4bl2

X-ray diffraction
2.72Å resolution

Crystal structure of PBP2a clinical mutant E150K from MRSA

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.
Biological process:
Cellular component:

Structure analysis Details

Assembly composition:
monomeric (preferred)
PDBe Complex ID:
PDB-CPX-101921 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Penicillin binding protein 2 prime Chains: A, B
Molecule details ›
Chains: A, B
Length: 643 amino acids
Theoretical weight: 73.42 KDa
Source organism: Staphylococcus aureus
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: A0A0H3JPA5 (Residues: 26-668; Coverage: 96%)
Gene names: SAV0041, mecA
Sequence domains:
Structure domains:

Ligands and Environments

2 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: BRUKER AXS MICROSTAR
Spacegroup: P212121
Unit cell:
a: 81.437Å b: 101.637Å c: 186.838Å
α: 90° β: 90° γ: 90°
R-values:
R R work R free
0.212 0.207 0.287
Expression system: Escherichia coli BL21(DE3)