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The Relation between Indel Length and Functional Divergence: A Formal Study

机译:插入缺失长度与功能发散之间的关系:一项正式研究

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Although insertions and deletions (indels) are a common type of evolutionary sequence variation, their origins and their functional consequences have not been comprehensively understood. There is evidence that, on one hand, classical alignment procedures only roughly reflect the evolutionary processes and, on the other hand, that they cause structural changes in the proteins' surfaces. We first demonstrate how to identify alignment gaps that have been introduced by evolution to a statistical significant degree, by means of a novel, sound statistical framework, based on pair hidden Markov models (HMMs). Second, we examine paralogous protein pairs in E. coli, obtained by computation of classical global alignments. Distinguishing between indel and non-indel pairs, according to our novel statistics, revealed that, despite having the same sequence identity, indel pairs are significantly less functionally similar than non-indel pairs, as measured by recently suggested GO based functional distances. This suggests that indels cause more severe functional changes than other types of sequence variation and that indel statistics should be taken into additional account to assess functional similarity between paralogous protein pairs.
机译:尽管插入和缺失(indels)是进化序列变异的一种常见类型,但其起源和功能后果尚未得到全面了解。有证据表明,一方面,经典比对程序仅大致反映了进化过程,另一方面,它们导致了蛋白质表面的结构变化。我们首先展示如何基于配对隐马尔可夫模型(HMM),通过新颖,合理的统计框架,识别出进化到统计学上显着程度引入的比对缺口。其次,我们检查了大肠杆菌中的同源蛋白质对,这是通过计算经典全局比对获得的。根据我们的新统计,区分插入/缺失和非插入/缺失对发现,尽管具有相同的序列同一性,但插入/缺失对的功能相似性远低于非插入/缺失对,如最近建议的基于GO的功能距离所测。这表明插入缺失引起比其他类型的序列变异更严重的功能改变,并且应该另外考虑插入缺失统计以评估旁源蛋白质对之间的功能相似性。

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