1vai

X-ray diffraction
1.8Å resolution

Structure of e. coli cyclophilin B K163T mutant bound to n-acetyl-ala-ala-pro-ala-7-amino-4-methylcoumarin

Released:

Function and Biology Details

Structure analysis Details

Assemblies composition:
monomeric
hetero dimer (preferred)
PDBe Complex ID:
PDB-CPX-142740 (preferred)
Entry contents:
2 distinct polypeptide molecules
Macromolecules (2 distinct):
Peptidyl-prolyl cis-trans isomerase A Chains: A, B
Molecule details ›
Chains: A, B
Length: 166 amino acids
Theoretical weight: 18.07 KDa
Source organism: Escherichia coli
Expression system: Escherichia coli
UniProt:
  • Canonical: P0AFL3 (Residues: 25-190; Coverage: 100%)
Gene names: JW3326, b3363, ppiA, rot, rotA
Sequence domains: Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD
Structure domains: Cyclophilin-like
(ACE)AAPA(MCM) Chain: C
Molecule details ›
Chain: C
Length: 6 amino acids
Theoretical weight: 512 Da
Source organism: Escherichia coli
Expression system: Not provided

Ligands and Environments

No bound ligands
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: PHOTON FACTORY BEAMLINE BL-6A
Spacegroup: P32
Unit cell:
a: 78.73Å b: 78.73Å c: 56.16Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.188 0.188 0.229
Expression systems:
  • Escherichia coli
  • Not provided