Mining graph patterns in the protein-RNA interfaces

Wen Cheng, Changhui Yan
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引用次数: 2

Abstract

Protein-RNA interactions play important roles in the biological systems. The goal of this study is to discover structural patterns in the protein-RNA interfaces that contribute the affinity of the interactions. We represented known protein-RNA interfaces using graphs and then identify common subgraphs enriched in the interfaces. Comparison of the discovered graph patterns with UniProt annotations showed that the graph patterns had a significant overlap with residue sites that had been proven by experimental methods to be crucial for RNA bindings. Using 200 patterns as input features, a Support Vector Machine method was able to classify protein surface patches into RNA-binding sites and non-RNA-biding sites with 84.0% accuracy and 88.9% precision. We built a simple scoring function that calculated the total number of the graph patterns that occurred in a protein-RNA interface. That scoring function was able to discriminate near native protein-RNA complexes from docking decoys with a performance comparable with a state-of-the-art complex scoring function.
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在蛋白质- rna界面中挖掘图形模式
蛋白质- rna相互作用在生物系统中起着重要作用。本研究的目的是发现蛋白质- rna界面的结构模式,这些结构模式有助于相互作用的亲和力。我们使用图形表示已知的蛋白质- rna界面,然后识别界面中丰富的公共子图。将发现的图形模式与UniProt注释进行比较,发现图形模式与实验方法证明对RNA结合至关重要的残基位点有显著重叠。使用200种模式作为输入特征,支持向量机方法能够将蛋白质表面斑块分为rna结合位点和非rna结合位点,准确率为84.0%,精密度为88.9%。我们建立了一个简单的评分函数来计算在蛋白质- rna界面中出现的图形模式的总数。该评分功能能够区分接近天然蛋白- rna复合物和对接诱饵,其性能可与最先进的复杂评分功能相媲美。
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