6vib

X-ray diffraction
1.84Å resolution

Observing a ring-cleaving dioxygenase in action through a crystalline lens - enol tautomers of ACMS bidentately bound structure

Released:
Primary publication:
Observing 3-hydroxyanthranilate-3,4-dioxygenase in action through a crystalline lens.
Proc Natl Acad Sci U S A 117 19720-19730 (2020)
PMID: 32732435

Function and Biology Details

Reaction catalysed:
3-hydroxyanthranilate + O(2) = 2-amino-3-carboxymuconate semialdehyde
Biochemical function:
Biological process:
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
homo dimer (preferred)
PDBe Complex ID:
PDB-CPX-172948 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecule:
3-hydroxyanthranilate 3,4-dioxygenase Chain: A
Molecule details ›
Chain: A
Length: 195 amino acids
Theoretical weight: 22.59 KDa
Source organism: Cupriavidus metallidurans CH34
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: Q1LCS4 (Residues: 1-174; Coverage: 100%)
Gene names: Rmet_5193, nbaC
Sequence domains: 3-hydroxyanthranilic acid dioxygenase

Ligands and Environments

3 bound ligands:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 19-ID
Spacegroup: P6522
Unit cell:
a: 58.33Å b: 58.33Å c: 232.04Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.201 0.197 0.246
Expression system: Escherichia coli BL21(DE3)