Microsomal cytochrome P450s participate in xenobiotic detoxification, procarcinogen activation, and steroid hormone synthesis. The first structure of a mammalian microsomal P450 suggests that the association of P450s with the endoplasmic reticulum involves a hydrophobic surface of the protein formed by noncontiguous portions of the polypeptide chain. This interaction places the entrance of the putative substrate access channel in or near the membrane and orients the face of the protein proximal to the heme cofactor perpendicular to the plane of the membrane for interaction with the P450 reductase. This structure offers a template for modeling other mammalian P450s and should aid drug discovery and the prediction of drug–drug interactions.
Copyright © 2000 Cell Press. All rights reserved.
, Vol 5, 121-131, January 2000
Article
Mammalian Microsomal Cytochrome P450 Monooxygenase: Structural Adaptations for Membrane Binding and Functional Diversity
1Department of Molecular Biology MB-8, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA
2Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA
Corresponding author
Duncan E. McRee
858 784 9235 (phone)
858 784 2279 (fax)
dem@scripps.edu
Summary
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