SOLUTION STRUCTURE OF SERINE-RICH DOMAIN FROM CRK-ASSOCIATED SUBSTRATE
SOLUTION STRUCTURE OF SERINE-RICH DOMAIN FROM CRK-ASSOCIATED SUBSTRATE
批准号:
7722363
负责人:
KATHRYN R. ELY
金额:
$0.32万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-05-01 至 2009-04-30
关键词:
Binding SitesCell AdhesionComputer Retrieval of Information on Scientific Projects DatabaseDockingFocal AdhesionsFundingGrantInstitutionOncogenicPhysiologicalPlayPositioning AttributeProteinsRegulationReportingResearchResearch PersonnelResourcesRoleSerineSignal TransductionSolutionsSourceStructureUnited States National Institutes of Healthmigrationprotein protein interaction
中文摘要
这个子项目是许多研究子项目中的一个
由NIH/NCRR资助的中心赠款提供的资源。子项目和
研究者(PI)可能从另一个NIH来源获得了主要资金,
因此可以在其他CRISP条目中表示。所列机构为
研究中心,而研究中心不一定是研究者所在的机构。
130 cas(Crk相关底物)是一种对接蛋白,参与粘着斑的组装和伴随的细胞信号传导。它在细胞粘附、迁移、存活和增殖的生理调节以及致癌转化中起作用。该分子由多个蛋白质-蛋白质相互作用基序组成,包括位于Crk和Src结合位点之间的富含丝氨酸的区域。本研究报告的第一个结构的功能域的Cas。
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
130cas (Crk-associated substrate) is a docking protein that is involved in assembly of focal adhesions and concomitant cellular signaling. It plays a role in physiological regulation of cell adhesion, migration, survival, and proliferation, as well as in oncogenic transformation. The molecule consists of multiple protein-protein interaction motifs, including a serine-rich region that is positioned between Crk and Src-binding sites. This study reports the first structure of a functional domain of Cas.
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资助金额:$0.02万
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财政年份:2009
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负责人:KATHRYN R. ELY
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依托单位:
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资助金额:--
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