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8hor

X-ray diffraction
1.95Å resolution

Crystal structure of the P450 BM3 heme domain mutant F87A in complex with Im-C6-Phe(4CH3)-Tyr

Released:
Model geometry
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Function and Biology Details

Reactions catalysed:
an organic molecule + reduced [NADPH--hemoprotein reductase] + O2 =an alcohol + oxidized [NADPH--hemoprotein reductase] + H2O + H(+).
2 oxidized [cytochrome P450] + NADPH = 2 reduced [cytochrome P450] +NADP(+) + H(+).
Biochemical function:
Biological process:
  • not assigned
Cellular component:
  • not assigned

Structure analysis Details

Assembly composition:
hetero tetramer (preferred)
PDBe Complex ID:
PDB-CPX-273225 (preferred)
Entry contents:
2 distinct polypeptide molecules
Macromolecules (2 distinct):
Bifunctional cytochrome P450/NADPH--P450 reductase Chains: A, B
Molecule details ›
Chains: A, B
Length: 465 amino acids
Theoretical weight: 53.35 KDa
Source organism: Priestia megaterium
Expression system: Escherichia coli BL21(DE3)
UniProt:
  • Canonical: P14779 (Residues: 1-456; Coverage: 44%)
Gene names: BG04_163, cyp102, cyp102A1
Sequence domains: Cytochrome P450
Im-C6-Phe(4CH3)-Tyr Chains: C, D
Molecule details ›
Chains: C, D
Length: 3 amino acids
Theoretical weight: 507 Da
Source organism: synthetic construct
Expression system: Not provided

Ligands and Environments


Cofactor: Ligand HEM 2 x HEM
No bound ligands
1 modified residue:

Experiments and Validation Details

wwPDB Validation report is not available for this entry.
X-ray source: SSRF BEAMLINE BL10U2
Spacegroup: P21
Unit cell:
a: 58.686Å b: 147.645Å c: 64.719Å
α: 90° β: 100.01° γ: 90°
R-values:
R R work R free
0.213 0.212 0.23
Expression systems:
  • Escherichia coli BL21(DE3)
  • Not provided