Publication | Open Access
GPS 5.0: An Update on the Prediction of Kinase-Specific Phosphorylation Sites in Proteins
315
Citations
34
References
2020
Year
Gps 5.0Molecular BiologyReceptor Tyrosine KinaseProteomicsCell SignalingProtein FunctionBiochemistryTyrosine KinasesKinase-specific Phosphorylation SitesProtein ModelingOmicsPathway AnalysisProtein Structure PredictionBioinformaticsFunctional GenomicsCell BiologyStructural BiologyProtein BioinformaticsProtein PhosphorylationSignal TransductionNatural SciencesComputational BiologyCellular BiochemistrySystems BiologyMedicine
Abstract In eukaryotes, protein phosphorylation is specifically catalyzed by numerous protein kinases (PKs), faithfully orchestrates various biological processes, and reversibly determines cellular dynamics and plasticity. Here we report an updated algorithm of Group-based Prediction System (GPS) 5.0 to improve the performance for predicting kinase-specific phosphorylation sites (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 dual-specificity kinase-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 http://gps.biocuckoo.cn.
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