Investigating human p450s involved in drug metabolism via homology with high-resolution p450 crystal structures of the CYP2C subfamily

被引:9
作者
Lewis, David F. V. [1 ]
Ito, Yuko
Goldfarb, Peter S.
机构
[1] Univ Surrey, Sch Biomed & Mol Sci, Guildford GU2 7XH, Surrey, England
[2] Kyushu Inst Technol, Dept Biosci & Bioinformat, Iizuka, Fukuoka 8208502, Japan
关键词
cytochromes p450; human drug metabolism; structural modeling;
D O I
10.2174/138920006778017812
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The important role of high-resolution crystal structures of cytochrome P450 (CYP) enzymes for the generation of P450 models by homology is discussed. The main focus is oil human P450 enzymes involved in drug metabolism, where the role of homology modelling has been emphasized in the recent literature. Report of the first human 11450 crystal structure has provided ail opportunity for comparison between those modelled from other crystallographic templates, and the recent substrate-bound rabbit CYP2C5 structure exemplifies the relevance Of high-resolution template structures to generating 3-D models of P450s where the homology is relatively high. In particular, the homology models of human CYP1 and CYP2 family enzymes are presented, where good agreement with experiment findings are apparent.
引用
收藏
页码:589 / 598
页数:10
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