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Binding Site Prediction for Protein-Protein Interactions and Novel Motif Discovery using Re-occurring Polypeptide Sequences

机译:蛋白质相互作用的结合位点预测和使用重复出现的多肽序列的新型基序发现

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摘要

BackgroundWhile there are many methods for predicting protein-protein interaction, very few can determine the specific site of interaction on each protein. Characterization of the specific sequence regions mediating interaction (binding sites) is crucial for an understanding of cellular pathways. Experimental methods often report false binding sites due to experimental limitations, while computational methods tend to require data which is not available at the proteome-scale. Here we present PIPE-Sites, a novel method of protein specific binding site prediction based on pairs of re-occurring polypeptide sequences, which have been previously shown to accurately predict protein-protein interactions. PIPE-Sites operates at high specificity and requires only the sequences of query proteins and a database of known binary interactions with no binding site data, making it applicable to binding site prediction at the proteome-scale.
机译:背景技术虽然有许多预测蛋白质相互作用的方法,但很少能确定每种蛋白质相互作用的特定位点。介导相互作用(结合位点)的特定序列区域的表征对于理解细胞途径至关重要。由于实验的局限性,实验方法通常会报告错误的结合位点,而计算方法往往需要蛋白质组规模无法获得的数据。在这里,我们介绍PIPE-Site,这是一种基于重复出现的多肽序列对的蛋白质特异性结合位点预测的新方法,以前已经证明该方法可以准确预测蛋白质-蛋白质相互作用。 PIPE-Site具有高特异性,仅需要查询蛋白的序列和已知二元相互作用的数据库,而没有结合位点数据,因此可用于蛋白质组规模的结合位点预测。

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