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GPS 5.0: An Update on the Prediction of Kinase-specific Phosphorylation Sites in Proteins

机译:GPS 5.0:关于蛋白质激酶特异性磷酸化位点预测的更新

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摘要

In eukaryotes, is specifically catalyzed by numerous (PKs), faithfully orchestrates various biological processes, and reversibly determines cellular dynamics and plasticity. Here we report an updated algorithm of (GPS) 5.0 to improve the performance for predicting (p-sites). Two novel methods, position weight determination (PWD) and scoring matrix optimization (SMO), were developed. Compared with other existing tools, GPS 5.0 exhibits a highly competitive accuracy. Besides serine/threonine or tyrosine kinases, GPS 5.0 also supports the prediction of -specific p-sites. In the classical module of GPS 5.0, 617 individual predictors were constructed for predicting p-sites of 479 human PKs. To extend the application of GPS 5.0, a species-specific module was implemented to predict kinase-specific p-sites for 44,795 PKs in 161 eukaryotes. The online service and local packages of GPS 5.0 are freely available for academic research at .
机译:在真核生物中,由许多(PKS)特异性催化,忠实地编制各种生物过程,并可逆地决定蜂窝动力学和可塑性。在这里,我们报告了一种更新的(GPS)5.0算法,以提高预测(P-Site)的性能。开发了两种新方法,位置重量确定(PWD)和评分矩阵优化(SMO)。与其他现有工具相比,GPS 5.0表现出具有较强竞争的准确性。除了丝氨酸/苏氨酸或酪氨酸激酶外,GPS 5.0还支持预测 - 特异性P-Sites。在GPS 5.0的经典模块中,构建了617个单独的预测因子,用于预测479个人p的P-sits。为了扩展GPS 5.0的应用,实施了物种特异性模块以预测161个真核生物中的44,795 PKS的基酶特异性P-位点。 GPS 5.0的在线服务和本地包装可自由参加学术研究。

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