Protein fold recognition by sequence threading: Tools and assessment techniques

被引:49
作者
Miller, RT
Jones, DT
Thornton, JM
机构
[1] UNIV LONDON UNIV COLL,DEPT BIOCHEM & MOLEC BIOL,BIOMOLEC STRUCT & MODELLING UNIT,LONDON WC1E 6BT,ENGLAND
[2] NATL INST MED RES,MATH BIOL LAB,LONDON NW7 7HX,ENGLAND
基金
英国惠康基金;
关键词
protein folding; protein structure prediction; protein threading;
D O I
10.1096/fasebj.10.1.8566539
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
Protein fold recognition has been approached by threading an amino acid sequence onto a library of folds, calculating a sequence-structure compatibility score, and ranking these scores, Due to imperfections in the empirically derived pairwise potential functions and the necessarily heuristic approach to the sequence-structure alignment problem, the method benefits from the assessment of threaded models to evaluate the most probable structures among the list of possible folds, THREADER and ANALYST, software tools available through the Internet, facilitate the alignment and assessment steps of a threading prediction, No process has been found to be universally reliable for the detection of folds related to the structure of a known input sequence, but several useful steps and approaches are discussed.
引用
收藏
页码:171 / 178
页数:8
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