EVALUATION OF CURRENT TECHNIQUES FOR AB-INITIO PROTEIN-STRUCTURE PREDICTION

被引:58
作者
DEFAY, T
COHEN, FE
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT MOLEC & CELLULAR PHARMACOL, SAN FRANCISCO, CA 94131 USA
[2] UNIV CALIF SAN FRANCISCO, GRAD GRP BIOPHYS, SAN FRANCISCO, CA 94131 USA
[3] UNIV CALIF SAN FRANCISCO, DEPT PHARMACEUT CHEM, SAN FRANCISCO, CA 94131 USA
[4] UNIV CALIF SAN FRANCISCO, DEPT MED BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94131 USA
关键词
PROTEIN STRUCTURE PREDICTION; SECONDARY STRUCTURE; EVALUATION;
D O I
10.1002/prot.340230317
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 results of a protein structure prediction contest are reviewed. Twelve different groups entered predictions on 14 proteins of known sequence whose structures had been determined but not yet disseminated to the scientific community. Thus, these represent true tests of the current state of structure prediction methodologies. From this work, it is clear that accurate tertiary structure prediction is not yet possible. However, protein fold and motif prediction are possible when the motif is recognizably similar to another known structure. Internal symmetry and the information inherent in an aligned family of homologous sequences facilitate predictive efforts. Novel folds remain a major challenge for prediction efforts. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:431 / 445
页数:15
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