4q2h

X-ray diffraction
1.8Å resolution

Crystal structure of probable proline racemase from agrobacterium radiobacter K84, TARGET EFI-506561, with bound carbonate

Released:
Entry authors: Patskovsky Y, Toro R, Bhosle R, Al Obaidi NF, Morisco LL, Wasserman SR, Sojitra S, Stead M, Washington E, Glenn AS, Chowdhury S, Evans B, Hammonds J, Hillerich B, Love J, Seidel RD, Gerlt JA, Almo SC, Enzyme Function Initiative (EFI)

Function and Biology Details

Reaction catalysed:
Trans-4-hydroxy-L-proline = cis-4-hydroxy-D-proline
Biological process:
  • not assigned
Cellular component:
  • not assigned
Sequence domain:

Structure analysis Details

Assembly composition:
homo dimer (preferred)
PDBe Complex ID:
PDB-CPX-110828 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
4-hydroxyproline 2-epimerase 1 Chains: A, B
Molecule details ›
Chains: A, B
Length: 367 amino acids
Theoretical weight: 39.41 KDa
Source organism: Agrobacterium radiobacter K84
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: B9J8G8 (Residues: 1-345; Coverage: 100%)
Gene name: Arad_0731
Sequence domains: Proline racemase
Structure domains: Diaminopimelate Epimerase; Chain A, domain 1

Ligands and Environments

2 bound ligands:
1 modified residue:

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 31-ID
Spacegroup: C2221
Unit cell:
a: 67.43Å b: 129.47Å c: 178.703Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.147 0.147 0.176
Expression system: Escherichia coli BL21(DE3)