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Cdc42Hs与Rho鸟苷酸解离抑制蛋白之间的相互作用是通过Rho插入区域介导的。

Interaction between Cdc42Hs and RhoGDI is mediated through the Rho insert region.

作者信息

Wu W J, Leonard D A, A-Cerione R, Manor D

机构信息

Department of Pharmacology, Veterinary Medical Center, Cornell University, Ithaca, New York 14853, USA.

出版信息

J Biol Chem. 1997 Oct 17;272(42):26153-8. doi: 10.1074/jbc.272.42.26153.

Abstract

Members of the Rho subfamily of GTP-binding proteins contain a region of amino acid sequence (residues 122-134) that is absent from other Ras-like proteins and is termed the Rho insert region. To address the functional role of this domain, we have constructed a Cdc42Hs/Ras chimera in which loop 8 from Ha-Ras was substituted for the region in Cdc42Hs that contains the 13-amino acid insert region. Our data indicate that the insert region of Cdc42Hs is not essential for its interactions with various target/effector molecules or for interactions with the guanine nucleotide exchange factor, Dbl, or the Cdc42 GTPase-activating protein (GAP). However, the regulation of GDP dissociation and GTP hydrolysis on Cdc42Hs by the Rho GDP-dissociation inhibitor (GDI) is extremely sensitive to changes in the insert region, such that a Cdc42Hs/Ha-Ras chimera that lacks this insert is no longer susceptible to a GDI-induced inhibition of GDP dissociation and GTP hydrolysis. The insensitivity to GDI activity is not due to the inability of the GDI molecule to bind to the Cdc42Hs/Ha-Ras chimera, and in fact, the GDI is fully capable of stimulating the release of this chimera from membranes.

摘要

GTP结合蛋白Rho亚家族的成员含有一段氨基酸序列区域(第122 - 134位氨基酸残基),该区域在其他类Ras蛋白中不存在,被称为Rho插入区域。为了研究该结构域的功能作用,我们构建了一种Cdc42Hs/Ras嵌合体,其中将Ha - Ras的环8替换为Cdc42Hs中包含13个氨基酸插入区域的部分。我们的数据表明,Cdc42Hs的插入区域对于其与各种靶标/效应分子的相互作用、与鸟嘌呤核苷酸交换因子Dbl或Cdc42 GTP酶激活蛋白(GAP)的相互作用并非必不可少。然而,Rho GDP解离抑制剂(GDI)对Cdc42Hs上GDP解离和GTP水解的调节对插入区域的变化极为敏感,以至于缺乏该插入区域的Cdc42Hs/Ha - Ras嵌合体不再易受GDI诱导的GDP解离和GTP水解抑制的影响。对GDI活性不敏感并非由于GDI分子无法与Cdc42Hs/Ha - Ras嵌合体结合,事实上,GDI完全能够刺激该嵌合体从膜上释放。

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