Brand  (β version)

  The number of atoms exceeds 100,000.
  So, it can not be displayed here.

Select unit:

Select hetatm:   

close
information
centroid:
interaction residue:

Select chain:   Sequence  

Data format:   

Color scheme of protein:

Ligands
Code Name Style Show Link
0ZZ 5-S-benzyl-3-({N-[(5-bromo-2-methoxyphenyl)acetyl]-L-valyl}amino)-2,3-dideoxy-5-thio-D-erythro-pentonic acid
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 1RHQ   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/hydrolase inhibitor
Title : CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A BROMOMETHOXYPHENYL INHIBITOR
Release Data : 2004-05-11
Compound :
mol_id molecule chains synonym
1 Caspase-3 A,D Cysteine protease CPP32, Yama protein, CPP-32, Apopain, CASP-3, SREBP cleavage activity 1, SCA-1
ec: 3.4.22.-
fragment: P17 SUBUNIT
mol_id molecule chains synonym
2 Caspase-3 B,E Cysteine protease CPP32, Yama protein, CPP-32, Apopain, CASP-3, SREBP cleavage activity 1, SCA-1
ec: 3.4.22.-
fragment: P12 SUBUNIT
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli BL21(DE3)  (taxid:469008)
gene: CASP3, CPP32
expression_system_strain: BL21(DE3)
expression_system_vector_type: PLASMID
mol_id organism_scientific organism_common expression_system
2 Homo sapiens  (taxid:9606) Human Escherichia coli BL21(DE3)  (taxid:469008)
gene: CASP3, CPP32
expression_system_strain: BL21(DE3)
expression_system_vector_type: PLASMID
Authors : Becker, J.W., Rotonda, J., Soisson, S.M.
Keywords : CYSTEINE PROTEASE, CASPASE-3, APOPAIN, CPP32, YAMA, HYDROLASE-hydrolase inhibitor complex
Exp. method : X-RAY DIFFRACTION ( 3.00 Å )
Citation :

Reducing the Peptidyl Features of Caspase-3 Inhibitors: A Structural Analysis.

Becker, J.W.,Rotonda, J.,Soisson, S.M.  et al.
(2004)  J.Med.Chem.  47 : 2466 - 2474

PubMed: 15115390
DOI: 10.1021/jm0305523

Chain : B, E
UniProt : P42574 (CASP3_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
Strict requirement for an Asp residue at positions P1 and P4. It has a preferred cleavage sequence of Asp-Xaa-Xaa-Asp-|- with a hydrophobic amino-acid residue at P2 and a hydrophilic amino-acid residue at P3, although Val or Ala are also accepted at this position. 3.4.22.56 PubMed:16374543, PubMed:18723680, PubMed:20566630, PubMed:23152800, PubMed:23650375, PubMed:23845944, PubMed:30878284, PubMed:33725486, PubMed:7596430
-