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

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

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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
通过单分子实时测序全基因组检测 UV DNA 损伤
  • 批准号:
    8807049
  • 财政年份:
    2014
  • 资助金额:
    $ 14.27万
  • 项目类别:

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