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Ligand:__I...
Compound type: RNA linking
The following list shows the 330 PDB entries that contain one or more instances of ligand __I. Where the structure contains more than one instance, the count is shown in brackets after the protein name.
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.PDB.Id
Title
1a31* Human reconstituted DNA topoisomerase i in covalent complex with a 22 base pair DNA duplex (x10)
1a6w* B1- 8 fv fragment complexed with a (4- hydroxy- 5- iodo- 3- nitrophenyl) acetate compound
1a6y* Crystal structure of reverb- DNA binding complex
1ais* Tata- binding protein/transcription factor (ii)b/tata- box complex from pyrococcus woesei (x2)
1alw* Inhibitor and calcium bound domain vi of porcine calpain (x2)
1arx* Crystal structures of cyanide- and triiodide- bound forms of arthromyces ramosus peroxidase at different ph values. Perturbations of active site residues and their implication in enzyme catalysis (x7)
1ary* Crystal structures of cyanide- and triiodide- bound forms of arthromyces ramosus peroxidase at different ph values. Perturbations of active site residues and their implication in enzyme catalysis (x7)
1b2k* Structural effects of monovalent anions on polymorphic lysozyme crystals (x17)
1bf4* Sso7d- gcgaacgc complex
1bke* Human serum albumin in a complex with myristic acid and tri- iodobenzoic acid (x6)
1bls* Beta- lactamase (cephalosporinase) complexed with a phosphonate inhibitor (x2)
1bsx* Structure and specificity of nuclear receptor- coactivator interactions (x6)
1c3x* Purine nucleoside phosphorylase from cellulomonas sp. In complex with 8- iodo- guanine (x3)
1c5n* Structural basis for selectivity of a small molecule, s1- binding, sub- micromolar inhibitor of urokinase type plasminogen activator
1c5q* Structural basis for selectivity of a small molecule, s1- binding, sub- micromolar inhibitor of urokinase type plasminogen activator
1c5r* Structural basis for selectivity of a small molecule, s1- binding, sub- micromolar inhibitor of urokinase type plasminogen activator
1c5w* Structural basis for selectivity of a small molecule, s1- binding, sub- micromolar inhibitor of urokinase type plasminogen activator
1c5x* Structural basis for selectivity of a small molecule, s1- binding, sub- micromolar inhibitor of urokinase type plasminogen activator
1cel* 1,4- beta- d- glucan cellobiohydrolase i (cellulase) (x2)
1ckt* Crystal structure of hmg1 domain a bound to a cisplatin- modified DNA duplex
1cqw* Nai cocrystallised with haloalkane dehalogenase from a rhodococcus species (x2)
1ctp* Camp- dependent protein kinase (capk) (catalytic subunit) (x2)
1czi* Chymosin complex with the inhibitor cp- 113972
1deh* Crystallization of human beta1 alcohol dehydrogenase (15 mg/ml) in 50 mm sodium phosphate (ph 7.5), 2.0 mm NAD+ and 1 mm 4- iodopyrazole at 25 oc, 13% (w/v) peg 8000 (x2)
1dh1* Structure of t. Gondii adenosine kinase bound to prodrug 2 7- iodotubercidin and amp- pcp
1ecv* Crystal structure of protein tyrosine phosphatase 1b complexed with 5- iodo- 2- (oxalyl- amino)- benzoic acid
1ek1* Crystal structure of murine soluble epoxide hydrolase complexed with ciu inhibitor (x2)
1eta* Transthyretin (prealbumin) naturally occurring variant with 1:1 mix of val and met at position 30 complexed with thyroxine (3,5,3',5'- tetraiodo- l- thyronine) (x8)
1etb* Transthyretin (prealbumin) mutant with ala 109 replaced by thr (a109t) complexed with thyroxine (3,5,3',5'- tetraiodo- l- thyronine) (x8)
1ewa* Dehaloperoxidase and 4- iodophenol (x2)
