A novel Greedy approach for Sequence based Computational prediction of Binding-Sites in Protein-Protein Interaction

Aishwarya Purohit, S. Acharya, James Green
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Abstract

Computational prediction of protein-protein interaction (PPI) from protein sequence is important as many cellular functions are made possible through PPI. The Protein Interaction Prediction Engine (PIPE) software suite was developed for such predictions. The specific location of interaction is predicted by the PIPE-Sites predictor, which depends on PIPE engine. This PIPE-Sites predictor is here updated through the use of a large high-quality dataset of known PPI sites. Additionally, a similarity-weighted score had been recently developed in PIPE4 and has been proven to be more accurate for the likelihood of PPI prediction. However, PIPE-Sites are shown to be ineffective when applied to similarity-weighted score data. Thus, we here propose and evaluate a new sequence-based PPI site prediction method, named Panorama. This new method leverages similarity-weighted score data to further increase performance over two different performance metrics when evaluated on both $\boldsymbol{H}$. sapiens and $\boldsymbol{S}$, cerevisiae PPI site data.
一种基于序列的蛋白质相互作用结合位点计算预测的贪心方法
蛋白质-蛋白质相互作用(PPI)的计算预测是重要的,因为许多细胞功能是通过PPI实现的。蛋白质相互作用预测引擎(PIPE)软件套件就是为了这样的预测而开发的。具体的交互位置由PIPE- sites预测器预测,它依赖于PIPE引擎。通过使用已知PPI位点的大型高质量数据集,这个PPI位点预测器在这里进行了更新。此外,最近在PIPE4中开发了一种相似性加权评分,并已被证明对PPI预测的可能性更准确。然而,当应用于相似加权分数数据时,PIPE-Sites被证明是无效的。因此,我们在此提出并评估了一种新的基于序列的PPI位点预测方法,名为Panorama。当在两个$\boldsymbol{H}$上进行评估时,这个新方法利用相似度加权得分数据在两个不同的性能指标上进一步提高性能。sapiens和$\boldsymbol{S}$,查看PPI站点数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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