicillopepsin | complex with phosphonate inhibitor methyl[cyclo-7[(2R)-((N-valyl)amino)-2-(hydroxyl-(1S)-1-methyloxycarbonyl-2-phenylethoxy)phosphinyloxy-ethyl]-1-naphthaleneacetamide] | 2WEA |
AA | A01.011 | penicillopepsin | complex with phosphonate inhibitor methyl (2S)-[1-((N-formyl)-l-valyl)amino-2-(2-naphthyl)ethyl)hydroxyphosphinyloxy]-3-phenyl propanoate | 2WEB |
AA | A01.011 | penicillopepsin | complex with phosphonate inhibitor methyl (2S)-[1-((N-(naphthaleneacetyl))-L-valyl)aminomethyl)hydroxyphosphinyloxy]-3-phenyl propanoate | 2WEC |
AA | A01.011 | penicillopepsin | complex with phosphonate macrocyclic inhibitor | 2WED |
AA | A01.011 | penicillopepsin | 3APP | |
AA | A01.012 | rhizopuspepsin | pH 4.6 | 1UH7 |
AA | A01.012 | rhizopuspepsin | pH 8.0 | 1UH8 |
AA | A01.012 | rhizopuspepsin | pH 7.0 | 1UH9 |
AA | A01.012 | rhizopuspepsin | 2APR | |
AA | A01.012 | rhizopuspepsin | complex with psi-(CH2-NH)-D-His-Pro-Phe-His-Phe-Phe-Val-Tyr | 3APR |
AA | A01.012 | rhizopuspepsin | complex with a pepstatin-like renin inhibitor | 4APR |
AA | A01.012 | rhizopuspepsin | complex with a pepstatin-like renin inhibitor | 5APR |
AA | A01.012 | rhizopuspepsin | complex with pepstatin | 6APR |
AA | A01.013 | mucorpepsin | 2ASI | |
AA | A01.013 | mucorpepsin | complex with pepstatin A | 2RMP_A |
AA | A01.013 | mucorpepsin | 1MPP | |
AA | A01.014 | candidapepsin SAP1 | 2QZW | |
AA | A01.016 | aspergillopepsin I | 1IZD | |
AA | A01.016 | aspergillopepsin I | 1IZE | |
AA | A01.016 | aspergillopepsin I | 1IBQ_A | |
AA | A01.017 | endothiapepsin | complex with inhibitor DB2 | 1E5O |
AA | A01.017 | endothiapepsin | complex with renin inhibitor Merck-KGAA-EMD56133 | 1E80 |
AA | A01.017 | endothiapepsin | complex with renin inhibitor Merck-KGAA-EMD61395 | 1E81 |
AA | A01.017 | endothiapepsin | complex with renin inhibitor Merck-KGAA-EMD59601 | 1E82 |
AA | A01.017 | endothiapepsin | complex with cyclohexyl renin inhibitor PD125754 | 1EED |
AA | A01.017 | endothiapepsin | complex with inhibitor PD130328 | 1ENT |
AA | A01.017 | endothiapepsin | complex with PS1 (Pro-Leu-Glu-PSA-Arg-Leu) | 1EPL |
AA | A01.017 | endothiapepsin | complex with PS2 (Thr-Phe-Gln-Ala-PSA-Leu-Arg-Glu) | 1EPM |
AA | A01.017 | endothiapepsin | complex with CP-80,794 (MOR-Phe-Cys-CH3-NOR) | 1EPN |
AA | A01.017 | endothiapepsin | complex with CP-81,282 (MOR-Phe-Nle-CHF-NME) | 1EPO |
AA | A01.017 | endothiapepsin | complex with PD-130,693 (MAS-Phe-Lys-MTF-Sta-MBA) | 1EPP |
AA | A01.017 | endothiapepsin | complex with PD-133,450 (SOT-Phe-Gly-SCC-GCL) | 1EPQ |
AA | A01.017 | endothiapepsin | complex with PD-135,040 (TSM-DPH-His-CHF-EMR) | 1EPR |
AA | A01.017 | endothiapepsin | complex with H-77 (D-His-Pro-Phe-His-Leu-Leu-Val-Tyr) | 1ER8_E |
AA | A01.017 | endothiapepsin | complex with transition state analogue inhibitor H261 | 1GKT |
AA | A01.017 | endothiapepsin | complex with CP-80,794 (N-carbonylmorphine-Phe-S-methyl-Cys-cyclohexyl-norstatine) inhibitor | 1GVT |
AA | A01.017 | endothiapepsin | complex with inhibitor H189 | 1GVU |
AA | A01.017 | endothiapepsin | complex with Glu-statine-Leu-meta-di(aminomethyl)benzene inhibitor | 1GVV |
AA | A01.017 | endothiapepsin | complex with PD-130,328 inhibitor | 1GVW |
AA | A01.017 | endothiapepsin | complex with inhibitor H256 | 1GVX |
AA | A01.017 | endothiapepsin | complex with PD135,040 | 1OD1 |
AA | A01.017 | endothiapepsin | 1OEW | |
AA | A01.017 | endothiapepsin | complex with transition state analogue inhibitor H261 | 1OEX |
AA | A01.017 | endothiapepsin | complex with L364,099 (IVA-His-Pro-Phe-His-CHS-Leu-Phe-NH2) | 2ER0 |
AA | A01.017 | endothiapepsin | complex with H-256 (Pro-Thr-Glu-Phe-Phe-Arg-Glu) | 2ER6 |
AA | A01.017 | endothiapepsin | complex with H-261 | 2ER7_E |
AA | A01.017 | endothiapepsin | complex with L636,564 | 2ER9 |
AA | A01.017 | endothiapepsin | complex with gem-diol inhibitor PD-135.040 | 2JJI_A |
AA | A01.017 | endothiapepsin | 2JJJ | |
AA | A01.017 | endothiapepsin | complex with compound 1 | 2V00 |
AA | A01.017 | endothiapepsin | neutron diffraction structure; complex with gem-diol inhibitor PD-135.040 . | 2VS2_A |
AA | A01.017 | endothiapepsin | complex with CP-71,362 | 3ER3 |
AA | A01.017 | endothiapepsin | complex with H-189 | 3ER5_E |
AA | A01.017 | endothiapepsin | 3LZY | |
AA | A01.017 | endothiapepsin | 3PB5 | |
AA | A01.017 | endothiapepsin | 3PBD | |
AA | A01.017 | endothiapepsin | 3PBZ | |
AA | A01.017 | endothiapepsin | 3PCW | |
AA | A01.017 | endothiapepsin | 3PCZ | |
AA | A01.017 | endothiapepsin | 3PGI | |
AA | A01.017 | endothiapepsin | 3PI0 | |
AA | A01.017 | endothiapepsin | 3PLD | |
AA | A01.017 | endothiapepsin | 3PLL | |
AA | A01.017 | endothiapepsin | 3PM4 | |
AA | A01.017 | endothiapepsin | 3PMU | |
AA | A01.017 | endothiapepsin | 3PMY | |
AA | A01.017 | endothiapepsin | 3PRS | |
AA | A01.017 | endothiapepsin | 3PSY | |
AA | A01.017 | endothiapepsin | 3PWW | |
AA | A01.017 | endothiapepsin | 3Q6Y | |
AA | A01.017 | endothiapepsin | 3T6I | |
AA | A01.017 | endothiapepsin | 3T7P | |
AA | A01.017 | endothiapepsin | 3T7Q | |
AA | A01.017 | endothiapepsin | 3T7X | |
AA | A01.017 | endothiapepsin | 3URI | |
AA | A01.017 | endothiapepsin | 3URJ | |
AA | A01.017 | endothiapepsin | 3URL | |
AA | A01.017 | endothiapepsin | 3WZ6 | |
AA | A01.017 | endothiapepsin | 3WZ7 | |
AA | A01.017 | endothiapepsin | 3WZ8 | |
AA | A01.017 | endothiapepsin | 4APE | |
AA | A01.017 | endothiapepsin | complex with PD125967 (BNA-His-CAL-DCI) | 4ER1 |
AA | A01.017 | endothiapepsin | complex with pepstatin | 4ER2 |
AA | A01.017 | endothiapepsin | complex with Pro-His-Pro-Phe-His-Leu-Val-Ile-His-Lys | 4ER4 |
AA | A01.017 | endothiapepsin | 4KUP | |
AA | A01.017 | endothiapepsin | 4L6B | |
AA | A01.017 | endothiapepsin | 4LAP | |
AA | A01.017 | endothiapepsin | 4LBT | |
AA | A01.017 | endothiapepsin | 4LHH | |
AA | A01.017 | endothiapepsin | 4LP9 | |
AA | A01.017 | endothiapepsin | complex with BW624 (LOL-CH2-Val-Ile-Phe-OMe) | 5ER1 |
AA | A01.017 | endothiapepsin | complex with CP-69,799 (BOC-Phe-His-AHS-Lys-Phe) | 5ER2 |
AA | A01.017 | endothiapepsin | endothiapepsin in complex with biacylhydrazone | 5HCT_A |
AA | A01.017 | endothiapepsin | treated with fragment 115 | 5P1W_A |
AA | A01.017 | endothiapepsin | treated with fragment 116 | 5P1X_A |
AA | A01.017 | endothiapepsin | treated with fragment 117 | 5P1Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 118 | 5P1Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 119 | 5P20_A |
AA | A01.017 | endothiapepsin | treated with fragment 120 | 5P22_A |
AA | A01.017 | endothiapepsin | treated with fragment 121 | 5P23_A |
AA | A01.017 | endothiapepsin | treated with fragment 122 | 5P24_A |
AA | A01.017 | endothiapepsin | treated with fragment 123 | 5P25_A |
AA | A01.017 | endothiapepsin | treated with fragment 124 | 5P26_A |
AA | A01.017 | endothiapepsin | treated with fragment 125 | 5P27_A |
AA | A01.017 | endothiapepsin | treated with fragment 126 | 5P28_A |
AA | A01.017 | endothiapepsin | treated with fragment 127 | 5P29_A |
AA | A01.017 | endothiapepsin | treated with fragment 128 | 5P2A_A |
AA | A01.017 | endothiapepsin | treated with fragment 129 | 5P2B_A |
AA | A01.017 | endothiapepsin | treated with fragment 130 | 5P2C_A |
AA | A01.017 | endothiapepsin | treated with fragment 131 | 5P2D_A |
AA | A01.017 | endothiapepsin | treated with fragment 132 | 5P2E_A |
AA | A01.017 | endothiapepsin | treated with fragment 133 | 5P2F_A |
AA | A01.017 | endothiapepsin | treated with fragment 134 | 5P2G_A |
AA | A01.017 | endothiapepsin | treated with fragment 135 | 5P2H_A |
AA | A01.017 | endothiapepsin | treated with fragment 136 | 5P2I_A |
AA | A01.017 | endothiapepsin | treated with fragment 137 | 5P2J_A |
AA | A01.017 | endothiapepsin | treated with fragment 138 | 5P2K_A |
AA | A01.017 | endothiapepsin | treated with fragment 139 | 5P2L_A |
AA | A01.017 | endothiapepsin | treated with fragment 140 | 5P2M_A |
AA | A01.017 | endothiapepsin | treated with fragment 141 | 5P2N_A |
AA | A01.017 | endothiapepsin | treated with fragment 142 | 5P2O_A |
AA | A01.017 | endothiapepsin | treated with fragment 143 | 5P2Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 144 | 5P2R_A |
AA | A01.017 | endothiapepsin | treated with fragment 145 | 5P2S_A |
AA | A01.017 | endothiapepsin | treated with fragment 146 | 5P2T_A |
AA | A01.017 | endothiapepsin | treated with fragment 147 | 5P2U_A |
AA | A01.017 | endothiapepsin | treated with fragment 148 | 5P2V_A |
AA | A01.017 | endothiapepsin | treated with fragment 149 | 5P2W_A |
AA | A01.017 | endothiapepsin | treated with fragment 150 | 5P2X_A |
AA | A01.017 | endothiapepsin | treated with fragment 151 | 5P2Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 152 | 5P2Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 153 | 5P30_A |
AA | A01.017 | endothiapepsin | treated with fragment 154 | 5P31_A |
AA | A01.017 | endothiapepsin | treated with fragment 155 | 5P32_A |
AA | A01.017 | endothiapepsin | treated with fragment 156 | 5P33_A |
AA | A01.017 | endothiapepsin | treated with fragment 157 | 5P34_A |
AA | A01.017 | endothiapepsin | treated with fragment 158 | 5P35_A |
AA | A01.017 | endothiapepsin | treated with fragment 159 | 5P36_A |
AA | A01.017 | endothiapepsin | treated with fragment 160 | 5P37_A |
AA | A01.017 | endothiapepsin | treated with fragment 161 | 5P38_A |
AA | A01.017 | endothiapepsin | treated with fragment 162 | 5P39_A |
AA | A01.017 | endothiapepsin | treated with fragment 163 | 5P3A_A |
AA | A01.017 | endothiapepsin | treated with fragment 164 | 5P3B_A |
AA | A01.017 | endothiapepsin | treated with fragment 165 | 5P3C_A |
AA | A01.017 | endothiapepsin | treated with fragment 166 | 5P3D_A |
AA | A01.017 | endothiapepsin | treated with fragment 167 | 5P3E_A |
AA | A01.017 | endothiapepsin | treated with fragment 168 | 5P3F_A |
AA | A01.017 | endothiapepsin | treated with fragment 169 | 5P3G_A |
AA | A01.017 | endothiapepsin | treated with fragment 170 | 5P3H_A |
AA | A01.017 | endothiapepsin | treated with fragment 171 | 5P3I_A |
AA | A01.017 | endothiapepsin | treated with fragment 172 | 5P3J_A |
AA | A01.017 | endothiapepsin | treated with fragment 173 | 5P3K_A |
AA | A01.017 | endothiapepsin | treated with fragment 174 | 5P3L_A |
AA | A01.017 | endothiapepsin | treated with fragment 175 | 5P3M_A |
AA | A01.017 | endothiapepsin | treated with fragment 176 | 5P3N_A |
AA | A01.017 | endothiapepsin | treated with fragment 177 | 5P3O_A |
AA | A01.017 | endothiapepsin | treated with fragment 178 | 5P3P_A |
AA | A01.017 | endothiapepsin | treated with fragment 179 | 5P3Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 180 | 5P3R_A |
AA | A01.017 | endothiapepsin | treated with fragment 181 | 5P3S_A |
AA | A01.017 | endothiapepsin | treated with fragment 182 | 5P3T_A |
AA | A01.017 | endothiapepsin | treated with fragment 183 | 5P3U_A |
AA | A01.017 | endothiapepsin | treated with fragment 184 | 5P3V_A |
AA | A01.017 | endothiapepsin | treated with fragment 185 | 5P3W_A |
AA | A01.017 | endothiapepsin | treated with fragment 186 | 5P3X_A |
AA | A01.017 | endothiapepsin | treated with fragment 187 | 5P3Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 188 | 5P3Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 189 | 5P40_A |
AA | A01.017 | endothiapepsin | treated with fragment 190 | 5P41_A |
AA | A01.017 | endothiapepsin | treated with fragment 191 | 5P42_A |
AA | A01.017 | endothiapepsin | treated with fragment 192 | 5P43_A |
AA | A01.017 | endothiapepsin | treated with fragment 193 | 5P44_A |
AA | A01.017 | endothiapepsin | treated with fragment 194 | 5P45_A |
AA | A01.017 | endothiapepsin | treated with fragment 195 | 5P46_A |
AA | A01.017 | endothiapepsin | treated with fragment 196 | 5P47_A |
AA | A01.017 | endothiapepsin | treated with fragment 197 | 5P48_A |
AA | A01.017 | endothiapepsin | treated with fragment 198 | 5P49_A |
AA | A01.017 | endothiapepsin | treated with fragment 199 | 5P4A_A |
AA | A01.017 | endothiapepsin | treated with fragment 200 | 5P4B_A |
AA | A01.017 | endothiapepsin | treated with fragment 201 | 5P4C_A |
AA | A01.017 | endothiapepsin | treated with fragment 202 | 5P4D_A |
AA | A01.017 | endothiapepsin | treated with fragment 203 | 5P4E_A |
AA | A01.017 | endothiapepsin | treated with fragment 204 | 5P4F_A |
AA | A01.017 | endothiapepsin | treated with fragment 205 | 5P4G_A |
AA | A01.017 | endothiapepsin | treated with fragment 206 | 5P4H_A |
AA | A01.017 | endothiapepsin | treated with fragment 207 | 5P4I_A |
AA | A01.017 | endothiapepsin | treated with fragment 208 | 5P4J_A |
AA | A01.017 | endothiapepsin | treated with fragment 209 | 5P4K_A |
AA | A01.017 | endothiapepsin | treated with fragment 210 | 5P4L_A |
AA | A01.017 | endothiapepsin | treated with fragment 211 | 5P4M_A |
AA | A01.017 | endothiapepsin | treated with fragment 212 | 5P4N_A |
AA | A01.017 | endothiapepsin | treated with fragment 213 | 5P4O_A |
AA | A01.017 | endothiapepsin | treated with fragment 214 | 5P4P_A |
AA | A01.017 | endothiapepsin | treated with fragment 215 | 5P4Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 216 | 5P4R_A |
AA | A01.017 | endothiapepsin | treated with fragment 217 | 5P4S_A |
AA | A01.017 | endothiapepsin | treated with fragment 218 | 5P4T_A |
AA | A01.017 | endothiapepsin | treated with fragment 219 | 5P4U_A |
AA | A01.017 | endothiapepsin | treated with fragment 220 | 5P4V_A |
AA | A01.017 | endothiapepsin | treated with fragment 221 | 5P4W_A |
AA | A01.017 | endothiapepsin | treated with fragment 222 | 5P4X_A |
AA | A01.017 | endothiapepsin | treated with fragment 223 | 5P4Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 224 | 5P4Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 225 | 5P50_A |
AA | A01.017 | endothiapepsin | treated with fragment 226 | 5P51_A |
AA | A01.017 | endothiapepsin | treated with fragment 227 | 5P52_A |
AA | A01.017 | endothiapepsin | treated with fragment 228 | 5P53_A |
AA | A01.017 | endothiapepsin | treated with fragment 229 | 5P54_A |
AA | A01.017 | endothiapepsin | treated with fragment 230 | 5P55_A |
AA | A01.017 | endothiapepsin | treated with fragment 231 | 5P56_A |
AA | A01.017 | endothiapepsin | treated with fragment 232 | 5P57_A |
AA | A01.017 | endothiapepsin | treated with fragment 233 | 5P58_A |
AA | A01.017 | endothiapepsin | treated with fragment 234 | 5P59_A |
AA | A01.017 | endothiapepsin | treated with fragment 235 | 5P5A_A |
AA | A01.017 | endothiapepsin | treated with fragment 236 | 5P5B_A |
AA | A01.017 | endothiapepsin | treated with fragment 237 | 5P5C_A |
AA | A01.017 | endothiapepsin | treated with fragment 238 | 5P5D_A |
AA | A01.017 | endothiapepsin | treated with fragment 239 | 5P5E_A |
AA | A01.017 | endothiapepsin | treated with fragment 240 | 5P5F_A |
AA | A01.017 | endothiapepsin | treated with fragment 241 | 5P5G_A |
AA | A01.017 | endothiapepsin | treated with fragment 242 | 5P5H_A |
AA | A01.017 | endothiapepsin | treated with fragment 243 | 5P5I_A |
AA | A01.017 | endothiapepsin | treated with fragment 244 | 5P5J_A |
AA | A01.017 | endothiapepsin | treated with fragment 245 | 5P5K_A |
AA | A01.017 | endothiapepsin | treated with fragment 246 | 5P5L_A |
AA | A01.017 | endothiapepsin | treated with fragment 247 | 5P5M_A |
AA | A01.017 | endothiapepsin | treated with fragment 248 | 5P5N_A |
AA | A01.017 | endothiapepsin | treated with fragment 249 | 5P5O_A |
AA | A01.017 | endothiapepsin | treated with fragment 250 | 5P5P_A |
AA | A01.017 | endothiapepsin | treated with fragment 251 | 5P5Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 252 | 5P5R_A |
AA | A01.017 | endothiapepsin | treated with fragment 253 | 5P5S_A |
AA | A01.017 | endothiapepsin | treated with fragment 254 | 5P5T_A |
AA | A01.017 | endothiapepsin | treated with fragment 255 | 5P5U_A |
AA | A01.017 | endothiapepsin | treated with fragment 256 | 5P5V_A |
AA | A01.017 | endothiapepsin | treated with fragment 257 | 5P5W_A |
AA | A01.017 | endothiapepsin | treated with fragment 258 | 5P5X_A |
AA | A01.017 | endothiapepsin | treated with fragment 259 | 5P5Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 260 | 5P5Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 261 | 5P60_A |
AA | A01.017 | endothiapepsin | treated with fragment 262 | 5P61_A |
AA | A01.017 | endothiapepsin | treated with fragment 263 | 5P62_A |
AA | A01.017 | endothiapepsin | treated with fragment 264 | 5P63_A |
AA | A01.017 | endothiapepsin | treated with fragment 265 | 5P64_A |
AA | A01.017 | endothiapepsin | treated with fragment 266 | 5P65_A |
AA | A01.017 | endothiapepsin | treated with fragment 267 | 5P66_A |
AA | A01.017 | endothiapepsin | treated with fragment 268 | 5P67_A |
AA | A01.017 | endothiapepsin | treated with fragment 269 | 5P68_A |
AA | A01.017 | endothiapepsin | treated with fragment 270 | 5P69_A |
AA | A01.017 | endothiapepsin | treated with fragment 271 | 5P6A_A |
AA | A01.017 | endothiapepsin | treated with fragment 272 | 5P6B_A |
AA | A01.017 | endothiapepsin | treated with fragment 273 | 5P6C_A |
AA | A01.017 | endothiapepsin | treated with fragment 274 | 5P6D_A |
AA | A01.017 | endothiapepsin | treated with fragment 275 | 5P6E_A |
AA | A01.017 | endothiapepsin | treated with fragment 276 | 5P6F_A |
AA | A01.017 | endothiapepsin | treated with fragment 277 | 5P6G_A |
AA | A01.017 | endothiapepsin | treated with fragment 278 | 5P6H_A |
AA | A01.017 | endothiapepsin | treated with fragment 279 | 5P6I_A |
AA | A01.017 | endothiapepsin | treated with fragment 280 | 5P6J_A |
AA | A01.017 | endothiapepsin | treated with fragment 281 | 5P6K_A |
AA | A01.017 | endothiapepsin | treated with fragment 282 | 5P6L_A |
AA | A01.017 | endothiapepsin | treated with fragment 283 | 5P6M_A |
AA | A01.017 | endothiapepsin | treated with fragment 284 | 5P6N_A |
AA | A01.017 | endothiapepsin | treated with fragment 285 | 5P6O_A |
AA | A01.017 | endothiapepsin | treated with fragment 286 | 5P6P_A |
AA | A01.017 | endothiapepsin | treated with fragment 287 | 5P6Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 288 | 5P6R_A |
AA | A01.017 | endothiapepsin | treated with fragment 289 | 5P6S_A |
AA | A01.017 | endothiapepsin | treated with fragment 290 | 5P6T_A |
AA | A01.017 | endothiapepsin | treated with fragment 291 | 5P6U_A |
AA | A01.017 | endothiapepsin | treated with fragment 292 | 5P6V_A |
AA | A01.017 | endothiapepsin | treated with fragment 293 | 5P6W_A |
AA | A01.017 | endothiapepsin | treated with fragment 294 | 5P6X_A |
AA | A01.017 | endothiapepsin | treated with fragment 295 | 5P6Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 296 | 5P6Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 297 | 5P70_A |
AA | A01.017 | endothiapepsin | treated with fragment 298 | 5P71_A |
AA | A01.017 | endothiapepsin | treated with fragment 299 | 5P72_A |
AA | A01.017 | endothiapepsin | treated with fragment 300 | 5P73_A |
AA | A01.017 | endothiapepsin | treated with fragment 301 | 5P74_A |
AA | A01.017 | endothiapepsin | treated with fragment 302 | 5P75_A |
AA | A01.017 | endothiapepsin | treated with fragment 303 | 5P76_A |
AA | A01.017 | endothiapepsin | treated with fragment 304 | 5P77_A |
AA | A01.017 | endothiapepsin | treated with fragment 305 | 5P78_A |
AA | A01.017 | endothiapepsin | treated with fragment 306 | 5P79_A |
AA | A01.017 | endothiapepsin | treated with fragment 307 | 5P7A_A |
AA | A01.017 | endothiapepsin | treated with fragment 308 | 5P7B_A |
AA | A01.017 | endothiapepsin | treated with fragment 309 | 5P7C_A |
AA | A01.017 | endothiapepsin | treated with fragment 310 | 5P7D_A |
AA | A01.017 | endothiapepsin | treated with fragment 311 | 5P7E_A |
AA | A01.017 | endothiapepsin | treated with fragment 312 | 5P7F_A |
AA | A01.017 | endothiapepsin | treated with fragment 313 | 5P7G_A |
AA | A01.017 | endothiapepsin | treated with fragment 314 | 5P7H_A |
AA | A01.017 | endothiapepsin | treated with fragment 315 | 5P7I_A |
AA | A01.017 | endothiapepsin | treated with fragment 316 | 5P7J_A |
AA | A01.017 | endothiapepsin | treated with fragment 317 | 5P7K_A |
AA | A01.017 | endothiapepsin | treated with fragment 318 | 5P7L_A |
AA | A01.017 | endothiapepsin | treated with fragment 319 | 5P7M_A |
AA | A01.017 | endothiapepsin | treated with fragment 320 | 5P7N_A |
AA | A01.017 | endothiapepsin | treated with fragment 321 | 5P7O_A |
AA | A01.017 | endothiapepsin | treated with fragment 322 | 5P7P_A |
AA | A01.017 | endothiapepsin | treated with fragment 323 | 5P7Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 324 | 5P7R_A |
AA | A01.017 | endothiapepsin | treated with fragment 325 | 5P7S_A |
AA | A01.017 | endothiapepsin | treated with fragment 326 | 5P7T_A |
AA | A01.017 | endothiapepsin | treated with fragment 327 | 5P7U_A |
AA | A01.017 | endothiapepsin | treated with fragment 328 | 5P7V_A |
AA | A01.017 | endothiapepsin | treated with fragment 329 | 5P7W_A |
AA | A01.017 | endothiapepsin | treated with fragment 330 | 5P7X_A |
AA | A01.017 | endothiapepsin | treated with fragment 331 | 5P7Y_A |
AA | A01.017 | endothiapepsin | treated with fragment 332 | 5P7Z_A |
AA | A01.017 | endothiapepsin | treated with fragment 333 | 5P80_A |
AA | A01.017 | endothiapepsin | treated with fragment 334 | 5P81_A |
AA | A01.017 | endothiapepsin | treated with fragment 335 | 5P82_A |
AA | A01.017 | endothiapepsin | treated with fragment 336 | 5P83_A |
AA | A01.017 | endothiapepsin | treated with fragment 337 | 5P84_A |
AA | A01.017 | endothiapepsin | treated with fragment 338 | 5P85_A |
AA | A01.017 | endothiapepsin | treated with fragment 339 | 5P86_A |
AA | A01.017 | endothiapepsin | treated with fragment 340 | 5P87_A |
AA | A01.017 | endothiapepsin | treated with fragment 341 | 5P88_A |
AA | A01.017 | endothiapepsin | treated with fragment 342 | 5P89_A |
AA | A01.017 | endothiapepsin | treated with fragment 343 | 5P8A_A |
AA | A01.017 | endothiapepsin | treated with fragment 344 | 5P8B_A |
AA | A01.017 | endothiapepsin | treated with fragment 345 | 5P8C_A |
AA | A01.017 | endothiapepsin | treated with fragment 346 | 5P8D_A |
AA | A01.017 | endothiapepsin | treated with fragment 347 | 5P8E_A |
AA | A01.017 | endothiapepsin | treated with fragment 348 | 5P8F_A |
AA | A01.017 | endothiapepsin | treated with fragment 349 | 5P8G_A |
AA | A01.017 | endothiapepsin | treated with fragment 350 | 5P8H_A |
AA | A01.017 | endothiapepsin | treated with fragment 351 | 5P8I_A |
AA | A01.017 | endothiapepsin | treated with fragment 352 | 5P8J_A |
AA | A01.017 | endothiapepsin | treated with fragment 353 | 5P8K_A |
AA | A01.017 | endothiapepsin | treated with fragment 354 | 5P8L_A |
AA | A01.017 | endothiapepsin | treated with fragment 355 | 5P8M_A |
AA | A01.017 | endothiapepsin | treated with fragment 356 | 5P8N_A |
AA | A01.017 | endothiapepsin | treated with fragment 357 | 5P8O_A |
AA | A01.017 | endothiapepsin | treated with fragment 358 | 5P8P_A |
AA | A01.017 | endothiapepsin | treated with fragment 359 | 5P8Q_A |
AA | A01.017 | endothiapepsin | treated with fragment 360 | 5P8R_A |
AA | A01.017 | endothiapepsin | treated with fragment 361 | 5P8S_A |
AA | A01.017 | endothiapepsin | treated with fragment 362 | 5P8T_A |
AA | A01.017 | endothiapepsin | treated with fragment 363 | 5P8U_A |
AA | A01.017 | endothiapepsin | treated with fragment 364 | 5P8V_A |
AA | A01.018 | saccharopepsin | complex with IA3 mutant inhibitor | 1DP5_A |
AA | A01.018 | saccharopepsin | complex with IA3 inhibitor | 1DPJ_A |
AA | A01.018 | saccharopepsin | 1FMU | |
AA | A01.018 | saccharopepsin | 1FMX | |
AA | A01.018 | saccharopepsin | complex with hydroxythylene inhibitor CP-108,420 | 1FQ4 |
AA | A01.018 | saccharopepsin | complex with cyclic statine inhibitor PD-129,541 | 1FQ5 |
AA | A01.018 | saccharopepsin | complex with glycol inhibitor PD-133,450 | 1FQ6 |
AA | A01.018 | saccharopepsin | complex with inhibitor CP-72,647 | 1FQ7 |
AA | A01.018 | saccharopepsin | complex with difluorostatine inhibitor CP81,198 | 1FQ8 |
AA | A01.018 | saccharopepsin | complex with proteinase A inhibitor 3 mutant | 1G0V_A |
AA | A01.018 | saccharopepsin | complex with N-carbonylmorpholine-Phe-norLeu-cyclohexylfluorostatone-methylamine | 2JXR |
AA | A01.019 | polyporopepsin | 1WKR | |
AA | A01.020 | phytepsin | zymogen | 1QDM |
AA | A01.020 | phytepsin | 1B5F_A | |
AA | A01.020 | phytepsin | 5NFG_A | |
AA | A01.021 | plasmepsin (Plasmodium sp.) | 1MIQ | |
AA | A01.021 | plasmepsin (Plasmodium sp.) | complex with pepstatin A inhibitor | 1QS8 |
AA | A01.021 | plasmepsin (Plasmodium sp.) | complex with allophenylnorstatine inhibitor KNI-764 | 2ANL |
