4.7 Article

KinasePhos 3.0: Redesign and Expansion of the Prediction on Kinase-specific Phosphorylation Sites

期刊

GENOMICS PROTEOMICS & BIOINFORMATICS
卷 21, 期 1, 页码 228-241

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ELSEVIER
DOI: 10.1016/j.gpb.2022.06.004

关键词

Kinase-specific phosphorylation; Phosphorylation site prediction; Phosphorylation; SHAP feature importance; Kinase

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The purpose of this work is to enhance the KinasePhos tool, which predicts kinase-specific phosphorylation sites using machine learning. Through collecting experimentally verified data, a total of 41,421 phosphorylation sites were identified, which cover 1380 unique kinases. Based on kinase classification, 771 predictive models were built, showing higher accuracy than other tools. The web interface of KinasePhos 3.0 has been redesigned to provide comprehensive annotations, and a downloadable prediction tool is available for large-scale phosphoproteomic data.
The purpose of this work is to enhance KinasePhos, a machine learning-based kinasespecific phosphorylation site prediction tool. Experimentally verified kinase-specific phosphorylation data were collected from PhosphoSitePlus, UniProtKB, the GPS 5.0, and Phospho.ELM. In total, 41,421 experimentally verified kinase-specific phosphorylation sites were identified. A total of 1380 unique kinases were identified, including 753 with existing classification information from KinBase and the remaining 627 annotated by building a phylogenetic tree. Based on this kinase classification, a total of 771 predictive models were built at the individual, family, and group levels, using at least 15 experimentally verified substrate sites in positive training datasets. The improved models demonstrated their effectiveness compared with other prediction tools. For example, the prediction of sites phosphorylated by the protein kinase B, casein kinase 2, and protein kinase A families had accuracies of 94.5%, 92.5%, and 90.0%, respectively. The average prediction accuracy for all 771 models was 87.2%. For enhancing interpretability, the SHapley Additive exPlanations (SHAP) method was employed to assess feature importance. The web interface of KinasePhos 3.0 has been redesigned to provide comprehensive annotations of kinase-specific phosphorylation sites on multiple proteins. Additionally, considering the large scale of phosphoproteomic data, a downloadable prediction tool is available at https://awi.cuhk.edu.cn/KinasePhos/download.html or https://github.com/tom-209/ KinasePhos-3.0-executable-file.

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