4.8 Review

The structure and function of G-protein-coupled receptors

期刊

NATURE
卷 459, 期 7245, 页码 356-363

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nature08144

关键词

-

资金

  1. US National Institute of General Medical Sciences [F32 GM082028, RO1GM083118]
  2. Lundbeck Foundation
  3. National Institute of Neurological Disorders and Stroke [RO1-NS28471]
  4. Mather Charitable Foundation
  5. Lundbeck Foundation [R19-2008-2113] Funding Source: researchfish

向作者/读者索取更多资源

G-protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants, and so have great potential as therapeutic targets for a broad spectrum of diseases. They are also fascinating molecules from the perspective of membrane-protein structure and biology. Great progress has been made over the past three decades in understanding diverse GPCRs, from pharmacology to functional characterization in vivo. Recent high-resolution structural studies have provided insights into the molecular mechanisms of GPCR activation and constitutive activity.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据