一种新的蛋白质序列相似性度量方法。

Kuen-Pin Wu, Hsin-Nan Lin, Ting-Yi Sung, Wen-Lian Hsu
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引用次数: 0

摘要

蛋白质序列分析是破解生命逻辑的重要工具。在这一领域,最重要的相似性度量之一是两个序列之间氨基酸的编辑距离。我们认为应该重新考虑这一标准,因为蛋白质的特征可能更多地与小肽片段有关,而不是与单个氨基酸有关。在本文中,我们设计了一组蛋白质序列中与高度转换区域相关的小模式。这些模式的使用类似于信息检索中的索引项。因此,我们不考虑模式中的间隙。这种新的相似性度量方法已应用于系统发育树的构建、蛋白质聚类和蛋白质二级结构的预测,并取得了令人满意的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new similarity measure among protein sequences.

Protein sequence analysis is an important tool to decode the logic of life. One of the most important similarity measures in this area is the edit distance between amino acids of two sequences. We believe this criterion should be reconsidered because protein features are probably associated more with small peptide fragments than with individual amino acids. In this paper, we design small patterns that are associated with highly conversed regions among a set of protein sequences. These patterns are used analogous to the index terms in information retrieval. Therefore, we do not consider gaps within patterns. This new similarity measure has been applied to phylogenetic tree construction, protein clustering and protein secondary structure prediction and has produced promising results.

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