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dc.contributor.authorKim, Do-Hee-
dc.contributor.authorSim, Taebo-
dc.date.accessioned2024-01-20T18:04:07Z-
dc.date.available2024-01-20T18:04:07Z-
dc.date.created2021-09-05-
dc.date.issued2010-11-30-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/130903-
dc.description.abstractKinomics is an emerging and promising approach for deciphering kinomes. Chemical kinomics is a discipline of chemical genomics that is also referred to as "chemogenomics", which is derived from chemistry and biology. Chemical kinomics has become a powerful approach to decipher complicated phosphorylation-based cellular signaling networks with the aid of small molecules that modulate kinase functions. Moreover, chemical kinomics has played a pivotal role in the field of kinase drug discovery as it enables identification of new molecular targets of small molecule kinase modulators and/or exploitation of novel functions of known kinases and has also provided novel chemical entities as hit/lead compounds. In this short review, contemporary chemical kinomics technologies such as activity-based protein profiling, T7 kinase-tagged phages, kinobeads, three-hybrid systems, fluorescent-tagged kinase binding assays, and chemical genomic profiling are discussed along with a novel allosteric Bcr-Abl kinase inhibitor (GNF-2/GNF-5) as a successful application of chemical kinomics approaches. [BMB reports 2010; 43(11): 711-719]-
dc.languageEnglish-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.subjectPROTEIN-KINASES-
dc.subjectBCR-ABL-
dc.subjectPEPTIDE ARRAYS-
dc.subjectPHOSPHOINOSITIDE 3-KINASE-
dc.subjectALLOSTERIC INHIBITORS-
dc.subjectBACTERIOPHAGE-T7 DNA-
dc.subjectCLINICAL RESISTANCE-
dc.subjectSTRUCTURAL BASIS-
dc.subjectWORTMANNIN-
dc.subjectPROTEOMICS-
dc.titleChemical kinomics: a powerful strategy for target deconvolution-
dc.typeArticle-
dc.identifier.doi10.5483/BMBRep.2010.43.11.711-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBMB REPORTS, v.43, no.11, pp.711 - 719-
dc.citation.titleBMB REPORTS-
dc.citation.volume43-
dc.citation.number11-
dc.citation.startPage711-
dc.citation.endPage719-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001495453-
dc.identifier.wosid000284974500001-
dc.identifier.scopusid2-s2.0-78649790001-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.type.docTypeReview-
dc.subject.keywordPlusPROTEIN-KINASES-
dc.subject.keywordPlusBCR-ABL-
dc.subject.keywordPlusPEPTIDE ARRAYS-
dc.subject.keywordPlusPHOSPHOINOSITIDE 3-KINASE-
dc.subject.keywordPlusALLOSTERIC INHIBITORS-
dc.subject.keywordPlusBACTERIOPHAGE-T7 DNA-
dc.subject.keywordPlusCLINICAL RESISTANCE-
dc.subject.keywordPlusSTRUCTURAL BASIS-
dc.subject.keywordPlusWORTMANNIN-
dc.subject.keywordPlusPROTEOMICS-
dc.subject.keywordAuthorChemical kinomics-
dc.subject.keywordAuthorKinase inhibitor-
dc.subject.keywordAuthorProtein kinase-
dc.subject.keywordAuthorTarget identification-
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