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5YFI

Crystal structure of the anti-human prostaglandin E receptor EP4 antibody Fab fragment

5YFI の概要
エントリーDOI10.2210/pdb5yfi/pdb
分子名称Light chain of Fab fragment, Heavy chain of Fab fragment, ZINC ION, ... (4 entities in total)
機能のキーワードantibody, immune system
由来する生物種Mus musculus
詳細
タンパク質・核酸の鎖数2
化学式量合計54581.40
構造登録者
Toyoda, Y.,Morimoto, K.,Suno, R.,Horita, S.,Iwata, S.,Kobayashi, T. (登録日: 2017-09-21, 公開日: 2018-12-05, 最終更新日: 2024-10-16)
主引用文献Toyoda, Y.,Morimoto, K.,Suno, R.,Horita, S.,Yamashita, K.,Hirata, K.,Sekiguchi, Y.,Yasuda, S.,Shiroishi, M.,Shimizu, T.,Urushibata, Y.,Kajiwara, Y.,Inazumi, T.,Hotta, Y.,Asada, H.,Nakane, T.,Shiimura, Y.,Nakagita, T.,Tsuge, K.,Yoshida, S.,Kuribara, T.,Hosoya, T.,Sugimoto, Y.,Nomura, N.,Sato, M.,Hirokawa, T.,Kinoshita, M.,Murata, T.,Takayama, K.,Yamamoto, M.,Narumiya, S.,Iwata, S.,Kobayashi, T.
Ligand binding to human prostaglandin E receptor EP4at the lipid-bilayer interface.
Nat. Chem. Biol., 15:18-26, 2019
Cited by
PubMed Abstract: Prostaglandin E receptor EP4, a G-protein-coupled receptor, is involved in disorders such as cancer and autoimmune disease. Here, we report the crystal structure of human EP4 in complex with its antagonist ONO-AE3-208 and an inhibitory antibody at 3.2 Å resolution. The structure reveals that the extracellular surface is occluded by the extracellular loops and that the antagonist lies at the interface with the lipid bilayer, proximal to the highly conserved Arg316 residue in the seventh transmembrane domain. Functional and docking studies demonstrate that the natural agonist PGE binds in a similar manner. This structural information also provides insight into the ligand entry pathway from the membrane bilayer to the EP4 binding pocket. Furthermore, the structure reveals that the antibody allosterically affects the ligand binding of EP4. These results should facilitate the design of new therapeutic drugs targeting both orthosteric and allosteric sites in this receptor family.
PubMed: 30510193
DOI: 10.1038/s41589-018-0131-3
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.848 Å)
構造検証レポート
Validation report summary of 5yfi
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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