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X-ray diffraction
3.2Å resolution

Crystal Structure of Human Calpain-3 Protease Core in Complex with Leupeptin

Released:

Function and Biology Details

Reaction catalysed:
Broad endopeptidase activity
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
hetero dimer (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-149063 (preferred)
Entry contents:
2 distinct polypeptide molecules
Macromolecules (2 distinct):
Calpain-3 Chains: A, B, C, D
Molecule details ›
Chains: A, B, C, D
Length: 382 amino acids
Theoretical weight: 44.46 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: P20807 (Residues: 46-419; Coverage: 46%)
Gene names: CANP3, CANPL3, CAPN3, NCL1
Sequence domains: Calpain family cysteine protease
Structure domains: Cysteine proteinases
Leupeptin Chains: F, G, H, I
Molecule details ›
Chains: F, G, H, I
Length: 4 amino acids
Theoretical weight: 430 Da
Source organism: Streptomyces roseus
Expression system: Not provided

Ligands and Environments

1 bound ligand:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 23-ID-B
Spacegroup: P212121
Unit cell:
a: 54.93Å b: 106.69Å c: 234.63Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.281 0.277 0.353
Expression systems:
  • Escherichia coli BL21(DE3)
  • Not provided