5YLU
Crystal structure of the gastric proton pump complexed with vonoprazan
5YLU の概要
エントリーDOI | 10.2210/pdb5ylu/pdb |
分子名称 | Potassium-transporting ATPase alpha chain 1, Potassium-transporting ATPase subunit beta, 1-[5-(2-fluorophenyl)-1-pyridin-3-ylsulfonyl-pyrrol-3-yl]-~{N}-methyl-methanamine, ... (8 entities in total) |
機能のキーワード | gastric, proton pump, h+, k+-atpase, p-type atpase, transporter, membrane protein |
由来する生物種 | Sus scrofa (Pig) 詳細 |
細胞内の位置 | Cell membrane ; Multi-pass membrane protein : P19156 Cell membrane ; Single-pass type II membrane protein : P18434 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 151124.46 |
構造登録者 | |
主引用文献 | Abe, K.,Irie, K.,Nakanishi, H.,Suzuki, H.,Fujiyoshi, Y. Crystal structures of the gastric proton pump Nature, 556:214-218, 2018 Cited by PubMed Abstract: The gastric proton pump-the H, K-ATPase-is a P-type ATPase responsible for acidifying the gastric juice down to pH 1. This corresponds to a million-fold proton gradient across the membrane of the parietal cell, the steepest known cation gradient of any mammalian tissue. The H, K-ATPase is an important target for drugs that treat gastric acid-related diseases. Here we present crystal structures of the H, K-ATPase in complex with two blockers, vonoprazan and SCH28080, in the luminal-open state, at 2.8 Å resolution. The drugs have partially overlapping but clearly distinct binding modes in the middle of a conduit running from the gastric lumen to the cation-binding site. The crystal structures suggest that the tight configuration at the cation-binding site lowers the pK value of Glu820 sufficiently to enable the release of a proton even into the pH 1 environment of the stomach. PubMed: 29618813DOI: 10.1038/s41586-018-0003-8 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.79988962319 Å) |
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