AA | A01.021 | plasmepsin (Plasmodium sp.) | theoretical model | 1KBX |
AA | A01.022 | plasmepsin-1 | theoretical model | 1LCR |
AA | A01.022 | plasmepsin-1 | 1LDU | |
AA | A01.022 | plasmepsin-1 | 3QRV | |
AA | A01.022 | plasmepsin-1 | complex with KNI-10006 inhibitor | 3QS1 |
AA | A01.023 | plasmepsin-2 | theoretical model | 1J8J |
AA | A01.023 | plasmepsin-2 | complex with inhibitor RS367 | 1LEE |
AA | A01.023 | plasmepsin-2 | complex with inhibitor RS370 | 1LF2 |
AA | A01.023 | plasmepsin-2 | complex with EH58 inhibitor | 1LF3 |
AA | A01.023 | plasmepsin-2 | 1LF4 | |
AA | A01.023 | plasmepsin-2 | complex with pepstatin A | 1M43 |
AA | A01.023 | plasmepsin-2 | complex with a statine based inhibitor | 1ME6 |
AA | A01.023 | plasmepsin-2 | precursor | 1PFZ |
AA | A01.023 | plasmepsin-2 | complex with pepstatin A | 1SME |
AA | A01.023 | plasmepsin-2 | complex with TIT inhibitor | 1W6H |
AA | A01.023 | plasmepsin-2 | complex with pepstatin A | 1W6I |
AA | A01.023 | plasmepsin-2 | complex with pepstatin A | 1XDH |
AA | A01.023 | plasmepsin-2 | complex with a pepstatin analogue | 1XE5 |
AA | A01.023 | plasmepsin-2 | complex with a pepstatin analogue | 1XE6 |
AA | A01.023 | plasmepsin-2 | complex with N-(R-carboxy-ethyl)-alpha-(S)-(2-phenylethyl) | 2BJU |
AA | A01.023 | plasmepsin-2 | 2BL3 | |
AA | A01.023 | plasmepsin-2 | achiral, cheap and potent inhibitors of plasmepsins ii | 2IGX_A |
AA | A01.023 | plasmepsin-2 | achiral, cheap and potent inhibitors of plasmepsins ii | 2IGY_A |
AA | A01.023 | plasmepsin-2 | complex with KPFS-(CH2-NH)-LQF | 2R9B_A |
AA | A01.023 | plasmepsin-2 | re-refinement of uncomplexed plasmepsin ii from plasmodium falciparum. | 3F9Q_A |
AA | A01.023 | plasmepsin-2 | 4CKU | |
AA | A01.023 | plasmepsin-2 | 4Y6M | |
AA | A01.023 | plasmepsin-2 | 4YA8 | |
AA | A01.027 | trichodermapepsin | 3C9X | |
AA | A01.027 | trichodermapepsin | complex with pepstatin A | 3C9Y |
AA | A01.027 | trichodermapepsin | complex with pepstatin A | 3EMY |
AA | A01.030 | yapsin-1 | theoretical model | 1YPS |
AA | A01.037 | canditropsin | Complex with Thr-Ile-Thr-Ser | 1J71 |
AA | A01.038 | candiparapsin | complex with pepstatin | 3FV3 |
AA | A01.038 | candiparapsin | 3TNE | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | complex with hydroxyethylenamine transition-state inhibitor N-(1S,2R)-1-benzyl-2-hydroxy-3-[(3-methylbenzyl)amino]propyldibenzo[B,F]oxepine-10-carboxamide | 2EWY_A |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKG | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKI | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKM | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKN | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKQ | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKS | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZKX | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZL7 | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 3ZLQ | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 4BEL | |
AA | A01.041 | BACE2 g.p. (Homo sapiens) | 4BFB | |
AA | A01.043 | histoaspartic peptidase (Plasmodium falciparum) | ON HOLD; apoenzyme | 3FNS |
AA | A01.043 | histoaspartic peptidase (Plasmodium falciparum) | complex with pepstatin A | 3FNT |
AA | A01.043 | histoaspartic peptidase (Plasmodium falciparum) | complex with inhibitor KNI-10006 | 3FNU |
AA | A01.043 | histoaspartic peptidase (Plasmodium falciparum) | 3QVC_A | |
AA | A01.043 | histoaspartic peptidase (Plasmodium falciparum) | complex with kni-10395 | 3QVI_A |
AA | A01.055 | Mername-AA047 peptidase | 1AM5 | |
AA | A01.059 | plasmepsin-4 | complex with pepstatin A | 1LS5_A |
AA | A01.060 | candidapepsin SAP2 | complex with A70450 | 1EAG_A |
AA | A01.060 | candidapepsin SAP2 | complex with N-ethyl-N-[(4-methylpiperazin-1-yl)carbonyl]- D-phenylalanyl-N-[(1S,2S,4R)-4-(butylcarbamoyl)- 1-(cyclohexylmethyl)-2-hydroxy-5-methylhexyl]- L-norleucinamide | 1ZAP |
AA | A01.061 | candidapepsin SAP3 | secreted aspartic proteinase (sap) 3 from candida albicans | 2H6S_A |
AA | A01.061 | candidapepsin SAP3 | complex with pepstatin A | 2H6T_A |
AA | A01.063 | candidapepsin SAP5 | complex with pepstatin A | 2QZX |
AA | A01.070 | pepsin A4 | Uropepsin | 1FLH |
AA | A01.070 | pepsin A4 | pepsin 3A | 1PSN |
AA | A01.070 | pepsin A4 | pepsin 3A; complex with pepstatin | 1PSO |
AA | A01.070 | pepsin A4 | complex with phosphonate inhibitor Iva-Val-Val-Leu(P)-(O)Phe-Ala-Ala-Ome | 1QRP |
AA | A01.070 | pepsin A4 | 3UTL | |
AA | A01.075 | plasmepsin-5 (Plasmodium sp.) | plasmepsin v from plasmodium vivax bound to a transition state mimetic(wehi-842) | 4ZL4_A |
AA | A01.075 | plasmepsin-5 (Plasmodium sp.) | plasmepsin v from plasmodium vivax bound to a transition state mimetic(wehi-601) | 6C4G_A |
AA | A01.076 | Sapp2p peptidase (Candida parapsilosis) | aspartic proteinase sapp2 secreted from candida parapsilosis at 0.82 aresolution. | 4Y9W_A |
AA | A01.076 | Sapp2p peptidase (Candida parapsilosis) | aspartic proteinase sapp2 secreted from candida parapsilosis at 1.25 aresolution | 4YBF_A |
AA | A01.950 | cockroach allergen | Asn93Gln mutant | 1YG9 |
AA | A01.950 | cockroach allergen | Asn93Gln mutant; complex with monoclonal antibody | 2NR6_A |
AA | A01.950 | cockroach allergen | 3LIZ | |
AA | A01.950 | cockroach allergen | 4RLD | |
AA | A01.974 | xylanase inhibitor precursor | 1T6E_X | |
AA | A01.974 | xylanase inhibitor precursor | complex with Aspergillus niger xylanase-I | 1T6G_A |
AA | A01.974 | xylanase inhibitor precursor | complex with Bacillus subtilis xylanase | 2B42_A |
AA | A01.974 | xylanase inhibitor precursor | complex with bacillus subtilis xylanase | 3HD8_A |
AA | A01.UNB | subfamily A1B non-peptidase homologues | 3VLA_A | |
AA | A01.UNB | subfamily A1B non-peptidase homologues | 3VLB_A | |
AA | A01.UNB | subfamily A1B non-peptidase homologues | 4PPH_A | |
AA | A01.UNB | subfamily A1B non-peptidase homologues | 3AUP | |
AA | A01.UPA | subfamily A1A unassigned peptidases | 1IZD | |
AA | A01.UPA | subfamily A1A unassigned peptidases | 1IZE | |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with the n-terminal octapeptide of the propeptid | 5N70_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | 5N71_A | |
AA | A01.UPA | subfamily A1A unassigned peptidases | zymogen | 5N7N_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with the inhibitor pepstatin a | 5N7Q_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with kni-10343 | 5YIA_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with kni-10743 | 5YIB_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with kni-10333 | 5YIC_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with kni-10395 | 5YID_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | complex with kni-10742 | 5YIE_A |
AA | A01.UPA | subfamily A1A unassigned peptidases | precursor | 5MKT_A |
AA | A02.001 | HIV-1 retropepsin | complex with Glu-Asp-Leu inhibitor | 1A30 |
AA | A02.001 | HIV-1 retropepsin | complex with SDZ283-910 inhibitor | 1A8G |
AA | A02.001 | HIV-1 retropepsin | complex with CA-P2 peptide substrate analogue | 1A8K |
AA | A02.001 | HIV-1 retropepsin | complex with Arg-Val-Leu-Phe-Glu-Ala-norLeu-NH2 | 1A94 |
AA | A02.001 | HIV-1 retropepsin | complex with U-89360E inhibitor | 1A9M |
AA | A02.001 | HIV-1 retropepsin | complex with methyl N-(4S,5S)-5-[(L-alanyl-L-alanyl)amino]- 4-hydroxy-6-phenylhexanoyl-L-valyl-L-valinate | 1AAQ |
AA | A02.001 | HIV-1 retropepsin | complex with UCSF8 inhibitor | 1AID |
AA | A02.001 | HIV-1 retropepsin | complex with AHA006 inhibitor | 1AJV |
AA | A02.001 | HIV-1 retropepsin | complex with AHA001 inhibitor | 1AJX |
AA | A02.001 | HIV-1 retropepsin | Ala28Ser mutant | 1AXA |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 1 | 1B6J |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 5 | 1B6K |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 4 | 1B6L |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 6 | 1B6M |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 3 | 1B6N |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 2 | 1B6O |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 7 | 1B6P |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with SB203386 inhibitor | 1BDL |
AA | A02.001 | HIV-1 retropepsin | complex with SB203386 inhibitor | 1BDQ |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with SB203386 inhibitor | 1BDR |
AA | A02.001 | HIV-1 retropepsin | Val3Ile, Ile64Val, Val77Ile mutant; complex with cyclic urea amide XV638 | 1BV7 |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with XV638 (Dupont Pharmaceuticals) | 1BV9 |
AA | A02.001 | HIV-1 retropepsin | NMR structure; complex with DMP323 | 1BVE |
AA | A02.001 | HIV-1 retropepsin | NMR structure; complex with DMP323 | 1BVG |
AA | A02.001 | HIV-1 retropepsin | Val82Phe and Ile84Val double mutant; complex with XV638 (Dupont Pharmaceuticals) | 1BWA |
AA | A02.001 | HIV-1 retropepsin | Val82Phe and Ile84Val double mutant; complex with SD146 (Dupont Pharmaceuticals) | 1BWB |
AA | A02.001 | HIV-1 retropepsin | complex with L-739,622 inhibitor | 1C6X |
AA | A02.001 | HIV-1 retropepsin | complex with L-735,524 inhibitor | 1C6Y |
AA | A02.001 | HIV-1 retropepsin | complex with ROC 505 inhibitor | 1C6Z |
AA | A02.001 | HIV-1 retropepsin | complex with L-756,423 inhibitor | 1C70 |
AA | A02.001 | HIV-1 retropepsin | complex with a cyclic peptide inhibitor | 1CPI |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA435 | 1D4H |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA425 | 1D4I |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MSL370 | 1D4J |
AA | A02.001 | HIV-1 retropepsin | complex with N-13-[(10S,13S)-9,12-dioxo-10-(2-butyl)-2-oxa-8,11-diazabicyclo [13.2.2] nonadeca-15,17,18-triene] (2R)-benzyl-(4S)-hydroxy-5-aminopentanoic (1R)- hydroxy-(2S)-indaneamide | 1D4K |
AA | A02.001 | HIV-1 retropepsin | complex with (10S,13S,1'R)-13-[1'-hydroxy-2'-(N-P-aminobenzenesulfonyl-1''-amino-3''-methylbutyl)ethyl]-8,11-dioxo-10-isopropyl-2-oxa-9,12-diazabicyclo [13.2.2]nonadeca-15,17,18-triene | 1D4L |
AA | A02.001 | HIV-1 retropepsin | Val82Phe, Ile84Val double mutant; complex with tipranavir inhibitor | 1D4S |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys, Leu33Ile, Leu63Ile mutant: complex with tipranavir | 1D4Y |
AA | A02.001 | HIV-1 retropepsin | drug resistant mutant; complex with peptide inhibitor | 1DAZ |
AA | A02.001 | HIV-1 retropepsin | complex with a difluoroketone containing inhibitor A79285 | 1DIF |
AA | A02.001 | HIV-1 retropepsin | complex with DMP450 (Dupont-Merck) | 1DMP |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor analogue of CA-P2 processing site | 1DW6 |
AA | A02.001 | HIV-1 retropepsin | drug-resistant mutant | 1EBK |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA322 | 1EBW |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA369 | 1EBY |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA388 | 1EBZ |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA403 | 1EC0 |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA409 | 1EC1 |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor BEA428 | 1EC2 |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MSA367 | 1EC3 |
AA | A02.001 | HIV-1 retropepsin | complex with Lys-Ala-Arg-Val-Leu-Ala-Glu-Ala-Met-Ser substrate | 1F7A |
AA | A02.001 | HIV-1 retropepsin | Val48Gly, Met90Leu mutant; complex with saquinavir | 1FB7 |
AA | A02.001 | HIV-1 retropepsin | complex with substrate acetyl-Thr-Ile-norLeu-norLeu-Gln-Arg | 1FEJ |
AA | A02.001 | HIV-1 retropepsin | engineered; complex with acetyl-Thr-Ile-norLeu-norLeu-Gln-Arg inhibitor | 1FF0 |
AA | A02.001 | HIV-1 retropepsin | engineered; complex with Arg-Val-2-amino-4-methyl-pentan-1-ol-Phe-Glu-Ala-norLeu-NH2 inhibitor | 1FFF |
AA | A02.001 | HIV-1 retropepsin | engineered; complex with acetyl-Thr-Ile-norLeu-norLeu-Gln-Arg inhibitor | 1FFI |
AA | A02.001 | HIV-1 retropepsin | engineered; complex with acetyl-Thr-Ile-norLeu-norLeu-Gln-Arg inhibitor | 1FG6 |
AA | A02.001 | HIV-1 retropepsin | engineered; complex with Arg-Val-2-amino-4-methyl-pentan-1-ol-Phe-Glu-Ala-norLeu-NH2 inhibitor | 1FG8 |
AA | A02.001 | HIV-1 retropepsin | engineered; complex with acetyl-Thr-Ile-norLeu-norLeu-Gln-Arg inhibitor | 1FGC |
AA | A02.001 | HIV-1 retropepsin | complex with Boc-3(S)-amino-4-phenyl-butan-2(S)-yl-Phe-Glu-Phe-NH2 inhibitor | 1FQX |
AA | A02.001 | HIV-1 retropepsin | complex with cyclic sulfamide inhibitor AHA047 | 1G2K |
AA | A02.001 | HIV-1 retropepsin | complex with AHA024 inhibitor | 1G35 |
AA | A02.001 | HIV-1 retropepsin | homodimer covalently linked through engineered pentapeptide linker | 1G6L |
AA | A02.001 | HIV-1 retropepsin | Val82Asp mutant; complex with U89360E inhibitor | 1GNM |
AA | A02.001 | HIV-1 retropepsin | Val82Asn mutant; complex with U89360E inhibitor | 1GNN |
AA | A02.001 | HIV-1 retropepsin | complex with U89360E inhibitor | 1GNO |
AA | A02.001 | HIV-1 retropepsin | complex with SB203238 | 1HBV |
AA | A02.001 | HIV-1 retropepsin | recombinant | 1HEF |
AA | A02.001 | HIV-1 retropepsin | recombinant | 1HEG |
AA | A02.001 | HIV-1 retropepsin | recombinant | 1HHP |
AA | A02.001 | HIV-1 retropepsin | complex with CGP 53820 | 1HIH |
AA | A02.001 | HIV-1 retropepsin | 1HIV | |
AA | A02.001 | HIV-1 retropepsin | complex with SB204144 | 1HOS |
AA | A02.001 | HIV-1 retropepsin | mutant form; complex with benzenesulfonamide inhibitor U103265 | 1HPO |
AA | A02.001 | HIV-1 retropepsin | 1HPS | |
AA | A02.001 | HIV-1 retropepsin | complex with VX-478 | 1HPV |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor KNI-272 | 1HPX |
AA | A02.001 | HIV-1 retropepsin | complex with L-735,524 | 1HSG |
AA | A02.001 | HIV-1 retropepsin | complex with GR123976 | 1HTE |
AA | A02.001 | HIV-1 retropepsin | complex with GR126045 | 1HTF |
AA | A02.001 | HIV-1 retropepsin | complex with GR137615 | 1HTG |
AA | A02.001 | HIV-1 retropepsin | complex with A-76928 | 1HVC |
AA | A02.001 | HIV-1 retropepsin | complex with Q8261 inhibitor | 1HVH |
AA | A02.001 | HIV-1 retropepsin | complex with A77003 | 1HVI |
AA | A02.001 | HIV-1 retropepsin | complex with A78791 | 1HVJ |
AA | A02.001 | HIV-1 retropepsin | complex with A-76928 | 1HVK |
AA | A02.001 | HIV-1 retropepsin | complex with A76889 | 1HVL |
AA | A02.001 | HIV-1 retropepsin | theoretical model | 1HVP |
AA | A02.001 | HIV-1 retropepsin | complex with XK263 | 1HVR |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with A77003 | 1HVS |
AA | A02.001 | HIV-1 retropepsin | complex with synthetic cyclic urea inhibitor XK216 | 1HWR |
AA | A02.001 | HIV-1 retropepsin | complex with RO 31-8959 | 1HXB |
AA | A02.001 | HIV-1 retropepsin | complex with A-84538 | 1HXW |
AA | A02.001 | HIV-1 retropepsin | 1IHV | |
AA | A02.001 | HIV-1 retropepsin | 1IHW | |
AA | A02.001 | HIV-1 retropepsin | complex with hydroxyethylamine peptidomimetic inhibitor Boc-Pso-Phe-Gln-Phe-NH2 | 1IIQ |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor Q50 | 1IZH |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor Q50 | 1IZI |
AA | A02.001 | HIV-1 retropepsin | engineered multiple mutant form | 1K1T |
AA | A02.001 | HIV-1 retropepsin | engineered multiple mutant form | 1K1U |
AA | A02.001 | HIV-1 retropepsin | engineered multiple mutant form | 1K2B |
AA | A02.001 | HIV-1 retropepsin | engineered multiple mutant form | 1K2C |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MK1 | 1K6C |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor XN3 | 1K6P |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor XN1 | 1K6T |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor XN2 | 1K6V |
AA | A02.001 | HIV-1 retropepsin | complex with GAG protein fragment | 1KJ4 |
AA | A02.001 | HIV-1 retropepsin | complex with GAG protein fragment | 1KJ7 |
AA | A02.001 | HIV-1 retropepsin | complex with GAG protein fragment | 1KJF |
AA | A02.001 | HIV-1 retropepsin | complex with decapeptide substrate | 1KJG |
AA | A02.001 | HIV-1 retropepsin | complex with POL protein fragment | 1KJH |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor JE-2147 | 1KZK |
AA | A02.001 | HIV-1 retropepsin | engineered tethered dimer | 1LV1 |
AA | A02.001 | HIV-1 retropepsin | Ala71Val, Val82Thr, Ile84Val mutant; complex with Boc-Phe-Psi[CH2CH2NH]-Phe-Glu-Phe-NH2 | 1LZQ |
AA | A02.001 | HIV-1 retropepsin | complex with Boc-Phe-Psi[CH2CH2NH]-Phe-Glu-Phe-NH2 | 1M0B_A |
AA | A02.001 | HIV-1 retropepsin | complex with DMP450 | 1MER |
AA | A02.001 | HIV-1 retropepsin | Ile84Val mutant; complex with DMP323 | 1MES |
AA | A02.001 | HIV-1 retropepsin | Val82Phe mutant; complex with DMP323 | 1MET |
AA | A02.001 | HIV-1 retropepsin | Val82Phe, Ile84Val mutant; complex with DMP323 | 1MEU |
AA | A02.001 | HIV-1 retropepsin | Gln7lys/Leu33Ile/Leu63Ile mutant; complex with kni-577 | 1MRW_A |
AA | A02.001 | HIV-1 retropepsin | mutant q7k l33i l63i v82f i84v; complex with kni-577 | 1MRX_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys, Leu33Ile, Leu63Ile mutant; complex with KNI-764 inhibitor | 1MSM_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys, Leu33Ile, Leu63Ile, Val82Phe, Ile84Valmutant; complex with KNI-764 inhibitor | 1MSN_A |
AA | A02.001 | HIV-1 retropepsin | complex with GAG protein fragment | 1MT7 |
AA | A02.001 | HIV-1 retropepsin | complex with GAG protein fragment | 1MT8 |
AA | A02.001 | HIV-1 retropepsin | complex with GAG protein fragment | 1MT9 |
AA | A02.001 | HIV-1 retropepsin | complex with Saquinavir | 1MTB |
AA | A02.001 | HIV-1 retropepsin | complex with a cyclic Phe-Ile-Val peptidomimetic inhibitor | 1MTR |
AA | A02.001 | HIV-1 retropepsin | complex with lopinavir | 1MUI |
AA | A02.001 | HIV-1 retropepsin | complex with Ritonavir | 1N49 |
AA | A02.001 | HIV-1 retropepsin | 1.03 a structure of hiv-1 protease: inhibitor binding inside and outside the active site | 1NH0_A |
AA | A02.001 | HIV-1 retropepsin | complex with LDC271 | 1NPV |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor LGZ479 | 1NPW |
AA | A02.001 | HIV-1 retropepsin | 1ODW | |
AA | A02.001 | HIV-1 retropepsin | Ala71Thr, Val82Ala mutant | 1ODX |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor LP-130 | 1ODY |
AA | A02.001 | HIV-1 retropepsin | complex with nelfinavir mesylate AG1343 inhibitor | 1OHR |
AA | A02.001 | HIV-1 retropepsin | dimer; complex with A-98881 | 1PRO |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor XV638 | 1QBR |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor DMP323 | 1QBS |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor SD146 | 1QBT |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor Q8467 (Dupont-Merck) | 1QBU |
AA | A02.001 | HIV-1 retropepsin | resistant strain (Val82Ala mutant); complex with ritonavir | 1RL8_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant hiv-1 protease | 1RV7_A |
AA | A02.001 | HIV-1 retropepsin | complex with SB203386 | 1SBG |
AA | A02.001 | HIV-1 retropepsin | Val82Ala and Ile90Met mutant; complex with indinavir | 1SDT_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala and Ile90Met mutant | 1SDU_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala and Ile90Met mutant | 1SDV_A |
AA | A02.001 | HIV-1 retropepsin | comparing the accumulation of active site and non-active site mutations in the hiv-1 protease | 1SGU_A |
AA | A02.001 | HIV-1 retropepsin | comparing the accumulation of active site and non-active site mutations in the hiv-1 protease | 1SH9_A |
AA | A02.001 | HIV-1 retropepsin | complex with a product of autoproteolysis | 1SP5_A |
AA | A02.001 | HIV-1 retropepsin | complex with TMC114 inhibitor | 1T3R_A |
AA | A02.001 | HIV-1 retropepsin | triple mutant; complex with SB203386 | 1TCX |
AA | A02.001 | HIV-1 retropepsin | Val82Ala/Asp25Asn mutant; complex with AP2V substrate variant of NC-P1 decamer peptide | 1TSQ_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala/Asp25Asn mutant; complex with AP2V substrate variant of NC-P1 decamer peptide | 1TSQ_P |
AA | A02.001 | HIV-1 retropepsin | wild-type Asp25Asn variant; complex with decamer NCP1 substrate peptide | 1TSU_A |
AA | A02.001 | HIV-1 retropepsin | wild-type Asp25Asn variant; complex with decamer NCP1 substrate peptide | 1TSU_P |
AA | A02.001 | HIV-1 retropepsin | peptidase domain only; multi-drug resistant isolate | 1TW7 |
AA | A02.001 | HIV-1 retropepsin | complex with peptidomimetic inhibitor KI2-Phe-Glu-Glu-NH2 | 1U8G_A |
AA | A02.001 | HIV-1 retropepsin | complex with [3-[1-(4-bromophenyl)isobutyl]-4-hydroxycoumarin (U095438) | 1UPJ |
AA | A02.001 | HIV-1 retropepsin | complex with HOE/BAY 793 inhibitor | 1VIJ |
AA | A02.001 | HIV-1 retropepsin | compex with HOE/BAY 793 inhibitor, orthorhombic form | 1VIK |
AA | A02.001 | HIV-1 retropepsin | complex with fluoro substituted diol- based c2-symmetric inhibitor N,N-[2,5-O-di-3-fluoro-benzyl-glucaryl]-di-[1-amino-indan-2-ol] | 1W5V_A |
AA | A02.001 | HIV-1 retropepsin | complex with fluoro substituted diol- based c2-symmetric inhibitor (2R,3R,4R,5R)-2,5-bis[(2,4-difluorobenzyl)oxy]-3,4-dihydroxy-N,N'-bis[(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]hexanediamide | 1W5W_A |
AA | A02.001 | HIV-1 retropepsin | complex with fluoro substituted diol- based c2-symmetric inhibitor (2R,3R,4R,5R)-2,5-bis[(2,3-difluorobenzyl)oxy]-3,4-dihydroxy-N,N'-bis[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]hexanediamide | 1W5X_A |
AA | A02.001 | HIV-1 retropepsin | complex with fluoro substituted diol- based c2-symmetric inhibitor (2R,3R,4R,5R)-2,5-bis[(2,5-difluorobenzyl)oxy]-3,4-dihydroxy-N,N'-bis[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]hexanediamide | 1W5Y_A |
AA | A02.001 | HIV-1 retropepsin | complex with asymmetric inhibitor BEA568 | 1WBK_A |
AA | A02.001 | HIV-1 retropepsin | complex with symmetric inhibitor BEA450 | 1WBM_A |
AA | A02.001 | HIV-1 retropepsin | complex with pyrrolidinmethanamine | 1XL2_A |
AA | A02.001 | HIV-1 retropepsin | complex with amidhyroxysulfone | 1XL5_A |
AA | A02.001 | HIV-1 retropepsin | complex with Pro-Ile-Val-NH2 peptide product | 1YTG |
AA | A02.001 | HIV-1 retropepsin | complex with ac-Ser-Leu-Asn-Phe peptide product | 1YTH |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 3 | 1Z1H_A |
AA | A02.001 | HIV-1 retropepsin | complex with macrocyclic peptidomimetic inhibitor 2 | 1Z1R_A |
AA | A02.001 | HIV-1 retropepsin | lle63Pro, Ala71Val, Val82Thr, Ile84Val mutant; complex with a hydroxyethylamine peptidomimetic inhibitor Boc-Phe-psi[r-CH(OH)CH2NH]-Phe-Glu-Phe-NH2 | 1Z8C_A |
AA | A02.001 | HIV-1 retropepsin | Ala71Val, Val82Thr, Ile84Val mutant; complex with a hydroxyethylamine peptidomimetic inhibitor Boc-Phe-psi[r-CH(OH)CH2NH]-Phe-Glu-Phe-NH2 | 1ZBG_A |
AA | A02.001 | HIV-1 retropepsin | Ala71Val, Val82Thr, Ile84Val mutant; complex with a hydroxyethylamine peptidomimetic inhibitor Boc-Phe-psi[r-CH(OH)CH2NH]-Phe-Glu-Phe-NH2 | 1ZJ7_A |
AA | A02.001 | HIV-1 retropepsin | Ala71Val, Val82Thr, Ile84Val mutant; complex with a hydroxyethylamine peptidomimetic inhibitor | 1ZLF_A |
AA | A02.001 | HIV-1 retropepsin | Ala71Val, Val82Thr, Ile84Val mutant; complex with a hydroxyethylamine peptidomimetic inhibitor Boc-Phe-psi[r-CH(OH)CH2NH]-Phe-Glu-Phe-NH2 | 1ZPK_A |
AA | A02.001 | HIV-1 retropepsin | complex with a hydroxyethylamine inhibitor N-(2R,3S)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-4-phenylbutyl-L-phenylalanyl-L-alpha-glutamyl-L-phenylalaninamide | 1ZSF_A |
AA | A02.001 | HIV-1 retropepsin | complex with a hydroxyethylamine peptidomimetic inhibitor Boc-Phe-psi[r-CH(OH)CH2NH]-Phe-Glu-Phe-NH2 | 1ZSR_A |
AA | A02.001 | HIV-1 retropepsin | complex with cobalt bis(1,2-dicarbollide) | 1ZTZ_A |
AA | A02.001 | HIV-1 retropepsin | complex with ts-126 | 2A1E_A |
AA | A02.001 | HIV-1 retropepsin | synthesis and activity of n-axyl azacyclic urea hiv-1 protease inhibitors with high potency against multiple drug resistant viral strains. | 2A4F_A |
AA | A02.001 | HIV-1 retropepsin | complex with UCSF8 inhibitor | 2AID |
AA | A02.001 | HIV-1 retropepsin | Ile84Val mutant; complex with a substrate analog p2-nc | 2AOC_A |
AA | A02.001 | HIV-1 retropepsin | complex with a substrate analog p2-nc | 2AOD_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with a substrate analog ca-p2 | 2AOE_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with a substrate analog p1-p6 | 2AOF_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with a substrate analog p2-nc | 2AOG_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with a substrate analog p6-pr | 2AOH_A |
