2ql7

X-ray diffraction
2.4Å resolution

Crystal Structure of Caspase-7 with inhibitor AC-IEPD-CHO

Released:

Function and Biology Details

Reaction catalysed:
Strict requirement for an Asp residue at position P1 and has a preferred cleavage sequence of Asp-Glu-Val-Asp-|-
Biochemical function:
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
hetero heptamer (preferred)
PDBe Complex ID:
PDB-CPX-157237 (preferred)
Entry contents:
4 distinct polypeptide molecules
Macromolecules (4 distinct):
Caspase-7 subunit p20 Chains: A, C
Molecule details ›
Chains: A, C
Length: 173 amino acids
Theoretical weight: 19.56 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli BL21
UniProt:
  • Canonical: P55210 (Residues: 24-196; Coverage: 57%)
Gene names: CASP7, MCH3
Sequence domains: Caspase domain
Structure domains: Rossmann fold
Caspase-7 subunit p11 Chains: B, D
Molecule details ›
Chains: B, D
Length: 97 amino acids
Theoretical weight: 11.35 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli BL21
UniProt:
  • Canonical: P55210 (Residues: 207-303; Coverage: 32%)
Gene names: CASP7, MCH3
Sequence domains: Caspase domain
Structure domains: Caspase-like
Inhibitor AC-IEPD_CHO Chains: E, F
Molecule details ›
Chains: E, F
Length: 5 amino acids
Theoretical weight: 485 Da
QGHGE Chain: G
Molecule details ›
Chain: G
Length: 5 amino acids
Theoretical weight: 528 Da

Ligands and Environments

1 bound ligand:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 22-ID
Spacegroup: P3221
Unit cell:
a: 87.942Å b: 87.942Å c: 187.551Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.202 0.196 0.237
Expression system: Escherichia coli BL21