8HJ1
GPR21(wt) and Gs complex
8HJ1 の概要
エントリーDOI | 10.2210/pdb8hj1/pdb |
EMDBエントリー | 33483 |
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, ... (5 entities in total) |
機能のキーワード | gpcr, orphan receptor, structural protein |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 5 |
化学式量合計 | 133550.97 |
構造登録者 | |
主引用文献 | Lin, X.,Chen, B.,Wu, Y.,Han, Y.,Qi, A.,Wang, J.,Yang, Z.,Wei, X.,Zhao, T.,Wu, L.,Xie, X.,Sun, J.,Zheng, J.,Zhao, S.,Xu, F. Cryo-EM structures of orphan GPR21 signaling complexes. Nat Commun, 14:216-216, 2023 Cited by PubMed Abstract: GPR21 is a class-A orphan G protein-coupled receptor (GPCR) and a potential therapeutic target for type 2 diabetes and other metabolic disorders. This receptor shows high basal activity in coupling to multiple G proteins in the absence of any known endogenous agonist or synthetic ligand. Here, we present the structures of ligand-free human GPR21 bound to heterotrimeric miniGs and miniG15 proteins, respectively. We identified an agonist-like motif in extracellular loop 2 (ECL2) that occupies the orthosteric pocket and promotes receptor activation. A side pocket that may be employed as a new ligand binding site was also uncovered. Remarkably, G protein binding is accommodated by a flexible cytoplasmic portion of transmembrane helix 6 (TM6) which adopts little or undetectable outward movement. These findings will enable the design of modulators for GPR21 for understanding its signal transduction and exploring opportunity for deorphanization. PubMed: 36639690DOI: 10.1038/s41467-023-35882-w 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.27 Å) |
構造検証レポート
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