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MULTICOM: a multi-level combination approach to protein structure prediction and its assessments in CASP8

机译:MULTICOM:CASP8中蛋白质结构预测及其评估的多级组合方法

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Motivation: Protein structure prediction is one of the most important problems in structural bioinformatics. Here we describe MULTICOM, a multi-level combination approach to improve the various steps in protein structure prediction. In contrast to those methods which look for the best templates, alignments and models, our approach tries to combine complementary and alternative templates, alignments and models to achieve on average better accuracy.Results: The multi-level combination approach was implemented via five automated protein structure prediction servers and one human predictor which participated in the eighth Critical Assessment of Techniques for Protein Structure Prediction (CASP8), 2008. The MULTICOM servers and human predictor were consistently ranked among the top predictors on the CASP8 benchmark. The methods can predict moderate-to high-resolution models for most template-based targets and low-resolution models for some template-free targets. The results show that the multi-level combination of complementary templates, alternative alignments and similar models aided by model quality assessment can systematically improve both template-based and template-free protein modeling.
机译:动机:蛋白质结构预测是结构生物信息学中最重要的问题之一。在这里,我们介绍MULTICOM,这是一种多级组合方法,可以改善蛋白质结构预测中的各个步骤。与那些寻找最佳模板,比对和模型的方法相反,我们的方法尝试将互补和替代模板,比对和模型组合在一起,以实现平均更好的准确性。结果:通过五个自动化蛋白质实现了多级组合方法结构预测服务器和一个人类预测因子参加了2008年第八次蛋白质结构预测技术关键评估(CASP8)。MULTICOM服务器和人类预测因子一直是CASP8基准测试中的顶级预测因子。这些方法可以预测大多数基于模板的目标的中到高分辨率模型,以及一些无模板目标的低分辨率模型。结果表明,互补的模板,替代比对和相似模型的多级组合在模型质量评估的帮助下可以系统地改善基于模板的蛋白质模型和无模板的蛋白质模型。

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