STRUCTURE OF PUMILIO NOVEL RNA BINDING DOMAIN
PUMILIO 新型 RNA 结合域的结构
基本信息
- 批准号:6491092
- 负责人:
- 金额:$ 14.27万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-08-15 至 2002-08-14
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The 90 kilodalton heat shock protein (hsp90) is a highly abundant,
highly conserved protein in both prokaryotes and eukaryotes. In
certain mammalian cell types, the isozymes of hsp90 can comprise as
much as 2% of total cellular protein under nonstess conditions. At
elevated temperatures, both the transcription and translation of hsp90
increase dramatically suggesting that it plays a major role in the
heat shock response. In fact, like several other heat shock proteins,
hsp90 has been shown to chaperone protein folding in vitro; that is,
addition of hsp90 prevents nonproductive aggregation of protein
molecules during refolding reactions. In addition, hsp90 has been
shown to modulate the activities of a variety of signal transduction
molecules including steroid hormone receptors (such as the
glucocorticoid and estrogen receptors) as well as nonreceptor tyrosine
kinases (such as v-src). Finally, hsp90 has been found to be
associated with molecules such as calmodulin, actin, tubulin and
serine/threonine kinases such as casein kinase II and eIF-2a kinase.
Overall, the studies of the interactions between hsp90 and these
various signal transduction molecules hint that the mechanism through
which hsp90 modulates the activities of these molecules and its role
as a chaperone may overlap; these signaling molecules may have
co-opted the ability of hsp90 to stabilize folding intermediates into
regulating conformational changes necessary for signaling. Therefore,
to begin probing these mechanisms, we have initiated a structural
study of htpG (high temperature production protein G), the Escherichia
coli member of the hsp90 family.
90千道尔顿热休克蛋白(hsp90)是一种非常丰富的,
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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ANEEL K. AGGARWAL其他文献
ANEEL K. AGGARWAL的其他文献
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{{ truncateString('ANEEL K. AGGARWAL', 18)}}的其他基金
Development of MS2045 for inhibition of Zika methyltransferase
开发用于抑制寨卡病毒甲基转移酶的 MS2045
- 批准号:
10645958 - 财政年份:2023
- 资助金额:
$ 14.27万 - 项目类别:
Structure and Specificity of Restriction-Modification (R-M) Systems
限制性修饰(R-M)系统的结构和特异性
- 批准号:
10241952 - 财政年份:2019
- 资助金额:
$ 14.27万 - 项目类别:
Structure and Specificity of Restriction-Modification (R-M) Systems
限制性修饰(R-M)系统的结构和特异性
- 批准号:
10470890 - 财政年份:2019
- 资助金额:
$ 14.27万 - 项目类别:
Structure and Specificity of Restriction-Modification (R-M) Systems
限制性修饰(R-M)系统的结构和特异性
- 批准号:
10686907 - 财政年份:2019
- 资助金额:
$ 14.27万 - 项目类别:
Structure and Specificity of Restriction-Modification (R-M) Systems
限制性修饰(R-M)系统的结构和特异性
- 批准号:
10797690 - 财政年份:2019
- 资助金额:
$ 14.27万 - 项目类别:
Structure and Specificity of Restriction-Modification (R-M) Systems
限制性修饰(R-M)系统的结构和特异性
- 批准号:
10727038 - 财政年份:2019
- 资助金额:
$ 14.27万 - 项目类别:
Structure and Specificity of Restriction-Modification (R-M) Systems
限制性修饰(R-M)系统的结构和特异性
- 批准号:
10599570 - 财政年份:2019
- 资助金额:
$ 14.27万 - 项目类别:
Structure and mechanism of multisubunit complexes of DNA polymerase zeta
DNA聚合酶zeta多亚基复合物的结构和机制
- 批准号:
10249252 - 财政年份:2018
- 资助金额:
$ 14.27万 - 项目类别:
Structure and mechanism of multisubunit complexes of DNA polymerase zeta
DNA聚合酶zeta多亚基复合物的结构和机制
- 批准号:
10018049 - 财政年份:2018
- 资助金额:
$ 14.27万 - 项目类别:
Genome-wide detection of UV DNA damage by single molecule real time sequencing
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- 批准号:
8807049 - 财政年份:2014
- 资助金额:
$ 14.27万 - 项目类别:
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