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Ligands
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Non-standard Residues
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Glycosylation
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Modification
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CF0 Fluoromethane
PHQ Benzyl chlorocarbonate
Code : 2H48   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : Crystal structure of human caspase-1 (Cys362->Ala, Cys364->Ala, Cys397->Ala) in complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl-butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-VAD-FMK)
Release Data : 2006-06-06
Compound :
mol_id molecule chains
1 Caspase 1, isoform gamma A
ec: 3.4.22.36
fragment: large subunit, residues, 120-297
mol_id molecule chains
2 Caspase 1, isoform gamma B
ec: 3.4.22.36
fragment: small subunit, residues 317-404
mutation: C362A, C364A, C397A
mol_id molecule chains
3 N-[(benzyloxy)carbonyl]-L-valyl-N-[(2S)-1-carboxy-4-fluoro-3-oxobutan-2-yl]-L-alaninamide C
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: CASP1
expression_system_strain: BL21(DE3)Star
expression_system_vector_type: Plasmid
expression_system_plasmid: pGEX6P-1
mol_id organism_scientific organism_common expression_system
2 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: CASP1
expression_system_strain: BL21(DE3)Star
expression_system_vector_type: Plasmid
expression_system_plasmid: pGEX6P-1
mol_id organism_scientific
3
synthetic: yes
Authors : Scheer, J.M., Wells, J.A., Romanowski, M.J.
Keywords : allosteric side, z-VAD-FMK, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
Exp. method : X-RAY DIFFRACTION ( 2.20 Å )
Citation :

A common allosteric site and mechanism in caspases

Scheer, J.M.,Romanowski, M.J.,Wells, J.A.
(2006)  Proc.Natl.Acad.Sci.USA  103 : 7595 - 7600

PubMed: 16682620
DOI: 10.1073/pnas.0602571103

Chain : B
UniProt : P29466 (CASP1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
Strict requirement for an Asp residue at position P1 and has a preferred cleavage sequence of Tyr-Val-Ala-Asp-|-. 3.4.22.36 PubMed:1574116, PubMed:22464733
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