ELUCIDATING THE FOLDING PROBLEM OF HELICAL PEPTIDES USING EMPIRICAL PARAMETERS

被引:616
作者
MUNOZ, V
SERRANO, L
机构
[1] EMBL, Heidelberg, D-69117
来源
NATURE STRUCTURAL BIOLOGY | 1994年 / 1卷 / 06期
关键词
D O I
10.1038/nsb0694-399
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
Using an empirical analysis of experimental data we have estimated a set of energy contributions which accounts for the stability of isolated alpha-helices. With this database and an algorithm based on statistical mechanics, we describe the average helical behaviour in solution of 323 peptides and the helicity per residue of those peptides analyzed by nuclear magnetic resonance. Moreover the algorithm successfully detects the alpha-helical tendency, in solution, of a peptide corresponding to a beta-strand of ubiquitin.
引用
收藏
页码:399 / 409
页数:11
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