PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection
Abstract Protein phosphorylation is a major form of post-translational modification (PTM) that regulates diverse cellular processes. In silico methods for phosphorylation site prediction can provide a useful and complementary strategy for complete phosphoproteome annotation. Here, we present a novel...
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doaj-f266672a200d45e199456ae3087541bc2020-12-08T00:46:10ZengNature Publishing GroupScientific Reports2045-23222017-07-017111910.1038/s41598-017-07199-4PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selectionJiangning Song0Huilin Wang1Jiawei Wang2André Leier3Tatiana Marquez-Lago4Bingjiao Yang5Ziding Zhang6Tatsuya Akutsu7Geoffrey I. Webb8Roger J. Daly9Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash UniversityDepartment of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen UniversityBiomedicine Discovery Institute and Department of Microbiology, Monash UniversityInformatics Institute and Department of Genetics, School of Medicine, University of Alabama at BirminghamInformatics Institute and Department of Genetics, School of Medicine, University of Alabama at BirminghamCollege of Mechanical Engineering, Yanshan UniversityState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural UniversityBioinformatics Center, Institute for Chemical Research, Kyoto UniversityMonash Centre for Data Science, Faculty of Information Technology, Monash UniversityBiomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash UniversityAbstract Protein phosphorylation is a major form of post-translational modification (PTM) that regulates diverse cellular processes. In silico methods for phosphorylation site prediction can provide a useful and complementary strategy for complete phosphoproteome annotation. Here, we present a novel bioinformatics tool, PhosphoPredict, that combines protein sequence and functional features to predict kinase-specific substrates and their associated phosphorylation sites for 12 human kinases and kinase families, including ATM, CDKs, GSK-3, MAPKs, PKA, PKB, PKC, and SRC. To elucidate critical determinants, we identified feature subsets that were most informative and relevant for predicting substrate specificity for each individual kinase family. Extensive benchmarking experiments based on both five-fold cross-validation and independent tests indicated that the performance of PhosphoPredict is competitive with that of several other popular prediction tools, including KinasePhos, PPSP, GPS, and Musite. We found that combining protein functional and sequence features significantly improves phosphorylation site prediction performance across all kinases. Application of PhosphoPredict to the entire human proteome identified 150 to 800 potential phosphorylation substrates for each of the 12 kinases or kinase families. PhosphoPredict significantly extends the bioinformatics portfolio for kinase function analysis and will facilitate high-throughput identification of kinase-specific phosphorylation sites, thereby contributing to both basic and translational research programs.https://doi.org/10.1038/s41598-017-07199-4 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jiangning Song Huilin Wang Jiawei Wang André Leier Tatiana Marquez-Lago Bingjiao Yang Ziding Zhang Tatsuya Akutsu Geoffrey I. Webb Roger J. Daly |
spellingShingle |
Jiangning Song Huilin Wang Jiawei Wang André Leier Tatiana Marquez-Lago Bingjiao Yang Ziding Zhang Tatsuya Akutsu Geoffrey I. Webb Roger J. Daly PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection Scientific Reports |
author_facet |
Jiangning Song Huilin Wang Jiawei Wang André Leier Tatiana Marquez-Lago Bingjiao Yang Ziding Zhang Tatsuya Akutsu Geoffrey I. Webb Roger J. Daly |
author_sort |
Jiangning Song |
title |
PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
title_short |
PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
title_full |
PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
title_fullStr |
PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
title_full_unstemmed |
PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
title_sort |
phosphopredict: a bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-07-01 |
description |
Abstract Protein phosphorylation is a major form of post-translational modification (PTM) that regulates diverse cellular processes. In silico methods for phosphorylation site prediction can provide a useful and complementary strategy for complete phosphoproteome annotation. Here, we present a novel bioinformatics tool, PhosphoPredict, that combines protein sequence and functional features to predict kinase-specific substrates and their associated phosphorylation sites for 12 human kinases and kinase families, including ATM, CDKs, GSK-3, MAPKs, PKA, PKB, PKC, and SRC. To elucidate critical determinants, we identified feature subsets that were most informative and relevant for predicting substrate specificity for each individual kinase family. Extensive benchmarking experiments based on both five-fold cross-validation and independent tests indicated that the performance of PhosphoPredict is competitive with that of several other popular prediction tools, including KinasePhos, PPSP, GPS, and Musite. We found that combining protein functional and sequence features significantly improves phosphorylation site prediction performance across all kinases. Application of PhosphoPredict to the entire human proteome identified 150 to 800 potential phosphorylation substrates for each of the 12 kinases or kinase families. PhosphoPredict significantly extends the bioinformatics portfolio for kinase function analysis and will facilitate high-throughput identification of kinase-specific phosphorylation sites, thereby contributing to both basic and translational research programs. |
url |
https://doi.org/10.1038/s41598-017-07199-4 |
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