TERTIARY STRUCTURE DATA |
Carica papaya
|
complex with carbobenzyloxy-Leu-leucinal inhibitor |
2.20 Å |
1BP4 |
1BP4 |
1BP4 |
1BP4 |
1BP4 |
1BP4 |
LaLonde et al., 1998 |
complex with carboxybenzyloxy-Leu-Leu-methoxymethylketone |
2.50 Å |
1BQI |
1BQI |
1BQI |
1BQI |
1BQI |
1BQI |
LaLonde et al., 1998 |
complex with inhibitor CLIK148 |
1.70 Å |
1CVZ |
1CVZ |
1CVZ |
1CVZ |
1CVZ |
1CVZ |
Tsuge et al., 1999 |
theoretical model; complex with N-acetyl-p-benzoquinone imine |
0.00 Å |
1EFF |
1EFF |
1EFF |
1EFF |
1EFF |
1EFF |
|
complex with Z-Leu-Phe-Gly-diazomethylketone inhibitor |
2.00 Å |
1KHP |
1KHP |
1KHP |
1KHP |
1KHP |
1KHP |
Janowski et al., 2004 |
complex with Z-Leu-Phe-Gly-diazomethylketone inhibitor (orthorhombic form) |
1.60 Å |
1KHQ |
1KHQ |
1KHQ |
1KHQ |
1KHQ |
1KHQ |
Janowski et al., 2004 |
Cys25Ac-Ala-Ala-Phe-methylenylAla derivative |
2.80 Å |
1PAD |
1PAD |
1PAD |
1PAD |
1PAD |
1PAD |
Drenth et al., 1976 |
complex with E64C |
2.10 Å |
1PE6 |
1PE6 |
1PE6 |
1PE6 |
1PE6 |
1PE6 |
Yamamoto et al., 1991 |
complex with Suc-Gln-Vla-Val-Ala-Ala-pNA |
1.70 Å |
1PIP |
1PIP |
1PIP |
1PIP |
1PIP |
1PIP |
Yamamoto et al., 1992 |
complex with leupeptin |
2.10 Å |
1POP |
1POP |
1POP |
1POP |
1POP |
1POP |
Schroder et al., 1993 |
hydroxyethylthiopapain |
2.00 Å |
1PPD |
1PPD |
1PPD |
1PPD |
1PPD |
1PPD |
|
Cys25 with bound atom |
1.60 Å |
1PPN |
1PPN |
1PPN |
1PPN |
1PPN |
1PPN |
|
complex with E64C |
1.90 Å |
1PPP |
1PPP |
1PPP |
1PPP |
1PPP |
1PPP |
Kim et al., 1992 |
complex with cystatin B Cys18Ser |
2.37 Å |
1STF |
1STF |
1STF |
1STF |
1STF |
1STF |
Stubbs et al., 1990 |
complex with ICP |
1.50 Å |
2CIO |
2CIO |
2CIO |
2CIO |
2CIO |
2CIO |
Alphey & Hunter, 2006 |
cysteinyl derivative of Cys25 |
2.80 Å |
2PAD |
2PAD |
2PAD |
2PAD |
2PAD |
2PAD |
Drenth et al., 1976 |
complex with chagasin |
1.86 Å |
3E1Z |
3E1Z |
3E1Z |
3E1Z |
3E1Z |
3E1Z |
Redzynia et al., 2009 |
complex with tarocystatin |
2.03 Å |
3IMA |
3IMA |
3IMA |
3IMA |
3IMA |
3IMA |
|
complex with CTD of tarocystatin |
2.60 Å |
3LFY |
3LFY |
3LFY |
3LFY |
3LFY |
3LFY |
|
precursor; thermostable variant |
2.62 Å |
3TNX |
3TNX |
3TNX |
3TNX |
3TNX |
3TNX |
|
precursor; thermostable variant from a crystal soaked at ph 4 |
3.80 Å |
3USV |
3USV |
3USV |
3USV |
3USV |
3USV |
|
TOS-methylenylLys derivative of Cys25 |
2.80 Å |
4PAD |
4PAD |
4PAD |
4PAD |
4PAD |
4PAD |
Drenth et al., 1976 |
Ile86Leu mutant |
2.50 Å |
4QRG |
4QRG |
4QRG |
4QRG |
4QRG |
4QRG |
|
Ile86Phe mutant |
1.98 Å |
4QRV |
4QRV |
4QRV |
4QRV |
4QRV |
4QRV |
|
precursor mutant at ph 4.0 |
3.14 Å |
4QRX |
4QRX |
4QRX |
4QRX |
4QRX |
4QRX |
|
benzyloxycarbonyl-Gly-Phe-methylenylGly derivative |
2.80 Å |
5PAD |
5PAD |
5PAD |
5PAD |
5PAD |
5PAD |
Drenth et al., 1976 |
modified by achiral ru(ii)complex |
2.10 Å |
6H8T |
6H8T |
6H8T |
6H8T |
6H8T |
6H8T |
|
benzyloxycarbonyl-Gly-Phe-methylenylGly derivative |
2.80 Å |
6PAD |
6PAD |
6PAD |
6PAD |
6PAD |
6PAD |
Drenth et al., 1976 |
Cys25 oxidized |
1.65 Å |
9PAP |
9PAP |
9PAP |
9PAP |
9PAP |
9PAP |
Kamphuis et al., 1984 |