Structure, Function and Inhibition of Human O-GlcNAc Transferase
Structure, Function and Inhibition of Human O-GlcNAc Transferase
批准号:
9025947
负责人:
Suzanne Walker
金额:
$2.75万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-02-01 至 2016-03-31
关键词:
Active SitesAddressAttenuatedBindingBiochemicalBiologicalCell ExtractsCell divisionCell physiologyCellsCommunitiesComplexComplications of Diabetes MellitusCysteineDevelopmentDiphosphatesDiseaseElementsEnzymesFamilyFoundationsGluconeogenesisGlycopeptidesGoalsHandHealthHumanInhibitory Concentration 50LaboratoriesLeadLightLinkLysineMalignant NeoplasmsMediatingMethodsModificationMolecularNutrientO-GlcNAc transferasePathologyPathway interactionsPatternPeptidesPlayPost-Translational Protein ProcessingProcessProtein MicrochipsProtein Profiling MicroarraysProteinsProteomeQuinolonesResearchRoleStress Response SignalingStructureStructure-Activity RelationshipSulfonamidesWorkanalogbasecrosslinkdesignenzyme structureenzyme substrateglucose metabolismglycosylationimprovedinhibitor/antagonistinsulin signalinginterestmutantnovelprotein protein interactionresearch studysmall moleculesugartherapeutic targettool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): O-GlcNAc transferase (OGT) is an essential mammalian enzyme that catalyzes a unique post-translational modification, O-GlcNAcylation. O-GlcNAcylation has been shown to modulate insulin signaling, gluconeogenesis, and other pathways connected to glucose metabolism. Hyper-O-GlcNAcylation leads to widespread transcriptional changes and has been linked to diabetic complications, cancer, and other pathologies. Therefore, it has been suggested that OGT could be a therapeutic target. A better understanding of the structure and function of OGT is critical for dissecting its biological roles, and small molecule inhibitors are widely sought by the scientific community. The goals of this proposal are i) to supply the structural basis for rational experiments to dissect the biochemical and cellular functions of OGT, ii) to provide validated small molecule inhibitors for use as cellular probes of OGT function, and iii) to develop a proteome-wide substrate profiling approach to identify OGT features required for substrate selection.
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