AA | A02.001 | HIV-1 retropepsin | complex with a substrate analog p1-p6 | 2AOI_A |
AA | A02.001 | HIV-1 retropepsin | complex with a substrate analog p6-pr | 2AOJ_A |
AA | A02.001 | HIV-1 retropepsin | complex with atazanavir | 2AQU_A |
AA | A02.001 | HIV-1 retropepsin | kinetics, stability, and structural changes in high resolution crystalstructures of hiv-1 protease with drug resistant mutations l24i, i50v, and g73s | 2AVM_A |
AA | A02.001 | HIV-1 retropepsin | kinetics, stability, and structural changes in high resolution crystalstructures of hiv-1 protease with drug resistant mutations l24i, i50v, and g73s | 2AVO_A |
AA | A02.001 | HIV-1 retropepsin | kinetics, stability, and structural changes in high resolution crystalstructures of hiv-1 protease with drug resistant mutations l24i, i50v, and g73s | 2AVQ_A |
AA | A02.001 | HIV-1 retropepsin | kinetics, stability, and structural changes in high resolution crystal structures of hiv-1 protease with drug resistant mutations l24i, i50v, and g73s | 2AVS_A |
AA | A02.001 | HIV-1 retropepsin | kinetics, stability, and structural changes in high resolution crystal structures of hiv-1 protease with drug resistant mutations l24i, i50v, and g73s | 2AVV_A |
AA | A02.001 | HIV-1 retropepsin | ML4-3 mutant; complex with inhibitorTL3 | 2AZ8_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease nl4-3 1x mutant | 2AZ9_A |
AA | A02.001 | HIV-1 retropepsin | NL4-3 3X mutant; complex with inhibitorTL-3 | 2AZB_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease nl4-3 6x mutant ***caveat 2azc incorrect chirality at ca of ala j 201 | 2AZC_A |
AA | A02.001 | HIV-1 retropepsin | complex with ritonavir | 2B60_A |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with indinavir | 2B7Z_B |
AA | A02.001 | HIV-1 retropepsin | complex with akc4p_133a | 2BB9_A |
AA | A02.001 | HIV-1 retropepsin | complex with hh1_173_3a | 2BBB_A |
AA | A02.001 | HIV-1 retropepsin | complex with L-738,317 inhibitor | 2BPV |
AA | A02.001 | HIV-1 retropepsin | complex with L-738,317 inhibitor | 2BPW |
AA | A02.001 | HIV-1 retropepsin | complex with L-735,524 inhibitor | 2BPX |
AA | A02.001 | HIV-1 retropepsin | complex with L-739,622 inhibitor | 2BPY |
AA | A02.001 | HIV-1 retropepsin | complex with L-739,622 inhibitor | 2BPZ |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor AHA455 | 2BQV_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with r01 | 2F3K_A |
AA | A02.001 | HIV-1 retropepsin | Asp30Asn mutant; complex with inhibitor TMC114 | 2F80_A |
AA | A02.001 | HIV-1 retropepsin | Leu90Met mutant; complex with inhibitor TMC114 | 2F81_A |
AA | A02.001 | HIV-1 retropepsin | Ile50Val mutant; complex with inhibitor TMC114 | 2F8G_A |
AA | A02.001 | HIV-1 retropepsin | Thr80Ser variant; complex with the inhibitor saquinavir | 2FGU_A |
AA | A02.001 | HIV-1 retropepsin | Thrt80Asn variant; complex with the inhibitor saquinavir | 2FGV_A |
AA | A02.001 | HIV-1 retropepsin | Asp25Asn mutant; complex with wild-type HIV-1 NC-P1 substrate. | 2FNS_A |
AA | A02.001 | HIV-1 retropepsin | drug-resistant (Val82Ala) inactive (Asp25Asn) mutant; complex with AP2V variant of hiv-1 NC-P1 substrate. | 2FNT_A |
AA | A02.001 | HIV-1 retropepsin | structure of hiv protease 6x mutant in apo form | 2HB2_A |
AA | A02.001 | HIV-1 retropepsin | complex with potent inhibitor GRL06579 | 2HB3_A |
AA | A02.001 | HIV-1 retropepsin | structure of hiv protease nl4-3 in an unliganded state | 2HB4_A |
AA | A02.001 | HIV-1 retropepsin | 6x mutant; complex with AB-2. | 2HC0_A |
AA | A02.001 | HIV-1 retropepsin | recombinant | 2HVP |
AA | A02.001 | HIV-1 retropepsin | complex with KB-19 | 2I0A_A |
AA | A02.001 | HIV-1 retropepsin | complex with AD-81 | 2I0D_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor jg-365 | 2J9J_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MVT-101 | 2J9K_A |
AA | A02.001 | HIV-1 retropepsin | complex with jg-365 | 2JE4_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with a inhibitor saquinavir | 2NMY_A |
AA | A02.001 | HIV-1 retropepsin | Val82Ala mutant; complex with a inhibitor saquinavir | 2NMZ_A |
AA | A02.001 | HIV-1 retropepsin | Ile84Val mutant; complex with a inhibitor saquinavir | 2NNK_A |
AA | A02.001 | HIV-1 retropepsin | Ile84Val mutant; complex with a inhibitor saquinavir | 2NNP_A |
AA | A02.001 | HIV-1 retropepsin | complex with product in situ | 2NPH_A |
AA | A02.001 | HIV-1 retropepsin | Asp25Asn mutant; complex with rt-rh analogue peptide gly-ala-asp-ile-phe*tyr-leu-asp-gly-ala | 2NXD_A |
AA | A02.001 | HIV-1 retropepsin | Asp25Asn mutant; complex with peptide Gly-Ala-Glu-Val-Phe*Tyr-Val-Asp-Gly-Ala | 2NXL_A |
AA | A02.001 | HIV-1 retropepsin | Asp25Asn mutant; complex with the rt-rh analogue peptide gly-ala-gln-thr-phe*tyr-val-asp-gly-ala | 2NXM_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys mutant; complex with Atazanavir | 2O4K_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys, Ile50Val mutant; complex with Tipranavir | 2O4L_A |
AA | A02.001 | HIV-1 retropepsin | TRM mutant; complex with Tipranavir | 2O4N_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys mutant; complex with Tipranavir | 2O4P_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys mutant; complex with Lopinavir | 2O4S_A |
AA | A02.001 | HIV-1 retropepsin | complex with TL-3 inhibitor | 2P3B_A |
AA | A02.001 | HIV-1 retropepsin | subtype F; complex with TL-3 inhibitor | 2P3C_A |
AA | A02.001 | HIV-1 retropepsin | multi-drug resistant mutant subtype F; complex with TL-3 inhibitor | 2P3D_A |
AA | A02.001 | HIV-1 retropepsin | apo wild-type hiv protease in the open conformation | 2PC0_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys, Leu33Ile, Leu63Ile mutant; complex with KNI-10075 | 2PK5_A |
AA | A02.001 | HIV-1 retropepsin | Gln7Lys, Leu33Ile, Leu63Ile mutant; complex with KNI-10033 | 2PK6_A |
AA | A02.001 | HIV-1 retropepsin | complex with N,N'-(3S,4S)-pyrrolidine-3,4-diylbis(N-benzylbenzenesulfonamide) | 2PQZ_A |
AA | A02.001 | HIV-1 retropepsin | complex with CARB-AD37 | 2PSU_A |
AA | A02.001 | HIV-1 retropepsin | complex with CARB-KB45 | 2PSV_A |
AA | A02.001 | HIV-1 retropepsin | complex with N,N'-(3S,4S)-pyrrolidine-3,4-diylbis(4-amino-N-benzylbenzenesulfonamide) | 2PWC_A |
AA | A02.001 | HIV-1 retropepsin | complex with 4,4'-(3S,4S)-pyrrolidine-3,4-diylbis[(benzylimino)sulfonyl]dibenzamide | 2PWR_A |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with nelfinavir | 2PYM_A |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with Nelfinavir | 2PYN_A |
AA | A02.001 | HIV-1 retropepsin | complex with a lysine sulfonamide inhibitor | 2Q3K_A |
AA | A02.001 | HIV-1 retropepsin | complex with KB73 | 2Q54_A |
AA | A02.001 | HIV-1 retropepsin | complex with KK44 | 2Q55_A |
AA | A02.001 | HIV-1 retropepsin | complex with lopinavir | 2Q5K_A |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with nelfinavir | 2Q63_A |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with nelfinavir | 2Q64_A |
AA | A02.001 | HIV-1 retropepsin | mutant; complex with nelfinavir | 2QAK_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease mutant d30n with potent antiviral inhibitor grl-98065 | 2QCI_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease mutant i50v with potent antiviral inhibitor grl-98065 | 2QD6_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease mutant v82a with potent antiviral inhibitor grl-98065 | 2QD7_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease mutant i84v with potent antiviral inhibitor grl-98065 | 2QD8_A |
AA | A02.001 | HIV-1 retropepsin | the influence of i47a mutation on reduced susceptibility to the protease inhibitor lopinavir | 2QHC_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-1-AC6 | 2QHY_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-1-AC87 | 2QHZ_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-1-KK80 | 2QI0_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-1-KK81 | 2QI1_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-2-AD94 | 2QI3_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-2-AD93 | 2QI4_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-2-KC08 | 2QI5_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-2-KB98 | 2QI6_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor MIT-2-AD86 | 2QI7_A |
AA | A02.001 | HIV-1 retropepsin | complex with PL-100 | 2QMP_A |
AA | A02.001 | HIV-1 retropepsin | complex with 4,4'-[(3S,4S)-pyrrolidine-3,4-diylbis([4- (trifluoromethyl)benzyl]iminosulfonyl)]dibenzamide | 2QNN_A |
AA | A02.001 | HIV-1 retropepsin | complex with | 2QNP_A |
AA | A02.001 | HIV-1 retropepsin | complex with a chloro decorated pyrrolidine-based inhibitor | 2QNQ_A |
AA | A02.001 | HIV-1 retropepsin | i84v hiv-1 protease mutant in complex with a carbamoyl decorated pyrrolidine-based inhibitor | 2R38_A |
AA | A02.001 | HIV-1 retropepsin | Ile50Val mutant; complex with a carbamoyl decorated pyrrolidine-based inhibitor | 2R3T_A |
AA | A02.001 | HIV-1 retropepsin | Ile84Val mutant; complex with a amino decorated pyrrolidine-based inhibitor | 2R3W_A |
AA | A02.001 | HIV-1 retropepsin | i50v hiv-1 protease in complex with an amino decorated pyrrolidine-based inhibitor | 2R43_A |
AA | A02.001 | HIV-1 retropepsin | subtype c protease; complex with indinavir | 2R5P_A |
AA | A02.001 | HIV-1 retropepsin | subtype c; complex with nelfinavir | 2R5Q_A |
AA | A02.001 | HIV-1 retropepsin | subtype C | 2R8N |
AA | A02.001 | HIV-1 retropepsin | complex with U100313 | 2UPJ |
AA | A02.001 | HIV-1 retropepsin | two-carbon-elongated hiv-1 protease inhibitors with a tertiary-alcohol-containing transition-state mimic | 2UXZ_A |
AA | A02.001 | HIV-1 retropepsin | two-carbon-elongated hiv-1 protease inhibitors with a tertiary-alcohol-containing transition-state mimic | 2UY0_A |
AA | A02.001 | HIV-1 retropepsin | hiv-1 protease inhibitors containing a tertiary alcohol in the transition-state mimic with improved cell-based antiviral activity | 2WKZ_A |
AA | A02.001 | HIV-1 retropepsin | wild type hiv-1 protease with potent antiviral inhibitor grl-98065 | 2Z4O_A |
AA | A02.001 | HIV-1 retropepsin | Ile47Ala mutant on reduced susceptibility to the protease inhibitor lopinavir | 2Z54_A |
AA | A02.001 | HIV-1 retropepsin | complex with (3S,4S),-3,4-Bis-[(4-carbamoyl-benzensulfonyl)- (3-methyl-but-2-enyl)-amino]-pyrrolidine | 2ZGA_A |
AA | A02.001 | HIV-1 retropepsin | complex with potent inhibitor KNI-272 | 2ZYE_A |
AA | A02.001 | HIV-1 retropepsin | complex with kni-1689 | 3A2O_A |
AA | A02.001 | HIV-1 retropepsin | complex with benzoylamino-benzyl-methyl-[2-hydroxy-3-[1-methyl-ethyl-oxy-N-formamidyl]-4-phenyl-butyl]-ammonium | 3AID |
AA | A02.001 | HIV-1 retropepsin | complex with gem-diol-amine tetrahedral intermediate nlltqi | 3B7V_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Val mutant; complex with gem-diol-amine intermediate nlltqi | 3B80_A |
AA | A02.001 | HIV-1 retropepsin | Ile84Val mutant; complex with a pyrrolidine diester | 3BC4_A |
AA | A02.001 | HIV-1 retropepsin | complex with N,N'-(iminodiethane-2,1-diyl)bis[4-amino- N-(2-methylpropyl)benzenesulfonamide] | 3BGB_A |
AA | A02.001 | HIV-1 retropepsin | complex with N,N'-(iminodiethane-2,1-diyl)bis(4-amino- N-benzylbenzenesulfonamide) | 3BGC_A |
AA | A02.001 | HIV-1 retropepsin | complex with a three armed pyrrolidine derivative | 3BHE_A |
AA | A02.001 | HIV-1 retropepsin | Asp25Asn mutant; complex with p2-nc analog inhibitor | 3BVA_A |
AA | A02.001 | HIV-1 retropepsin | cystal structure of hiv-1 active site mutant d25n and inhibitor darunavir | 3BVB_A |
AA | A02.001 | HIV-1 retropepsin | crystal structures of highly constrained substrate and hydrolysis products bound to hiv-1 protease. implications for catalytic mechanism | 3BXR_A |
AA | A02.001 | HIV-1 retropepsin | crystal structures of highly constrained substrate and hydrolysis products bound to hiv-1 protease. implications for catalytic mechanism | 3BXS_A |
AA | A02.001 | HIV-1 retropepsin | complex with (3S,4S),-3,4-Bis-[(4-carbamoyl-benzensulfonyl)- (3-methyl-but-2-enyl)-amino]-pyrrolidine (orthorhombic space group) | 3CKT_A |
AA | A02.001 | HIV-1 retropepsin | effect of flap mutations inhibition by saquinavir and darunavir | 3CYW_A |
AA | A02.001 | HIV-1 retropepsin | Ile50Val mutant; complex with inhibitor saquinavir | 3CYX_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Met mutant; complex with inhibitor saquinavir | 3D1X_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Val mutant; complex with inhibitor saquinavir | 3D1Y_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Met mutant; complex with inhibitor darunavir | 3D1Z_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Val mutant; complex with inhibitor darunavia | 3D20_A |
AA | A02.001 | HIV-1 retropepsin | complex with substrate p1-p6 | 3D3T_A |
AA | A02.001 | HIV-1 retropepsin | wild type hiv-1 protease with potent antiviral inhibitor grl-0255a | 3DJK_A |
AA | A02.001 | HIV-1 retropepsin | wild type hiv-1 protease with potent antiviral inhibitor grl-0105a | 3DK1_A |
AA | A02.001 | HIV-1 retropepsin | multidrug resistant variant (Leu10Ile/Gly48Val/Ile54Val/Val64Ile/Val82Ala); complex with inhibitor amprenavir (apv) | 3EKP_A |
AA | A02.001 | HIV-1 retropepsin | multi-drug resistant form (Leu63Pro/Val82Thr/Ile84Val); complex with inhibitor saquinavir (sqv) | 3EKQ_A |
AA | A02.001 | HIV-1 retropepsin | multi-drug resistant variant (Leu10Phe/Gly48Val/Ile54Val/Val64Ile/Val82Ala); complex with darunavir (drv) | 3EKT_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with the inhibitor, amprenavir | 3EKV_A |
AA | A02.001 | HIV-1 retropepsin | multi-drug resistance variant (Leu10Ile/Gly48Val/Ile54Val/Val64Ile/Val82Ala); complex with the inhibitor atazanavir (atv) in complex with a refer: flap+ in citation. | 3EKW_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with the inhibitor nelfinavir | 3EKX_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with the inhibitor, atazanavir | 3EKY_A |
AA | A02.001 | HIV-1 retropepsin | multi-drug resistant variant (Leu10Ile/Gly48Val/Ile54Val/Val64Ile/Val82Ala); in complex with inhibitor nelfinavir (nfv) | 3EL0_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with the inhibitor, atazanavir | 3EL1_A |
AA | A02.001 | HIV-1 retropepsin | drug resistant Ile50Leu/Ala71Val variant; complex with amprenavir (apv) | 3EM3_A |
AA | A02.001 | HIV-1 retropepsin | drug- resistant Ile50Val/Ala71Val variant; complex with the protease inhibitor atazanavir | 3EM4_A |
AA | A02.001 | HIV-1 retropepsin | Ile50Leu/Ala71val mutant; complex with inhibitor darunavir | 3EM6_A |
AA | A02.001 | HIV-1 retropepsin | complex with potent inhibitor KNI-272 | 3FX5_A |
AA | A02.001 | HIV-1 retropepsin | hiv protease inhibitors with pseudo-symmetric cores | 3GGA_G |
AA | A02.001 | HIV-1 retropepsin | hiv protease, pseudo-symmetric inhibitors | 3GGV_B |
AA | A02.001 | HIV-1 retropepsin | hiv protease, pseudo-symmetric inhibitors | 3GGX_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with inhibitor kb60 | 3GI4_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with inhibitor kb62 | 3GI5_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with inhibitor ad78 | 3GI6_A |
AA | A02.001 | HIV-1 retropepsin | Cys replaced with alpha-amino-N-butyric acid | 3HVP |
AA | A02.001 | HIV-1 retropepsin | complex with mutant resistant inhibitor uic-98038 | 3I7E_A |
AA | A02.001 | HIV-1 retropepsin | complex with saquinavir | 3K4V_A |
AA | A02.001 | HIV-1 retropepsin | complex with darunavir | 3LZS_A |
AA | A02.001 | HIV-1 retropepsin | nelfinavir resistant variant (Asn88Ser); complex with the protease inhibitor darunavir. | 3LZU_B |
AA | A02.001 | HIV-1 retropepsin | nelfinavir-resistant variant (Asp30Asn/Asn88Asp); complex with darunavir. | 3LZV_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with inhibitor kc53 | 3MXD_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with inhibitor kc32 | 3MXE_A |
AA | A02.001 | HIV-1 retropepsin | complex with saquinavir:ritonavir 1:1 | 3NDT_A |
AA | A02.001 | HIV-1 retropepsin | complex with saquinavir:ritonavir 1:5 | 3NDU_A |
AA | A02.001 | HIV-1 retropepsin | complex with saquinavir:ritonavir 1:15 | 3NDW_A |
AA | A02.001 | HIV-1 retropepsin | complex with saquinavir:ritonavir 1:50 | 3NDX_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with antiviral drug amprenavir | 3NU3_A |
AA | A02.001 | HIV-1 retropepsin | Val32Ile mutant; complex with antiviral drug amprenavir | 3NU4_A |
AA | A02.001 | HIV-1 retropepsin | Ile50Val mutant; complex with antiviral drug amprenavir | 3NU5_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Met mutant; complex with antiviral drug amprenavir | 3NU6_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Val mutant; complex with antiviral drug amprenavir | 3NU9_A |
AA | A02.001 | HIV-1 retropepsin | Ile54Val mutant; complex with antiviral drug amprenavir | 3NUJ_A |
AA | A02.001 | HIV-1 retropepsin | Ile90Met mutant; complex with antiviral drug amprenavir | 3NUO_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd13 | 3O99_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd14 | 3O9A_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd25 | 3O9B_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd20 | 3O9C_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd19 | 3O9D_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af60 | 3O9E_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd27 | 3O9F_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af53 | 3O9G_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kd26 | 3O9H_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af61 | 3O9I_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with oxatricyclic designed inhibitor GRL-0519a | 3OK9_A |
AA | A02.001 | HIV-1 retropepsin | complex with saquinavir | 3OXC_A |
AA | A02.001 | HIV-1 retropepsin | Ile50Val, Ala71 variant; complex with the protease inhibitor amprenavir. | 3OXV_B |
AA | A02.001 | HIV-1 retropepsin | Ile50Val/Ala71Val variant; complex with the protease inhibitor darunavir | 3OXW_B |
AA | A02.001 | HIV-1 retropepsin | drug- resistant Ile50Val/Ala71Val variant; complex with the protease inhibitor atazanavir | 3OXX_B |
AA | A02.001 | HIV-1 retropepsin | Leu76Val variant; complex with the protease inhibitor darunavir. | 3OY4_A |
AA | A02.001 | HIV-1 retropepsin | recombinant | 3PHV |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with a substituted bis-tetrahydrofuran inhibitor, GRL-044-10a | 3QAA_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with tmc310911 | 3R4B_A |
AA | A02.001 | HIV-1 retropepsin | Val32Ile/Ile47Val/Val82Ile mutant; complex with antiviral drug amprenavir | 3S43_A |
AA | A02.001 | HIV-1 retropepsin | triple mutant Val32Ile/Ile47Val/Val82Ile; complex with antiviral drug darunavir in space group p212121 | 3S53_A |
AA | A02.001 | HIV-1 retropepsin | triple mutant Val32Ile/Ile47Val/Val82Ile; complex with antiviral drug darunavir in space group p21212 | 3S54_A |
AA | A02.001 | HIV-1 retropepsin | triple mutants Val32Ile, Ile47Val, Val82Ile with antiviral drug saquinavir | 3S56_A |
AA | A02.001 | HIV-1 retropepsin | discovery of new hiv protease inhibitors with potential for convenientdosing and reduced side effects: a-790742 and a-792611. | 3S85_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with ag23 | 3SA3_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af72 | 3SA4_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af69 | 3SA5_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af71 | 3SA6_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af55 | 3SA7_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with kb83 | 3SA8_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af68 | 3SA9_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af77 | 3SAA_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af78 | 3SAB_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with af80 | 3SAC_A |
AA | A02.001 | HIV-1 retropepsin | complex with TL-3-093 inhibitor | 3TLH |
AA | A02.001 | HIV-1 retropepsin | South African wild type subtype c | 3U71_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with mkp56 | 4DJO_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with mkp73 | 4DJP_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with mkp86 | 4DJQ_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with mkp97 | 4DJR_A |
AA | A02.001 | HIV-1 retropepsin | hiv protease (pr) dimer with acetate in exo site and peptide in activesite | 4E43_A |
AA | A02.001 | HIV-1 retropepsin | apo hiv protease (pr) dimer in closed form with fragment 1f1 in the outside/top of flap | 4EJ8_A |
AA | A02.001 | HIV-1 retropepsin | dimer in closed form with pepstatin in active site and fragment 1f1 in the outside/top of flap | 4EJD_A |
AA | A02.001 | HIV-1 retropepsin | dimer in closed form with pepstatin in active site and fragment 1f1-n in the outside/top of flap | 4EJK_A |
AA | A02.001 | HIV-1 retropepsin | apo hiv protease (pr) dimer in closed form with fragment 1f1-n in the outside/top of flap | 4EJL_A |
AA | A02.001 | HIV-1 retropepsin | inactive single chain wild-type; complex with the substrate rt-rh | 4EP2_A |
AA | A02.001 | HIV-1 retropepsin | inactive single chain wild-type; complex with the substrate rt-rh | 4EP2_B |
AA | A02.001 | HIV-1 retropepsin | inactive single chain variant; complex with the substrate ca-p2 | 4EP3_A |
AA | A02.001 | HIV-1 retropepsin | inactive single chain variant; complex with the substrate p2-nc | 4EPJ_A |
AA | A02.001 | HIV-1 retropepsin | inactive single chain variant; complex with the substrate p2-nc | 4EQ0_A |
AA | A02.001 | HIV-1 retropepsin | inactive single chain variant; complex with the substrate rt-rh | 4EQJ_A |
AA | A02.001 | HIV-1 retropepsin | inactive single chain variant; complex with the substrate rt-rh | 4EQJ_G |
AA | A02.001 | HIV-1 retropepsin | complex with the n terminal product of ca-p2 cleavage site | 4F73_A |
AA | A02.001 | HIV-1 retropepsin | complex with the n terminal product of the substrate ma-ca. | 4F74_A |
AA | A02.001 | HIV-1 retropepsin | complex with the n terminal product of the substrate rh-in | 4F75_A |
AA | A02.001 | HIV-1 retropepsin | complex with the products of p1-p6 substrate | 4F76_A |
AA | A02.001 | HIV-1 retropepsin | complex with N-Ac-Thr-Ile-Nle-PSI(CH2-NH)-Nle-Gln-Arg amide | 4HVP |
AA | A02.001 | HIV-1 retropepsin | tl-3 inhibited trp6ala hiv protease | 4K4P_A |
AA | A02.001 | HIV-1 retropepsin | tl-3 inhibited trp6ala hiv protease with 3-bromo-2,6-dimethoxybenzoic acid bound in flap site ***caveat 4k4q chirality error on c10 center of 3tl 108 a | 4K4Q_A |
AA | A02.001 | HIV-1 retropepsin | tl-3 inhibited trp6ala hiv protease with 1-bromo-2-napthoic acid boundin exosite | 4K4R_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with novel tricyclic p2-ligands GRL-0739a | 4KB9_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with darunavir | 4LL3_A |
AA | A02.001 | HIV-1 retropepsin | gs-8374, a novel phosphonate-containing inhibitor of hiv-1 protease, effectively inhibits hiv pr mutants with amino acid insertions | 4M8X_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with non-peptidic inhibitor, GRL008 | 4NJS_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with darunavir | 4NJT_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with tipranavir | 4NJU_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with ritonavir | 4NJV_A |
AA | A02.001 | HIV-1 retropepsin | nelfinavir-resistant, inactive Asp30Asn/Asn88Asp; complex with the p1-p6 substrate variant (Leu449Phe/Ser451Asn) | 4OBD_A |
AA | A02.001 | HIV-1 retropepsin | nelfinavir-resistant, inactive Asp30Asn/Asn88Asp; complex with the p1-p6 substrate variant (Ser451Asn) | 4OBF_A |
AA | A02.001 | HIV-1 retropepsin | nelfinavir-resistant, inactive Asp30Asn/Asn88Asp; complex with the p1-p6 substrate. | 4OBG_A |
AA | A02.001 | HIV-1 retropepsin | complex with N,N-bis(2(R)-hydroxy-1(S)-indanyl)-2,6-(R,R)-diphenylmethyl-4-hydroxy-1,7,-heptandiamide | 4PHV |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with non-peptidic inhibitor, GRL0519 | 4RVI_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with amprenavir | 4RVJ_A |
AA | A02.001 | HIV-1 retropepsin | multidrug-resistant clinical isolate; complex with non-peptidic inhibitor, GRL079 | 4RVX_A |
AA | A02.001 | HIV-1 retropepsin | dimer in closed form with pepstatin in active site and fragment ak-2097 in the outside/top of flap | 4TVG_A |
