Structure for peptidase S01.133: cathepsin G
 
| PDB | Organism | Resolution | Comment |
|---|---|---|---|
| 1CGH | Homo sapiens | 1.80 Å | complex with Suc-Val-Pro-PhEP inhibitor |
| Catalytic residues are shown in ball-and-stick representation: His64 in purple, Asp108 in pink and Ser201 in orange. Bound inhibitor is shown in grey in ball-and-stick representation. | |||
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| TERTIARY STRUCTURE DATA | ||||||||
|---|---|---|---|---|---|---|---|---|
| Comment | Resolution | PDB | PDBe | SCOP | CATH | PDBSum | Proteopedia | Reference |
| Homo sapiens | ||||||||
| complex with phosophonate inhibitor Suc-Val-Pro-LysP-(OPh)2 | 1.90 Å | 1AU8 | 1AU8 | 1AU8 | 1AU8 | 1AU8 | 1AU8 | |
| complex with Suc-Val-Pro-PhEP inhibitor | 1.80 Å | 1CGH | 1CGH | 1CGH | 1CGH | 1CGH | 1CGH | Hof et al., 1996 |
| complex with beta-ketophosphonic acid inhibitor KTP | 3.50 Å | 1KYN | 1KYN | 1KYN | 1KYN | 1KYN | 1KYN | Greco et al., 2002 |
| a dual inhibitor of the leukocyte proteases cathepsin g and chymase with therapeutic efficacy in animals models of inflammation | 1.85 Å | 1T32 | 1T32 | 1T32 | 1T32 | 1T32 | 1T32 | de et al., 2005 |


