Suppr超能文献

G蛋白偶联受体中对配体识别重要的残基的位置和性质。

Location and nature of the residues important for ligand recognition in G-protein coupled receptors.

作者信息

Bywater Robert P

机构信息

Adelard Institute, London, UK and Division of Molecular Neurobiology, Wallenberg Neuroscience Center, Lund University, Lund, Sweden.

出版信息

J Mol Recognit. 2005 Jan-Feb;18(1):60-72. doi: 10.1002/jmr.685.

Abstract

The overall structure of the biogenic amine subclass of the G-protein-coupled receptors, and of their ligand binding sites, is discussed with the aim of highlighting the major structural features of these receptors that are responsible for ligand recognition. A comparison is made between biogenic amine receptors, peptide receptors of the rhodopsin class, and the secretin receptors which all have peptide ligands. The question of where the peptide ligands bind, whether at extracellular sites or within the transmembrane helix bundle, is discussed. The suitability of the rhodopsin crystal structure as a template for construction of homology models is discussed and it is concluded that there are many reasons why a caution should be issued against using it uncritically.

摘要

讨论了G蛋白偶联受体生物胺亚类及其配体结合位点的整体结构,目的是突出这些受体负责配体识别的主要结构特征。对生物胺受体、视紫红质类肽受体和均具有肽配体的促胰液素受体进行了比较。讨论了肽配体的结合位置问题,即其是结合在细胞外位点还是跨膜螺旋束内。讨论了视紫红质晶体结构作为构建同源模型模板的适用性,并得出结论,有许多理由应谨慎使用它,而不应不加批判地使用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验