3isa

X-ray diffraction
1.76Å resolution

CRYSTAL STRUCTURE OF putative enoyl-CoA hydratase/isomerase FROM Bordetella parapertussis

Released:
Source organism: Bordetella parapertussis
Entry authors: Patskovsky Y, Malashkevich V, Toro R, Foti R, Dickey M, Miller S, Sauder JM, Burley SK, Almo SC, New York SGX Research Center for Structural Genomics (NYSGXRC)

Function and Biology Details

Biochemical function:
  • not assigned
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
homo hexamer (preferred)
PDBe Complex ID:
PDB-CPX-182102 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Enoyl-CoA hydratase/isomerase Chains: A, B, C, D, E, F
Molecule details ›
Chains: A, B, C, D, E, F
Length: 254 amino acids
Theoretical weight: 27.63 KDa
Source organism: Bordetella parapertussis
Expression system: Escherichia coli
UniProt:
  • Canonical: Q7W3D6 (Residues: 5-247; Coverage: 98%)
Gene name: BPP4107
Sequence domains: Enoyl-CoA hydratase/isomerase
Structure domains: 2-enoyl-CoA Hydratase; Chain A, domain 1

Ligands and Environments

2 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: NSLS BEAMLINE X29A
Spacegroup: C2
Unit cell:
a: 203.837Å b: 120.825Å c: 78.577Å
α: 90° β: 110.37° γ: 90°
R-values:
R R work R free
0.167 0.166 0.208
Expression system: Escherichia coli