Mechanism of allosteric signal integration in Src tyrosine kinase
Mechanism of allosteric signal integration in Src tyrosine kinase
批准号:
8594641
负责人:
Zachariah Hussein Foda
金额:
$3.12万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-07-01 至 2016-06-30
关键词:
Active SitesAffinityAllosteric SiteAmino AcidsAnimal ModelApoptosisBindingBinding SitesBiochemicalBiological AssayCatalytic DomainCell CycleCell DeathCell SurvivalCell physiologyCellsCellular AssayChronicClinicalComputer SimulationCyclic AMP-Dependent Protein KinasesCyclinsDataDevelopmentDiabetes MellitusDiseaseDistantDockingDrug TargetingDrug resistanceEnzymesFamilyFutureGastrointestinal Stromal TumorsGoalsGrowthHumanImatinibIndividualLaboratoriesLengthLigand BindingLigandsLinkLobeLyticMalignant NeoplasmsMolecularMutationMyelogenousNeoplasm MetastasisPDGFRB genePathogenesisPathway interactionsPatientsPhosphorylationPhosphotransferasesPhysiologicalPost-Translational Protein ProcessingPrevalenceProcessPropertyProtein KinaseProtein Tyrosine KinaseProteinsProto-OncogenesRegulationResistanceRouteSignal TransductionSiteSpecificityTherapeuticTherapeutic InterventionTissuesTranslatingWorkangiogenesisbasebiological adaptation to stresscell motilityclinically relevantinhibitor/antagonistkinase inhibitormembermolecular dynamicsnovelnovel therapeuticspreventpublic health relevanceresearch studysimulationsmall moleculesmall molecule librariessrc-Family Kinasestherapeutic targettumor progression
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Protein kinases, as key cellular pathway regulators, are frequently linked to disease and provide opportunities for therapeutic intervention. Due to their prevalence and importance, strict regulation of kinase activity is necessary to control essential cellular processes including the cell cycle, proliferation, differentiation, motility, an cell death or survival. Small molecule kinase inhibitors selected for their ability to target the kinase
ATP-binding pocket have achieved clinical utility. However, the high sequence and structural conservation of the pocket found in the more than 500 human protein kinases has created a challenge to developing inhibitors specific for individual kinases. Many limitations in using these
small molecule inhibitors derive from their cross-inhibition of other kinases unconnected to the targeted disease process. Part of the mechanism through which protein kinases achieve precise regulation, though, involves integration of many inter- and intramolecular signals via sites that are considerably less well conserved in sequence and function. These non-conserved mechanisms of regulation therefore provide the opportunity for more precise therapeutic targeting, for example, through the development of allosteric inhibitors based on high-affinity and high-specificity ligands. However, it is challenging to identify such allosteric sites in detai. Recently, my sponsor's laboratory identified a previously unknown allosteric network of amino acids that spans the length of the kinase and may thus facilitate integration of allosteric signals
into the regulation of protein kinase catalytic domain activity. I propose to experimentally probe the allosteric network and identify ligands that stabilize a predicted allosteric pocket. The findings from this work will deepen our understanding of the fundamental regulatory mechanisms for this important class of drug targets and potentially open the way to the development of more specific therapeutics.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Mechanism of allosteric signal integration in Src tyrosine kinase
-
批准号:8867868
-
项目类别:
-
资助金额:$4.64万
-
财政年份:2013
-
负责人:Zachariah Hussein Foda
-
依托单位:
Mechanism of allosteric signal integration in Src tyrosine kinase
-
批准号:8793682
-
项目类别:
-
资助金额:$3.16万
-
财政年份:2013
-
负责人:Zachariah Hussein Foda
-
依托单位:
海外基金