1f09* Crystal structure of the green fluorescent protein (gfp) variant yfp- h148q with two bound iodides (x2)
1f3m* Crystal structure of human serine/threonine kinase pak1 (x28)
1f64* Leu55pro ttr- idox theoretical model
1f86* Transthyretin thr119met protein stabilisation (x8)
1f9o* Crystal structure of the cellulase cel48f from c. Cellulolyticum with the thiooligosaccharide inhibitor pips- ig3 (x2)
1fz9* Methane monooxygenase hydroxylase, form ii cocrystallized with iodoethane (x8)
1ga1* Crystal structure analysis of pscp (pseudomonas serine- carboxyl proteinase) complexed with a fragment of iodotyrostatin (this enzyme renamed "sedolisin" in 2003)
1ga4* Crystal structure analysis of pscp (pseudomonas serine- carboxyl proteinase) complexed with inhibitor pseudoiodotyrostatin (this enzyme renamed "sedolisin" in 2003)
1ga5* Crystal structure of the orphan nuclear receptor rev- erb(alpha) DNA- binding domain bound to its cognate response element (x2)
1gjd* Engineering inhibitors highly selective for the s1 sites of ser190 trypsin- like serine protease drug targets
1gte* Dihydropyrimidine dehydrogenase (dpd) from pig, binary complex with 5- iodouracil (x4)
1gth* Dihydropyrimidine dehydrogenase (dpd) from pig, ternary complex with NADPH and 5- iodouracil (x2)
1gul* Human glutathione transferase a4- 4 complex with iodobenzyl glutathione (x8)
1gw9* Tri- iodide derivative of xylose isomerase from streptomyces rubiginosus (x29)
1gwa* Triiodide derivative of porcine pancreas elastase (x23)
1gwd* Tri- iodide derivative of hen egg- white lysozyme (x5)
1gwg* Tri- iodide derivative of apoferritin (x9)
1gza* Peroxidase
1hc0* Structure of lysozyme with periodate (x10)
1hc9* A- bungarotoxin complexed with high affinity peptide (x2)
1hdy* Alcohol dehydrogenase (beta- 2 isoenzyme, human) complexed with NAD+ and 4- iodopyrazole (x2)
1hk1* Human serum albumin complexed with thyroxine (3,3',5,5'- tetraiodo- l- thyronine) (x16)
1hk2* Human serum albumin mutant r218h complexed with thyroxine (3,3',5,5'- tetraiodo- l- thyronine) (x16)
1hk3* Human serum albumin mutant r218p complexed with thyroxine (3,3',5,5'- tetraiodo- l- thyronine) (x16)
1hk4* Human serum albumin complexed with thyroxine (3,3',5,5'- tetraiodo- l- thyronine) and myristic acid (tetradecanoic acid) (x4)
1hk5* Human serum albumin mutant r218h complexed with thyroxine (3,3',5,5'- tetraiodo- l- thyronine) and myristic acid (tetradecanoic acid) (x4)
1hp6* Crystal structure of a hairpin ribozyme in the catalytically- active conformation (x2)
1hso* Human alpha alcohol dehydrogenase (adh1a) (x2)
1htb* Crystallization of human beta3 alcohol dehydrogenase (10 mg/ml) in 100 mm sodium phosphate (ph 7.5), 7.5 mm NAD+ and 1 mm 4- iodopyrazole at 25 c (x2)
1huh* Differences in anionic inhibition of human carbonic anhydrase i revealed from the structures of iodide and gold cyanide inhibitor complexes (x5)
1ian* Human p38 map kinase inhibitor complex (x3)
1ict* Monoclinic form of human transthyretin complexed with thyroxine (t4) (x8)
1ie4* Rat transthyretin complex with thyroxine (t4) (x8)
1igb* Aeromonas proteolytica aminopeptidase complexed with the inhibitor para- iodo- d- phenylalanine hydroxamate
1imr* DNA (5'- d( Tp Gp Tp Ap Cp A)- 3'). Heterogen: 4'- deoxy- 4'- iododoxorubicin
1ims* DNA (5'- d( Cp Gp Ap Tp Cp G)- 3'). Heterogen: 4'- deoxy- 4'- iododoxorubicin
1j2j* Crystal structure of gga1 gat n- terminal region in complex with arf1 gtp form (x2)
1j99* Crystal structure of human dehydroepiandrosterone sulfotransferase in complex with substrate (x7)
1jj6* Testing the water- mediated hin recombinase DNA recognition by systematic mutations.
