Loading
PDBj
メニューPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

8HSC

Gi bound Orphan GPR20 complex with Fab046 in ligand-free state

8HSC の概要
エントリーDOI10.2210/pdb8hsc/pdb
EMDBエントリー34993
分子名称light chain of Fab046, Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (7 entities in total)
機能のキーワードorphan receptor, gpcr, gpr20, gi-coupled, gpr20-gi-fab046, membrane protein
由来する生物種Rattus
詳細
タンパク質・核酸の鎖数7
化学式量合計224707.03
構造登録者
Lin, X.,Jiang, S.,Xu, F. (登録日: 2022-12-19, 公開日: 2023-03-08, 最終更新日: 2024-10-23)
主引用文献Lin, X.,Jiang, S.,Wu, Y.,Wei, X.,Han, G.W.,Wu, L.,Liu, J.,Chen, B.,Zhang, Z.,Zhao, S.,Cherezov, V.,Xu, F.
The activation mechanism and antibody binding mode for orphan GPR20.
Cell Discov, 9:23-23, 2023
Cited by
PubMed Abstract: GPR20 is a class-A orphan G protein-coupled receptor (GPCR) and a potential therapeutic target for gastrointestinal stromal tumors (GIST) owing to its differentially high expression. An antibody-drug conjugate (ADC) containing a GPR20-binding antibody (Ab046) was recently developed in clinical trials for GIST treatment. GPR20 constitutively activates Gi proteins in the absence of any known ligand, but it remains obscure how this high basal activity is achieved. Here we report three cryo-EM structures of human GPR20 complexes including Gi-coupled GPR20 in the absence or presence of the Fab fragment of Ab046 and Gi-free GPR20. Remarkably, the structures demonstrate a uniquely folded N-terminal helix capping onto the transmembrane domain and our mutagenesis study suggests a key role of this cap region in stimulating the basal activity of GPR20. We also uncover the molecular interactions between GPR20 and Ab046, which may enable the design of tool antibodies with enhanced affinity or new functionality for GPR20. Furthermore, we report the orthosteric pocket occupied by an unassigned density which might be essential for exploring opportunities for deorphanization.
PubMed: 36849514
DOI: 10.1038/s41421-023-00520-8
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.22 Å)
構造検証レポート
Validation report summary of 8hsc
検証レポート(詳細版)ダウンロードをダウンロード

227111

件を2024-11-06に公開中

PDB statisticsPDBj update infoContact PDBjnumon