3fkv

X-ray diffraction
1.85Å resolution

AmpC K67R mutant complexed with benzo(b)thiophene-2-boronic acid (bzb)

Released:
Source organism: Escherichia coli
Primary publication:
Re-examining the role of Lys67 in class C beta-lactamase catalysis.
Protein Sci 18 662-9 (2009)
PMID: 19241376

Function and Biology Details

Reaction catalysed:
A beta-lactam + H(2)O = a substituted beta-amino acid
Biochemical function:
Biological process:
Cellular component:

Structure analysis Details

Assemblies composition:
monomeric
homo dimer (preferred)
Assembly name:
PDBe Complex ID:
PDB-CPX-133600 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Beta-lactamase Chains: A, B
Molecule details ›
Chains: A, B
Length: 358 amino acids
Theoretical weight: 39.62 KDa
Source organism: Escherichia coli
Expression system: Escherichia coli
UniProt:
  • Canonical: P00811 (Residues: 20-377; Coverage: 100%)
Gene names: JW4111, ampA, ampC, b4150
Sequence domains: Beta-lactamase
Structure domains: DD-peptidase/beta-lactamase superfamily

Ligands and Environments

3 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: ALS BEAMLINE 8.3.1
Spacegroup: C2
Unit cell:
a: 118.043Å b: 76.949Å c: 97.831Å
α: 90° β: 116.23° γ: 90°
R-values:
R R work R free
0.165 0.163 0.203
Expression system: Escherichia coli