3juv

X-ray diffraction
3.12Å resolution

Crystal structure of human lanosterol 14alpha-demethylase (CYP51)

Released:
Source organism: Homo sapiens
Primary publication:
Structural basis of human CYP51 inhibition by antifungal azoles.
J Mol Biol 397 1067-78 (2010)
PMID: 20149798

Function and Biology Details

Reaction catalysed:
(1a) a 14-alpha-methylsteroid + [reduced NADPH--hemoprotein reductase] + O(2) = a 14-alpha-hydroxysteroid + [oxidized NADPH--hemoprotein reductase] + H(2)O
Biochemical function:
Biological process:
  • not assigned
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
homo dimer (preferred)
PDBe Complex ID:
PDB-CPX-172598 (preferred)
Entry contents:
1 distinct polypeptide molecule
Macromolecules (2 distinct):
Lanosterol 14-alpha demethylase Chain: A
Molecule details ›
Chain: A
Length: 461 amino acids
Theoretical weight: 52.77 KDa
Source organism: Homo sapiens
Expression system: Escherichia coli
UniProt:
  • Canonical: Q16850 (Residues: 60-508; Coverage: 88%)
Gene names: CYP51, CYP51A1
Sequence domains: Cytochrome P450
Structure domains: Cytochrome P450

Ligands and Environments

Carbohydrate polymer : NEW Components: GLC
1 bound ligand:
No modified residues

Experiments and Validation Details

Entry percentile scores
X-ray source: APS BEAMLINE 23-ID-B
Spacegroup: R32
Unit cell:
a: 174.144Å b: 174.144Å c: 244.269Å
α: 90° β: 90° γ: 120°
R-values:
R R work R free
0.199 0.198 0.227
Expression system: Escherichia coli