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dc.contributor.authorFerguson, Fleur M.-
dc.contributor.authorDoctor, Zainab M.-
dc.contributor.authorFicarro, Scott B.-
dc.contributor.authorBrowne, Christopher M.-
dc.contributor.authorMarto, Jarrod A.-
dc.contributor.authorJohnson, Jared L.-
dc.contributor.authorYaron, Tomer M.-
dc.contributor.authorCantley, Lewis C.-
dc.contributor.authorKim, Nam Doo-
dc.contributor.authorSim, Taebo-
dc.contributor.authorBerberich, Matthew J.-
dc.contributor.authorKalocsay, Marian-
dc.contributor.authorSorger, Peter K.-
dc.contributor.authorGray, Nathanael S.-
dc.date.accessioned2024-01-19T20:00:53Z-
dc.date.available2024-01-19T20:00:53Z-
dc.date.created2022-01-25-
dc.date.issued2019-06-
dc.identifier.issn2451-9448-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/119898-
dc.description.abstractCyclin-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.-
dc.languageEnglish-
dc.publisherCELL PRESS-
dc.titleDiscovery of Covalent CDK14 Inhibitors with Pan-TAIRE Family Specificity-
dc.typeArticle-
dc.identifier.doi10.1016/j.chembiol.2019.02.015-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCELL CHEMICAL BIOLOGY, v.26, no.6, pp.804 - +-
dc.citation.titleCELL CHEMICAL BIOLOGY-
dc.citation.volume26-
dc.citation.number6-
dc.citation.startPage804-
dc.citation.endPage+-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000472159700004-
dc.identifier.scopusid2-s2.0-85066461252-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.type.docTypeArticle-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusTARGET-
dc.subject.keywordPlusPFTK1-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusINVASION-
dc.subject.keywordPlusKINASES-
dc.subject.keywordPlusPOTENT-
dc.subject.keywordAuthorCDK14-
dc.subject.keywordAuthorcell cycle-
dc.subject.keywordAuthorcovalent inhibitor-
dc.subject.keywordAuthordruggable genome-
dc.subject.keywordAuthormitosis-
dc.subject.keywordAuthorTAIRE kinase-
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