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8WKY

Crystal structure of the Melanocortin-4 Receptor (MC4R) in complex with S25

8WKY の概要
エントリーDOI10.2210/pdb8wky/pdb
分子名称Melanocortin receptor 4, N-(2-aminoethyl)-5-(2-{[4-(morpholin-4-yl)pyridin-2-yl]amino}-1,3-thiazol-5-yl)pyridine-3-carboxamide, CALCIUM ION, ... (5 entities in total)
機能のキーワードca++ cofactor, gpcr, pgs fusion, membrane protein, lcp
由来する生物種Homo sapiens (human)
詳細
タンパク質・核酸の鎖数2
化学式量合計63026.48
構造登録者
主引用文献Gimenez, L.E.,Martin, C.,Yu, J.,Hollanders, C.,Hernandez, C.C.,Wu, Y.,Yao, D.,Han, G.W.,Dahir, N.S.,Wu, L.,Van der Poorten, O.,Lamouroux, A.,Mannes, M.,Zhao, S.,Tourwe, D.,Stevens, R.C.,Cone, R.D.,Ballet, S.
Novel Cocrystal Structures of Peptide Antagonists Bound to the Human Melanocortin Receptor 4 Unveil Unexplored Grounds for Structure-Based Drug Design.
J.Med.Chem., 67:2690-2711, 2024
Cited by
PubMed Abstract: Melanocortin 4 receptor (MC4-R) antagonists are actively sought for treating cancer cachexia. We determined the structures of complexes with and . These peptides differ from by substituting His with Pro and inserting Gly or Arg. The structures revealed two subpockets at the TM7-TM1-TM2 domains, separated by N285. Two peptide series based on the complexed peptides led to an antagonist activity and selectivity SAR study. Most ligands retained the potency, but several -derived peptides significantly enhanced MC4-R selectivity over MC1-R by 60- to 132-fold. We also investigated MC4-R coupling to the K channel, Kir7.1. Some peptides activated the channel, whereas others induced channel closure independently of G protein coupling. In cell culture studies, channel activation correlated with increased feeding, while a peptide with Kir7.1 inhibitory activity reduced eating. These results highlight the potential for targeting the MC4-R:Kir7.1 complex for treating positive and restrictive eating disorders.
PubMed: 38345933
DOI: 10.1021/acs.jmedchem.3c01822
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.9 Å)
構造検証レポート
Validation report summary of 8wky
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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