NADPH-cytochrome P-450 oxidoreductase gene organization correlates with structural domains of the protein
doi: 10.1021/bi00494a009
pmid: 2125483
NADPH-cytochrome P-450 oxidoreductase gene organization correlates with structural domains of the protein
cDNA clones to rat liver NADPH-cytochrome P-450 oxidoreductase were used to isolate genomic clones from a Wistar-Furth inbred rat genomic DNA library. Fifteen exons containing the coding region and 3'-nontranslated segment of the P-450 reductase gene were identified, spanning 20 kilobases of DNA contained in 3 lambda-Charon 35 clones. The organization of this single copy gene reveals a general correspondence between exons and structural domains of the protein, with the segment responsible for anchoring the reductase to the microsomal membrane and several segments involved in FMN, FAD, and NADPH binding encoded by discrete exons.
- University of Wisconsin–Oshkosh United States
- University of Wisconsin–Madison United States
Binding Sites, Base Sequence, Flavin Mononucleotide, Molecular Sequence Data, Rats, Inbred WF, DNA, Exons, Endoplasmic Reticulum, Rats, Cytochrome P-450 Enzyme System, Genes, Flavin-Adenine Dinucleotide, Animals, Amino Acid Sequence, NADP, NADPH-Ferrihemoprotein Reductase, Protein Binding
Binding Sites, Base Sequence, Flavin Mononucleotide, Molecular Sequence Data, Rats, Inbred WF, DNA, Exons, Endoplasmic Reticulum, Rats, Cytochrome P-450 Enzyme System, Genes, Flavin-Adenine Dinucleotide, Animals, Amino Acid Sequence, NADP, NADPH-Ferrihemoprotein Reductase, Protein Binding
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