Probing the Mechanism of Receptor Activity–Modifying Protein Modulation of GPCR Ligand Selectivity through Rational Design of Potent Adrenomedullin and Calcitonin Gene-Related Peptide Antagonists-Reference-Cited by-同舟云学术

Probing the Mechanism of Receptor Activity–Modifying Protein Modulation of GPCR Ligand Selectivity through Rational Design of Potent Adrenomedullin and Calcitonin Gene-Related Peptide Antagonists

Published:2018-01-23 Issue:4 Volume:93 Page:355-367
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Booe Jason M.,Warner Margaret L.,Roehrkasse Amanda M.,Hay Debbie L.,Pioszak Augen A.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference37 articles.

1. PHENIX: a comprehensive Python-based system for macromolecular structure solution

2. A Novel α-Calcitonin Gene-Related Peptide Analogue Protects Against End-Organ Damage in Experimental Hypertension, Cardiac Hypertrophy, and Heart Failure

3. Pharmacology of the human CGRP1 receptor in Cos 7 cells

4. Calcitonin and calcitonin receptor-like receptors: common themes with family B GPCRs?

5. Structural Basis for Receptor Activity-Modifying Protein-Dependent Selective Peptide Recognition by a G Protein-Coupled Receptor

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