启发式
结构线形
成对比较
多序列比对
计算机科学
蛋白质结构预测
合并(版本控制)
数据结构
序列比对
自由序列分析
蛋白质结构
理论计算机科学
算法
线程(蛋白质序列)
人工智能
数据挖掘
情报检索
生物
操作系统
肽序列
基因
生物化学
程序设计语言
出处
期刊:Advances in protein chemistry and structural biology
日期:2014-01-01
卷期号:: 121-175
被引量:56
标识
DOI:10.1016/b978-0-12-800168-4.00005-6
摘要
As a fundamental problem in computational structure biology, protein structure alignment has attracted the focus of the community for more than 20 years. While the pairwise structure alignment could be applied to measure the similarity between two proteins, which is a first step for homology search and fold space construction, the multiple structure alignment could be used to understand evolutionary conservation and divergence from a family of protein structures. Structure alignment is an NP-hard problem, which is only computationally tractable by using heuristics. Three levels of heuristics for pairwise structure alignment have been proposed, from the representations of protein structure, the perspectives of viewing protein as a rigid-body or flexible, to the scoring functions as well as the search algorithms for the alignment. For multiple structure alignment, the fourth level of heuristics is applied on how to merge all input structures to a multiple structure alignment. In this review, we first present a small survey of current methods for protein pairwise and multiple alignment, focusing on those that are publicly available as web servers. In more detail, we also discuss the advancements on the development of the new approaches to increase the pairwise alignment accuracy, to efficiently and reliably merge input structures to the multiple structure alignment. Finally, besides broadening the spectrum of the applications of structure alignment for protein template-based prediction, we also list several open problems that need to be solved in the future, such as the large complex alignment and the fast database search.
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