G蛋白偶联受体
变构调节
计算生物学
资源(消歧)
受体
计算机科学
药物发现
结构生物学
生物
生物信息学
细胞生物学
生物化学
计算机网络
作者
Christian Munk,Eshita Mutt,Vignir Ísberg,Louise F. Nikolajsen,Janne M. Bibbe,Tilman Flock,Michael A. Hanson,Raymond C. Stevens,Xavier Deupí,David E. Gloriam
出处
期刊:Nature Methods
[Springer Nature]
日期:2019-01-21
卷期号:16 (2): 151-162
被引量:110
标识
DOI:10.1038/s41592-018-0302-x
摘要
G-protein-coupled receptors (GPCRs) transduce physiological and sensory stimuli into appropriate cellular responses and mediate the actions of one-third of drugs. GPCR structural studies have revealed the general bases of receptor activation, signaling, drug action and allosteric modulation, but so far cover only 13% of nonolfactory receptors. We broadly surveyed the receptor modifications/engineering and methods used to produce all available GPCR crystal and cryo-electron microscopy (cryo-EM) structures, and present an interactive resource integrated in GPCRdb ( http://www.gpcrdb.org ) to assist users in designing constructs and browsing appropriate experimental conditions for structure studies. An interactive online resource integrated in the GPCRdb hub presents tools to design GPCR constructs and determine appropriate experimental conditions for structural studies by crystallography and cryo-EM.
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