KEA3: improved kinase enrichment analysis via data integration

Maxim V. Kuleshov(Icahn School of Medicine at Mount Sinai), Zhuorui Xie(Icahn School of Medicine at Mount Sinai), Alexandra B. London(Icahn School of Medicine at Mount Sinai), Janice Yang(Icahn School of Medicine at Mount Sinai), John Erol Evangelista(Icahn School of Medicine at Mount Sinai), Alexander Lachmann(Icahn School of Medicine at Mount Sinai), Ingrid Shu(Icahn School of Medicine at Mount Sinai), Denis Torre(Icahn School of Medicine at Mount Sinai), Avi Ma’ayan(Icahn School of Medicine at Mount Sinai)
Nucleic Acids Research
April 23, 2021
Cited by 155Open Access
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Abstract

Phosphoproteomics and proteomics experiments capture a global snapshot of the cellular signaling network, but these methods do not directly measure kinase state. Kinase Enrichment Analysis 3 (KEA3) is a webserver application that infers overrepresentation of upstream kinases whose putative substrates are in a user-inputted list of proteins. KEA3 can be applied to analyze data from phosphoproteomics and proteomics studies to predict the upstream kinases responsible for observed differential phosphorylations. The KEA3 background database contains measured and predicted kinase-substrate interactions (KSI), kinase-protein interactions (KPI), and interactions supported by co-expression and co-occurrence data. To benchmark the performance of KEA3, we examined whether KEA3 can predict the perturbed kinase from single-kinase perturbation followed by gene expression experiments, and phosphoproteomics data collected from kinase-targeting small molecules. We show that integrating KSIs and KPIs across data sources to produce a composite ranking improves the recovery of the expected kinase. The KEA3 webserver is available at https://maayanlab.cloud/kea3.


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