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7ZGO

Cryo-EM structure of human NKCC1 (TM domain)

7ZGO の概要
エントリーDOI10.2210/pdb7zgo/pdb
EMDBエントリー14709
分子名称Solute carrier family 12 member 2, SODIUM ION, POTASSIUM ION, ... (7 entities in total)
機能のキーワードslc12 family, nkcc1 in complex with na+, k+ and 2cl-, leut-fold, transport protein
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数2
化学式量合計272146.13
構造登録者
主引用文献Neumann, C.,Rosenbaek, L.L.,Flygaard, R.K.,Habeck, M.,Karlsen, J.L.,Wang, Y.,Lindorff-Larsen, K.,Gad, H.H.,Hartmann, R.,Lyons, J.A.,Fenton, R.A.,Nissen, P.
Cryo-EM structure of the human NKCC1 transporter reveals mechanisms of ion coupling and specificity.
Embo J., 41:e110169-e110169, 2022
Cited by
PubMed Abstract: The sodium-potassium-chloride transporter NKCC1 of the SLC12 family performs Na -dependent Cl - and K -ion uptake across plasma membranes. NKCC1 is important for regulating cell volume, hearing, blood pressure, and regulation of hyperpolarizing GABAergic and glycinergic signaling in the central nervous system. Here, we present a 2.6 Å resolution cryo-electron microscopy structure of human NKCC1 in the substrate-loaded (Na , K , and 2 Cl ) and occluded, inward-facing state that has also been observed for the SLC6-type transporters MhsT and LeuT. Cl binding at the Cl1 site together with the nearby K ion provides a crucial bridge between the LeuT-fold scaffold and bundle domains. Cl -ion binding at the Cl2 site seems to undertake a structural role similar to conserved glutamate of SLC6 transporters and may allow for Cl -sensitive regulation of transport. Supported by functional studies in mammalian cells and computational simulations, we describe a putative Na release pathway along transmembrane helix 5 coupled to the Cl2 site. The results provide insight into the structure-function relationship of NKCC1 with broader implications for other SLC12 family members.
PubMed: 36239040
DOI: 10.15252/embj.2021110169
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.55 Å)
構造検証レポート
Validation report summary of 7zgo
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-06-18に公開中

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