Information of Binding Sites Improves Prediction of Protein-Protein Interaction

Tapan P. Patel, Manoj Pillay, Rahul Jawa, Li Liao
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引用次数: 10

Abstract

Protein-protein interaction is essential to cellular functions. In this work, we describe a simple, novel approach to improve the accuracy of predicting protein-protein interaction by incorporating the binding site information. First, we assess the importance of the seven attributes that are used by Bradford et. al (2005) for predicting protein binding sites. The leave-one-out cross validation experiments and principal component analysis indicate that some attributes such as residue propensity and hydrophobicity are more important than other attributes such as curvedness and shape index in differentiating a binding patch from nonbinding patch. Second, we incorporate those attributes to predict protein-protein interaction by simple concatenation of the attribute vectors of candidate interacting partners. A support vector machine is trained to predict the interacting partners. This is combined with using the attributes directly derived from the primary sequence at the binding sites. The results from the leave-one-out cross validation experiments show significant improvement in prediction accuracy by incorporating the structural information at the binding sites
结合位点的信息改善了蛋白质相互作用的预测
蛋白质之间的相互作用对细胞功能至关重要。在这项工作中,我们描述了一种简单、新颖的方法,通过结合结合位点信息来提高预测蛋白质-蛋白质相互作用的准确性。首先,我们评估了Bradford等人(2005)用于预测蛋白质结合位点的七个属性的重要性。通过留一交叉验证实验和主成分分析表明,残留倾向和疏水性等属性比曲线度和形状指数等属性更能有效地区分结合贴片与非结合贴片。其次,我们结合这些属性,通过简单的候选相互作用伙伴属性向量的连接来预测蛋白质-蛋白质相互作用。训练支持向量机来预测交互伙伴。这与使用直接从结合位点的初级序列派生的属性相结合。留一交叉验证实验结果表明,结合结合位点的结构信息显著提高了预测精度
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