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首页> 外文期刊>Journal of computational biology >Learning Sequence Determinants of Protein:Protein Interaction Specificity with Sparse Graphical Models
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Learning Sequence Determinants of Protein:Protein Interaction Specificity with Sparse Graphical Models

机译:学习蛋白质的序列决定因素:蛋白质与稀疏图形模型的相互作用特异性

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Abstract In studying the strength and specificity of interaction between members of two protein families, key questions center on which pairs of possible partners actually interact, how well they interact, and why they interact while others do not. The advent of large-scale experimental studies of interactions between members of a target family and a diverse set of possible interaction partners offers the opportunity to address these questions. We develop here a method, DgSpi (data-driven graphical models of specificity in protein:protein interactions), for learning and using graphical models that explicitly represent the amino acid basis for interaction specificity (why) and extend earlier classification-oriented approaches (which) to predict the ΔG of binding (how well). We demonstrate the effectiveness of our approach in analyzing and predicting interactions between a set of 82 PDZ recognition modules against a panel of 217 possible peptide partners, based on data from MacBeath and colleagues. Our pred..." />展开▼
机译:摘要在研究两个蛋白质家族成员之间相互作用的强度和特异性时,关键问题集中在可能的一对伴侣之间实际相互作用,相互作用的程度以及为什么彼此不相互作用的原因。目标家庭成员与各种可能的相互作用伙伴之间相互作用的大规模实验研究的出现提供了解决这些问题的机会。我们在这里开发一种方法DgSpi(蛋白质:蛋白质相互作用的数据驱动的特异性图形模型),用于学习和使用可明确表示相互作用特异性氨基酸基础的图形模型(为什么)并扩展早期的面向分类的方法(该方法)以预测结合的ΔG(水平)。我们基于MacBeath及其同事的数据,证明了我们的方法在分析和预测82个PDZ识别模块与217种可能的肽伴侣组成的组之间的相互作用时的有效性。我们的调查对象...“ />

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