AA | A02.001 | HIV-1 retropepsin | hiv protease (pr) dimer in closed form with tl-3 in active site and fragment ak-2097 in the outside/top of flap ***caveat 4tvh chiral center atom c10 of 3tl a 200 has sp2 hybridization ***caveat 2 4tvh instead of sp3 | 4TVH_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-050-10a (a gem-difluoro-bis- tetrahydrofuran as p2-ligand) | 4U8W_A |
AA | A02.001 | HIV-1 retropepsin | multidrug resistant clinical isolate pr20; complex with inhibitor GRL-4410a | 4YE3_A |
AA | A02.001 | HIV-1 retropepsin | multidrug resistant clinical isolate pr20; complex with inhibitor GRL-5010a | 4YHQ_A |
AA | A02.001 | HIV-1 retropepsin | multidrug resistant clinical isolate pr20d25n with open flap | 4Z4X_A |
AA | A02.001 | HIV-1 retropepsin | crystal structure of multidrug resistant hiv-1 protease clinical isolate pr20d25n with tucked flap | 4Z50_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-0648a (a isophthalamide-derived p2- ligand) | 4ZIP_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-096-13a (a boc-derivative p2-ligand,3,-5-dimethylbiphenyl p1-ligand) | 4ZLS_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-011-11a (a methylamine bis- tetrahydrofuran p2-ligand, sulfonamide isostere derivate) | 5BRY_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-047-11a (a methylamine bis- tetrahydrofuran p2-ligand, 4-amino sulfonamide derivative) | 5BS4_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor GRL-004-11a containing substituted fused-tetrahydropyranyl tetrahydrofuran as P2-ligand | 5DGU_A |
AA | A02.001 | HIV-1 retropepsin | complex with inhibitor GRL-105-11a containing substituted fused-tetrahydropyranyl tetrahydrofuran as p2-ligand | 5DGW_A |
AA | A02.001 | HIV-1 retropepsin | triple mutant (Val32Ile/Ile47Val/Val82Ile); complex with darunavir at ph 6.0 | 5E5J_A |
AA | A02.001 | HIV-1 retropepsin | complex with acetyl-pepstatin | 5HVP |
AA | A02.001 | HIV-1 retropepsin | complex with methyl n-[(1s)-1- benzhydryl-2-(3-morpholin-4-ium-2-ylpropylamino)-2-oxo- ethyl]carbamate | 5IVQ_A |
AA | A02.001 | HIV-1 retropepsin | complex with methyl n-[(1s)-1-[[2-[(3s)-3-[(4-aminophenyl)methylamino]-4-hydroxy- butyl]phenyl]carbamoyl]-2,2-diphenyl-ethyl]carbamate | 5IVR_A |
AA | A02.001 | HIV-1 retropepsin | complex with methyl n-[(1s)-1- benzhydryl-2-[2-[2-[(2r,5s)-5-(benzylcarbamoyloxymethyl)morpholin-2- yl]ethyl]anilino]-2-oxo-ethyl]carbamate | 5IVS_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL- 10413 | 5KAO_A |
AA | A02.001 | HIV-1 retropepsin | Val32Ile/Ile47Val/Val82Ile mutant; complex with amprenavir at ph 6.0 | 5T8H_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-09510 | 5V4Y_A |
AA | A02.001 | HIV-1 retropepsin | hiv protease (pr) with tl-3 in active site and 4-methylbenzene-1,2- diamine in exosite | 5VEA_A |
AA | A02.001 | HIV-1 retropepsin | hiv protease (pr) in open form with mg2+ in active site and hive-9 in eye site | 5VJ3_A |
AA | A02.001 | HIV-1 retropepsin | hiv protease (pr) in open form with mg2+ in active site and hive-9 in eye site | 5W5W_A |
AA | A02.001 | HIV-1 retropepsin | complex with (s)-n-(3-fluoro-2-(2-(1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3-bis(4- fluorophenyl)propanamide | 6B36_A |
AA | A02.001 | HIV-1 retropepsin | complex with n-(3-fluoro-2-(2- ((2s,6r)-6-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3-bis(4-fluorophenyl)propanamide | 6B38_A |
AA | A02.001 | HIV-1 retropepsin | complex with n-(3-fluoro-2-(2- ((2s,6r)-6-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3-bis(4-fluorophenyl)propanamide | 6B3C_A |
AA | A02.001 | HIV-1 retropepsin | complex with n-(3-fluoro-2-(2- ((2s,5s)-5-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3-bis(4-fluorophenyl)propanamide | 6B3F_A |
AA | A02.001 | HIV-1 retropepsin | complex with n-(3-fluoro-2-(2- ((2s,6s)-6-methyl-1-(phenylsulfonyl)piperazin-2-yl)ethyl)phenyl)-3,3-bis(4-fluorophenyl)propanamide | 6B3G_A |
AA | A02.001 | HIV-1 retropepsin | complex with n-(2-(2-((6r,9s)-2,2-dioxido-2-thia-1,7-diazabicyclo[4.3.1]decan-9-yl)ethyl)-3- fluorophenyl)-3,3-bis(4-fluorophenyl)propanamide | 6B3H_A |
AA | A02.001 | HIV-1 retropepsin | nl4-3 wt; complex with darunavir | 6DGX_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 wt; complex with umass1 | 6DGY_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 wt; complex with umass6 | 6DGZ_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 v82i mutant; complex with darunavir | 6DH3_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 Val82Ile mutant; complex with umass1 | 6DH4_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 Val82Ile mutant; complex with umass6 | 6DH5_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 i50v mutant; complex with darunavir | 6DH6_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 Ile50Val mutant; complex with umass1 | 6DH7_B |
AA | A02.001 | HIV-1 retropepsin | nl4-3 Ile50Val mutant; complex with umass6 | 6DH8_B |
AA | A02.001 | HIV-1 retropepsin | wild-type hiv-1 protease in complex with tipranavir | 6DIF_A |
AA | A02.001 | HIV-1 retropepsin | Leu76Val mutant; complex with tipranavir | 6DIL_A |
AA | A02.001 | HIV-1 retropepsin | wild-type; complex with lopinavir | 6DJ1_A |
AA | A02.001 | HIV-1 retropepsin | Leu76Val mutant; complex with lopinavir | 6DJ2_A |
AA | A02.001 | HIV-1 retropepsin | Leu76Val mutant; complex with GRL-0519 (tris- tetrahydrofuran as p2 ligand) | 6DJ5_A |
AA | A02.001 | HIV-1 retropepsin | Leu76Val mutant; complex with GRL-5010 (gem- difluoro-bis-tetrahydrofuran as p2 ligand) | 6DJ7_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-02815a, a thiochroman heterocycle with (s)-boc-amine functionality as the p2 ligand | 6DV0_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-04315a, a tetrahydronaphthalene carboxamide with (r)-boc-amine and (s)-hydroxyl functionalities as the p2 ligand | 6DV4_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-042-17a, 3-phenylhexahydro-2h- cyclopenta[d]oxazol-2-one with a bicyclic oxazolidinone scaffold as the p2 ligand | 6E7J_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-034-17a, (3as, 5r, 6ar)-2-oxohexahydcyclopenta[d]-5-oxazolyl urethane with a bicyclic oxazolidinone scaffas the p2 ligand | 6E9A_A |
AA | A02.001 | HIV-1 retropepsin | complex with bpi-11 | 6IXD_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-001 | 6MCR_A |
AA | A02.001 | HIV-1 retropepsin | wild type; complex with GRL-003 | 6MCS_A |
AA | A02.001 | HIV-1 retropepsin | wild-type hiv-1 protease in complex with a substrate analog ca-p2 | 6O48_A |
AA | A02.001 | HIV-1 retropepsin | Val32Ile/Ile47Val/Val82Ile mutant; complex with GRL-011-11a (a methylamine bis-tetrahydrofuran p2-ligand, sulfonamide isostere derivate) | 6OTG_A |
AA | A02.001 | HIV-1 retropepsin | complex with ACE-Ser-Leu-Asn-Phe-PSI(CH(OH)-CH2)-Pro-Ile-Val-OME | 7HVP |
AA | A02.001 | HIV-1 retropepsin | complex with U101935 | 7UPJ |
AA | A02.001 | HIV-1 retropepsin | complex with Val-Ser-Gln-Asn-Leu-PSI(CH(OH)-CH2)-Val-Ile-Val | 8HVP |
AA | A02.001 | HIV-1 retropepsin | complex with A-74704l | 9HVP |
AA | A02.002 | HIV-2 retropepsin | complex with inhibitor CGP 53820 | 1HII |
AA | A02.002 | HIV-2 retropepsin | 1HSH | |
AA | A02.002 | HIV-2 retropepsin | 1HSI | |
AA | A02.002 | HIV-2 retropepsin | complex with BILA 1906 | 1IDA |
AA | A02.002 | HIV-2 retropepsin | complex with BILA 2450 | 1IDB |
AA | A02.002 | HIV-2 retropepsin | Lys57Leu mutant; complex with NOA-His-CHA-PSI[CH(OH)CH(OH)]Val-Ile-APY | 1IVP |
AA | A02.002 | HIV-2 retropepsin | Lys57Leu mutant; complex with QNC-Asn-CHA-PSI[CH(OH)CH(OH)]Val-NPT | 1IVQ |
AA | A02.002 | HIV-2 retropepsin | complex with inhibitor containing an (hydroxyethyl) amide isostere | 1JLD |
AA | A02.002 | HIV-2 retropepsin | theoretical model; complex with N-ac-Val-Val-Sta-Ala-Sta | 1PHV |
AA | A02.002 | HIV-2 retropepsin | Lys57Leu mutant | 2HPE |
AA | A02.002 | HIV-2 retropepsin | Lys57Leu mutant | 2HPF |
AA | A02.002 | HIV-2 retropepsin | complex with Phe-Val-Phe-PSI(CH2NH)-Leu-Glu-Ile amide inhibitor | 2MIP |
AA | A02.002 | HIV-2 retropepsin | theoretical model; complex with renin inhibitor H261 | 2PHV |
AA | A02.002 | HIV-2 retropepsin | complex with clinical drug darunavir | 3EBZ_A |
AA | A02.002 | HIV-2 retropepsin | complex with antiviral inhibitor GRL-06579a | 3EC0_A |
AA | A02.002 | HIV-2 retropepsin | complex with antiviral inhibitor GRL-98065 | 3ECG_A |
AA | A02.002 | HIV-2 retropepsin | wild-type; complex with antiviral drug amprenavir | 3S45_A |
AA | A02.002 | HIV-2 retropepsin | complex with U096333 | 3UPJ |
AA | A02.002 | HIV-2 retropepsin | complex with U097410 | 4UPJ |
AA | A02.002 | HIV-2 retropepsin | complex with U99283 | 5UPJ |
AA | A02.002 | HIV-2 retropepsin | complex with U99294 | 6UPJ |
AA | A02.004 | equine infectious anaemia virus retropepsin | theoretical model | 1EQI |
AA | A02.004 | equine infectious anaemia virus retropepsin | complex with inhibitor HBY-793 | 1FMB |
AA | A02.004 | equine infectious anaemia virus retropepsin | complex with inhibitor LP-130 | 2FMB |
AA | A02.005 | bovine immunodeficiency virus retropepsin | 3KKR | |
AA | A02.005 | bovine immunodeficiency virus retropepsin | 3KKS | |
AA | A02.006 | Visna lentivirus-type retropepsin | 3HPG | |
AA | A02.006 | Visna lentivirus-type retropepsin | 3HPH | |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with TL-3-093 inhibitor | 1B11 |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with acAla-Val-Sta-Glu-Ala-NH2 | 1FIV |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with Ac-naphylAla-Val-Sta-Glu-naphthylaminoAla substrate | 2FIV |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with tl-3 | 2HAH_A |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with Ac-naphthylAla-Val-Leu-Ala-Glu-naphthylaminoAla substrate | 3FIV |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with darunavir | 3OGP_A |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with lopinavir | 3OGQ_A |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with LP-130 inhibitor | 4FIV |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with TL-3-093 inhibitor | 5FIV |
AA | A02.007 | feline immunodeficiency virus retropepsin | complex with TL-3-093 inhibitor | 6FIV |
AA | A02.008 | murine leukemia virus-type retropepsin | 1D0E | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1D1U | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1I6J | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1MML | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1N4L | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1NND | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1QAI | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1QAJ | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1ZTT | |
AA | A02.008 | murine leukemia virus-type retropepsin | 1ZTW | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FJV | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FJW | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FJX | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FVP | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FVQ | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FVR | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2FVS | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2HB5 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2M9U | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2MQV | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2MS0 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2MS1 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2R2R | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2R2S | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2R2T | |
AA | A02.008 | murine leukemia virus-type retropepsin | 2R2U | |
AA | A02.008 | murine leukemia virus-type retropepsin | 3FSI | |
AA | A02.008 | murine leukemia virus-type retropepsin | 3NNQ | |
AA | A02.008 | murine leukemia virus-type retropepsin | peptidase domain only; complex with TL-3 | 3SLZ |
AA | A02.008 | murine leukemia virus-type retropepsin | peptidase domain only; complex with pepstatin | 3SM1 |
AA | A02.008 | murine leukemia virus-type retropepsin | peptidase domain only; complex with amprenavir | 3SM2 |
AA | A02.008 | murine leukemia virus-type retropepsin | complex with acetyl-pepstatin | 4EXH_A |
AA | A02.008 | murine leukemia virus-type retropepsin | 4M94 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4M95 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4MH8 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4NZG | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4XO0 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4XPC | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4XPE | |
AA | A02.008 | murine leukemia virus-type retropepsin | 3NR6_A | |
AA | A02.008 | murine leukemia virus-type retropepsin | 3P1G | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4E89 | |
AA | A02.008 | murine leukemia virus-type retropepsin | 4HKQ | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 1NSO | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 2D4L | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 2D4M | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 2D4N | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 3SQF | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 3TP1 | |
AA | A02.009 | Mason-Pfizer leukemia virus retropepsin | 3TPW | |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | 2B7F | |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with the inhibitor, kni- 10562 | 3LIN_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with the inhibitor, kni- 10673 | 3LIQ_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with the inhibitor kni-10681 | 3LIT_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with the inhibitor kni- 10683 | 3LIV_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with the inhibitor kni- 10729 | 3LIX_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with statine-containing peptide inhibitor | 3LIY_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with the hiv-1 protease inhibitor indinavir | 3WSJ_A |
AA | A02.012 | retropepsin (human T-cell leukemia virus) | complex with compound 9 | 4YDF_A |
AA | A02.013 | bovine leukemia virus retropepsin | 2IM6 | |
AA | A02.013 | bovine leukemia virus retropepsin | 2IM7 | |
AA | A02.015 | Rous sarcoma virus retropepsin | NMR structure | 1A6S |
AA | A02.015 | Rous sarcoma virus retropepsin | complex with Arg-Val-Leu-Phe-Glu-Ala-norLeu-NH2 inhibitor | 1BAI |
AA | A02.015 | Rous sarcoma virus retropepsin | 1EM9 | |
AA | A02.015 | Rous sarcoma virus retropepsin | 1EOQ | |
AA | A02.015 | Rous sarcoma virus retropepsin | 1P7N | |
AA | A02.015 | Rous sarcoma virus retropepsin | 2IHX | |
AA | A02.015 | Rous sarcoma virus retropepsin | 2RSP_B | |
AA | A02.015 | Rous sarcoma virus retropepsin | 2X8Q | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G0V | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G1G | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G1I | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G21 | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G26 | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G28 | |
AA | A02.015 | Rous sarcoma virus retropepsin | 3G29 | |
AA | A02.015 | Rous sarcoma virus retropepsin | 5A9E | |
AA | A02.018 | simian T-cell lymphotropic virus retropepsin | 1JVR | |
AA | A02.022 | Ty3 transposon peptidase | 4OL8 | |
AA | A02.UPA | subfamily A2A unassigned peptidases | open conformation | 1AZ5 |
AA | A02.UPA | subfamily A2A unassigned peptidases | 1C6V | |
AA | A02.UPA | subfamily A2A unassigned peptidases | 1ECW | |
AA | A02.UPA | subfamily A2A unassigned peptidases | 1ED1 | |
AA | A02.UPA | subfamily A2A unassigned peptidases | 1SIP | |
AA | A02.UPA | subfamily A2A unassigned peptidases | complex with SKF107457 | 1SIV |
AA | A02.UPA | subfamily A2A unassigned peptidases | complex with SB203386 | 1TCW |
AA | A02.UPA | subfamily A2A unassigned peptidases | complex with Phe-Leu-Glu-Lys peptide product | 1YTI |
AA | A02.UPA | subfamily A2A unassigned peptidases | complex with p-nitroPhe-Glu-Ala-norLeu-Ser peptide product | 1YTJ |
AA | A02.UPA | subfamily A2A unassigned peptidases | mutant Ser4His | 2SAM |
AA | A02.UPA | subfamily A2A unassigned peptidases | 3JTS | |
AA | A02.UPW | family A2 unassigned peptidases | 1MVP | |
AA | A02.UPW | family A2 unassigned peptidases | theoretical model | 2MVP |
AA | A02.UPW | family A2 unassigned peptidases | 1BV7_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1BV9_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1BVE_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1BVG_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1BWA_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1BWB_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1C0T | |
AA | A02.UPW | family A2 unassigned peptidases | 1C0U | |
AA | A02.UPW | family A2 unassigned peptidases | 1C1B | |
AA | A02.UPW | family A2 unassigned peptidases | 1C1C | |
AA | A02.UPW | family A2 unassigned peptidases | 1DMP_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1DTQ | |
AA | A02.UPW | family A2 unassigned peptidases | 1DTT | |
AA | A02.UPW | family A2 unassigned peptidases | 1E6J | |
AA | A02.UPW | family A2 unassigned peptidases | 1EP4 | |
AA | A02.UPW | family A2 unassigned peptidases | 1ESK | |
AA | A02.UPW | family A2 unassigned peptidases | 1EX4 | |
AA | A02.UPW | family A2 unassigned peptidases | 1EXQ | |
AA | A02.UPW | family A2 unassigned peptidases | Val48Gly, Met90Leu mutant; complex with saquinavir | 1FB7 |
AA | A02.UPW | family A2 unassigned peptidases | 1FK9 | |
AA | A02.UPW | family A2 unassigned peptidases | 1FKO | |
AA | A02.UPW | family A2 unassigned peptidases | 1FKP | |
AA | A02.UPW | family A2 unassigned peptidases | 1G6L_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1HIV_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1HVH_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1HVR_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1HWR_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1HXB_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1JKH | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLA | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLB | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLC | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLE | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLF | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLG | |
AA | A02.UPW | family A2 unassigned peptidases | 1JLQ | |
AA | A02.UPW | family A2 unassigned peptidases | 1KLM | |
AA | A02.UPW | family A2 unassigned peptidases | 1LV1_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1LW0 | |
AA | A02.UPW | family A2 unassigned peptidases | 1LW2 | |
AA | A02.UPW | family A2 unassigned peptidases | 1LWC | |
AA | A02.UPW | family A2 unassigned peptidases | 1LWE | |
AA | A02.UPW | family A2 unassigned peptidases | 1LWF | |
AA | A02.UPW | family A2 unassigned peptidases | 1NCP_N | |
AA | A02.UPW | family A2 unassigned peptidases | 1O1W | |
AA | A02.UPW | family A2 unassigned peptidases | 1ODW_A | |
AA | A02.UPW | family A2 unassigned peptidases | complex with inhibitor LP-130 | 1ODY |
AA | A02.UPW | family A2 unassigned peptidases | 1QBR_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1QBS_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1QBT_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1QBU_A | |
AA | A02.UPW | family A2 unassigned peptidases | 1REV | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT1 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT2 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT3 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT4 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT5 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT6 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RT7 | |
AA | A02.UPW | family A2 unassigned peptidases | 1RTD | |
AA | A02.UPW | family A2 unassigned peptidases | 1RTH | |
AA | A02.UPW | family A2 unassigned peptidases | 1RTI | |
AA | A02.UPW | family A2 unassigned peptidases | 1RTJ | |
AA | A02.UPW | family A2 unassigned peptidases | 1S1T | |
AA | A02.UPW | family A2 unassigned peptidases | 1S1U | |
AA | A02.UPW | family A2 unassigned peptidases | 1S1V | |
AA | A02.UPW | family A2 unassigned peptidases | 1S1W | |
AA | A02.UPW | family A2 unassigned peptidases | 1S1X | |
AA | A02.UPW | family A2 unassigned peptidases | 1T05 | |
AA | A02.UPW | family A2 unassigned peptidases | 1TAM | |
AA | A02.UPW | family A2 unassigned peptidases | 1TKT | |
AA | A02.UPW | family A2 unassigned peptidases | 1TKX | |
AA | A02.UPW | family A2 unassigned peptidases | 1TKZ | |
AA | A02.UPW | family A2 unassigned peptidases | 1TL1 | |
AA | A02.UPW | family A2 unassigned peptidases | 1TL3 | |
AA | A02.UPW | family A2 unassigned peptidases | 1VRT | |
AA | A02.UPW | family A2 unassigned peptidases | 1VRU | |
AA | A02.UPW | family A2 unassigned peptidases | 2HND | |
AA | A02.UPW | family A2 unassigned peptidases | 2HNY | |
AA | A02.UPW | family A2 unassigned peptidases | 2HNZ | |
AA | A02.UPW | family A2 unassigned peptidases | 2KOD | |
AA | A02.UPW | family A2 unassigned peptidases | 2NPH | |
AA | A02.UPW | family A2 unassigned peptidases | 2OPP | |
AA | A02.UPW | family A2 unassigned peptidases | 2OPQ | |
AA | A02.UPW | family A2 unassigned peptidases | 2OPR | |
AA | A02.UPW | family A2 unassigned peptidases | 2OPS | |
AA | A02.UPW | family A2 unassigned peptidases | 2RF2 | |
AA | A02.UPW | family A2 unassigned peptidases | 2RKI | |
AA | A02.UPW | family A2 unassigned peptidases | 2WHH | |
AA | A02.UPW | family A2 unassigned peptidases | 2WOM | |
AA | A02.UPW | family A2 unassigned peptidases | 2WON | |
AA | A02.UPW | family A2 unassigned peptidases | 2YNF | |
AA | A02.UPW | family A2 unassigned peptidases | 2YNG | |
AA | A02.UPW | family A2 unassigned peptidases | 2YNH | |
AA | A02.UPW | family A2 unassigned peptidases | 2YNI | |
AA | A02.UPW | family A2 unassigned peptidases | 3AO2 | |
AA | A02.UPW | family A2 unassigned peptidases | 3C6T | |
AA | A02.UPW | family A2 unassigned peptidases | 3C6U | |
AA | A02.UPW | family A2 unassigned peptidases | 3DI6 | |
AA | A02.UPW | family A2 unassigned peptidases | 3DLE | |
AA | A02.UPW | family A2 unassigned peptidases | 3DLG | |
AA | A02.UPW | family A2 unassigned peptidases | 3DM2 | |
AA | A02.UPW | family A2 unassigned peptidases | 3DMJ | |
AA | A02.UPW | family A2 unassigned peptidases | 3DOK | |
AA | A02.UPW | family A2 unassigned peptidases | 3DOL | |
AA | A02.UPW | family A2 unassigned peptidases | 3DOX | |
AA | A02.UPW | family A2 unassigned peptidases | 3DRP | |
AA | A02.UPW | family A2 unassigned peptidases | 3DRR | |
AA | A02.UPW | family A2 unassigned peptidases | 3DRS | |
AA | A02.UPW | family A2 unassigned peptidases | 3DYA | |
AA | A02.UPW | family A2 unassigned peptidases | 3E01 | |
AA | A02.UPW | family A2 unassigned peptidases | 3FFI | |
AA | A02.UPW | family A2 unassigned peptidases | 3I0R | |
AA | A02.UPW | family A2 unassigned peptidases | 3I0S | |
AA | A02.UPW | family A2 unassigned peptidases | 3KJV | |
AA | A02.UPW | family A2 unassigned peptidases | 3KK1 | |
AA | A02.UPW | family A2 unassigned peptidases | 3KK2 | |
AA | A02.UPW | family A2 unassigned peptidases | 3KK3 | |
AA | A02.UPW | family A2 unassigned peptidases | 3KT2 | |
AA | A02.UPW | family A2 unassigned peptidases | 3KT5 | |
AA | A02.UPW | family A2 unassigned peptidases | 3LAK | |
AA | A02.UPW | family A2 unassigned peptidases | 3LAL | |
AA | A02.UPW | family A2 unassigned peptidases | 3LAM | |
AA | A02.UPW | family A2 unassigned peptidases | 3LAN | |
AA | A02.UPW | family A2 unassigned peptidases | 3LP0 | |
AA | A02.UPW | family A2 unassigned peptidases | 3LP1 | |
AA | A02.UPW | family A2 unassigned peptidases | 3LP2 | |
AA | A02.UPW | family A2 unassigned peptidases | 3M8P | |
AA | A02.UPW | family A2 unassigned peptidases | 3M8Q | |
AA | A02.UPW | family A2 unassigned peptidases | 3MEC | |
AA | A02.UPW | family A2 unassigned peptidases | 3MED | |
AA | A02.UPW | family A2 unassigned peptidases | 3MEE | |
AA | A02.UPW | family A2 unassigned peptidases | 3MEG | |
AA | A02.UPW | family A2 unassigned peptidases | 3MIM | |
AA | A02.UPW | family A2 unassigned peptidases | 3N3I | |
AA | A02.UPW | family A2 unassigned peptidases | 3NBP | |
AA | A02.UPW | family A2 unassigned peptidases | 3PHV_A | |
AA | A02.UPW | family A2 unassigned peptidases | 3QIN | |
AA | A02.UPW | family A2 unassigned peptidases | 3QIO | |
AA | A02.UPW | family A2 unassigned peptidases | 3QIP | |
