COBRE: U KS: P1: ID OF HSP90 COCHAPERONES, IMMUNOPHILINS & PROTEINS

COBRE：UK KS：P1：HSP90 辅助伴侣、免疫亲和素的 ID

• 批准号: 7381953
• 负责人: Brian S J Blagg
• 金额: $ 2.72万
• 依托单位: UNIVERSITY OF KANSAS LAWRENCE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-01 至 2007-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7381953
• 关键词: COBRE; KS; P1; ID; HSP90

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. Hsp90 molecular chaperones are responsible for the conformational maturation of linear peptides into active three-dimensional enzymes and receptors. Examples of proteins dependent on the Hsp90 protein folding machinery include steroid hormone receptors, Src kinase, Her-2 kinase, Raf, p185, mutant p53, telomerase, PKR, telomerase, nitric oxide synthase, CDK-4 and CDK-6 to name a few. As Hsp90 continues to evolve into a popular target for the treatment of cancer more information is required to validate its role in the maturation of key regulatory proteins. For example, it is not known how many client proteins require Hsp90 for folding, or which of the four known forms of Hsp90 (a, b, GRP94, or TRP), immunophilin (FKBP51, FKBP52, or Cyp40), or cochaperone participate in the folding of various individual client proteins.

本子项目是利用由NIH/NCRR资助的中心赠款提供的资源的众多研究子项目之一。子项目和研究者（PI）可能已经从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。列出的机构是中心的，不一定是研究者的机构。Hsp90分子伴侣负责线性肽的构象成熟为活跃的三维酶和受体。依赖于Hsp90蛋白折叠机制的蛋白质包括类固醇激素受体、Src激酶、Her-2激酶、Raf、p185、突变型p53、端粒酶、PKR、端粒酶、一氧化氮合酶、CDK-4和CDK-6等等。随着Hsp90不断发展成为癌症治疗的热门靶点，需要更多的信息来验证其在关键调节蛋白成熟中的作用。例如，目前尚不清楚有多少客户蛋白需要Hsp90才能折叠，也不知道四种已知形式的Hsp90 （a、b、GRP94或TRP）、亲免疫蛋白（FKBP51、FKBP52或Cyp40）或cochaperone中的哪一种参与各种客户蛋白的折叠。