A REVISED SET OF POTENTIALS FOR BETA-TURN FORMATION IN PROTEINS

被引:856
作者
HUTCHINSON, EG
THORNTON, JM
机构
[1] Biomolecular Structure and Modelling Unit, Department of Biochemistry and Molecular Biology, University College, London, WC1E 6BT, Gower Street
关键词
PROTEIN STRUCTURE ANALYSIS; SEQUENCE PREFERENCE;
D O I
10.1002/pro.5560031206
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
Three thousand eight hundred ninety-nine beta-turns have been identified and classified using a nonhomologous data set of 205 protein chains. These were used to derive beta-turn positional potentials for turn types I' and II' for the first time and to provide updated potentials for formation of the more common types I, II, and VIII. Many of the sequence preferences for each of the 4 positions in turns can be rationalized. in terms of the formation of stabilizing hydrogen bonds, preferences for amino acids to adopt a particular conformation in phi, psi space, and the involvement of turn types I' and II' in beta-hairpins. Only 1,632 (42%) of the turns occur in isolation; the remainder have at least 1 residue in common with another turn and have hence been classified as multiple turns. Several types of multiple turn have been identified and analyzed.
引用
收藏
页码:2207 / 2216
页数:10
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