AA | A02.UPW | family A2 unassigned peptidases | 3T19 | |
AA | A02.UPW | family A2 unassigned peptidases | 3T1A | |
AA | A02.UPW | family A2 unassigned peptidases | 3TAM | |
AA | A02.UPW | family A2 unassigned peptidases | 4B3O | |
AA | A02.UPW | family A2 unassigned peptidases | 4B3P | |
AA | A02.UPW | family A2 unassigned peptidases | 4B3Q | |
AA | A02.UPW | family A2 unassigned peptidases | 4I7F | |
AA | A02.UPW | family A2 unassigned peptidases | 4KSE | |
AA | A02.UPW | family A2 unassigned peptidases | 4KV8 | |
AA | A02.UPW | family A2 unassigned peptidases | 4NCG | |
AA | A02.UPW | family A2 unassigned peptidases | 4Q1W | |
AA | A02.UPW | family A2 unassigned peptidases | 4Q1X | |
AA | A02.UPW | family A2 unassigned peptidases | 4Q1Y | |
AA | A02.UPW | family A2 unassigned peptidases | 4Q5M | |
AA | A02.UPW | family A2 unassigned peptidases | 4QLH | |
AA | A02.UPW | family A2 unassigned peptidases | 4U1H | |
AA | A02.UPW | family A2 unassigned peptidases | 4U1I | |
AA | A02.UPW | family A2 unassigned peptidases | 4U1J | |
AA | A02.UPW | family A2 unassigned peptidases | 4U7Q | |
AA | A02.UPW | family A2 unassigned peptidases | 4U7V | |
AA | A02.UPW | family A2 unassigned peptidases | x-ray snapshot of hiv-1 protease in action: observation of tetrahedralintermediate and its sihb with catalytic aspartate | 5YRS_A |
AC | A08.UPW | family A8 unassigned peptidases | 5DIR | |
AC | A08.UPW | family A8 unassigned peptidases | imisx-ep of se-lspa | 6FMS_A |
AA | A09.001 | spumapepsin | 2LSN | |
AA | A09.001 | spumapepsin | 2X6N | |
AA | A09.001 | spumapepsin | 2X6S | |
AA | A09.001 | spumapepsin | 2X74 | |
AA | A09.001 | spumapepsin | 2X78 | |
AA | A09.001 | spumapepsin | 3DLR | |
AA | A09.001 | spumapepsin | 3L2Q | |
AA | A09.001 | spumapepsin | 3L2R | |
AA | A09.001 | spumapepsin | 3L2U | |
AA | A09.001 | spumapepsin | 3L2V | |
AA | A09.001 | spumapepsin | 3L2W | |
AA | A09.001 | spumapepsin | 3OS0 | |
AA | A09.001 | spumapepsin | 3OS1 | |
AA | A09.001 | spumapepsin | 3OS2 | |
AA | A09.001 | spumapepsin | 3OY9 | |
AA | A09.001 | spumapepsin | 3OYA | |
AA | A09.001 | spumapepsin | 3OYB | |
AA | A09.001 | spumapepsin | 3OYC | |
AA | A09.001 | spumapepsin | 3OYD | |
AA | A09.001 | spumapepsin | 3OYE | |
AA | A09.001 | spumapepsin | 3OYF | |
AA | A09.001 | spumapepsin | 3OYG | |
AA | A09.001 | spumapepsin | 3OYH | |
AA | A09.001 | spumapepsin | 3OYI | |
AA | A09.001 | spumapepsin | 3OYJ | |
AA | A09.001 | spumapepsin | 3OYK | |
AA | A09.001 | spumapepsin | 3OYL | |
AA | A09.001 | spumapepsin | 3OYM | |
AA | A09.001 | spumapepsin | 3OYN | |
AA | A09.001 | spumapepsin | 3S3M | |
AA | A09.001 | spumapepsin | 3S3N | |
AA | A09.001 | spumapepsin | 3S3O | |
AA | A09.001 | spumapepsin | 4BAC | |
AA | A09.001 | spumapepsin | 4BDY | |
AA | A09.001 | spumapepsin | 4BDZ | |
AA | A09.001 | spumapepsin | 4BE0 | |
AA | A09.001 | spumapepsin | 4BE1 | |
AA | A09.001 | spumapepsin | 4BE2 | |
AA | A09.001 | spumapepsin | 4E7H | |
AA | A09.001 | spumapepsin | 4E7I | |
AA | A09.001 | spumapepsin | 4E7J | |
AA | A09.001 | spumapepsin | 4E7K | |
AA | A09.001 | spumapepsin | 4E7L | |
AA | A09.001 | spumapepsin | 4IKF | |
AA | A09.001 | spumapepsin | 4ZTF | |
AA | A09.001 | spumapepsin | 4ZTJ | |
AA | A09.001 | spumapepsin | NMR structure | 2JYS |
AD | A22.001 | presenilin 1 | NMR structure; CTF subunit | 2KR6 |
AD | A22.001 | presenilin 1 | 4UIS | |
AD | A22.001 | presenilin 1 | 5A63 | |
AD | A22.001 | presenilin 1 | 5FN2 | |
AD | A22.001 | presenilin 1 | 5FN3 | |
AD | A22.001 | presenilin 1 | 5FN4 | |
AD | A22.001 | presenilin 1 | 5FN5 | |
AD | A22.001 | presenilin 1 | complex with a notch fragment | 6IDF_B |
AD | A22.001 | presenilin 1 | recognition of the amyloid precursor protein by human gamma-secretase | 6IYC_B |
AD | A22.007 | signal peptide peptidase-like protein 2A | 2FC7 | |
AD | A22.007 | signal peptide peptidase-like protein 2A | 2YUM | |
AD | A22.015 | intramembrane aspartyl peptidase (Methanoculleus marisnigri JR1) | 4HYC | |
AD | A22.015 | intramembrane aspartyl peptidase (Methanoculleus marisnigri JR1) | 4HYD | |
AD | A22.015 | intramembrane aspartyl peptidase (Methanoculleus marisnigri JR1) | 4HYG | |
AD | A22.015 | intramembrane aspartyl peptidase (Methanoculleus marisnigri JR1) | complex with an inhibitor | 4Y6K_A |
AD | A24.016 | FlaK peptidase | 3S0X | |
AE | A25.001 | gpr peptidase | precursor | 1C8B_A |
AF | A26.001 | omptin | 1I78_A | |
AF | A26.003 | plasminogen activator Pla | Ala106Asp mutant | 2X4M |
AF | A26.003 | plasminogen activator Pla | 2X55 | |
AF | A26.003 | plasminogen activator Pla | 2X56 | |
AF | A26.003 | plasminogen activator Pla | 4DCB_A | |
AA | A28.001 | DNA-damage inducible protein 1 | 2I1A | |
AA | A28.001 | DNA-damage inducible protein 1 | 2MR9 | |
AA | A28.001 | DNA-damage inducible protein 1 | 2MRO | |
AA | A28.001 | DNA-damage inducible protein 1 | 2MRP | |
AA | A28.001 | DNA-damage inducible protein 1 | 2MWS | |
AA | A28.001 | DNA-damage inducible protein 1 | 4Z2Z | |
AA | A28.001 | DNA-damage inducible protein 1 | 3S8I_A | |
AA | A28.003 | DNA-damage inducible protein 2 | human dna damage-inducible protein: from protein chemistry and 3d structure to deciphering its cellular role | 4RGH_A |
AA | A28.A01 | gene name 1700011N24Rik (Mus musculus) | NMR structure | 1V5O |
AA | A28.UPA | subfamily A28A unassigned peptidases | protease-like domain | 5YQ8_A |
AA | A28.UPA | subfamily A28A unassigned peptidases | protease-like domain | 5YS4_A |
AE | A31.001 | HybD peptidase | 1CFZ_A | |
AE | A31.001 | HybD peptidase | NMR structure | 2KML |
AE | A31.003 | HycI peptidase | 3PU6_A | |
AE | A31.007 | TK2004 peptidase | 5ZBY | |
AE | A31.008 | TK2066 peptidase | 5IJA | |
AE | A31.UPW | family A31 unassigned peptidases | 5TTX_A | |
AE | A31.UPW | family A31 unassigned peptidases | 2E85_A | |
AA | A32.002 | RC1339 g.p. (Rickettsia conorii) | 5C9B | |
AA | A32.002 | RC1339 g.p. (Rickettsia conorii) | 5C9D | |
AA | A32.002 | RC1339 g.p. (Rickettsia conorii) | 5C9F | |
CA | C01.001 | papain | complex with carbobenzyloxy-Leu-leucinal inhibitor | 1BP4 |
CA | C01.001 | papain | complex with carboxybenzyloxy-Leu-Leu-methoxymethylketone | 1BQI |
CA | C01.001 | papain | complex with inhibitor CLIK148 | 1CVZ |
CA | C01.001 | papain | theoretical model; complex with N-acetyl-p-benzoquinone imine | 1EFF |
CA | C01.001 | papain | complex with Z-Leu-Phe-Gly-diazomethylketone inhibitor | 1KHP |
CA | C01.001 | papain | complex with Z-Leu-Phe-Gly-diazomethylketone inhibitor (orthorhombic form) | 1KHQ |
CA | C01.001 | papain | Cys25Ac-Ala-Ala-Phe-methylenylAla derivative | 1PAD |
CA | C01.001 | papain | complex with E64C | 1PE6 |
CA | C01.001 | papain | complex with Suc-Gln-Vla-Val-Ala-Ala-pNA | 1PIP |
CA | C01.001 | papain | complex with leupeptin | 1POP |
CA | C01.001 | papain | hydroxyethylthiopapain | 1PPD |
CA | C01.001 | papain | Cys25 with bound atom | 1PPN |
CA | C01.001 | papain | complex with E64C | 1PPP |
CA | C01.001 | papain | complex with cystatin B Cys18Ser | 1STF_E |
CA | C01.001 | papain | complex with ICP | 2CIO_A |
CA | C01.001 | papain | cysteinyl derivative of Cys25 | 2PAD |
CA | C01.001 | papain | complex with chagasin | 3E1Z_B |
CA | C01.001 | papain | complex with tarocystatin | 3IMA_A |
CA | C01.001 | papain | complex with CTD of tarocystatin | 3LFY_A |
CA | C01.001 | papain | precursor; thermostable variant | 3TNX_A |
CA | C01.001 | papain | precursor; thermostable variant from a crystal soaked at ph 4 | 3USV_A |
CA | C01.001 | papain | TOS-methylenylLys derivative of Cys25 | 4PAD |
CA | C01.001 | papain | Ile86Leu mutant | 4QRG_A |
CA | C01.001 | papain | Ile86Phe mutant | 4QRV_A |
CA | C01.001 | papain | precursor mutant at ph 4.0 | 4QRX_A |
CA | C01.001 | papain | benzyloxycarbonyl-Gly-Phe-methylenylGly derivative | 5PAD |
CA | C01.001 | papain | modified by achiral ru(ii)complex | 6H8T_A |
CA | C01.001 | papain | benzyloxycarbonyl-Gly-Phe-methylenylGly derivative | 6PAD |
CA | C01.001 | papain | Cys25 oxidized | 9PAP |
CA | C01.002 | chymopapain | 1YAL | |
CA | C01.003 | caricain | theoretical model; Asp158Glu mutant; complex with carbobenzoxy-Phe-3-amino-butan-2-one | 1C7X |
CA | C01.003 | caricain | theoretical model; Asp158Glu mutant in complex with E64c | 1EUX |
CA | C01.003 | caricain | theoretical model; Asp158Glu mutant in complex with leupeptin | 1F1I |
CA | C01.003 | caricain | Asp185Glu mutant; complex with E64 | 1MEG |
CA | C01.003 | caricain | precursor | 1PCI |
CA | C01.003 | caricain | Cys25 with bound mercury | 1PPO |
CA | C01.004 | glycyl endopeptidase | complex with benzyloxycarbonyl-Leu-Val-Gly-methylene bound to Cys25 | 1GEC |
CA | C01.005 | stem bromelain | 1W0Q | |
CA | C01.007 | actinidin | complex with E64 | 1AEC |
CA | C01.007 | actinidin | theoretical model; complex with ZPACK (Z-Phe-Ala-Ala-chloromethyl ketone) | 1F3Q |
CA | C01.007 | actinidin | theoretical model; complex with leupeptin | 1FOG |
CA | C01.007 | actinidin | theoretical model; complex with E64c | 1FTV |
CA | C01.007 | actinidin | 2ACT | |
CA | C01.009 | cathepsin V | complex with 4-methylpiperazin-1-ylcarbonyl-Phe-3-amino-5-phenylpentane inhibitor | 1FH0 |
CA | C01.009 | cathepsin V | complex with clitocypin | 3H6S_A |
CA | C01.010 | vignain | complex with D-Val-Leu-dexoxy-methyl-Lys. | 1S4V_A |
CA | C01.011 | calotropain | 0CDI | |
CA | C01.013 | cathepsin X | precursor | 1DEU |
CA | C01.013 | cathepsin X | 1EF7 | |
CA | C01.017 | zingipain | tetramer | 1CQD |
CA | C01.018 | cathepsin F | theoretical model | 1D5U |
CA | C01.018 | cathepsin F | 1M6D_A | |
CA | C01.024 | endopeptidase-B (Hordeum-type) | isoform 2 (EP-B2); complex with leupeptin | 2FO5_A |
CA | C01.026 | ananain | complex with E-64 | 6MIS_A |
CA | C01.026 | ananain | native ananain from ananas comosus | 6OKJ_A |
CA | C01.032 | cathepsin L | precursor | 1CJL |
CA | C01.032 | cathepsin L | procathepsin L | 1CJL_P |
CA | C01.032 | cathepsin L | precursor | 1CS8_A |
CA | C01.032 | cathepsin L | procathepsin L | 1CS8_P |
CA | C01.032 | cathepsin L | complex with MHC class II associated P41 II fragment | 1ICF_A |
CA | C01.032 | cathepsin L | complex with propeptide-based inhibitor biphenyl-4-yl-acetaldehyde-Cys-D-Arg-Tyr-2-phenylethylamine | 1MHW |
CA | C01.032 | cathepsin L | complex with chagasin | 2NQD_B |
CA | C01.032 | cathepsin L | cathsilicatein, a chimera | 2VHS_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2XU1_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2XU3_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2XU4_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2XU5_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2YJ2_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2YJ8_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2YJ9_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2YJB_A |
CA | C01.032 | cathepsin L | complex with a nitrile inhibitor | 2YJC_A |
CA | C01.032 | cathepsin L | exploring inhibitor binding at the s subsites of cathepsin l | 3BC3_A |
CA | C01.032 | cathepsin L | complex with retro-binding inhibitor compound 4 | 3H89_A |
CA | C01.032 | cathepsin L | complex with retro-binding inhibitor compound 9 | 3H8B_A |
CA | C01.032 | cathepsin L | complex with retro-binding inhibitor compound 14 | 3H8C_A |
CA | C01.032 | cathepsin L | complex with az12878478 | 3HHA_A |
CA | C01.032 | cathepsin L | cathepsin l with az13010160 | 3HWN_A |
CA | C01.032 | cathepsin L | Cys25Ala mutant | 3IV2_A |
CA | C01.032 | cathepsin L | Cys25Ala mutant; complex with Gln-Leu-Ala peptide | 3K24_A |
CA | C01.032 | cathepsin L | complex with dipeptidyl glyoxal and diazomethylketone inhibitors | 3OF8_A |
CA | C01.032 | cathepsin L | complex with adiazomethylketone inhibitor | 3OF9_A |
CA | C01.032 | cathepsin L | human cathepsin l apo form with zn | 4AXL_A |
CA | C01.032 | cathepsin L | triazine cathepsin inhibitor complex | 4AXM_A |
CA | C01.032 | cathepsin L | complex with (2s,4r)-4-(2-chloro-4-methoxy- benzenesulfonyl)-1-[3-(5-chloro-pyridin-2-yl)-azetidine-3-carbonyl]- pyrrolidine-2-carboxylic acid (1-cyano-cyclopropyl)-amide | 5F02_A |
CA | C01.032 | cathepsin L | cleaved cathepsin L bound to the active site of cathepsin L | 5I4H_A |
CA | C01.032 | cathepsin L | complex with (2s,4r)-4-(2-chloro-4-methoxy- benzenesulfonyl)-1-[3-(5-chloro-pyridin-2-yl)-azetidine-3-carbonyl]- pyrrolidine-2-car boxylic acid (1-cyano-cyclopropyl)-amide | 5MAE_A |
CA | C01.032 | cathepsin L | complex with 4-[cyclopentyl(imidazo[1,2-a]pyridin-2- ylmethyl)amino]-6-morpholino-1,3,5-triazine-2-carbonitrile | 5MAJ_A |
CA | C01.032 | cathepsin L | complex with 4-[1,3-benzodioxol-5-ylmethyl(2- phenoxyethyl)amino]-5-fluoropyrimidine-2-carbonitrile | 5MQY_A |
CA | C01.032 | cathepsin L | complex with (3s,14e)-19-chloro-n-(1-cyanocyclopropyl)-5-oxo-12,17-dioxa-4-azatricyclo[16.2.2.06,11]docosa-1(21),6(11),7,9, 14,18(22),19-heptaene-3-carboxamide | 6EZP_A |
CA | C01.032 | cathepsin L | complex with (3s,14e)-19-chloro-n-(1-cyanocyclopropyl)-5-oxo-17-oxa-4-azatricyclo[16.2.2.06,11]docosa-1(21),6,8,10,14, 18(22),19-heptaene-3-carboxamide | 6EZX_A |
CA | C01.032 | cathepsin L | complex with (3s,14e)-8-(azetidin-3-yl)-19-chloro-n-(1-cyanocyclopropyl)-5-oxo-12,17-dioxa-4-azatricyclo[16.2.2.06, 11]docosa-1(21),6,8,10,14,18(22),19-heptaene-3-carboxamide | 6F06_A |
CA | C01.032 | cathepsin L | theoretical model | 1MVV |
CA | C01.033 | cathepsin L1 (Fasciola sp.) | precursor | 2O6X |
CA | C01.034 | cathepsin S | theoretical model | 1BXF |
CA | C01.034 | cathepsin S | Cys25Ser mutant | 1GLO |
CA | C01.034 | cathepsin S | complex with dipeptide nitrile inhibitor BLN | 1MS6 |
CA | C01.034 | cathepsin S | complex with inhibitor C1P | 1NPZ |
CA | C01.034 | cathepsin S | complex with inhibitor C4P | 1NQC |
CA | C01.034 | cathepsin S | precursor Cys25Ala mutant | 2C0Y_A |
CA | C01.034 | cathepsin S | complex with non-covalent 2-(benzoxazol-2- ylamino)-acetamide | 2F1G_A |
CA | C01.034 | cathepsin S | complex with CRA-27934, a nitrile inhibitor | 2FRA_A |
CA | C01.034 | cathepsin S | complex with inhibitor CRA-26871 | 2FRQ_A |
CA | C01.034 | cathepsin S | complex with inhibitor CRA-29728 | 2FT2_A |
CA | C01.034 | cathepsin S | complex with inhibitor CRA-27566 | 2FUD_A |
CA | C01.034 | cathepsin S | complex with irreversible inhibitor CRA-14013 | 2FYE_A |
CA | C01.034 | cathepsin S | complex with vinyl sulfone inhibitor CRA-14009 | 2G6D_A |
CA | C01.034 | cathepsin S | complex with inhibitor CRA-16981 | 2G7Y_A |
CA | C01.034 | cathepsin S | complex with N-[(1S)-1-1-[(1R,3E)-1-acetylpent-3-en-1-yl]-1H-1,2,3-triazol-4-yl-1,2-dimethylpropyl]benzamide | 2H7J_A |
CA | C01.034 | cathepsin S | complex with N-[(1R)-1-[(benzylsulfonyl)methyl]-2-[(1S)-1-methyl-2-[4-(trifluoromethoxy)phenyl]aminoethyl]amino-2-oxoethyl]morpholine-4-carboxamide | 2HH5_A |
CA | C01.034 | cathepsin S | complex with non covalent arylaminoethyl amide. | 2HHN_A |
CA | C01.034 | cathepsin S | complex with N-[(1S)-1-1-[(1R,3E)-1-acetylpent-3-en-1-yl]-1H-1,2,3-triazol-4-yl-1,2-dimethylpropyl]benzamide | 2HXZ_A |
CA | C01.034 | cathepsin S | complex with a novel 2- arylphenoxyacetaldehyde inhibitor derived by the substrate activity screening (sas) method | 2OP3_A |
CA | C01.034 | cathepsin S | complex with compound 15 | 2R9M_A |
CA | C01.034 | cathepsin S | complex with compound 26 | 2R9N_A |
CA | C01.034 | cathepsin S | complex with compound 8 | 2R9O_A |
CA | C01.034 | cathepsin S | complex with a pyrazole-based inhibitor with an arylalkynes as P1 binding element | 3IEJ_A |
CA | C01.034 | cathepsin S | complex with 4-(3-trifluoromethylphenyl)-pyrimidine-2-carbonitrile | 3N3G_A |
CA | C01.034 | cathepsin S | complex with 6-phenyl-1h-imidazo[4,5-c]pyridine-4-carbonitrile | 3N4C_A |
CA | C01.034 | cathepsin S | complex with a covalent inhibitor with an aldehyde warhead | 3OVX_A |
CA | C01.034 | cathepsin S | complex with a non-covalent inhibitor | 4P6E_A |
CA | C01.034 | cathepsin S | complex with a non-covalent inhibitor. | 4P6G_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QBU_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QBV_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QBW_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QBX_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QBY_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QBZ_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC0_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC1_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC2_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC3_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC4_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC5_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC6_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC7_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC8_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QC9_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCA_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCB_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCC_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCE_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCF_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCG_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCH_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCI_A |
CA | C01.034 | cathepsin S | complex with bound ligand | 5QCJ_A |
CA | C01.034 | cathepsin S | theoretical model; precursor | 1M0H |
CA | C01.034 | cathepsin S | 4BPV | |
CA | C01.034 | cathepsin S | 4BQV | |
CA | C01.034 | cathepsin S | 4BS5 | |
CA | C01.034 | cathepsin S | 4BS6 | |
CA | C01.034 | cathepsin S | 4BSQ | |
CA | C01.034 | cathepsin S | 4MZO | |
CA | C01.034 | cathepsin S | 4MZS | |
CA | C01.036 | cathepsin K | complex with E64 | 1ATK |
CA | C01.036 | cathepsin K | complex with a covalent symmetric diacylaminomethyl ketone inhibitor | 1AU0 |
CA | C01.036 | cathepsin K | complex with a covant propanone inhibitor | 1AU2 |
CA | C01.036 | cathepsin K | complex with 1-[N[(phenylmethoxy)carbonyl]-l-leucyl-4-[[N/N-[(phenylmethoxy)carbonyl]-/NL-leucyl]amino]-3-pyrrolidinone | 1AU3 |
CA | C01.036 | cathepsin K | complex with 4-[[N-[(phenylmethoxy)carbonyl]-L-leucyl]amino]-1[(2S)-2-[[[4-(pyridinylmethoxy)carbonyl]amino]-4-methylpentyl]-3-pyrrolidinone | 1AU4 |
CA | C01.036 | cathepsin K | complex with 1,5-bis(N-benzyloxycarbonyl-L-leucinyl)carbohydrazide | 1AYU |
CA | C01.036 | cathepsin K | complex with N-[2-[1-(N-benzyloxycarbonylamino)-3-methylbutyl]thiazol-4-ylcarbonyl]-N'-(benzyloxycarbonyl-L-leucinyl)hydrazide | 1AYV |
CA | C01.036 | cathepsin K | complex with 1-(N-benzyloxycarbonyl-L-leucinyl)-5-(3-benzyloxy benzoyl)carbohydrazide | 1AYW |
CA | C01.036 | cathepsin K | complex with covalent peptidomimetic inhibitor 1-[2-(3-bipheyl)-4-methylvaleryl)]-amino-3-(2-pyridylsulfonyl)amino-2-propanone | 1BGO |
CA | C01.036 | cathepsin K | precursor | 1BY8 |
CA | C01.036 | cathepsin K | Ser149Ala mutant; complex with vinyl sulfone inhibitor | 1MEM |
CA | C01.036 | cathepsin K | complex with covalent azepanone 5-(2-morpholin-4-ylethoxy)benzofuran-2-carboxylic acid ((S)-3-methyl-1-(S)-3-oxo-1-[2-(3-pyridin-2-ylphenyl)acetyl]azepan-4-ylcarbamoylbutyl)amide | 1NL6 |
CA | C01.036 | cathepsin K | complex with covalent azepanone benzofuran-2-carboxylic acid (S)-3-methyl-1-[3-oxo-1-(pyridin-2-ylsulfonyl)azepan-4-ylcarbamoyl]butylamide | 1NLJ |
CA | C01.036 | cathepsin K | complex with T-butyl(1S)-1-cyclohexyl-2- oxoethylcarbamate | 1Q6K_A |
CA | C01.036 | cathepsin K | complex with N2-([(4-bromophenyl)methyl]oxycarbonyl)-N1-[(1S)-1-formylpentyl]-L-leucinamide | 1SNK |
CA | C01.036 | cathepsin K | complex with ketoamide inhibitor [1-(4-fluorobenzyl)cyclobutyl]methyl (1S)-1-[oxo(1h-pyrazol-5-ylamino)acetyl]pentylcarbamate | 1TU6 |
CA | C01.036 | cathepsin K | complex with the covalent inhibitor NVP-ABE854 | 1U9V_A |
CA | C01.036 | cathepsin K | complex with the covalent inhibitor NVP-ABI491 | 1U9W_A |
CA | C01.036 | cathepsin K | complex with the covalent inhibitor NVP-ABJ688 | 1U9X_A |
CA | C01.036 | cathepsin K | complex with N-(2-aminoethyl)-N~2~-(1S)-1-[4'-(aminosulfonyl)biphenyl-4-yl]-2,2,2-trifluoroethyl-L-leucinamide | 1VSN_A |
CA | C01.036 | cathepsin K | complex with cyanopyrrolidine inhibitor N2-[(benzyloxy)carbonyl]-N1-[(3S)-1-cyanopyrrolidin-3-yl]-L-leucinamide | 1YK7 |
CA | C01.036 | cathepsin K | complex with cyanamide-based inhibitor tert-butyl 2-cyano-2-methylhydrazinecarboxylate | 1YK8_A |
CA | C01.036 | cathepsin K | complex with (1R)-2,2-dimethyl-1-(5-[4-(trifluoromethyl)phenyl]-1,3,4-oxadiazol-2-ylmethyl)propyl (1S)-1-oxo[(2-oxo-1,3-oxazolidin-3-yl)amino]acetylpentylcarbamate | 1YT7 |
CA | C01.036 | cathepsin K | complex with myocrisin | 2ATO_A |
CA | C01.036 | cathepsin K | complex with semicarbazone inhibitor (1R)-2-methyl-1-(phenylmethyl)propyl[(1S)-1-formylpentyl]carbamate | 2AUX |
CA | C01.036 | cathepsin K | complex with semicarbazone inhibitor 1-(phenylmethyl)cyclopentyl[(1S)-1-formylpentyl]carbamate | 2AUZ_A |
CA | C01.036 | cathepsin K | complex with (3S)-1-[(3,5-dimethylisoxazol-4-yl)amino]carbonyl-4,4-dimethylpyrrolidin-3-yl(1s)-1-[1-hydroxy-2-oxo-2-[(1R)-1-phenylethyl]aminoethyl]pentylcarbamate | 2BDL |
CA | C01.036 | cathepsin K | complex with a pyrrolopyrimidine inhibitor | 2R6N_A |
CA | C01.036 | cathepsin K | complex with chondroitin sulfate | 3C9E |
CA | C01.036 | cathepsin K | variant M5; complex with chondroitin-4-sulfate | 3H7D_A |
CA | C01.036 | cathepsin K | complex with a triazine ligand | 3KW9_A |
CA | C01.036 | cathepsin K | complex with a dioxo-triazine inhibitor | 3KWB_X |
CA | C01.036 | cathepsin K | complex with a non-selective 2-cyano-pyrimidine inhibitor | 3KWZ_A |
CA | C01.036 | cathepsin K | complex with a selective 2-cyano-pyrimidine inhibitor | 3KX1_A |
CA | C01.036 | cathepsin K | complex with a cyano-pyrimidine inhibitor | 3O0U_A |
CA | C01.036 | cathepsin K | complex with a 2-cyano pyrimidine inhibitor with a benzyl p3 group. | 3O1G_A |
CA | C01.036 | cathepsin K | complex with a covalent inhibitor with a ketoamide warhead | 3OVZ_A |
CA | C01.036 | cathepsin K | cathepsin k inhibitor | 4DMX_A |
CA | C01.036 | cathepsin K | cathepsin k inhibitor | 4DMY_A |
CA | C01.036 | cathepsin K | complex with dermatan sulfate | 4N79_A |
CA | C01.036 | cathepsin K | complex with chondroitin sulfate | 4N8W_A |
CA | C01.036 | cathepsin K | development of n-(functionalized benzoyl)-homocycloleucyl- glycinonitriles as potent cathepsin k inhibitors. | 4X6H_A |
CA | C01.036 | cathepsin K | development of n-(functionalized benzoyl)-homocycloleucyl- glycinonitriles as potent cathepsin k inhibitors. | 4X6I_A |
CA | C01.036 | cathepsin K | development of n-(functionalized benzoyl)-homocycloleucyl- glycinonitriles as potent cathepsin k inhibitors. | 4X6J_A |
CA | C01.036 | cathepsin K | complex with lichostatinal | 4YV8_A |
CA | C01.036 | cathepsin K | co-crystallized with actinomycetes extract | 4YVA_A |
CA | C01.036 | cathepsin K | Cys25Ser mutant; complex with the allosteric effector nsc13345 | 5J94_A |
CA | C01.036 | cathepsin K | Cys25Ser mutant; complex with the allosteric effector nsc94914 | 5JA7_A |
CA | C01.036 | cathepsin K | Cys25Ser mutant | 5JH3_A |
CA | C01.036 | cathepsin K | complex with a covalently-linked inhibitor | 5TDI_A |
CA | C01.036 | cathepsin K | 5TUN_A | |
CA | C01.036 | cathepsin K | pycnonodysostosis disease related Ile249Thr mutant | 5Z5O_A |
CA | C01.036 | cathepsin K | complex with a non-active site inhibitor | 6ASH_A |
CA | C01.036 | cathepsin K | complex with n-desmethyl thalassospiramide c | 6HGY_A |
CA | C01.036 | cathepsin K | complex with an alkyne moiety | 6QBS_A |
CA | C01.036 | cathepsin K | 7PCK | |
CA | C01.036 | cathepsin K | 5T6U_A | |
CA | C01.036 | cathepsin K | Thr101Ala variant | 6BKI_A |
CA | C01.040 | cathepsin H | theoretical model | 1BZN |
CA | C01.040 | cathepsin H | precursor | 6CZK_A |
CA | C01.040 | cathepsin H | Cys26Ser mutant | 6CZS_A |
CA | C01.040 | cathepsin H | complex with cystatin A | 1NB3_A |
CA | C01.040 | cathepsin H | complex with cystatin A | 1NB5_A |
CA | C01.040 | cathepsin H | 8PCH | |
CA | C01.046 | falcipain-2 | complex with egg-white cystatin | 1YVB_A |
CA | C01.046 | falcipain-2 | complex with E64 | 3BPF_A |
CA | C01.046 | falcipain-2 | complex with PBICP-C | 3PNR_A |
CA | C01.060 | cathepsin B | 1CSB | |
CA | C01.060 | cathepsin B | 1CSB_A | |
CA | C01.060 | cathepsin B | complex with a dipeptidyl nitrile inhibitor | 1GMY |
CA | C01.060 | cathepsin B | 1GMY_A | |
