Structure of a cytochrome P450-redox partner electron-transfer complex.

Article Details

Citation

Sevrioukova IF, Li H, Zhang H, Peterson JA, Poulos TL

Structure of a cytochrome P450-redox partner electron-transfer complex.

Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):1863-8.

PubMed ID
10051560 [ View in PubMed
]
Abstract

The crystal structure of the complex between the heme- and FMN-binding domains of bacterial cytochrome P450BM-3, a prototype for the complex between eukaryotic microsomal P450s and P450 reductase, has been determined at 2.03 A resolution. The flavodoxin-like flavin domain is positioned at the proximal face of the heme domain with the FMN 4.0 and 18.4 A from the peptide that precedes the heme-binding loop and the heme iron, respectively. The heme-binding peptide represents the most efficient and coupled through-bond electron pathway to the heme iron. Substantial differences between the FMN-binding domains of P450BM-3 and microsomal P450 reductase, observed around the flavin-binding sites, are responsible for different redox properties of the FMN, which, in turn, control electron flow to the P450.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Bifunctional cytochrome P450/NADPH--P450 reductaseP14779Details