1jj8* Testing the water- mediated hin recombinase DNA recognition by systematic mutations
1jwg* Vhs domain of human gga1 complexed with cation- independent m6pr c- terminal peptide (x6)
1jzv* Crystal structure of a bulged RNA from the sl2 stem- loop of the HIV- 1 psi- RNA (x2)
1k4s* Human DNA topoisomerase i in covalent complex with a 22 base pair DNA duplex (x15)
1k61* Matalpha2 homeodomain bound to DNA
1ked* Human transthyretin (also called prealbumin) complex with 3, 3',5,5'- tetraiodothyroacetic acid (t4ac) (x8)
1kgi* Rat transthyretin (also called prealbumin) complex with 3, 3',5,5'- tetraiodothyroacetic acid (t4ac) (x8)
1ki6* Crystal structure of thymidine kinase from herpes simplex virus type i complexed with a 5- iodouracil anhydrohexitol nucleoside (x2)
1ki7* Crystal structure of thymidine kinase from herpes simplex virus type i complexed with 5- iododeoxyuridine (x2)
1l0s* Choristoneura fumiferana (spruce budworm) antifreeze protein isoform 337 (x8)
1lei* The kb DNA sequence from the hlv- ltr functions as an allosteric regulator of HIV transcription (x4)
1lij* Structure of t. Gondii adenosine kinase bound to prodrug 2 7- iodotubercidin and amp- pcp
1lkr* Monoclinic hen egg white lysozyme iodide (x17)
1m5k* Crystal structure of a hairpin ribozyme in the catalytically- active conformation (x2)
1m9b* Crystal structure of the 26 kda glutathione s- transferase from schistosoma japonicum complexed with gamma- glutamyl[s- (2- iodobenzyl)cysteinyl]glycine
1mey* Crystal structure of a designed zinc finger protein bound to DNA (x2)
1ml7* Crystal structure of nitrophorin 4 complexed with 4- iodopyrazole (x2)
1mou* Crystal structure of coral pigment (x5)
1mov* Crystal structure of coral protein mutant (x5)
1mqg* Crystal structure of the glur2 ligand binding core (s1s2j) in complex with iodo- willardiine at 2.15 angstroms resolution (x2)
1mxi* Structure of yibk from haemophilus influenzae (hi0766): a methyltransferase with a cofactor bound at a site formed by a knot
1my4* Crystal structure of glutamate receptor ligand- binding core in complex with iodo- willardiine in the zn crystal form (x3)
1n4g* Structure of cyp121, a mycobacterial p450, in complex with iodopyrazole
1n5m* Crystal structure of the mouse acetylcholinesterase- gallamine complex (x10)
1n7j* The structure of phenylethanolamine n- methyltransferase in complex with s- adenosylhomocysteine and an iodinated inhibitor (x2)
1n92* Horse liver alcohol dehydrogenase complexed with NAD+ and 4- iodopyrazole (x2)
1nh2* Crystal structure of a yeast tfiia/tbp/DNA complex (x2)
1njk* Crystal structure of escherichia coli hypothetical protein ybaw (x4)
1nlu* Pseudomonas sedolisin (serine- carboxyl proteinase) complexed with two molecules of pseudo- iodotyrostatin (x2)
1nq0* Tr receptor mutations conferring hormone resistance and reduced corepressor release exhibit decreased stability in the nterminal lbd (x3)
1nq1* Tr receptor mutations conferring hormone resistance and reduced corepressor release exhibit decreased stability in the nterminal lbd (x3)
1nq2* Two rth mutants with impaired hormone binding (x3)
1nuo* Two rth mutants with impaired hormone binding (x3)
1nx3* Calpain domain vi in complex with the inhibitor pd150606
1nzb* Crystal structure of wild type cre recombinase- loxp synapse (x2)
1o5b* Dissecting and designing inhibitor selectivity determinants at the s1 site using an artificial ala190 protease (ala190 upa)
1oj5* Crystal structure of the nco- a1 pas- b domain bound to the stat6 transactivation domain lxxll motif (x5)
1omk* The crystal structure of d(cacg(5iu)g) (x2)
1opm* Oxidized (cu2+) peptidylglycine alpha- hydroxylating monooxygenase (phm) with bound substrate (x4)
1orw* Crystal structure of porcine dipeptidyl peptidase iv (cd26) in complex with a peptidomimetic inhibitor (x4)
