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首页> 外文期刊>Journal of computational biology: A journal of computational molecular cell biology >Protein local structure alignment under the discrete Frechet distance
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Protein local structure alignment under the discrete Frechet distance

机译:离散Frechet距离下的蛋白质局部结构比对

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摘要

Protein structure alignment is a fundamental problem in computational and structural biology. While there has been lots of experimental/heuristic methods and empirical results, very few results are known regarding the algorithmic/complexity aspects of the problem, especially on protein local structure alignment. A well-known measure to characterize the similarity of two polygonal chains is the famous Frechet distance, and with the application of protein-related research, a related discrete Frechet distance has been used recently. In this paper, following the recent work of Jiang et al. we investigate the protein local structural alignment problem using bounded discrete Frechet distance. Given m proteins (or protein backbones, which are 3D polygonal chains), each of length O(n), our main results are summarized as follows: If the number of proteins, m, is not part of the input, then the problem is NP-complete; moreover, under bounded discrete Frechet distance it is NP-hard to approximate the maximum size common local structure within a factor of n(1-epsilon). These results hold both when all the proteins are static and when translation/rotation are allowed. If the number of proteins, m, is a constant, then there is a polynomial time solution for the problem.
机译:蛋白质结构比对是计算和结构生物学中的基本问题。尽管有许多实验/启发式方法和经验结果,但是关于该问题的算法/复杂性方面(尤其是蛋白质局部结构比对)的结果很少。表征两个多边形链相似性的一个著名方法是著名的Frechet距离,并且随着蛋白质相关研究的应用,最近已经使用了相关的离散Frechet距离。在本文中,根据江等人的最新工作。我们使用有界离散弗雷谢距离研究蛋白质局部结构比对问题。给定m个蛋白质(或蛋白质骨架,它们是3D多边形链),每个蛋白质的长度为O(n),我们的主要结果总结如下:如果蛋白质的数量m不属于输入的一部分,那么问题是NP完全;此外,在有界的离散弗雷切特距离下,要在n(1-ε)因子内近似最大尺寸的公共局部结构是NP难的。当所有蛋白质都是静态的以及允许翻译/旋转时,这些结果均成立。如果蛋白质的数量m为常数,则存在针对该问题的多项式时间解。

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