3lub

X-ray diffraction
2.11Å resolution

Crystal structure of Putative creatinine amidohydrolase (YP_211512.1) from Bacteroides fragilis NCTC 9343 at 2.11 A resolution

Released:
Entry author: Joint Center for Structural Genomics (JCSG)

Function and Biology Details

Reaction catalysed:
Creatinine + H(2)O = creatine
Biochemical function:
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
homo hexamer (preferred)
PDBe Complex ID:
PDB-CPX-177476 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Putative creatinine amidohydrolase Chains: A, B, C, D, E, F, G, H, I, J, K, L
Molecule details ›
Chains: A, B, C, D, E, F, G, H, I, J, K, L
Length: 254 amino acids
Theoretical weight: 28.54 KDa
Source organism: Bacteroides fragilis NCTC 9343
Expression system: Escherichia coli
UniProt:
  • Canonical: Q5LE76 (Residues: 1-253; Coverage: 100%)
Gene name: BF9343_1795
Sequence domains: Creatinine amidohydrolase
Structure domains: Creatininase

Ligands and Environments

1 modified residue:

Experiments and Validation Details

Entry percentile scores
X-ray source: SSRL BEAMLINE BL9-2
Spacegroup: P21
Unit cell:
a: 55.906Å b: 156.79Å c: 170.161Å
α: 90° β: 95.29° γ: 90°
R-values:
R R work R free
0.153 0.151 0.193
Expression system: Escherichia coli