1ouq* Crystal structure of wild- type cre recombinase- loxp synapse (x2)
1ovl* Crystal structure of nurr1 lbd
1oxs* Crystal structure of glcv, the abc- atpase of the glucose abc transporter from sulfolobus solfataricus (x28)
1oxu* Crystal structure of glcv, the abc- atpase of the glucose abc transporter from sulfolobus solfataricus (x60)
1oxv* Crystal structure of glcv, the abc- atpase of the glucose abc transporter from sulfolobus solfataricus (x38)
1oxx* Crystal structure of glcv, the abc- atpase of the glucose abc transporter from sulfolobus solfataricus (x32)
1p59* Structure of a non- covalent endonuclease iii- DNA complex (x3)
1pge* Prostaglandin h2 synthase- 1 complexed with p- (2'- iodo- 5'- thenoyl)hydrotropic acid (iodosuprofen) (x2)
1pgf* Prostaglandin h2 synthase- 1 complexed with 1- (4- iodobenzoyl)- 5- methoxy- 2- methylindole- 3- acetic acid (iodoindomethacin), cis model (x2)
1pgg* Prostaglandin h2 synthase- 1 complexed with 1- (4- iodobenzoyl)- 5- methoxy- 2- methylindole- 3- acetic acid (iodoindomethacin), trans model (x2)
1pnn* Peptide nucleic acid (pna) complexed with DNA (x2)
1pvh* Crystal structure of leukemia inhibitory factor in complex with gp130 (x2)
1q0t* Ternary structure of t4dam with adohcy and DNA (x2)
1q3u* Crystal structure of a wild- type cre recombinase- loxp synapse: pre- cleavage complex (x2)
1q3v* Crystal structure of a wild- type cre recombinase- loxp synapse: phosphotyrosine covalent intermediate (x2)
1q8c* A conserved hypothetical protein from mycoplasma genitalium shows structural homology to nusb proteins (x7)
1qi9* X- ray siras structure determination of a vanadium- dependent haloperoxidase from ascophyllum nodosum at 2.0 a resolution (x5)
1qin* Human glyoxalase i complexed with s- (n- hydroxy- n- p- iodophenylcarbamoyl) glutathione (x2)
1qk0* Cel6a in complex with m- iodobenzyl beta- d- glucopyranosyl- beta(1,4)- d- xylopyranoside (x3)
1qms* Head- to- tail dimer of calicheamicin gamma- 1- i oligosaccharide bound to DNA duplex, nmr, 9 structures (x2)
1qon* Ache from drosophila melanogaster complex with tacrine derivative 9- (3- iodobenzylamino)- 1,2,3,4- tetrahydroacridine
1r60* A homology- derived model of human tripeptidyl- peptidase i (cln2)
1rlj* Structural genomics, a flavoprotein nrdi from bacillus subtilis (x2)
1rox* Human transthyretin complexed with thyroxine (x8)
1rrk* Crystal structure analysis of the bb segment of factor b (x2)
1rs0* Crystal structure analysis of the bb segment of factor b complexed with di- isopropyl- phosphate (dip) (x2)
1rtk* Crystal structure analysis of the bb segment of factor b complexed with 4- guanidinobenzoic acid (x2)
1s1m* Crystal structure of e. Coli ctp synthetase (x16)
1s6r* 908r class c beta- lactamase bound to iodo- acetamido- phenyl boronic acid
1s6v* Structure of a cytochromE C peroxidase- cytochromE C site specific cross- link
1s9i* X- ray structure of the human mitogen- activated protein kinase kinase 2 (mek2)in a complex with ligand and mgatp (x2)
1s9j* X- ray structure of the human mitogen- activated protein kinase kinase 1 (mek1) in a complex with ligand and mgatp
1sd5* Crystal structure of rv1626 (x15)
1sdw* Reduced (cu+) peptidylglycine alpha- hydroxylating monooxygenase with bound peptide and dioxygen (x6)
1sn0* Crystal structure of sea bream transthyretin in complex with thyroxine at 1.9a resolution (x8)
1sn5* Crystal structure of sea bream transthyretin in complex with triiodothyronine at 1.90a resolution (x6)
1so2* Catalytic domain of human phosphodiesterase 3b in complex with a dihydropyridazine inhibitor (x4)
1srs* Serum response factor (srf) core complexed with specific sre DNA
1t1f* Crystal structure of native antithrombin in its monomeric form (x21)
1t4e* Structure of human mdm2 in complex with a benzodiazepine inhibitor (x2)
