3p2f

X-ray diffraction
2.3Å resolution

Crystal structure of TofI in an apo form

Released:
Source organism: Burkholderia glumae
Primary publication:
Small-molecule inhibitor binding to an N-acyl-homoserine lactone synthase.
Proc Natl Acad Sci U S A 108 12089-94 (2011)
PMID: 21730159

Function and Biology Details

Reaction catalysed:
An acyl-[acyl-carrier-protein] + S-adenosyl-L-methionine = [acyl-carrier-protein] + S-methyl-5'-thioadenosine + an N-acyl-L-homoserine lactone
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
monomeric (preferred)
PDBe Complex ID:
PDB-CPX-175780 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
Acyl-homoserine-lactone synthase Chain: A
Molecule details ›
Chain: A
Length: 201 amino acids
Theoretical weight: 22.22 KDa
Source organism: Burkholderia glumae
Expression system: Escherichia coli
UniProt:
  • Canonical: Q4VSJ8 (Residues: 1-203; Coverage: 99%)
Gene names: bglu_2g14490, tofI
Sequence domains: Autoinducer synthase
Structure domains: Aminopeptidase

Ligands and Environments

No bound ligands
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: PAL/PLS BEAMLINE 6C1
Spacegroup: P3221
Unit cell:
a: 65.971Å b: 65.971Å c: 104.768Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.228 0.228 0.27
Expression system: Escherichia coli