3eqv

X-ray diffraction
2.4Å resolution

Crystal structure of penicillin-binding protein 2 from Neisseria gonorrhoeae containing four mutations associated with penicillin resistance

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-139932 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Probable peptidoglycan D,D-transpeptidase PenA Chains: A, B
Molecule details ›
Chains: A, B
Length: 542 amino acids
Theoretical weight: 59.11 KDa
Source organism: Neisseria gonorrhoeae
Expression system: Escherichia coli
UniProt:
  • Canonical: P08149 (Residues: 44-581; Coverage: 93%)
Gene name: penA
Sequence domains:
Structure domains:

Ligands and Environments

2 bound ligands:
1 modified residue:

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 22-ID
Spacegroup: P212121
Unit cell:
a: 57.6Å b: 137.2Å c: 229.8Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.219 0.217 0.253
Expression system: Escherichia coli