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8JSR

Cryo-EM structure of the anamorelin-bound ghrelin receptor and Gq complex

Summary for 8JSR
Entry DOI10.2210/pdb8jsr/pdb
EMDB information36627
DescriptorGrowth hormone secretagogue receptor type 1, Engineered G-alpha-q, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (7 entities in total)
Functional Keywordsgpcr, sbdd, cachexia, membrane protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight193042.94
Authors
Im, D.,Shiimura, Y.,Asada, H.,Iwata, S. (deposition date: 2023-06-20, release date: 2025-01-22, Last modification date: 2025-12-10)
Primary citationShiimura, Y.,Im, D.,Tany, R.,Asada, H.,Kise, R.,Kurumiya, E.,Wakasugi-Masuho, H.,Yasuda, S.,Matsui, K.,Kishikawa, J.I.,Kato, T.,Murata, T.,Kojima, M.,Iwata, S.,Masuho, I.
The structure and function of the ghrelin receptor coding for drug actions.
Nat.Struct.Mol.Biol., 32:531-542, 2025
Cited by
PubMed Abstract: Drugs targeting the ghrelin receptor hold therapeutic potential in anorexia, obesity and diabetes. However, developing effective drugs is challenging. To tackle this common issue across a broad drug target, this study aims to understand how anamorelin, the only approved drug targeting the ghrelin receptor, operates compared to other synthetic drugs. Our research elucidated the receptor's structure with anamorelin and miniG, unveiling anamorelin's superagonistic activity. We demonstrated that ligands with distinct chemical structures uniquely bind to the receptor, resulting in diverse conformations and biasing signal transduction. Moreover, our study showcased the utility of structural information in effectively identifying natural genetic variations altering drug action and causing severe functional deficiencies, offering a basis for selecting the right medication on the basis of the individual's genomic sequence. Thus, by building on structural analysis, this study enhances the foundational framework for selecting therapeutic agents targeting the ghrelin receptor, by effectively leveraging signaling bias and genetic variations.
PubMed: 39833471
DOI: 10.1038/s41594-024-01481-6
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.9 Å)
Structure validation

248335

건을2026-01-28부터공개중

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