7DDF

Crystal structures of Na+,K+-ATPase in complex with beryllium fluoride

「6KPU」から置き換えられました

7DDF の概要

• エントリーDOI: 10.2210/pdb7ddf/pdb
• 関連するPDBエントリー: 6kpv 6kpw 6kpx 6kpy 6kpz 6kq0 7d91 7d92 7d93 7d94
• 分子名称: Sodium/potassium-transporting ATPase subunit alpha-1, Sodium/potassium-transporting ATPase subunit beta-1, FXYD domain-containing ion transport regulator, ... (10 entities in total)
• 機能のキーワード: na+, k+-atpase, membrane protein, ion transport, cardiotonic steroids
• 由来する生物種: Sus scrofa (Pig); 詳細
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 320275.07

構造登録者

Ogawa, H.,Cornelius, F.,Kanai, R.,Motoyama, K.,Vilsen, B.,Toyoshima, C. (登録日: 2020-10-29, 公開日: 2021-01-27, 最終更新日: 2025-03-12)

主引用文献

Kanai, R.,Cornelius, F.,Ogawa, H.,Motoyama, K.,Vilsen, B.,Toyoshima, C.
Binding of cardiotonic steroids to Na + ,K + -ATPase in the E2P state.
Proc.Natl.Acad.Sci.USA, 118:-, 2021

PubMed Abstract: The sodium pump (Na, K-ATPase, NKA) is vital for animal cells, as it actively maintains Na and K electrochemical gradients across the cell membrane. It is a target of cardiotonic steroids (CTSs) such as ouabain and digoxin. As CTSs are almost unique strong inhibitors specific to NKA, a wide range of derivatives has been developed for potential therapeutic use. Several crystal structures have been published for NKA-CTS complexes, but they fail to explain the largely different inhibitory properties of the various CTSs. For instance, although CTSs are thought to inhibit ATPase activity by binding to NKA in the E2P state, we do not know if large conformational changes accompany binding, as no crystal structure is available for the E2P state free of CTS. Here, we describe crystal structures of the BeF complex of NKA representing the E2P ground state and then eight crystal structures of seven CTSs, including rostafuroxin and istaroxime, two new members under clinical trials, in complex with NKA in the E2P state. The conformations of NKA are virtually identical in all complexes with and without CTSs, showing that CTSs bind to a preformed cavity in NKA. By comparing the inhibitory potency of the CTSs measured under four different conditions, we elucidate how different structural features of the CTSs result in different inhibitory properties. The crystal structures also explain K-antagonism and suggest a route to isoform specific CTSs.

PubMed: 33318128
DOI: 10.1073/pnas.2020438118

実験手法

X-RAY DIFFRACTION (4.62 Å)