Incremental threading optimization (TITO) to help alignment and modelling of remote homologues

被引:60
作者
Labesse, G
Mornon, JP
机构
[1] Univ Paris 06, Lab Mineral Cristallog, CNRS URA 09, F-75252 Paris 05, France
[2] Univ Paris 07, Lab Mineral Cristallog, CNRS URA 09, F-75252 Paris 05, France
关键词
D O I
10.1093/bioinformatics/14.2.206
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Protein sequence comparison has become a major tool for biologists. Various methods have been designed in order to reveal even I-emote homologies among proteins. Sequence analyses are powerful, but the lower the identity score, the more skill and time are required to perform them accurately. While necessary to confirm the sequence comparison through the potential of mean force, sequence alignment and molecular modelling are still tedious and time-consuming tasks. Results: In order to help sequence threading onto known three-dimensional (3D) structures, we have developed a new program, named TITO (Tool for Incremental Threading Optimization), which uses a multiple alignment to validate and help the refinement of a sequence/structure comparison. It measures the compatibility of a family of related sequences with a known 3D structure. The coordinates of the common core are extracted, allowing further molecular modelling and 30 survey.
引用
收藏
页码:206 / 211
页数:6
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