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新型普列克底物蛋白同源(PH)结构域的鉴定为PH结构域的功能提供了一种假设。

Identification of novel pleckstrin homology (PH) domains provides a hypothesis for PH domain function.

作者信息

Shaw G

机构信息

Department of Neuroscience, JHM Health Center, Gainesville, Florida 32610.

出版信息

Biochem Biophys Res Commun. 1993 Sep 15;195(2):1145-51. doi: 10.1006/bbrc.1993.2164.

Abstract

Pleckstrin homology (PH) domains are difficult to find in protein sequence databases with widely used computer programs. A simple program developed to overcome this difficulty identified three proteins containing previously unrecognized PH domains; the beta-adrenergic receptor kinase (beta-ARK), the tecA protein kinase and the insulin receptor substrate protein IRS-1. The region of beta-ARK containing the novel PH domain coincides with that previously shown to bind the beta gamma subunits of trimeric G-proteins, suggesting a general hypothesis for PH domain function. PH domains were then found at the N-termini of the tecA homologues Btk and itk. In line with the hypothesis a point mutation in the PH domain of Btk is associated with defects in signal transduction.

摘要

普列克底物蛋白同源(PH)结构域很难通过广泛使用的计算机程序在蛋白质序列数据库中找到。为克服这一困难而开发的一个简单程序鉴定出了三种含有此前未被识别的PH结构域的蛋白质;β-肾上腺素能受体激酶(β-ARK)、tecA蛋白激酶和胰岛素受体底物蛋白IRS-1。β-ARK中含有新PH结构域的区域与先前显示能结合三聚体G蛋白βγ亚基的区域重合,这提示了一个关于PH结构域功能的普遍假说。随后在tecA同源物Btk和itk的N端发现了PH结构域。与该假说一致,Btk的PH结构域中的一个点突变与信号转导缺陷有关。

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