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7D68

Cryo-EM structure of the human glucagon-like peptide-2 receptor-Gs protein complex

7D68 の概要
エントリーDOI10.2210/pdb7d68/pdb
EMDBエントリー30590
分子名称Guanine nucleotide-binding protein G(s) subunit alpha isoforms short, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (7 entities in total)
機能のキーワードglucagon-like peptide-2 receptor, drug target, class b gpcr, biosynthetic protein
由来する生物種Bos taurus
詳細
タンパク質・核酸の鎖数6
化学式量合計185001.18
構造登録者
主引用文献Sun, W.,Chen, L.N.,Zhou, Q.,Zhao, L.H.,Yang, D.,Zhang, H.,Cong, Z.,Shen, D.D.,Zhao, F.,Zhou, F.,Cai, X.,Chen, Y.,Zhou, Y.,Gadgaard, S.,van der Velden, W.J.C.,Zhao, S.,Jiang, Y.,Rosenkilde, M.M.,Xu, H.E.,Zhang, Y.,Wang, M.W.
A unique hormonal recognition feature of the human glucagon-like peptide-2 receptor.
Cell Res., 30:1098-1108, 2020
Cited by
PubMed Abstract: Glucagon-like peptides (GLP-1 and GLP-2) are two proglucagon-derived intestinal hormones that mediate distinct physiological functions through two related receptors (GLP-1R and GLP-2R) which are important drug targets for metabolic disorders and Crohn's disease, respectively. Despite great progress in GLP-1R structure determination, our understanding on the differences of peptide binding and signal transduction between these two receptors remains elusive. Here we report the electron microscopy structure of the human GLP-2R in complex with GLP-2 and a G heterotrimer. To accommodate GLP-2 rather than GLP-1, GLP-2R fine-tunes the conformations of the extracellular parts of transmembrane helices (TMs) 1, 5, 7 and extracellular loop 1 (ECL1). In contrast to GLP-1, the N-terminal histidine of GLP-2 penetrates into the receptor core with a unique orientation. The middle region of GLP-2 engages with TM1 and TM7 more extensively than with ECL2, and the GLP-2 C-terminus closely attaches to ECL1, which is the most protruded among 9 class B G protein-coupled receptors (GPCRs). Functional studies revealed that the above three segments of GLP-2 are essential for GLP-2 recognition and receptor activation, especially the middle region. These results provide new insights into the molecular basis of ligand specificity in class B GPCRs and may facilitate the development of more specific therapeutics.
PubMed: 33239759
DOI: 10.1038/s41422-020-00442-0
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3 Å)
構造検証レポート
Validation report summary of 7d68
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-06に公開中

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