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 DooSim, TaeboBerberich, Matthew J.Kalocsay, MarianSorger, 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
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE