Structural and functional insights into the juxtamembranous amino-terminal tail and extracellular loop regions of class B GPCRs

Author:

Dong M1,Koole C2,Wootten D2,Sexton P M2,Miller L J1

Affiliation:

1. Department of Molecular Pharmacology and Experimental Therapeutics; Mayo Clinic; Scottsdale AZ USA

2. Drug Discovery Biology; Monash Institute of Pharmaceutical Sciences; Department of Pharmacology; Monash University; Parkville Vic. Australia

Publisher

Wiley

Subject

Pharmacology

Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Activation of Class B GPCR by Peptide Ligands: General Structural Aspects;GPCRs as Therapeutic Targets;2022-09-16

2. Discovery of HTL26119;Contemporary Accounts in Drug Discovery and Development;2022-03-07

3. Synthetic protease-activated class B GPCRs;Biochemical and Biophysical Research Communications;2020-09

4. Development of a Testing Funnel for Identification of Small-Molecule Modulators Targeting Secretin Receptors;SLAS DISCOVERY: Advancing the Science of Drug Discovery;2020-08-04

5. Full-length human GLP-1 receptor structure without orthosteric ligands;Nature Communications;2020-03-09

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