1t6c* Structural characterization of the ppx/gppa protein family: crystal structure of the aquifex aeolicus family member
1t6h* Crystal structure t4 lysozyme incorporating an unnatural amino acid p- iodo- l- phenylalanine at position 153
1tb4* Crystal structure of aspartate- semialdehyde dehydrogenase from haemophilus influenzae with a bound periodate
1tf9* Streptomyces griseus aminopeptidase complexed with p- iodo- l- phenylalanine
1tha* Transthyretin (also called prealbumin) complex with 3,3'- diiodo- l- thyronine (x4)
1tuk* Crystal stucture of liganted type 2 non specific lipid transfer protein from wheat (x2)
1u12* M. Loti cyclic nucleotide binding domain mutant (x31)
1u65* Ache w. Cpt- 11
1ue2* Crystal structure of d(gi5cgaaagct)
1uhi* Crystal structure of i- aequorin (x2)
1ujk* Vhs domain of human gga1 complexed with c- terminal phosphopeptide from bace (x6)
1uo4* Structure based engineering of internal molecular surfaces of four helix bundles
1uo5* Structure based engineering of internal molecular surfaces of four helix bundles
1utx* Regulation of cytolysin expression by enterococcus faecalis: role of cylr2 (x9)
1v1f* Structure of the arabidopsis thaliana sos3 complexed with calcium(ii) and manganese(ii) ions (x7)
1v1g* Structure of the arabidopsis thaliana sos3 complexed with calcium(ii) ion (x7)
1v3o* Crystal structure of d(gcgagagc): the DNA quadruplex structure split from the octaplex (x2)
1v3p* Crystal structure of d(gcgagagc): the DNA octaplex structure with i- motif of g- quartet (x2)
1vat* Iodine derivative of hen egg- white lysozyme (x2)
1vj5* Human soluble epoxide hydrolase- n- cyclohexyl- n'- (4- iodophenyl)urea complex
1vkc* Putative acetyl transferase from pyrococcus furiosus (x13)
1vko* Crystal structure of inositol- 3- phosphate synthase (ce21227) from caenorhabditis elegans at 2.30 a resolution (x2)
1w2z* Psao and xenon (x176)
1w50* Apo structure of bace (beta secretase) (x4)
1w51* Bace (beta secretase) in complex with a nanomolar non- peptidic inhibitor (x4)
1wc7* Fab fragment of plp- dependent catalytic antibody 15a9 in complex with phosphopyridoxyl- l- alanine (x5)
1wcb* Plp- dependent catalytic antibody 15a9 in complex with its hapten (x9)
1wcv* Structure of the bacterial chromosome segregation protein soj (x5)
1wnw* D136n mutant of heme oxygenase from corynebacterium diphtheriae (hmuo) (x9)
1wy4* Chicken villin subdomain hp- 35, k65(nle), n68h, ph5.1 (x2)
1xb7* X- ray structure of erralpha lbd in complex with a pgc- 1alpha peptide at 2.5a resolution
1xbu* Streptomyces griseus aminopeptidase complexed with p- iodo- d- phenylalanine
1xc6* Native structure of beta- galactosidase from penicillium sp. In complex with galactose (x52)
1xp4* Crystal structure of a peptidoglycan synthesis regulatory factor (pbp3) from streptococcus pneumoniae (x16)
1xzx* Thyroxine- thyroid hormone receptor interactions (x3)
1y0s* Crystal structure of ppar delta complexed with gw2331 (x11)
1y0x* Thyroxine- thyroid hormone receptor interactions (x4)
1ydo* Crystal structure of the bacillis subtilis hmg- coa lyase, northeast structural genomics target sr181. (x4)
1yku* Crystal structure of a sensor domain homolog (x26)
1yri* Chicken villin subdomain hp- 35, n68h, ph6.4 (x3)
1yvp* Ro autoantigen complexed with rnas (x8)
1z7j* Human transthyretin (also called prealbumin) complex with 3, 3',5,5'- tetraiodothyroacetic acid (t4ac) (x8)
1zcr* Crystal structure of human transthyretin with bound iodide (x6)
1zme* Crystal structure of put3/DNA complex (x2)
1zvv* Crystal structure of a ccpa- crh- DNA complex (x11)
2a0n* Crystal structure of imidazole glycerol phosphate synthase subunit hisf (ec 4.1.3.- ) (Tm1036) from thermotoga maritima at 1.64 a resolution (x7)
2af6* Crystal structure of mycobacterium tuberculosis flavin dependent thymidylate synthase (mtb thyx) in the presence of co- factor fad and substrate analog 5- bromo- 2'- deoxyuridine- 5'- monophosphate (brdump) (x10)
