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序列分析揭示了G蛋白偶联受体如何将信号传导至G蛋白。

Sequence analysis reveals how G protein-coupled receptors transduce the signal to the G protein.

作者信息

Oliveira Laerte, Paiva Paulo B, Paiva Antonio C M, Vriend Gerrit

机构信息

Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.

出版信息

Proteins. 2003 Sep 1;52(4):553-60. doi: 10.1002/prot.10489.

Abstract

Sequence entropy-variability plots based on alignments of very large numbers of sequences-can indicate the location in proteins of the main active site and modulator sites. In the previous article in this issue, we applied this observation to a series of well-studied proteins and concluded that it was possible to detect most of the residues with a known functional role. Here, we apply the method to rhodopsin-like G protein-coupled receptors. Our conclusion is that G protein binding is the main evolutionary constraint on these receptors, and that other ligands, such as agonists, act as modulators. The activation of the receptors can be described as a simple, two-step process, and the residues involved in signal transduction can be identified.

摘要

基于大量序列比对的序列熵变图——可以指示蛋白质中主要活性位点和调节剂位点的位置。在本期的上一篇文章中,我们将这一观察结果应用于一系列经过充分研究的蛋白质,并得出结论,即有可能检测到大多数具有已知功能作用的残基。在这里,我们将该方法应用于视紫红质样G蛋白偶联受体。我们的结论是,G蛋白结合是这些受体的主要进化限制因素,而其他配体,如激动剂,则作为调节剂起作用。受体的激活可以描述为一个简单的两步过程,并且可以识别参与信号转导的残基。

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