CA | C01.060 | cathepsin B | 1HUC | |
CA | C01.060 | cathepsin B | 1HUC_A | |
CA | C01.060 | cathepsin B | recombinant precursor | 1PBH |
CA | C01.060 | cathepsin B | recombinant precursor | 1PBH_A |
CA | C01.060 | cathepsin B | tetragonal form | 2IPP_A |
CA | C01.060 | cathepsin B | recombinant precursor | 2PBH |
CA | C01.060 | cathepsin B | recombinant precursor | 2PBH_A |
CA | C01.060 | cathepsin B | 3AI8 | |
CA | C01.060 | cathepsin B | complex with chagasin | 3CBJ_A |
CA | C01.060 | cathepsin B | complex with chagasin | 3CBK_A |
CA | C01.060 | cathepsin B | 3K9M_A | |
CA | C01.060 | cathepsin B | recombinant precursor | 3PBH |
CA | C01.060 | cathepsin B | recombinant precursor | 3PBH_A |
CA | C01.060 | cathepsin B | complex with darpin 81 | 5MBL_A |
CA | C01.060 | cathepsin B | complex with covalently linked compound 28 | 6AY2_A |
CA | C01.060 | cathepsin B | complex with E64c | 1ITO |
CA | C01.060 | cathepsin B | complex with CA074 inhibitor | 1QDQ |
CA | C01.060 | cathepsin B | complex with NS-134, a two headed epoxysuccinyl inhibitor | 1SP4_A |
CA | C01.060 | cathepsin B | 2DC6 | |
CA | C01.060 | cathepsin B | 2DC7 | |
CA | C01.060 | cathepsin B | 2DC8 | |
CA | C01.060 | cathepsin B | 2DC9 | |
CA | C01.060 | cathepsin B | 2DCA | |
CA | C01.060 | cathepsin B | 2DCB | |
CA | C01.060 | cathepsin B | 2DCC | |
CA | C01.060 | cathepsin B | 2DCD | |
CA | C01.060 | cathepsin B | Ser115Ala mutant | 1CPJ |
CA | C01.060 | cathepsin B | 1CTE | |
CA | C01.060 | cathepsin B | precursor | 1MIR |
CA | C01.060 | cathepsin B | Ser115Ala mutant; complex with Z-Arg-Ser(OBzl) chloromethylketone | 1THE_B |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | complex with ca074 inhibitor | 3QSD_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | complex with k11017 inhibitor | 3S3Q_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | complex with k11777 inhibitor | 3S3R_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | zymogen | 4I04_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | structure of intermediate processing form of cathepsin b1 from schistosoma mansoni | 4I05_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | mature form | 4I07_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | complex with wrr391 inhibitor | 5OGQ_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | complex with wrr286 inhibitor | 5OGR_A |
CA | C01.062 | cathepsin B-like peptidase (platyhelminth) | theoretical model | 1MF3 |
CA | C01.063 | falcipain-3 | complex with leupeptin | 3BPM_A |
CA | C01.063 | falcipain-3 | complex with the vinyl sulfone derived inhibitor K11017 | 3BWK_A |
CA | C01.068 | vitellogenic cathepsin B | theoretical model | 1MHG |
CA | C01.070 | dipeptidyl-peptidase I | 1JQP | |
CA | C01.070 | dipeptidyl-peptidase I | exclusion domain | 1K3B_A |
CA | C01.070 | dipeptidyl-peptidase I | complex with the inhibitor Gly-Phe-CHN2 | 2DJF_A |
CA | C01.070 | dipeptidyl-peptidase I | re-refinement of the native structure of human dipeptidyl peptidase i (cathepsin c) | 2DJG_A |
CA | C01.070 | dipeptidyl-peptidase I | discovery of novel cyanamide-based inhibitors of cathepsin c | 3PDF_A |
CA | C01.070 | dipeptidyl-peptidase I | human dpp1 in complex with (2s)-2-amino-n-((1s)-1-cyano-2-(4- phenylphenyl)ethyl)butanamide | 4CDC_A |
CA | C01.070 | dipeptidyl-peptidase I | human dpp1 in complex with (2s)-n-((1s)-1-cyano-2-(4-(4-cyanophenyl) phenyl)ethyl)piperidine-2-carboxamide | 4CDD_A |
CA | C01.070 | dipeptidyl-peptidase I | human dpp1 in complex with 4-amino-n-((1s)-1-cyano-2-(4-(4- cyanophenyl)phenyl)ethyl)tetrahydropyran-4-carboxamide | 4CDE_A |
CA | C01.070 | dipeptidyl-peptidase I | human dpp1 in complex with (2s,4s)-n-((1s)-1-cyano-2-(4-(4- cyanophenyl)phenyl)ethyl)-4-hydroxy-piperidine-2-carboxamide | 4CDF_A |
CA | C01.070 | dipeptidyl-peptidase I | complex with dipeptide substrates | 4OEL_A |
CA | C01.070 | dipeptidyl-peptidase I | complex with dipeptide substrates | 4OEM_A |
CA | C01.070 | dipeptidyl-peptidase I | complex with dipeptidyl cyclopropyl nitrile inhibitor 2 | 6IC5_A |
CA | C01.070 | dipeptidyl-peptidase I | complex with cyclopropyl peptidyl nitrile inhibitor 1 | 6IC6_A |
CA | C01.070 | dipeptidyl-peptidase I | complex with dipeptidyl cyclopropyl nitrile inhibitor 3 | 6IC7_A |
CA | C01.070 | dipeptidyl-peptidase I | theoretical model | 1BMU |
CA | C01.072 | rhodesain | complex with the vinyl sulfone derived inhibitor K11777 | 2P7U_A |
CA | C01.072 | rhodesain | complex with the vinyl sulfone derived inhibitor K11002 | 2P86_A |
CA | C01.072 | rhodesain | complex with a macrolactam inhibitor | 6EX8_A |
CA | C01.072 | rhodesain | complex with a macrolactam inhibitor | 6EXO_A |
CA | C01.072 | rhodesain | complex with a macrolactam inhibitor | 6EXQ_A |
CA | C01.073 | peptidase 1 (mite) | precursor; mutant form | 1XKG |
CA | C01.073 | peptidase 1 (mite) | 2AS8_A | |
CA | C01.073 | peptidase 1 (mite) | c2 crystal form of mite allergen der p 1 | 3F5V_A |
CA | C01.073 | peptidase 1 (mite) | 3RVW | |
CA | C01.073 | peptidase 1 (mite) | 3RVX | |
CA | C01.073 | peptidase 1 (mite) | 4PP1 | |
CA | C01.073 | peptidase 1 (mite) | 4PP2 | |
CA | C01.073 | peptidase 1 (mite) | complex with fab fragment of mab 5h8 | 5VCN_A |
CA | C01.073 | peptidase 1 (mite) | complex with fab fragment of mab 10b9 | 5VCO_A |
CA | C01.073 | peptidase 1 (mite) | complex with fab 4c1 | 5VPG_A |
CA | C01.073 | peptidase 1 (mite) | complex with fab 4c1 | 5VPH_A |
CA | C01.073 | peptidase 1 (mite) | 3D6S_A | |
CA | C01.073 | peptidase 1 (mite) | 3RVV | |
CA | C01.073 | peptidase 1 (mite) | 5VPK_A | |
CA | C01.073 | peptidase 1 (mite) | complex with fab 4c1 | 5VPL_A |
CA | C01.074 | CPB peptidase | theoretical model | 1BMJ |
CA | C01.075 | cruzipain | catalytic domain, Gly213 stop. | 1AIM |
CA | C01.075 | cruzipain | complex with WRR-99 | 1EWL_A |
CA | C01.075 | cruzipain | complex with WRR-112 | 1EWM |
CA | C01.075 | cruzipain | complex with WRR-204 | 1EWO |
CA | C01.075 | cruzipain | complex with N-carbonylmorpholine-Leu-homophenylalanylmethane inhibitor | 1EWP |
CA | C01.075 | cruzipain | complex with vinyl sulfone-derived inhibitor VS1 | 1F29 |
CA | C01.075 | cruzipain | complex with vinyl sulfone-derived inhibitor VS2 | 1F2A |
CA | C01.075 | cruzipain | complex with vinyl sulfone-derived inhibitor VS3 | 1F2B |
CA | C01.075 | cruzipain | complex with vinyl sulfone-derived inhibitor VS4 | 1F2C |
CA | C01.075 | cruzipain | complex with [1-(3-hydroxy-2-oxo-1-phenethyl-propylcarbamoyl)2-phenyl-ethyl]-carbamic acid pyridin-4-ylmethyl ester | 1ME3 |
CA | C01.075 | cruzipain | complex with [1-(1-benzyl-3-hydroxy-2-oxo-propylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester | 1ME4 |
CA | C01.075 | cruzipain | complex with [1-(1-methyl-4,5-dioxo-pent-2-enylcarbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester | 1U9Q_X |
CA | C01.075 | cruzipain | catalytic domain; complex with Bz-Arg-Ala-fluoromethylketone | 2AIM |
CA | C01.075 | cruzipain | complex with vinyl sulfone derived inhibitor WR483 | 2EFM_A |
CA | C01.075 | cruzipain | complex with the vinyl sulfone derived inhibitor K11777 | 2OZ2_A |
CA | C01.075 | cruzipain | 3HD3 | |
CA | C01.075 | cruzipain | 3I06 | |
CA | C01.075 | cruzipain | 3IUT | |
CA | C01.075 | cruzipain | 3KKU | |
CA | C01.075 | cruzipain | 3LXS | |
CA | C01.075 | cruzipain | 4KLB | |
CA | C01.075 | cruzipain | 4PI3 | |
CA | C01.075 | cruzipain | 4QH6 | |
CA | C01.075 | cruzipain | 4W5B | |
CA | C01.075 | cruzipain | 4W5C | |
CA | C01.075 | cruzipain | 4XUI | |
CA | C01.075 | cruzipain | apo-form | 6N3S_A |
CA | C01.075 | cruzipain | complex with mmts inhibitor | 6O2X_A |
CA | C01.084 | bleomycin hydrolase (animal) | 1CB5 | |
CA | C01.084 | bleomycin hydrolase (animal) | Cys73Ser mutant | 2CB5 |
CA | C01.085 | bleomycin hydrolase (yeast) | Cys73Ala mutant | 1A6R |
CA | C01.085 | bleomycin hydrolase (yeast) | 1GCB | |
CA | C01.085 | bleomycin hydrolase (yeast) | Asn392Ala mutant | 2DZY_A |
CA | C01.085 | bleomycin hydrolase (yeast) | Asn392Val mutant | 2DZZ_A |
CA | C01.085 | bleomycin hydrolase (yeast) | Asn392Leu mutant | 2E00_A |
CA | C01.085 | bleomycin hydrolase (yeast) | His369la mutant | 2E01_A |
CA | C01.085 | bleomycin hydrolase (yeast) | His369Leu mutant | 2E02_A |
CA | C01.085 | bleomycin hydrolase (yeast) | Asnq67e mutant | 2E03_A |
CA | C01.085 | bleomycin hydrolase (yeast) | Cys73Ala mutant | 3GCB |
CA | C01.098 | CPC peptidase | theoretical model | 1MJ6 |
CA | C01.098 | CPC peptidase | theoretical model | 1BF7 |
CA | C01.098 | CPC peptidase | complex with ca074 | 3HHI_A |
CA | C01.098 | CPC peptidase | 3MOR_A | |
CA | C01.098 | CPC peptidase | 4HWY_A | |
CA | C01.098 | CPC peptidase | trypanosoma brucei procathepsin b structure solved by serial microcrystallography using synchrotron radiation | 4N4Z_A |
CA | C01.098 | CPC peptidase | procathepsin b s9 from trypanosoma congolense | 5FPW_A |
CA | C01.099 | ervatamin B | 1IWD | |
CA | C01.101 | cathepsin B-like peptidase, nematode | theoretical model | 1MNW |
CA | C01.116 | ervatamin C | 1O0E_A | |
CA | C01.116 | ervatamin C | 2PNS_A | |
CA | C01.125 | Cwp84 peptidase | 4CI7 | |
CA | C01.125 | Cwp84 peptidase | Cys116Ala mutant; mature protein | 4D59 |
CA | C01.125 | Cwp84 peptidase | Cys116Ala mutant; mature protein | 4D5A |
CA | C01.128 | xylellain | 3OIS | |
CA | C01.134 | mexicain | 2BDZ | |
CA | C01.137 | ervatamin A | complex with E64 | 2PSC |
CA | C01.137 | ervatamin A | complex with E64 | 3BCN |
CA | C01.137 | ervatamin A | 2PNS | |
CA | C01.137 | ervatamin A | ervatamin-C; complex with E64 | 2PRE_A |
CA | C01.149 | TgCPL peptidase (Toxoplasma-type) | complex with propeptide | 3F75_A |
CA | C01.171 | Pd_dinase (Parabacteroides distasonis) | 3PW3 | |
CA | C01.171 | Pd_dinase (Parabacteroides distasonis) | 5WDK_A | |
CA | C01.171 | Pd_dinase (Parabacteroides distasonis) | 5WDL_A | |
CA | C01.984 | serine-repeat antigen (Plasmodium sp.) | 2WBF | |
CA | C01.984 | serine-repeat antigen (Plasmodium sp.) | 3CH2 | |
CA | C01.984 | serine-repeat antigen (Plasmodium sp.) | 3CH3 | |
CA | C01.987 | papain-like protein SPE31 (Pachyrhizus erosus) | 2B1M | |
CA | C01.987 | papain-like protein SPE31 (Pachyrhizus erosus) | 2B1N | |
CA | C01.UPA | subfamily C1A unassigned peptidases | complex with N-[(1S)-1-([(3S,4S,7R)-3-hydroxy-7-methyl-1-(pyridin-2-ylsulfonyl)-2,3,4,7-tetrahydro-1H-azepin-4-yl]aminocarbonyl)-3-methylbutyl]-1-benzofuran-2-carboxamide | 2FTD |
CA | C01.UPA | subfamily C1A unassigned peptidases | structural basis for the limited antibody cross reactivity between themite allergens blo t 1 and der p 1 | 5JT8_A |
CA | C01.UPA | subfamily C1A unassigned peptidases | structure of digestive procathepsin l2 proteinase from tenebrio molitor larval midgut | 3QJ3_A |
CA | C01.UPA | subfamily C1A unassigned peptidases | precursor | 5EF4_A |
CA | C01.UPA | subfamily C1A unassigned peptidases | precursor | 5EGW_A |
CA | C02.001 | calpain-1 | complex with inhibitor Z-Leu-Leu-Tyr-CH2F | 1ZCM |
CA | C02.001 | calpain-1 | catalytic domain only | 2ARY |
CA | C02.001 | calpain-1 | catalytic domain only | 1KXR_A |
CA | C02.001 | calpain-1 | 1QXP_A | |
CA | C02.001 | calpain-1 | protease core; complex with leupeptin | 1TL9_A |
CA | C02.001 | calpain-1 | peptidase unit only; complex with E64 | 1TLO |
CA | C02.001 | calpain-1 | calpain 1 proteolytic core;ncomplex with snj-1715, a cyclic hemiacetal-type inhibitor | 2G8E_A |
CA | C02.001 | calpain-1 | proteolytic core; complex with snj-1945, a alpha-ketoamide-type inhibitor. | 2G8J_A |
CA | C02.001 | calpain-1 | calpain 1 proteolytic core inactivated by wr18(s,s), an epoxysuccinyl-type inhibitor. | 2NQG_A |
CA | C02.001 | calpain-1 | calpain 1 proteolytic core inactivated by wr13(r,r), an epoxysuccinyl-type inhibitor. | 2NQI_A |
CA | C02.001 | calpain-1 | calpain 1 proteolytic core inactivated by zlak-3001, an alpha-ketoamide | 2R9C_A |
CA | C02.001 | calpain-1 | calpain 1 proteolytic core inactivated by zlak-3002, an alpha-ketoamide | 2R9F_A |
CA | C02.002 | calpain-2 | 1KFU_L | |
CA | C02.002 | calpain-2 | 1KFX_L | |
CA | C02.002 | calpain-2 | 2NQA | |
CA | C02.002 | calpain-2 | Complex with light chain | 1DF0_A |
CA | C02.002 | calpain-2 | protease core | 1MDW_A |
CA | C02.002 | calpain-2 | 1QXP_A | |
CA | C02.002 | calpain-2 | Lys10Thr mutant | 1U5I_A |
CA | C02.002 | calpain-2 | complex with light chain with calpastatin | 3BOW_A |
CA | C02.002 | calpain-2 | complex with light chain and calpastatin | 3DF0_A |
CA | C02.004 | calpain-3 | 1Y9V | |
CA | C02.004 | calpain-3 | 4OKH | |
CA | C02.004 | calpain-3 | crystal structure of human calpain-3 protease core mutant-Cys129Ser | 6BDT_A |
CA | C02.004 | calpain-3 | crystal structure of human calpain-3 protease core mutant-Cys129Ala | 6BGP_A |
CA | C02.004 | calpain-3 | protease core; complex with E-64 | 6BJD_A |
CA | C02.004 | calpain-3 | protease core; complex with leupeptin | 6BKJ_A |
CA | C02.006 | calpain-9 | catalytic domain only | 1ZIV |
CA | C02.006 | calpain-9 | complex with leupeptin | 2P0R_A |
CA | C02.011 | calpain-5 | core peptidase domain | 6P3Q |
CA | C02.020 | calpain-13 | 2I7A | |
CA | C02.029 | calpain (Plasmodium-type) | C2 domain | 2QFE |
PA | C03.001 | poliovirus-type picornain 3C | 1L1N_A | |
PA | C03.001 | poliovirus-type picornain 3C | coxsackievirus Ala24Val mutant; complex with the d1-d2 fragment of icam-1 | 6EIT_3 |
PA | C03.005 | hepatitis A virus-type picornain 3C | 1HAV_A | |
PA | C03.005 | hepatitis A virus-type picornain 3C | complex with inhibitor iodoacetyl-Val-Phe-amide | 1QA7 |
PA | C03.005 | hepatitis A virus-type picornain 3C | complex with peptide-based ketone inhibitor N-acetyl-L-leucyl-L-alanyl-N-[(1S)-4-(dimethylamino)-1-(fluoroacetyl)-4-oxobutyl]-L-alaninamide | 2H6M |
PA | C03.005 | hepatitis A virus-type picornain 3C | complex with peptide-based ketone inhibitor N-acetyl-L-Leu-L-Ala-N-[(1S)-4-(dimethylamino)-1-(fluoroacetyl)-4-oxobutyl]-L-alaninamide | 2H9H |
PA | C03.005 | hepatitis A virus-type picornain 3C | complex with peptide-based ketone inhibitor N-acetyl-L-Leu-L-Phe-N-[(1S,2R)-1-(2-carboxyethyl)-3-fluoro-2-hydroxypropyl]-L-phenylalaninamide | 2HAL |
PA | C03.007 | human rhinovirus 2-type picornain 3C | complex with AG7088 inhibitor | 1CQQ_A |
PA | C03.007 | human rhinovirus 2-type picornain 3C | 1AYM_4 | |
PA | C03.007 | human rhinovirus 2-type picornain 3C | 1AYN_4 | |
PA | C03.007 | human rhinovirus 2-type picornain 3C | 1R1A | |
PA | C03.007 | human rhinovirus 2-type picornain 3C | 2HWD | |
PA | C03.007 | human rhinovirus 2-type picornain 3C | 2HWE | |
PA | C03.007 | human rhinovirus 2-type picornain 3C | 2HWF | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | type A10(61); crystal packing mutant (Lys51Gln) | 2J92_A |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | complex with a decameric peptide corresponding to the vp1-2a cleavage junction | 2WV4_A |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | complex with a decameric peptide corresponding to the vp1-2a cleavage junction with a gln to glu substitution at p1 | 2WV5_A |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | crystal structure of the 3c protease from south african territories type 2 foot-and-mouth disease virus | 5HM2_A |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | 1QMY | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | 1QOL_A | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | 1QQP | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | 2JQF_R | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | 2JQG | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | 4QBB | |
PA | C03.008 | foot-and-mouth disease virus picornain 3C | fmdv leader protease bound to substrate isg15 | 6FFA_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | coxsackievirus b3 coat protein | 1COV_1 |
PA | C03.011 | Coxsackievirus-type picornain 3C | 2VB0_A | |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with epdtc | 2ZTX_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | space group c2 | 2ZTY_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | space group p21 | 2ZTZ_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | Cys147Ala mutant | 2ZU1_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | 2ZU3_A | |
PA | C03.011 | Coxsackievirus-type picornain 3C | the novel asymmetric entry intermediate of a picornavirus captured with nanodiscs | 3JD7_1 |
PA | C03.011 | Coxsackievirus-type picornain 3C | crystal structure of 3c protease of coxsackievirus b3 | 3ZYD_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | Thr68Ala mutant | 3ZYE_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | crystal structure of 3c protease mutant (Asn126Tyr) of coxsackievirus b3 | 3ZZ3_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | Thr68Ala and Asn126Tyr mutant | 3ZZ4_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with alpha, beta-unsaturated ethyl ester inhibitor 74 | 3ZZ5_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with michael receptor inhibitor 75 | 3ZZ6_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with alpha, beta-unsaturated ethyl ester inhibitor 81 | 3ZZ7_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with alpha, beta-unsaturated ethyl ester inhibitor 82 | 3ZZ8_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with alpha, beta-unsaturated ethyl ester inhibitor 83 | 3ZZ9_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with alpha, beta-unsaturated ethyl ester inhibitor 84 | 3ZZA_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with alpha, beta-unsaturated ethyl ester inhibitor 85 | 3ZZB_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | Thr68Ala and Asn126Tyr mutant; complex with alpha, beta-unsaturated ethyl ester inhibitor 83 | 3ZZC_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | Thr68Ala and Asn126Tyr mutant; complex with alpha, beta-unsaturated ethyl ester inhibitor 85 | 3ZZD_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | echovirus 18 native particle | 6HBG_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | echovirus 18 a-particle | 6HBH_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | echovirus 18 empty particle | 6HBJ_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | echovirus 18 open particle without one pentamer | 6HBK_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | echovirus 18 open particle without three pentamers | 6HBL_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | 3ZV8 | |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 74 | 3ZV9 |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 75 | 3ZVA |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 81 | 3ZVB |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 82 | 3ZVC |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 83 | 3ZVD |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 84 | 3ZVE |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 85 | 3ZVF |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with Michael receptor inhibitor 98 | 3ZVG |
PA | C03.011 | Coxsackievirus-type picornain 3C | crystal structure of the main protease (3c) from human enterovirus b ev93 | 3Q3X_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with compound 1 (ag7404) | 3Q3Y_A |
PA | C03.011 | Coxsackievirus-type picornain 3C | complex with rupintrivir (ag7088) | 3RUO_A |
PA | C03.014 | human enterovirus 71 3C peptidase | human enterovirus 71 3c protease | 3OSY_A |
PA | C03.014 | human enterovirus 71 3C peptidase | Glu71Asp mutant; complex with rupintrivir | 3QZQ_A |
PA | C03.014 | human enterovirus 71 3C peptidase | Glu71Ala mutant; complex with rupintrivir | 3QZR_A |
PA | C03.014 | human enterovirus 71 3C peptidase | His133Gly mutant; complex with rupintrivir | 3R0F_A |
PA | C03.014 | human enterovirus 71 3C peptidase | human enterovirus 71 in complex with capsid binding inhibitor win51711 | 3ZFE_A |
PA | C03.014 | human enterovirus 71 3C peptidase | human enterovirus 71 in complex with capsid binding inhibitor win51711 | 3ZFF_A |
PA | C03.014 | human enterovirus 71 3C peptidase | human enterovirus 71 in complex with capsid binding inhibitor win51711 | 3ZFG_A |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 | 4AED_A |
PA | C03.014 | human enterovirus 71 3C peptidase | cryo-em reconstruction of enterovirus 71 in complex with a neutralizing antibody e18 | 4C0U_A |
PA | C03.014 | human enterovirus 71 3C peptidase | cryo-em reconstruction of empty enterovirus 71 in complex with a neutralizing antibody e18 | 4C0Y_A |
PA | C03.014 | human enterovirus 71 3C peptidase | cryo-em reconstruction of empty enterovirus 71 in complex with a neutralizing antibody e19 | 4C10_4 |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 in complex with the uncoating inhibitor gpp2 | 4CDQ_A |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 in complex with the uncoating inhibitor gpp3 | 4CDU_A |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 in complex with the uncoating inhibitor gpp4 | 4CDW_A |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 in complex with the uncoating inhibitor gpp12 | 4CDX_A |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 in complex with the uncoating inhibitor ald | 4CEW_A |
PA | C03.014 | human enterovirus 71 3C peptidase | crystal structure of human enterovirus 71 in complex with the uncoating inhibitor nld | 4CEY_A |
PA | C03.014 | human enterovirus 71 3C peptidase | Cys110Ala mutant | 4FVB_A |
PA | C03.014 | human enterovirus 71 3C peptidase | Cys110Ala mutant; complex with substrate | 4FVD_A |
PA | C03.014 | human enterovirus 71 3C peptidase | 4GHQ_A | |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with ag7088 | 4GHT_A |
PA | C03.014 | human enterovirus 71 3C peptidase | human enterovirus 71 uncoating intermediate captured at atomic resolution | 4N43_C |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound xb | 5C1U_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound viii | 5C1X_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 1 | 5C1Y_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 2 | 5C20_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 2 | 5DP3_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 3 | 5DP4_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 4 | 5DP5_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 7 | 5DP6_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 5 | 5DP7_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 8 | 5DP8_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 9 | 5DP9_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with compound 6 | 5DPA_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with nk-1.8k | 5GSO_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with n69s 1.8k | 5GSW_A |
PA | C03.014 | human enterovirus 71 3C peptidase | complex with rupintrivir | 5WQ2_A |
PA | C03.014 | human enterovirus 71 3C peptidase | cryo-em structure of cva6 vlp | 5YHQ_C |
PA | C03.020 | enterovirus picornain 2A | 2IJD_1 | |
PA | C03.020 | enterovirus picornain 2A | poliovirus type 3 (strain saukett) stabilized virus-like particle | 5O5B_4 |
PA | C03.020 | enterovirus picornain 2A | poliovirus type 3 (strain saukett) stabilized virus-like particle in complex with the pocket factor compound gpp3 | 5O5P_4 |
PA | C03.020 | enterovirus picornain 2A | complex with antiviral agent sch48973 | 1EAH_1 |
PA | C03.020 | enterovirus picornain 2A | NMR structure | 1Z8R |
PA | C03.020 | enterovirus picornain 2A | identification of a druggable vp1-vp3 interprotomer pocket in the capsid of enteroviruses | 6GZV_A |
PA | C03.020 | enterovirus picornain 2A | 4MG3 | |
PA | C03.020 | enterovirus picornain 2A | 5C8C | |
PA | C03.020 | enterovirus picornain 2A | human enterovirus 71 uncoating intermediate captured at atomic resolution | 4N43_B |
PA | C03.020 | enterovirus picornain 2A | structural model of human decay-accelerating factor bound to echovirus7 from cryo-electron microscopy | 1M11_1 |
PA | C03.020 | enterovirus picornain 2A | 5X45 | |
PA | C03.021 | rhinovirus picornain 2A | 2HRV_A | |
PA | C03.023 | parechovirus picornain 3C | 4UDF | |
PA | C03.023 | parechovirus picornain 3C | 4Z92 | |
PA | C03.UNA | subfamily C3A non-peptidase homologues | 1QGC | |
PA | C03.UNA | subfamily C3A non-peptidase homologues | 4WYL | |
PA | C03.UNA | subfamily C3A non-peptidase homologues | 4WYW | |
PA | C03.UNA | subfamily C3A non-peptidase homologues | 4WZM | |
PA | C03.UNA | subfamily C3A non-peptidase homologues | 4WZQ | |
