CHARACTERIZATION AND MODELING OF MEMBRANE-PROTEINS USING SEQUENCE-ANALYSIS

被引:140
作者
REITHMEIER, RAF
机构
[1] Department of Medicine, University of Toronto, Toronto, M5S 1A8
关键词
D O I
10.1016/0959-440X(95)80034-4
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 current libraries of amino acid sequences of membrane proteins are a valuable resource for the analysis of elements common to these proteins. Multiple-sequence alignment techniques and the identification of conserved features of transmembrane segments have improved the prediction of membrane protein topology. Molecular modeling in combination with structural studies or site-directed mutagenesis is proving to be a powerful link between theory and experiment. Unfortunately, the number of high-resolution structures of intrinsic membrane proteins, although increased recently, presents a restricted and perhaps biased view of membrane protein structure.
引用
收藏
页码:491 / 500
页数:10
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