Structural Insight into the MC4R Conformational Changes via Different Agonist-Mediated Receptor Signaling
Author:
Affiliation:
1. Department of Surgery, State University of New York at Buffalo, Buffalo, New York 14203, United States
2. Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama 35233, United States
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi500856x
Reference29 articles.
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1. MC4R biased signalling and the conformational basis of biological function selections;Journal of Cellular and Molecular Medicine;2022-07-11
2. Insights into the Allosteric Mechanism of Setmelanotide (RM-493) as a Potent and First-in-Class Melanocortin-4 Receptor (MC4R) Agonist To Treat Rare Genetic Disorders of Obesity through an in Silico Approach;ACS Chemical Neuroscience;2018-07-26
3. Structural Insights into Selective Ligand–Receptor Interactions Leading to Receptor Inactivation Utilizing Selective Melanocortin 3 Receptor Antagonists;Biochemistry;2017-08-01
4. Adrenocorticotropic Hormone (ACTH) Responses Require Actions of the Melanocortin-2 Receptor Accessory Protein on the Extracellular Surface of the Plasma Membrane;Journal of Biological Chemistry;2015-11
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