8VPP

Phosphorylated human NCC in complex with chlorthalidone

8VPP の概要

• エントリーDOI: 10.2210/pdb8vpp/pdb
• EMDBエントリー: 43412
• 分子名称: Solute carrier family 12 member 3, 2-chloro-5-[(1S)-1-hydroxy-3-oxo-2H-isoindol-1-yl]benzenesulfonamide (3 entities in total)
• 機能のキーワード: sodium chloride cotransporter, phosphorylation, thiazide-like diuretics, chlorthalidone, 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: 227068.06

構造登録者

Zhao, Y.X.,Cao, E.H. (登録日: 2024-01-16, 公開日: 2024-09-04, 最終更新日: 2025-05-14)

主引用文献

Zhao, Y.,Schubert, H.,Blakely, A.,Forbush, B.,Smith, M.D.,Rinehart, J.,Cao, E.
Structural bases for Na + -Cl - cotransporter inhibition by thiazide diuretic drugs and activation by kinases.
Nat Commun, 15:7006-7006, 2024

PubMed Abstract: The Na-Cl cotransporter (NCC) drives salt reabsorption in the kidney and plays a decisive role in balancing electrolytes and blood pressure. Thiazide and thiazide-like diuretics inhibit NCC-mediated renal salt retention and have been cornerstones for treating hypertension and edema since the 1950s. Here we determine NCC co-structures individually complexed with the thiazide drug hydrochlorothiazide, and two thiazide-like drugs chlorthalidone and indapamide, revealing that they fit into an orthosteric site and occlude the NCC ion translocation pathway. Aberrant NCC activation by the WNKs-SPAK kinase cascade underlies Familial Hyperkalemic Hypertension, but it remains unknown whether/how phosphorylation transforms the NCC structure to accelerate ion translocation. We show that an intracellular amino-terminal motif of NCC, once phosphorylated, associates with the carboxyl-terminal domain, and together, they interact with the transmembrane domain. These interactions suggest a phosphorylation-dependent allosteric network that directly influences NCC ion translocation.

PubMed: 39143061
DOI: 10.1038/s41467-024-51381-y

実験手法

ELECTRON MICROSCOPY (2.9 Å)