2ak4* Crystal structure of sb27 tcr in complex with hla- b 3508- 13Mer peptide (x22)
2anv* Crystal structure of p22 lysozyme mutant l86m (x6)
2anx* Crystal structure of bacteriophage p22 lysozyme mutant l87m (x8)
2aqw* Structure of putative orotidine- monophosphate- decarboxylase from plasmodium yoelii (py01515) (x6)
2arl* The 2.0 angstroms crystal structure of a pocilloporin at ph 3.5: the structural basis for the linkage between color transition and halide binding (x4)
2axe* Iodinated complex of acetyl xylan esterase at 1.80 angstroms (x4)
2b5j* Crystal structure of HIV- 1 reverse transcriptase (rt) in complex with janssen- r165481
2b9x* Crystal structure of cla- producing fatty acid isomerase from p. Acnes (x11)
2be2* Crystal structure of HIV- 1 reverse transcriptase (rt) in complex with r221239
2biv* Crystal structure of the wild- type mbt domains of human scml2 (x10)
2bmk* Fab fragment of plp- dependent catalytic antibody 15a9 in complex with phosphopyridoxyl- d- alanine (x6)
2bsq* Fitab bound to DNA (x2)
2bxl* Human serum albumin complexed with myristate and 3,5- diiodosalicylic acid (x2)
2bxn* Human serum albumin complexed with myristate and iodipamide (x9)
2c3n* Human glutathione- s- transferase t1- 1, apo form (x15)
2c3q* Human glutathione- s- transferase t1- 1 w234r mutant, complex with s- hexylglutathione (x31)
2c3v* Structure of iodinated cbm25 from bacillus halodurans amylase (x6)
2c6c* Membrane- bound glutamate carboxypeptidase ii (gcpii) in complex with gpi- 18431 (s)- 2- (4- iodobenzylphosphonomethyl)- pentanedioic acid
2ceo* Thyroxine- binding globulin complex with thyroxine (x8)
2ciw* Chloroperoxidase iodide complex (x7)
2cj6* Crystal structure of a cell wall invertase inhibitor from tobacco (ph 7.5) (x24)
2cj7* Crystal structure of a cell wall invertase inhibitor from tobacco (ph 9.0) (x32)
2cj8* Crystal structure of a cell wall invertase inhibitor from tobacco (ph 9.5) (x18)
2ckk* High resolution crystal structure of the human kin17 c- terminal domain containing a kow motif kin17. (x12)
2ckl* Ring1b- bmi1 e3 catalytic domain structure (x2)
2d8o* Structure of vil- thaumatin (x5)
2d8p* Structure of hyper- vil- thaumatin (x13)
2d8w* Structure of hyper- vil- trypsin (x5)
2d91* Structure of hyper- vil- lysozyme (x2)
2d97* Structure of vil- xylanase (x2)
2d98* Structure of vil (extra ki/i2 added)- xylanase (x5)
2dfb* Xylanase ii from tricoderma reesei at 100k (x6)
2dfc* Xylanase ii from tricoderma reesei at 293k
2dgm* Crystal structure of escherichia coli gadb in complex with iodide (x32)
2eda* Crystallographic and fluorescence studies of the interaction of haloalkane dehalogenase with halide ions: studies with halide compounds reveal a halide binding site in the active site
2edc* Crystallographic and fluorescence studies of the interaction of haloalkane dehalogenase with halide ions: studies with halide compounds reveal a halide binding site in the active site
2eix* The structure of physarum polycephalum cytochrome b5 reductase (x4)
2es4* Crystal structure of the burkholderia glumae lipase- specific foldase in complex with its cognate lipase (x8)
2esv* Structure of the hla- e- vmaprtlil/kk50.4 tcr complex (x5)
2ewj* Escherichia coli replication terminator protein (tus) complexed with DNA- locked form (x3)
2fds* Crystal structure of plasmodium berghei orotidine 5'- monophosphate decarboxylase (ortholog of plasmodium falciparum pf10_0225) (x2)
2fwe* Crystal structure of thE C- terminal domain of the electron transfer catalyst dsbd (oxidized form) (x7)
2fwf* High resolution crystal structure of thE C- terminal domain of the electron transfer catalyst dsbd (reduced form) (x7)
2fwh* Atomic resolution crystal structure of thE C- terminal domain of the electron transfer catalyst dsbd (reduced form at ph7) (x3)