Ensemble approach to predict specificity determinants: benchmarking and validation

被引:24
作者
Chakrabarti, Saikat [1 ]
Panchenko, Anna R. [1 ]
机构
[1] NIH, Natl Ctr Biotechnol Informat, Natl Lib Med, Bethesda, MD 20892 USA
来源
BMC BIOINFORMATICS | 2009年 / 10卷
基金
美国国家卫生研究院;
关键词
FUNCTIONAL SPECIFICITY; DETERMINING RESIDUES; SEQUENCE ALIGNMENTS; PROTEIN FAMILIES; DIVERGENCE; SERVER; COMMON;
D O I
10.1186/1471-2105-10-207
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: It is extremely important and challenging to identify the sites that are responsible for functional specification or diversification in protein families. In this study, a rigorous comparative benchmarking protocol was employed to provide a reliable evaluation of methods which predict the specificity determining sites. Subsequently, three best performing methods were applied to identify new potential specificity determining sites through ensemble approach and common agreement of their prediction results. Results: It was shown that the analysis of structural characteristics of predicted specificity determining sites might provide the means to validate their prediction accuracy. For example, we found that for smaller distances it holds true that the more reliable the prediction method is, the closer predicted specificity determining sites are to each other and to the ligand. Conclusion: We observed certain similarities of structural features between predicted and actual subsites which might point to their functional relevance. We speculate that majority of the identified potential specificity determining sites might be indirectly involved in specific interactions and could be ideal target for mutagenesis experiments.
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页数:11
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