| Literature DB >> 30930164 |
Fleur M Ferguson1, Zainab M Doctor1, Scott B Ficarro2, Christopher M Browne1, Jarrod A Marto3, Jared L Johnson4, Tomer M Yaron5, Lewis C Cantley4, Nam Doo Kim6, Taebo Sim7, Matthew J Berberich8, Marian Kalocsay8, Peter K Sorger8, Nathanael S Gray9.
Abstract
Cyclin-dependent kinase 14 (CDK14) and other TAIRE family kinases (CDKs 15-18) are proteins that lack functional annotation but are frequent off-targets of clinical kinase inhibitors. In this study we develop and characterize FMF-04-159-2, a tool compound that specifically targets CDK14 covalently and possesses a TAIRE kinase-biased selectivity profile. This tool compound and its reversible analog were used to characterize the cellular consequences of covalent CDK14 inhibition, including an unbiased investigation using phospho-proteomics. To reduce confounding off-target activity, washout conditions were used to deconvolute CDK14-specific effects. This investigation suggested that CDK14 plays a supporting role in cell-cycle regulation, particularly mitotic progression, and identified putative CDK14 substrates. Together, these results represent an important step forward in understanding the cellular consequences of inhibiting CDK14 kinase activity.Entities:
Keywords: CDK14; TAIRE kinase; cell cycle; covalent inhibitor; druggable genome; mitosis
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Year: 2019 PMID: 30930164 PMCID: PMC6588450 DOI: 10.1016/j.chembiol.2019.02.015
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116