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A new algorithm for sequential and non-sequential protein multiple structure alignment

机译:顺序和非顺序蛋白质多结构比对的新算法

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摘要

A fundamental issue in studies of protein structure and function is how to identify the conserved common core in multiple protein structures. The existing algorithms work well for proteins family such as those in HOMSTRAD but are not satisfactory for general multiple structure alignment problems, especially in some challenging cases, such as the occurrence of circular permutations. In this paper, an efficient approach called SANA-mult for multiple structure alignment is presented. Specifically, the alignment problem is first mapped on to a mixed integer programming problem via introducing a structural template, and then the algorithm decomposes the problem into two subproblems, i.e. solving the pairwise alignment and updating the template chain. We show that the proposed method can obtain sequential and non-sequential solutions for multiple structure alignment in an accurate manner, which is competitive or superior to the existing methods. The effectiveness of the new algorithm SANA-mult is tested using various protein structure sets and benchmark examples.
机译:蛋白质结构和功能研究中的一个基本问题是如何识别多种蛋白质结构中的保守共有核心。现有的算法对于蛋白质家族(例如,HOMSTRAD中的那些)运作良好,但是对于一般的多结构比对问题(特别是在某些挑战性情况下,例如圆置换的发生)并不令人满意。在本文中,提出了一种用于多结构对齐的称为SANA-mult的有效方法。具体地,首先通过引入结构模板将对齐问题映射到混合整数规划问题,然后该算法将该问题分解为两个子问题,即,解决成对对齐并更新模板链。我们表明,所提出的方法可以以精确的方式获得用于多个结构对准的顺序和非顺序解决方案,这比现有方法具有竞争性或优越性。使用各种蛋白质结构集和基准示例测试了新算法SANA-mult的有效性。

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