2ex6

X-ray diffraction
1.6Å resolution

Crystal structure of penicillin binding protein 4 (dacB) from Escherichia coli, complexed with ampicillin

Released:

Function and Biology Details

Reaction catalysed:
Preferential cleavage: (Ac)(2)-L-Lys-D-Ala-|-D-Ala. Also transpeptidation of peptidyl-alanyl moieties that are N-acyl substituents of D-alanine.
Biochemical function:
Biological process:
Cellular component:

Structure analysis Details

Assemblies composition:
monomeric (preferred)
homo dimer
PDBe Complex ID:
PDB-CPX-150177 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
D-alanyl-D-alanine carboxypeptidase DacB Chain: A
Molecule details ›
Chain: A
Length: 458 amino acids
Theoretical weight: 49.8 KDa
Source organism: Escherichia coli
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: P24228 (Residues: 21-477; Coverage: 100%)
Gene names: JW3149, b3182, dacB
Sequence domains: D-Ala-D-Ala carboxypeptidase 3 (S13) family
Structure domains:

Ligands and Environments

2 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: PHOTON FACTORY BEAMLINE BL-5A
Spacegroup: P41212
Unit cell:
a: 95.704Å b: 95.704Å c: 115.952Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.218 0.216 0.25
Expression system: Escherichia coli BL21(DE3)