PA | C03.UNA | subfamily C3A non-peptidase homologues | 4X2B | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 1MEC | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 2M7Y | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 2MEV | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 2MMH | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 2MMI | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 2MMK | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 2MML | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 4NYZ | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 4NZ0 | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 4Y2C | |
PA | C03.UPA | subfamily C3A unassigned peptidases | 4Y3C | |
PA | C03.UPA | subfamily C3A unassigned peptidases | crystal structure of the 3c protease from coxsackievirus a16 | 3SJ8_A |
PA | C03.UPA | subfamily C3A unassigned peptidases | Cys147Ala mutant; complex with faglrqavtq peptide | 3SJ9_A |
PA | C03.UPA | subfamily C3A unassigned peptidases | complex with rupintrivir (ag7088) | 3SJI_A |
PA | C03.UPC | subfamily C3C unassigned peptidases | 3CJI | |
PA | C04.004 | tobacco etch virus NIa peptidase | inactive form; complex with substrate | 1LVB_A |
PA | C04.004 | tobacco etch virus NIa peptidase | complex with product | 1LVM |
PA | C04.004 | tobacco etch virus NIa peptidase | Cys151Ala mutant | 1Q31 |
CE | C05.001 | adenain | complex with peptide cofactor | 1AVP_A |
CE | C05.001 | adenain | complex with 11 amino acid cofactor | 1NLN_A |
CE | C05.001 | adenain | 4EKF | |
CE | C05.001 | adenain | complex with N-benzyl-2-[(Z)-iminomethyl]pyrimidine-5- carboxamide | 4PID |
CE | C05.001 | adenain | complex with N-(2S)-2-(3-chlorophenyl)-2-[(methylsulfonyl)amino]acetyl- L-phenylalanyl-N-[(2Z)-2-iminoethyl]glycinamide | 4PIE |
CE | C05.001 | adenain | structure of human adenovirus 2 protease with cofactor pvic | 5FGY_A |
CE | C05.001 | adenain | complex with N-[(3,5-dichlorophenyl)acetyl]-L-threonyl- N-[(2Z)-2-iminoethyl]glycinamide | 4PIQ |
CE | C05.001 | adenain | complex with N~2~-[(2R)-2-(3,5-dichlorophenyl)-2-(dimethylamino)acetyl]- N-(2-[(Z)-iminomethyl]pyrimidin-4-ylmethyl)- L-isoleucinamide | 4PIS |
CE | C05.001 | adenain | complex with a nitrile inhibitor | 4WX4_A |
CE | C05.001 | adenain | crystal structure of human adenovirus 8 protease with an irreversible vinyl sulfone inhibitor | 4WX6_A |
CE | C05.001 | adenain | crystal structure of adenovirus 8 protease with a nitrile inhibitor | 4WX7_A |
CA | C06.001 | potato virus Y-type helper component peptidase | 1LVM_A | |
CA | C06.001 | potato virus Y-type helper component peptidase | 1Q31_A | |
CA | C06.001 | potato virus Y-type helper component peptidase | 3MMG | |
CA | C06.001 | potato virus Y-type helper component peptidase | 3RNV | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 4GUA | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 3GPG | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 3GPO | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 3GPQ | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 3TRK | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 4TU0 | |
CN | C09.001 | sindbis virus-type nsP2 peptidase | 4ZTB | |
CN | C09.002 | equine encephalitis alphavirus nsP2 peptidase | 2HWK | |
CN | C09.002 | equine encephalitis alphavirus nsP2 peptidase | venezuelan equine encephalitis virus (veev) nonstructural protein 2 (nsp2) cysteine protease | 5EZQ_A |
CN | C09.002 | equine encephalitis alphavirus nsP2 peptidase | complex with E64d | 5EZS_A |
CA | C10.001 | streptopain | precursor; Cys47Ser mutant | 1DKI_A |
CA | C10.001 | streptopain | complex with inhibitor | 1PVJ |
CA | C10.001 | streptopain | mature peptidase | 2UZJ |
CA | C10.004 | interpain A | structure of prevotella intermedia prointerpain a fragment 39-359 (mutant c154a) | 3BB7_A |
CA | C10.004 | interpain A | structure of active wild-type prevotella intermedia interpain a cysteine protease | 3BBA_A |
CA | C100.001 | agglutinin peptidase (Marasmius oreades) | complex with trisaccharide Gal-Gla-GlcNAc | 2IHO |
CA | C100.001 | agglutinin peptidase (Marasmius oreades) | complex with trisaccharide Galalpha(1,3)[Fucalpha(1,2)]Gal | 3EF2 |
CA | C100.001 | agglutinin peptidase (Marasmius oreades) | complex with Z-Val-Ala-Asp-CH(2)F, direct orientation | 5D61 |
CA | C100.001 | agglutinin peptidase (Marasmius oreades) | complex with Z-Val-Ala-Asp-CH(2)F, inverted orientation | 5D62 |
CA | C100.001 | agglutinin peptidase (Marasmius oreades) | complex with Z-Val-Ala-Asp-CH(2)F, dual orientation | 5D63 |
CA | C100.UNW | family C100 non-peptidase homologues | complex with trisaccharide Neu5Aca2-6Galb1-4GlcNAc | 3PHZ |
CA | C100.UPW | family C100 unassigned peptidases | complex with E64 | 5MUA |
CA | C101.001 | OTULIN peptidase | 3ZNV | |
CA | C101.001 | OTULIN peptidase | 3ZNX | |
CA | C101.001 | OTULIN peptidase | 3ZNZ | |
CA | C101.001 | OTULIN peptidase | OTU domain | 4KSJ |
CA | C101.001 | OTULIN peptidase | complex with ubiquitin | 4KSK |
CA | C101.001 | OTULIN peptidase | complex with linear di-ubiquitin | 4KSL |
CA | C101.001 | OTULIN peptidase | 4OYK | |
CA | C101.001 | OTULIN peptidase | 4P0B | |
CA | C101.001 | OTULIN peptidase | structure of otulin bound to the met1-linked diubiquitin activity probe | 5OE7_A |
CA | C101.001 | OTULIN peptidase | structure of the otu domain of otulin g281r mutant | 6I9C_A |
CA | C101.950 | protein FAM105A | otu domain of fam105a | 6DRM_A |
CA | C102.001 | GtgE peptidase | 4MI7 | |
CA | C102.001 | GtgE peptidase | 5KDG | |
CA | C104.001 | PlyC phage lysin | complex with PlyCB | 4F88 |
PA | C107.UPW | family C107 unassigned peptidases | semet labeled derivative of cavally virus 3cl protease | 5LAC_A |
PA | C107.UPW | family C107 unassigned peptidases | ligand-bound structure of cavally virus 3cl protease ***caveat 5lak tyr i 2 has wrong chirality at atom ca tyr k 2 has wrong ***caveat 2 5lak chirality at atom ca | 5LAK_A |
CR | C108.001 | Prp peptidase (Staphylococcus aureus) | 2P92 | |
CR | C108.001 | Prp peptidase (Staphylococcus aureus) | 2IDL | |
CR | C108.001 | Prp peptidase (Staphylococcus aureus) | 2G0I | |
CR | C108.UPW | family C108 unassigned peptidases | 1S12 | |
CD | C11.003 | PmC11 peptidase (Parabacteroides merdae) | 3UWS | |
CD | C11.003 | PmC11 peptidase (Parabacteroides merdae) | complex with peptide inhibitor Ac-VLTK-AOMK | 4YEC |
CD | C11.004 | fragipain (Bacteroides fragilis) | 5DYN_A | |
CD | C11.005 | thetapain | ||
CD | C11.006 | clostripain-related protein (Bacteroides thetaiotaomicron) | complex with biotin-Val-Leu-Thr-Lys-AOMK | 5L20 |
CD | C11.006 | clostripain-related protein (Bacteroides thetaiotaomicron) | Arg154Ala mutant | 6NAG |
CD | C11.007 | distapain (Parabacteroides distasonis) | zymogen | 6MZO |
CA | C111.001 | coagulation factor XIIIa | with bound calcium | 1EVU |
CA | C111.001 | coagulation factor XIIIa | zymogen; Trp279Phe mutant | 1EX0 |
CA | C111.001 | coagulation factor XIIIa | recombinant form | 1F13 |
CA | C111.001 | coagulation factor XIIIa | recombinant form | 1FIE |
CA | C111.001 | coagulation factor XIIIa | 1GGT | |
CA | C111.001 | coagulation factor XIIIa | with bound calcium | 1GGU |
CA | C111.001 | coagulation factor XIIIa | with bound ytterbium | 1GGY |
CA | C111.001 | coagulation factor XIIIa | with bound strontium | 1QRK |
CA | C111.001 | coagulation factor XIIIa | complex with peptide-like ligand | 4KTY |
C- | C116.001 | dermonecrotic toxin (Pasteurella multocida) | 2EBF | |
C- | C116.001 | dermonecrotic toxin (Pasteurella multocida) | 2EBH | |
C- | C116.001 | dermonecrotic toxin (Pasteurella multocida) | 2EC5 | |
CA | C117.001 | SpvD g.p. (Salmonella enterica) | Arg161 variant | 5LQ6 |
CA | C117.001 | SpvD g.p. (Salmonella enterica) | Gly161 variant | 5LQ7 |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 2ETL | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 2LEN | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 3IFW | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 3IRT | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 3KVF | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 3KW5 | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 4DM9 | |
CA | C12.001 | ubiquitinyl hydrolase-L1 | 4JKJ | |
CA | C12.002 | ubiquitinyl hydrolase-YUH1 | complex with human ubiquitin | 1CMX |
CA | C12.003 | ubiquitinyl hydrolase-L3 | 1UCH | |
CA | C12.003 | ubiquitinyl hydrolase-L3 | complex with ubiquitin | 1XD3 |
CA | C12.003 | ubiquitinyl hydrolase-L3 | complex with Lys27-linked di-ubiquitin | 6ISU_A |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 3A7S | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 3IHR | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | catalytic domain only | 3RII |
CA | C12.005 | ubiquitinyl hydrolase-L5 | catalytic domain only | 3RIS |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 3TB3 | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4UEL | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4UEM | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4UF5 | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4UF6 | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4WLP | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4WLQ | |
CA | C12.005 | ubiquitinyl hydrolase-L5 | 4WLR | |
CA | C12.A09 | CG8445 g.p. (Drosophila melanogaster) | complex with pr | 6CGA_A |
CA | C12.A09 | CG8445 g.p. (Drosophila melanogaster) | complex with DEUBAD of ASX | 6HGC |
CE | C122.001 | SdeA (Legionella pneumophila) | 5CRA | |
CE | C122.001 | SdeA (Legionella pneumophila) | 5CRB | |
CE | C122.001 | SdeA (Legionella pneumophila) | 5CRC | |
CE | C122.001 | SdeA (Legionella pneumophila) | 5YSI | |
CE | C122.001 | SdeA (Legionella pneumophila) | 5YSJ | |
CE | C122.001 | SdeA (Legionella pneumophila) | 5YSK | |
CE | C122.001 | SdeA (Legionella pneumophila) | 6B7Q | |
CE | C122.001 | SdeA (Legionella pneumophila) | 6G0C | |
CD | C13.001 | legumain (plant beta form) | complex with AAN peptide | 6AZT |
CD | C13.004 | legumain, animal-type | complex with Ac-Tyr-Val-Ala-Asp-chloromethylketone | 4AW9 |
CD | C13.004 | legumain, animal-type | complex with Ac-Tyr-Val-Ala-Asp-chloromethylketone at pH 5.0 | 4AWA |
CD | C13.004 | legumain, animal-type | complex with Z-Ala-Ala-AzaAsn-chloromethylketone | 4AWB |
CD | C13.004 | legumain, animal-type | precursor | 4FGU |
CD | C13.004 | legumain, animal-type | oxidised form in complex with cystatin E/M | 4N6N_A |
CD | C13.004 | legumain, animal-type | complex with cystatin E/M | 4N6O_A |
CD | C13.004 | legumain, animal-type | YVAD-CMK bound form; complex with compound 11b | 5LU8_C |
CD | C13.004 | legumain, animal-type | YVAD-CMK bound form; complex with compound 11 | 5LU9_C |
CD | C13.004 | legumain, animal-type | complex with compound 11b | 5LUA_A |
CD | C13.004 | legumain, animal-type | complex with compound 11 | 5LUB_B |
CD | C13.004 | legumain, animal-type | activated at pH 3.5 | 4NOJ |
CD | C13.004 | legumain, animal-type | precxursor at pH 7.5 | 4NOK |
CD | C13.004 | legumain, animal-type | Asp223Ala mutant; precursor at pH 7.5 | 4NOL |
CD | C13.004 | legumain, animal-type | activated at pH 4.5 | 4NOM |
CD | C13.004 | legumain, animal-type | 4D3X | |
CD | C13.004 | legumain, animal-type | precursor | 4D3Y |
CD | C13.004 | legumain, animal-type | precursor; trigonal space group | 4D3Z |
CD | C13.006 | legumain (plant gamma form) | two-chain activation state | 5NIJ |
CD | C13.006 | legumain (plant gamma form) | isoform gamma in complex with Ac-YVAD-CMK | 5OBT |
CD | C13.010 | OaAEP1 (Oldenlandia affinis) | 5H0I | |
CD | C14.001 | caspase-1 | complex with (3S)-N-methanesulfonyl-3-(1-[N-(2-naphtoyl)-Val]-Proamino)-4-oxobutanamide inhibitor | 1BMQ |
CD | C14.001 | caspase-1 | complex with inhibitor ac-Trp-Glu-His-Asp | 1IBC |
CD | C14.001 | caspase-1 | complex with inhibitor Ac-Tyr-Val-Ala-Asp-H | 1ICE |
CD | C14.001 | caspase-1 | complex with 3-(2- mercapto-acetylamino)-4-oxo-pentanoic acid | 1RWK_A |
CD | C14.001 | caspase-1 | complex with 4-oxo- 3-[2-(5-[4-(quinoxalin-2-ylamino)-benzoylamino]-methyl- thiophen-2-yl)-acetylamino]-pentanoic acid | 1RWM_A |
CD | C14.001 | caspase-1 | complex with 3-2- ethyl-6-[4-(quinoxalin-2-ylamino)-benzoylamino]- hexanoylamino-4-oxo-butyric acid | 1RWN_A |
CD | C14.001 | caspase-1 | complex with 4-oxo- 3-6-[4-(quinoxalin-2-ylamino)-benzoylamino]-2-thiophen-2- yl-hexanoylamino-pentanoic acid | 1RWO_A |
CD | C14.001 | caspase-1 | complex with 3-6- [(8-hydroxy-quinoline-2-carbonyl)-amino]-2-thiophen-2-yl- hexanoylamino-4-oxo-butyric acid | 1RWP_A |
CD | C14.001 | caspase-1 | complex with 5-[5- (1-carboxymethyl-2-oxo-propylcarbamoyl)-5-phenyl- pentylsulfamoyl]-2-hydroxy-benzoic acid | 1RWV_A |
CD | C14.001 | caspase-1 | complex with 4-oxo- 3-[(6-[4-(quinoxalin-2-ylamino)-benzoylamino]-methyl- pyridine-3-carbonyl)-amino]-butyric acid | 1RWW_A |
CD | C14.001 | caspase-1 | complex with 4-oxo- 3-6-[4-(quinoxalin-2-yloxy)-benzoylamino]-2-thiophen-2-yl- hexanoylamino-butyric acid | 1RWX_A |
CD | C14.001 | caspase-1 | Cys285Ala mutant | 1SC1 |
CD | C14.001 | caspase-1 | Cys285Ala mutant; complex with malonate | 1SC3 |
CD | C14.001 | caspase-1 | Cys285Ala mutant; after malonate complex dissociation | 1SC4 |
CD | C14.001 | caspase-1 | Cys285Ala, Cys362Ala, Cys364Ala, Cys397Ala mutant; complex with 1-methyl-3- trifluoromethyl-1H-thieno[2,3-C]pyrazole-5-carboxylic acid (2-mercapto-ethyl)-amide | 2FQQ_A |
CD | C14.001 | caspase-1 | Cys362Ala, Cys364Ala, Cys397Ala mutant; complex with 3-[2-(2- benzyloxycarbonylamino-3-methyl-butyrylamino)- propionylamino]-4-oxo-pentanoic acid (z-VAD-FMK) | 2H48_A |
CD | C14.001 | caspase-1 | Glu390Asp mutant; complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl- butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-vad- fmk) | 2H4W_A |
CD | C14.001 | caspase-1 | Arg286Lys mutant; complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl- butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-vad- fmk) | 2H4Y_A |
CD | C14.001 | caspase-1 | Glu390Asp, Arg286Lys mutant; complex with 3-[2-(2- benzyloxycarbonylamino-3-methyl-butyrylamino)- propionylamino]-4-oxo-pentanoic acid | 2H51_A |
CD | C14.001 | caspase-1 | Thr388Ala mutant; complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl- butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-vad- fmk) | 2H54_A |
CD | C14.001 | caspase-1 | complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl-butyrylamino)- propionylamino]-4-oxo-pentanoic acid (z-VAD-FMK) | 2HBQ_A |
CD | C14.001 | caspase-1 | Arg286Ala mutant; complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl- butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-VAD- FMK) | 2HBR_A |
CD | C14.001 | caspase-1 | Glu390Ala mutant; complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl- butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-VAD- FMK) | 2HBY_A |
CD | C14.001 | caspase-1 | Arg286Ala, Glu390Ala mutant; complex with 3-[2-(2-benzyloxycarbonylamino-3- methyl-butyrylamino)-propionylamino]-4-oxo-pentanoic acid (Z-VAD-FMK) | 2HBZ_A |
CD | C14.001 | caspase-1 | 3D6F | |
CD | C14.001 | caspase-1 | 3D6H | |
CD | C14.001 | caspase-1 | 3D6M | |
CD | C14.001 | caspase-1 | procaspase-1 zymogen domain crystal strucutre | 3E4C_A |
CD | C14.001 | caspase-1 | 3NS7 | |
CD | C14.001 | caspase-1 | crystal structure of human caspase-1 with 2-((2-naphthoyl)-l-valyl)-4-hydroxy-n-((3s)-2-hydroxy-5-oxotetrahydrofuran-3-yl)-2- azabicyclo[2.2.2]octane-3-carboxamide (compound 1) | 5MMV_A |
CD | C14.001 | caspase-1 | crystal structure of human caspase-1 with (3s,6s,10as)-n-((2s,3s)-2- hydroxy-5-oxotetrahydrofuran-3-yl)-6-(isoquinoline-1-carboxamido)-5- oxodecahydropyrrolo[1,2-a]azocine-3-carboxamide (pge-3935199) | 5MTK_A |
CD | C14.001 | caspase-1 | complex with ac-fltd-cmk | 6BZ9_A |
CD | C14.001 | caspase-1 | crystal structure of human caspase-1 with n-3-[1-((s)-2-hydroxy-5- oxo-tetrahydro-furan-3-ylcarbamoyl)-ethyl]-1-methyl-2,4-dioxo-1,2,3, 4-tetrahydro-pyrimidin-5-yl-4-(quinoxalin-2-ylamino)-benzamide | 6F6R_A |
CD | C14.002 | CED-3 peptidase | 4M9R | |
CD | C14.003 | caspase-3 | complex with tetrapeptide inhibitor acetyl-Asp-Val-Ala-Asp-fluoromethylketone | 1CP3 |
CD | C14.003 | caspase-3 | complex with isatin sulfonamide inhibitor 1-methyl-5-(2-phenoxymethyl-pyrrolidine-1-sulfonyl)-1H-indole-2,3-dione | 1GFW |
CD | C14.003 | caspase-3 | complex with BIRC-4 protein | 1I3O_A |
CD | C14.003 | caspase-3 | 1NME | |
CD | C14.003 | caspase-3 | 1NMQ | |
CD | C14.003 | caspase-3 | 1NMS | |
CD | C14.003 | caspase-3 | complex with acetyl-Asp-Glu-Val-Asp-CHO | 1PAU_A |
CD | C14.003 | caspase-3 | 1QX3 | |
CD | C14.003 | caspase-3 | complex with nicotinic acid aldehyde (3S)-3-[(5-bromopyridin-3-yl)carbonyl]amino-4-oxobutanoic acid | 1RE1_A |
CD | C14.003 | caspase-3 | complex with pryazinone inhibitor 3-(2-5-tert-butyl-3-[(4-methyl-furazan-3-ylmethyl)-amino]-2-oxo-2H-pyrazin-1-yl-butyrylamino)-5-(hexyl-methyl-amino)-4-oxo-pentanoic acid anion | 1RHJ_A |
CD | C14.003 | caspase-3 | complex with phenyl- propyl-ketone N-acetyl-L-alpha-aspartyl-L-alpha-glutamyl-N-[(1S)-1-(carboxymethyl)-2-oxo-5-phenylpentyl]-L-valinamide | 1RHK_A |
CD | C14.003 | caspase-3 | complex with nicotinic acid aldehyde 4-[5-(2-carboxy-1-formyl-ethylcarbamoyl)-pyridin-3-yl]-benzoic acid | 1RHM_A |
CD | C14.003 | caspase-3 | complex with bromomethoxyphenyl inhibitor 5-S-benzyl-3-(N-[(5-bromo-2-methoxyphenyl)acetyl]- L-valylamino)-2,3-dideoxy-5-thio-D-erythro- pentonic acid | 1RHQ_A |
CD | C14.003 | caspase-3 | complex with cinnamic acid methyl ester (3S)-5-[(2-chloro-6-fluorobenzyl)sulfanyl]-3-[N-(2-ethoxy-5-[(1E)-3-methoxy-3-oxoprop-1-enyl]phenylacetyl)-D-valyl]amino-4-oxopentanoic acid | 1RHR_A |
CD | C14.003 | caspase-3 | complex with 5,6,7 tricyclic peptidomimetic inhibitor (3S)-3-[((2S)-5-[(N-acetyl-L-alpha-aspartyl)amino]-4-oxo-1,2,4,5,6,7-hexahydroazepino[3,2,1-hi]indol-2-ylcarbonyl)amino]-5-(benzylsulfanyl)-4-oxopentanoic acid | 1RHU_A |
CD | C14.003 | caspase-3 | complex with (5S,8R,11S)-8-(2-carboxyethyl)-5-(carboxymethyl)-14-(4-ethoxy-4-oxobutanoyl)-11-(1-methylethyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13,14-pentaazahexadecan-16-oic acid | 2C1E_A |
CD | C14.003 | caspase-3 | complex with (5S,8R,11S)-8-(2-carboxyethyl)-5-(carboxymethyl)-14-(4-ethoxy-4-oxobutanoyl)-11-(1-methylethyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13,14-pentaazahexadecan-16-oic acid | 2C2K_A |
CD | C14.003 | caspase-3 | complex with (5S,8R,11S)-14-[4-(benzyloxy)-4-oxobutanoyl]-8-(2-carboxyethyl)-5-(carboxymethyl)-11-(1-methylethyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13,14-pentaazahexadecan-16-oic acid | 2C2M_A |
CD | C14.003 | caspase-3 | complex with Cbz-Asp-Glu-Val-AAsp-CHCH-CON(CH3)CH2Ph | 2C2O_A |
CD | C14.003 | caspase-3 | complex with CBZ-Asp-Glu-Val-azaAsp-EP-CO-N(CH2PH)2 | 2CDR_A |
CD | C14.003 | caspase-3 | extended substrate recognition in caspase-3 revealed by high resolution x-ray structure analysis | 2CJX_A |
CD | C14.003 | caspase-3 | extended substrate recognition in caspase-3 revealed by high resolution x-ray structure analysis | 2CJY_A |
CD | C14.003 | caspase-3 | complex with CBZ-Asp-Glu-Val-azaAsp-EP-COO-CH2Ph | 2CNK_A |
CD | C14.003 | caspase-3 | complex with CBZ-Asp-Glu-Val-azaAsp-EP-CO-NH-CH2Ph | 2CNL_A |
CD | C14.003 | caspase-3 | complex with CBZ-Ile-Glu-Thr-azaAsp-EP-CO-Ala-NH-CH2-Ph | 2CNN_A |
CD | C14.003 | caspase-3 | complex with CBZ-Glu-Val-azaAsp-(S,S)EP-CO-NHCH2CH2Ph | 2CNO_A |
CD | C14.003 | caspase-3 | extended substrate recognition in caspase-3 revealed by high resolution x-ray structure analysis | 2DKO_A |
CD | C14.003 | caspase-3 | complex with inhibitor Ac-DEVD-CHO | 2H5I_A |
CD | C14.003 | caspase-3 | complex with inhibitor Ac-DMQD-CHO | 2H5J_A |
CD | C14.003 | caspase-3 | complex with inhibitor Ac-VDVAD-CHO | 2H65_A |
CD | C14.003 | caspase-3 | 2J30 | |
CD | C14.003 | caspase-3 | 2J31 | |
CD | C14.003 | caspase-3 | 2J32 | |
CD | C14.003 | caspase-3 | 2J33 | |
CD | C14.003 | caspase-3 | 2XYG | |
CD | C14.003 | caspase-3 | 2XYH | |
CD | C14.003 | caspase-3 | 2XYP | |
CD | C14.003 | caspase-3 | 2XZD | |
CD | C14.003 | caspase-3 | 2XZT | |
CD | C14.003 | caspase-3 | 2Y0B | |
CD | C14.003 | caspase-3 | 3DEH | |
CD | C14.003 | caspase-3 | 3DEI | |
CD | C14.003 | caspase-3 | 3DEJ | |
CD | C14.003 | caspase-3 | 3DEK | |
CD | C14.003 | caspase-3 | complex with inhibitor Ac-LDESD-CHO | 3EDQ_A |
CD | C14.003 | caspase-3 | caspase-3 binds diverse p4 residues in peptides | 3GJQ_A |
CD | C14.003 | caspase-3 | caspase-3 binds diverse p4 residues in peptides | 3GJR_A |
CD | C14.003 | caspase-3 | caspase-3 binds diverse p4 residues in peptides | 3GJS_A |
CD | C14.003 | caspase-3 | caspase-3 binds diverse p4 residues in peptides | 3GJT_A |
CD | C14.003 | caspase-3 | 3H0E | |
CD | C14.003 | caspase-3 | 3ITN | |
CD | C14.003 | caspase-3 | 3KJF | |
CD | C14.003 | caspase-3 | 3PCX | |
CD | C14.003 | caspase-3 | 3PD0 | |
CD | C14.003 | caspase-3 | 3PD1 | |
CD | C14.003 | caspase-3 | 4DCJ | |
CD | C14.003 | caspase-3 | 4DCO | |
CD | C14.003 | caspase-3 | 4DCP | |
CD | C14.003 | caspase-3 | 4EHA | |
CD | C14.003 | caspase-3 | 4EHD | |
CD | C14.003 | caspase-3 | 4EHF | |
CD | C14.003 | caspase-3 | 4EHH | |
CD | C14.003 | caspase-3 | 4EHK | |
CD | C14.003 | caspase-3 | 4EHL | |
CD | C14.003 | caspase-3 | 4EHN | |
CD | C14.003 | caspase-3 | 4JJE | |
CD | C14.003 | caspase-3 | 4JQY | |
CD | C14.003 | caspase-3 | 4JQZ | |
CD | C14.003 | caspase-3 | 4JR0 | |
CD | C14.003 | caspase-3 | 4PRY | |
CD | C14.003 | caspase-3 | 4PS0 | |
CD | C14.003 | caspase-3 | 4QTX | |
CD | C14.003 | caspase-3 | 4QTY | |
CD | C14.003 | caspase-3 | 4QU0 | |
CD | C14.003 | caspase-3 | 4QU5 | |
CD | C14.003 | caspase-3 | 4QU8 | |
CD | C14.003 | caspase-3 | 4QU9 | |
CD | C14.003 | caspase-3 | 4QUA | |
CD | C14.003 | caspase-3 | 4QUB | |
CD | C14.003 | caspase-3 | 4QUD | |
CD | C14.003 | caspase-3 | 4QUE | |
CD | C14.003 | caspase-3 | 4QUG | |
CD | C14.003 | caspase-3 | 4QUH | |
CD | C14.003 | caspase-3 | 4QUI | |
CD | C14.003 | caspase-3 | 4QUJ | |
CD | C14.003 | caspase-3 | 4QUL | |
CD | C14.003 | caspase-3 | Val266Ala mutant | 5I9B_A |
CD | C14.003 | caspase-3 | Val266Cys mutant | 5I9T_A |
CD | C14.003 | caspase-3 | Val266Asp mutant | 5IAB_A |
CD | C14.003 | caspase-3 | Val266Phe mutant | 5IAE_A |
CD | C14.003 | caspase-3 | Val266Gln mutant | 5IAG_A |
CD | C14.003 | caspase-3 | Val266Leu mutant | 5IAJ_A |
CD | C14.003 | caspase-3 | Val266Ser mutant | 5IAK_A |
CD | C14.003 | caspase-3 | Val266Asn mutant | 5IAN_A |
CD | C14.003 | caspase-3 | Val266Trp mutant | 5IAR_A |
CD | C14.003 | caspase-3 | Val266Tyr mutant | 5IAS_A |
CD | C14.003 | caspase-3 | Val266Ile mutant | 5IBC_A |
CD | C14.003 | caspase-3 | Val266Met mutant | 5IBP_A |
CD | C14.003 | caspase-3 | Val266Lys mutant | 5IBR_A |
CD | C14.003 | caspase-3 | complex with DEVE peptide | 5IC4_A |
CD | C14.003 | caspase-3 | caspase-3 mutant - t245d,s249d | 6BFJ_A |
CD | C14.003 | caspase-3 | caspase-3 mutant- t245a | 6BFK_A |
CD | C14.003 | caspase-3 | caspase-3 mutant- d9a,d28a,t245d | 6BFL_A |
CD | C14.003 | caspase-3 | caspase-3 mutant- t245d | 6BFO_A |
CD | C14.003 | caspase-3 | Asp9Ala/Asp28Ala/Ser150Asp mutant | 6BG0_A |
CD | C14.003 | caspase-3 | Asp9Ala/Asp28Ala/Ser150Glu mutant | 6BG1_A |
CD | C14.003 | caspase-3 | caspase-3 mutant- t152d | 6BG4_A |
CD | C14.003 | caspase-3 | caspase-3 mutant- d9a,d28a,t152d | 6BGK_A |
CD | C14.003 | caspase-3 | Ser150Asp mutant | 6BGQ_A |
CD | C14.003 | caspase-3 | caspase-3 mutant - s150e | 6BGR_A |
CD | C14.003 | caspase-3 | caspase-3 mutant - s150y | 6BGS_A |
CD | C14.003 | caspase-3 | caspase-3 mutant - t152a | 6BH9_A |
CD | C14.003 | caspase-3 | caspase-3 mutant - t152v | 6BHA_A |
CD | C14.003 | caspase-3 | complex with ac-dw3-ke | 6CKZ_A |
CD | C14.003 | caspase-3 | complex with ac-ats009-ke | 6CL0_A |
CD | C14.003 | caspase-3 | zebra fish caspase-3 ***caveat 5jft caspase should be connected to the chloromethyl ketone ***caveat 2 5jft residual terminus of the inhibitor through hemithioacetal ***caveat 3 5jft bond, but the model does not reflect the ideal ***caveat 4 5jft hemithio | 5JFT_A |
CD | C14.004 | caspase-7 | complex with acetyl-Asp-Glu-Val-Asp-CHO | 1F1J |
CD | C14.004 | caspase-7 | precursor | 1GQF |
CD | C14.004 | caspase-7 | complex with XIAP | 1I4O_A |
CD | C14.004 | caspase-7 | complex with XIAP inhibitor | 1I51_A |
CD | C14.004 | caspase-7 | 1K86 | |
CD | C14.004 | caspase-7 | precursor | 1K88 |
CD | C14.004 | caspase-7 | complex with XIAP-BIR2 | 1KMC_A |
CD | C14.004 | caspase-7 | theoretical model; complex with AC-DEVD inhibitor | 1MIA |
