Diversity in the Oxidation of Substrates by Cytochrome P450 2D6: Lack of an Obligatory Role of Aspartate 301−Substrate Electrostatic Bonding-Reference-Cited by-同舟云学术

Diversity in the Oxidation of Substrates by Cytochrome P450 2D6: Lack of an Obligatory Role of Aspartate 301−Substrate Electrostatic Bonding

Published:2002-08-15 Issue:36 Volume:41 Page:11025-11034
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Guengerich F. Peter¹,Miller Grover P.¹,Hanna Imad H.¹,Martin Martha V.¹,Léger Serge¹,Black Cameron¹,Chauret Nathalie¹,Silva José M.¹,Trimble Laird A.¹,Yergey James A.¹,Nicoll-Griffith Deborah A.¹

Affiliation:

1. Department of Biochemistry and Center in Molecular Toxicology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, and Department of Medicinal Chemistry, Merck Frosst Centre for Therapeutic Research, P.O. Box 1005, Pointe Claire Dorval, Quebec H9H 4P8, Canada

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi020341k

Reference65 articles.

1. Identification of molecular aggregates containing glycoproteins III, J, K (carboxypeptidase H), and H (Kex2-related proteases) in the soluble and membrane fractions of adrenal medullary chromaffin granules.

2. Guengerich, F. P. (1997) inBiotransformation, Vol. 3, Comprehensive Toxicology(Guengerich, F. P., Ed.) pp 37−68, Elsevier Science Ltd., Oxford.

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