Discovery of Covalent CDK14 Inhibitors with Pan-TAIRE Family Specificity
- Authors
- Ferguson, Fleur M.; Doctor, Zainab M.; Ficarro, Scott B.; Browne, Christopher M.; Marto, Jarrod A.; Johnson, Jared L.; Yaron, Tomer M.; Cantley, Lewis C.; Kim, Nam Doo; Sim, Taebo; Berberich, Matthew J.; Kalocsay, Marian; Sorger, Peter K.; Gray, Nathanael S.
- Issue Date
- 2019-06
- Publisher
- CELL PRESS
- Citation
- CELL CHEMICAL BIOLOGY, v.26, no.6, pp.804 - +
- 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.
- Keywords
- IDENTIFICATION; TARGET; PFTK1; PHOSPHORYLATION; PROLIFERATION; PATHWAYS; PROTEINS; INVASION; KINASES; POTENT; CDK14; cell cycle; covalent inhibitor; druggable genome; mitosis; TAIRE kinase
- ISSN
- 2451-9448
- URI
- https://pubs.kist.re.kr/handle/201004/119898
- DOI
- 10.1016/j.chembiol.2019.02.015
- Appears in Collections:
- KIST Article > 2019
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