CD | C14.004 | caspase-7 | complex with dica allosteric inhibitor | 1SHJ_A |
CD | C14.004 | caspase-7 | complex with FICA allosteric inhibitor | 1SHL |
CD | C14.004 | caspase-7 | complex with inhibitor Ac-DMQD-CHO | 2QL5_A |
CD | C14.004 | caspase-7 | complex with inhibitor Ac-IEPD-CHO | 2QL7_A |
CD | C14.004 | caspase-7 | complex with inhibitor Ac-DQMD-CHO | 2QL9_A |
CD | C14.004 | caspase-7 | complex with inhibitor Ac-ESMD-CHO | 2QLB_A |
CD | C14.004 | caspase-7 | complex with inhibitor Ac-DNLD-CHO | 2QLF_A |
CD | C14.004 | caspase-7 | complex with inhibitor Ac-WEHD-CHO | 2QLJ_A |
CD | C14.004 | caspase-7 | complex with acetyl- LDESD-CHO | 3EDR_A |
CD | C14.004 | caspase-7 | mature caspase-7 i213a with devd-cho inhibitor bound to active site | 3H1P_A |
CD | C14.004 | caspase-7 | complex with acetyl-yvad- cho | 3IBC_A |
CD | C14.004 | caspase-7 | crystal structure of unliganded caspase-7 | 3IBF_A |
CD | C14.004 | caspase-7 | redox-controlled | 3R5K_A |
CD | C14.004 | caspase-7 | crystal structure of caspase-7 | 4FDL_A |
CD | C14.004 | caspase-7 | complex with allosteric inhibitor | 4FEA_A |
CD | C14.004 | caspase-7 | crystal structure of mutant form of caspase-7 | 4HQ0_A |
CD | C14.004 | caspase-7 | crystal structure of mutant form of caspase-7 | 4HQR_A |
CD | C14.004 | caspase-7 | complex with darpin c7_16 | 4JB8_A |
CD | C14.004 | caspase-7 | caspase-3 specific unnatural amino acid peptides | 4JJ8_A |
CD | C14.004 | caspase-7 | precursor in complex with Ac-DEVD-CMK | 4JR1 |
CD | C14.004 | caspase-7 | human procaspase-7/caspase-7 heterodimer bound to ac-devd-cmk | 4JR2_A |
CD | C14.004 | caspase-7 | complex with darpin d7.18 | 4LSZ_A |
CD | C14.004 | caspase-7 | caspase-7 variant 4 (v4) with reprogrammed substrate specificity due to y230v/w232y/s234v/q276d substitutions bound to veid inhibitor. | 4ZVO_A |
CD | C14.004 | caspase-7 | caspase-7 variant 2 (v2) with reprogrammed substrate specificity due to y230v/w232m/q276c substitutions bound to devd inhibitor. | 4ZVP_A |
CD | C14.004 | caspase-7 | caspase-7 variant 2 (v2) with reprogrammed substrate specificity due to y230v/w232m/q276c substitutions bound to veid inhibitor. | 4ZVQ_A |
CD | C14.004 | caspase-7 | caspase-7 variant 4 (v4) with reprogrammed substrate specificity due to y230v/w232y/s234v/q276d substitutions bound to devd inhibitor. | 4ZVR_A |
CD | C14.004 | caspase-7 | caspase-7 variant 1 (v1) with reprogrammed substrate specificity due to y230a/w232m/s234n substitutions, bound to devd inhibitor. | 4ZVS_A |
CD | C14.004 | caspase-7 | caspase-7 variant 1 (v1) with reprogrammed substrate specificity due to y230a/w232m/s234n substitutions, bound to veid inhibitor. | 4ZVT_A |
CD | C14.004 | caspase-7 | caspase-7 wild-type bound to the caspase-6 cognate tetrapeptide inhibitor ac-veid-cho | 4ZVU_A |
CD | C14.004 | caspase-7 | complex with DEVE peptide | 5IC6_A |
CD | C14.004 | caspase-7 | caspase-7 s239e phosphomimetic | 5K20_A |
CD | C14.004 | caspase-7 | crystal structure of human caspase-7 soaked with allosteric inhibitor 2-[(2-acetylphenyl)sulfanyl]benzoic acid | 5V6U_A |
CD | C14.004 | caspase-7 | crystal structure of human caspase-7 soaked with allosteric inhibitor 2-[2-(4-chlorophenyl)-2-oxoethyl]sulfanylbenzoic acid | 5V6Z_A |
CD | C14.004 | caspase-7 | complex with ac-dw3-ke | 6CL1_A |
CD | C14.004 | caspase-7 | complex with ac-ats009-ke | 6CL2_A |
CD | C14.005 | caspase-6 | theoretical model; complex with AC-IETD inhibitor | 1MI9 |
CD | C14.005 | caspase-6 | 2WDP | |
CD | C14.005 | caspase-6 | 3K7E | |
CD | C14.005 | caspase-6 | 3NKF | |
CD | C14.005 | caspase-6 | 3NR2 | |
CD | C14.005 | caspase-6 | 3OD5 | |
CD | C14.005 | caspase-6 | 3P45 | |
CD | C14.005 | caspase-6 | 3P4U | |
CD | C14.005 | caspase-6 | 3QNW | |
CD | C14.005 | caspase-6 | 3S70 | |
CD | C14.005 | caspase-6 | 3S8E | |
CD | C14.005 | caspase-6 | 3V6L | |
CD | C14.005 | caspase-6 | 3V6M | |
CD | C14.005 | caspase-6 | 4EJF | |
CD | C14.005 | caspase-6 | 4FXO | |
CD | C14.005 | caspase-6 | 4HVA | |
CD | C14.005 | caspase-6 | 4IYR | |
CD | C14.005 | caspase-6 | 4N5D | |
CD | C14.005 | caspase-6 | 4N6G | |
CD | C14.005 | caspase-6 | 4N7J | |
CD | C14.005 | caspase-6 | 4N7M | |
CD | C14.005 | caspase-6 | 4NBK | |
CD | C14.005 | caspase-6 | 4NBL | |
CD | C14.005 | caspase-6 | 4NBN | |
CD | C14.005 | caspase-6 | Ala109Thr mutant | 6DEU_A |
CD | C14.005 | caspase-6 | Glu35Lys mutant | 6DEV_A |
CD | C14.006 | caspase-2 | complex with acetyl-Leu-Asp-Glu-Ser-Asp-CHO | 1PYO_A |
CD | C14.006 | caspase-2 | inhibition of caspase-2 by a designed ankyrin repeat protein (darpin) | 2P2C_A |
CD | C14.006 | caspase-2 | crystal structure of active caspase-2 bound with ac-advad-cho | 3R5J_A |
CD | C14.006 | caspase-2 | crystal structure of active caspase-2 bound with ac-vdvad-cho | 3R6G_A |
CD | C14.006 | caspase-2 | caspase-2 t380a bound with ac-vdvad-cho | 3R6L_A |
CD | C14.006 | caspase-2 | complex with one molecule of Ac-DVAD-CHO | 3R7B_A |
CD | C14.006 | caspase-2 | complex with two molecules of Ac-DVAD-CHO | 3R7N_A |
CD | C14.006 | caspase-2 | crystal structure of apo caspase2 | 3R7S_A |
CD | C14.006 | caspase-2 | complex with chdi ligand 33c | 3RJM_A |
CD | C14.009 | caspase-8 | complex with Z-Asp-Glu-Val-Asp-CHO inhibitor | 1F9E |
CD | C14.009 | caspase-8 | complex with baculovirus P35 inhibitor | 1I4E_B |
CD | C14.009 | caspase-8 | complex with tripeptide ketone inhibitor Z-Glu-Val-Asp-dichloromethylketone | 1QDU |
CD | C14.009 | caspase-8 | complex with acetyl-Ile-Glu-Thr-aspartic aldehyde | 1QTN |
CD | C14.009 | caspase-8 | complex with | 2C2Z_A |
CD | C14.009 | caspase-8 | alternative p35-caspase-8 complex | 2FUN_B |
CD | C14.009 | caspase-8 | complex with darpin-8.4 | 2Y1L_A |
CD | C14.009 | caspase-8 | zymogen; complex with c-flipl | 3H11_B |
CD | C14.009 | caspase-8 | complex with a covalent inhibitor | 3KJN_A |
CD | C14.009 | caspase-8 | complex with a covalent inhibitor | 3KJQ_A |
CD | C14.009 | caspase-8 | caspase-3 specific unnatural amino acid-based peptides | 4JJ7_A |
CD | C14.009 | caspase-8 | caspase-8 specific unnatural amino acid peptides | 4PRZ_A |
CD | C14.009 | caspase-8 | caspase-8 specific unnatural amino acid peptides | 4PS1_A |
CD | C14.010 | caspase-9 | cleaved form lacking caspase recruitment domain | 1JXQ |
CD | C14.010 | caspase-9 | complex with BIR-4 protein | 1NW9_B |
CD | C14.010 | caspase-9 | dimeric form | 2AR9_A |
CD | C14.010 | caspase-9 | ciap1-bir3 in complex with n-terminal peptide from caspase- 9 (atpfqe) | 3D9T_C |
CD | C14.010 | caspase-9 | complex with NleF | 3V3K_A |
CD | C14.010 | caspase-9 | propeptide only; complex with apoptotic protease activating factor 1 | 3YGS |
CD | C14.015 | caspase (insect 1) | 1M72 | |
CD | C14.015 | caspase (insect 1) | structure of pro-sf-caspase-1 | 2NN3_C |
CD | C14.015 | caspase (insect 1) | 3SIP_A | |
CD | C14.015 | caspase (insect 1) | 3SIR | |
CD | C14.019 | caspase DRONC (Drosophila melanogaster) | complex with DIAP1 | 1Q4Q_K |
CD | C14.019 | caspase DRONC (Drosophila melanogaster) | Cys284Arg, Cys318Ala double mutant | 2FP3 |
CD | C14.019 | caspase DRONC (Drosophila melanogaster) | 3J9K | |
CD | C14.026 | paracaspase | 2G7R | |
CD | C14.026 | paracaspase | 3BFO | |
CD | C14.026 | paracaspase | 3K0W | |
CD | C14.026 | paracaspase | complex with Val-Arg-Pro-Arg inhibitor | 3UO8 |
CD | C14.026 | paracaspase | complex with Val-Arg-Pro-Arg inhibitor | 3UOA |
CD | C14.026 | paracaspase | 3V4O | |
CD | C14.026 | paracaspase | 3V55 | |
CD | C14.026 | paracaspase | 4I1P | |
CD | C14.026 | paracaspase | 4I1R | |
CD | C14.026 | paracaspase | human malt1(329-728) in complex with mlt-747 | 6F7I_A |
CD | C14.026 | paracaspase | human malt1(329-728) in complex with mlt-748 | 6H4A_A |
CD | C14.026 | paracaspase | 3V4L | |
CD | C14.033 | metacaspase-4 (Arabidopsis-type) | 6W8R | |
CD | C14.035 | metacaspase Yca1 (Saccharomyces cerevisiae-type) | 4F6O | |
CD | C14.035 | metacaspase Yca1 (Saccharomyces cerevisiae-type) | 4F6P | |
CD | C14.044 | metacaspase TbMCA2 | 4AF8 | |
CD | C14.044 | metacaspase TbMCA2 | in presence of Samarium | 4AFP |
CD | C14.044 | metacaspase TbMCA2 | Cys213Ala mutant | 4AFR |
CD | C14.044 | metacaspase TbMCA2 | in presence of calcium chloride | 4AFV |
CD | C14.048 | bacterial metacaspase | 3BIJ_A | |
CD | C14.971 | FLIP protein | zymogen; complex with caspase-8 | 3H11_A |
CD | C14.971 | FLIP protein | c-flipl protease-like domain | 3H13_A |
CD | C14.UPA | subfamily C14A unassigned peptidases | complex with ACE-DEVD inhibitor | 6WI4 |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 1AUG | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 3RNZ | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 3RO0 | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 3GIU_A | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 1A2Z_A | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 1IOF | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | Cys142, C188 deletion mutant | 1IOI |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | structure of mutant pyrrolidone carboxyl peptidase (e192a) from a hyperthermophile, pyrococcus furiosus | 1X10_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | structure of mutant pyrrolidone carboxyl peptidase (e192d) from a hyperthermophile, pyrococcus furiosus | 1X12_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | structure of mutant pyrrolidone carboxyl peptidase (e192q) from a hyperthermophile, pyrococcus furiosus | 1Z8T_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | structure of mutant pyrrolidone carboxyl peptidase (e192i) from a hyperthermophile, pyrococcus furiosus | 1Z8W_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | structure of mutant pyrrolidone carboxyl peptidase (e192v) from a hyperthermophile, pyrococcus furiosus | 1Z8X_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | fragment 1-204 | 2DF5_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | Ala199Pro mutant | 2EO8 |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 1IU8 | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | crystal structure of pyrrolidone carboxylate peptidase i from deionococcus radiodurans r1 | 5Z40_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | crystal structure of pyrrolidone carboxylate peptidase i with disordered loop a from deinococcus radiodurans r1 | 5Z47_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | crystal structure of pyrrolidone carboxylate peptidase i from deinococcus radiodurans r1 bound to pyroglutamate | 5Z48_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 3LAC | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | 2EBJ | |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | crystal structure of a pyrrolidone-carboxylate peptidase 1 (target id nysgrc-012831) from xenorhabdus bovienii ss-2004 | 4GXH_A |
CF | C15.001 | pyroglutamyl-peptidase I (prokaryote) | crystal structure of a pyrrolidone-carboxylate peptidase 1 (target id nysgrc-012831) from xenorhabdus bovienii ss-2004 in space group p21 | 4HPS_A |
CA | C16.005 | avian infectious bronchitis coronavirus papain-like peptidase | 3EJF | |
CA | C16.005 | avian infectious bronchitis coronavirus papain-like peptidase | 3EKE | |
CA | C16.005 | avian infectious bronchitis coronavirus papain-like peptidase | 4X2Z | |
CA | C16.005 | avian infectious bronchitis coronavirus papain-like peptidase | Cys101Ser mutant; complex with ubiquitin | 5BZ0_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1P76 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1P9T | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1PA5 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1PUK | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1Q1X | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1Q2W | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1QZ8 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1UJ1 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1UK2 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1UK3 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1UW7 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1WOF | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1YSY | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1Z1I | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 1Z1J | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2A5A | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2A5I | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2A5K | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2ACF | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2AHM | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2AJ5 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2ALV | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2AMD | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2AMQ | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2BX3 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2BX4 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2C3S | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2D2D | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2DUC | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2FAV | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2FE8 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2FYG | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2G9T | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GA6 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GDT | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GRI | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GX4 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GZ7 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GZ8 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2GZ9 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2H2Z | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2HOB | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2HSX | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2IDY | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2KAF | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2KQV | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2KQW | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2KYS | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2LIZ | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2OP9 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | Gly11Ala mutant | 2PWX_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | Asn214Ala mutant | 2QC2_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | monomeric form of mutant | 2QCY_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | structure-based design and synthesis and biological evaluation of peptidomimetic sars-3clpro inhibitors | 2QIQ_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2W2G | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2WCT | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2YY4_A | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2Z3C | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2Z3D | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2Z3E | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | complex with tdt | 2Z94_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | complex with pma | 2Z9G_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | complex with epdtc | 2Z9J_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | complex with jmf1600 | 2Z9K_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | complex with jmf1586 | 2Z9L_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2ZU4 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 2ZU5 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3ATW | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3AVZ | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3AW0 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3AW1 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | development of broad-spectrum halomethyl ketone inhibitors against coronavirus main protease 3clpro | 3D62_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3E91 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | a new class of papain-like protease/deubiquitinase inhibitors blocks sars virus replication | 3E9S_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3EA7 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3EA8 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3EA9 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3EAJ | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3EE7 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3F9E | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3F9F | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3F9G | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3F9H | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3FZD | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3IWM | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3M3S | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3M3T | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3M3V | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3MJ5 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3R24 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SN8 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SNA | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SNB | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SNC | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SND | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SNE | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3SZN | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3TIT | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3TIU | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3TNS | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3TNT | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3V3M | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3VB3 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3VB4 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3VB5 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3VB6 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 3VB7 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 4HI3 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 4M0W | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 4MDS | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 4MM3 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 4OVZ | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | 4OW0 | |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | complex with glycerol | 5Y3E_A |
CA | C16.009 | severe acute respiratory syndrome coronavirus papain-like peptidase | crystal structure of sars coronavirus papain-like protease conjugated with beta-mercaptoethanol | 5Y3Q_A |
CA | C16.011 | Middle East respiratory syndrome coronavirus papain-like peptidase | 5KO3 | |
CA | C16.011 | Middle East respiratory syndrome coronavirus papain-like peptidase | 4P16 | |
CM | C18.001 | hepatitis C virus peptidase 2 | 2A4G | |
CM | C18.001 | hepatitis C virus peptidase 2 | 2GVF | |
CM | C18.001 | hepatitis C virus peptidase 2 | catalytic domain of the NS2 protein only | 2HD0 |
CM | C18.001 | hepatitis C virus peptidase 2 | 3HKW | |
CM | C18.001 | hepatitis C virus peptidase 2 | 3KN2 | |
CM | C18.001 | hepatitis C virus peptidase 2 | avoiding drug resistance against hcv ns3/4a protease inhibitors | 3M5M_C |
CM | C18.001 | hepatitis C virus peptidase 2 | visualizing atp-dependent rna translocation by the ns3 helicase from hcv | 3O8B_A |
CM | C18.001 | hepatitis C virus peptidase 2 | visualizing atp-dependent rna translocation by the ns3 helicase from hcv | 3O8C_A |
CM | C18.001 | hepatitis C virus peptidase 2 | visualizing atp-dependent rna translocation by the ns3 helicase from hcv | 3O8D_A |
CM | C18.001 | hepatitis C virus peptidase 2 | visualizing atp-dependent rna translocation by the ns3 helicase from hcv | 3O8R_A |
CM | C18.001 | hepatitis C virus peptidase 2 | 3QGH | |
CM | C18.001 | hepatitis C virus peptidase 2 | 3QGI | |
CM | C18.001 | hepatitis C virus peptidase 2 | 3RC4 | |
CM | C18.001 | hepatitis C virus peptidase 2 | 3RC5 | |
CM | C18.001 | hepatitis C virus peptidase 2 | crystal structure of hepatitis c virus ns3 helicase inhibitor co- complex with fragment 1 [(5-bromo-1h-indol-3-yl)acetic acid] | 4OJQ_A |
CM | C18.001 | hepatitis C virus peptidase 2 | crystal structure of hepatitis c virus ns3 helicase inhibitor co- complex with compound 7 [[1-(3-chlorobenzyl)-1h-indol-3-yl]acetic acid] | 4OK3_A |
CM | C18.001 | hepatitis C virus peptidase 2 | crystal structure of hepatitis c virus ns3 helicase inhibitor co- complex with compound 9 [1-(3-ethynylbenzyl)-1h-indol-3-yl]acetic acid] | 4OK5_A |
CM | C18.001 | hepatitis C virus peptidase 2 | crystal structure of hepatitis c virus ns3 helicase inhibitor co- complex with compound 13 [[1-(2-methoxy-5-nitrobenzyl)-1h-indol-3- yl]acetic acid] | 4OK6_A |
CM | C18.001 | hepatitis C virus peptidase 2 | crystal structure of hepatitis c virus ns3 helicase inhibitor co- complex with compound 19 [[6-(3,5-diaminophenyl)-1-(2-methoxy-5- nitrobenzyl)-1h-indol-3-yl]acetic acid] | 4OKS_A |
CA | C19.001 | ubiquitin-specific peptidase 5 | 2DAG | |
CA | C19.001 | ubiquitin-specific peptidase 5 | 2DAK | |
CA | C19.001 | ubiquitin-specific peptidase 5 | 2G43 | |
CA | C19.001 | ubiquitin-specific peptidase 5 | 2G45 | |
CA | C19.001 | ubiquitin-specific peptidase 5 | 3IHP | |
CA | C19.004 | Ubp3 ubiquitin peptidase | 2QIY | |
CA | C19.010 | ubiquitin-specific peptidase 4 | 2Y6E | |
CA | C19.010 | ubiquitin-specific peptidase 4 | 3JYU | |
CA | C19.011 | ubiquitin-specific peptidase 8 | 1WHB | |
CA | C19.011 | ubiquitin-specific peptidase 8 | N-terminal domain | 2A9U |
CA | C19.011 | ubiquitin-specific peptidase 8 | catalytic domain only | 2GFO |
CA | C19.011 | ubiquitin-specific peptidase 8 | complex with RING finger protein 41 | 2GWF |
CA | C19.011 | ubiquitin-specific peptidase 8 | 3N3K | |
CA | C19.011 | ubiquitin-specific peptidase 8 | 1UJ0 | |
CA | C19.012 | ubiquitin-specific peptidase 13 | 2L80 | |
CA | C19.012 | ubiquitin-specific peptidase 13 | 2LBC | |
CA | C19.013 | ubiquitin-specific peptidase 2 | complex with ubiquitin | 2HD5 |
CA | C19.013 | ubiquitin-specific peptidase 2 | complex with ubiquitin | 2IBI |
CA | C19.013 | ubiquitin-specific peptidase 2 | 3NHE | |
CA | C19.013 | ubiquitin-specific peptidase 2 | 3V6C | |
CA | C19.013 | ubiquitin-specific peptidase 2 | 3V6E | |
CA | C19.013 | ubiquitin-specific peptidase 2 | complex with ubiquitin and 6- thioguanine | 5XU8_A |
CA | C19.013 | ubiquitin-specific peptidase 2 | Cys276Ser mutant; complex with ubiquitin | 5XVE_A |
CA | C19.013 | ubiquitin-specific peptidase 2 | ubiquitin variant bound to usp2 | 6DGF_A |
CA | C19.014 | ubiquitin-specific peptidase 11 | 4MEL | |
CA | C19.015 | ubiquitin-specific peptidase 14 | 2AYN | |
CA | C19.015 | ubiquitin-specific peptidase 14 | complex with ubiquitin aldehyde | 2AYO |
CA | C19.015 | ubiquitin-specific peptidase 14 | 26S proteasome; complex with USP14-UbAl | 5GJQ_x |
CA | C19.015 | ubiquitin-specific peptidase 14 | usp14 catalytic domain with iu1 | 6IIK_A |
CA | C19.015 | ubiquitin-specific peptidase 14 | catalytic domain; complex with iu1-47 | 6IIL_A |
CA | C19.015 | ubiquitin-specific peptidase 14 | usp14 catalytic domain with iu1-206 | 6IIM_A |
CA | C19.015 | ubiquitin-specific peptidase 14 | usp14 catalytic domain with iu1-248 | 6IIN_A |
CA | C19.015 | ubiquitin-specific peptidase 14 | 1WGG | |
CA | C19.016 | ubiquitin-specific peptidase 7 | catalytic domain only | 1NB8_A |
CA | C19.016 | ubiquitin-specific peptidase 7 | complex with ubiquitin aldehyde | 1NBF |
CA | C19.016 | ubiquitin-specific peptidase 7 | 1YY6 | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 1YZE | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2F1W | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2F1X | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2F1Y | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2F1Z | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2FOJ | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2FOO | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2FOP | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2KVR | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2XXN | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 2YLM | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 3MQR | |
CA | C19.016 | ubiquitin-specific peptidase 7 | 3MQS | |
CA |