7TTI
Human KCC1 bound with VU0463271 In an outward-open state
Summary for 7TTI
Entry DOI | 10.2210/pdb7tti/pdb |
EMDB information | 26115 26116 |
Descriptor | Solute carrier family 12 member 4, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, N-cyclopropyl-N-(4-methyl-1,3-thiazol-2-yl)-2-[(6-phenylpyridazin-3-yl)sulfanyl]acetamide (3 entities in total) |
Functional Keywords | slc12a4, vu0463271, outward-open state, transport protein-inhibitor complex, transport protein/inhibitor |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 2 |
Total formula weight | 244003.59 |
Authors | Zhao, Y.X.,Cao, E.H. (deposition date: 2022-02-01, release date: 2022-06-29, Last modification date: 2025-05-21) |
Primary citation | Zhao, Y.,Shen, J.,Wang, Q.,Ruiz Munevar, M.J.,Vidossich, P.,De Vivo, M.,Zhou, M.,Cao, E. Structure of the human cation-chloride cotransport KCC1 in an outward-open state. Proc.Natl.Acad.Sci.USA, 119:e2109083119-e2109083119, 2022 Cited by PubMed Abstract: Cation-chloride cotransporters (CCCs) catalyze electroneutral symport of Cl with Na and/or K across membranes. CCCs are fundamental in cell volume homeostasis, transepithelia ion movement, maintenance of intracellular Cl concentration, and neuronal excitability. Here, we present a cryoelectron microscopy structure of human K-Cl cotransporter (KCC)1 bound with the VU0463271 inhibitor in an outward-open state. In contrast to many other amino acid-polyamine-organocation transporter cousins, our first outward-open CCC structure reveals that opening the KCC1 extracellular ion permeation path does not involve hinge-bending motions of the transmembrane (TM) 1 and TM6 half-helices. Instead, rocking of TM3 and TM8, together with displacements of TM4, TM9, and a conserved intracellular loop 1 helix, underlie alternate opening and closing of extracellular and cytoplasmic vestibules. We show that KCC1 intriguingly exists in one of two distinct dimeric states via different intersubunit interfaces. Our studies provide a blueprint for understanding the mechanisms of CCCs and their inhibition by small molecule compounds. PubMed: 35759661DOI: 10.1073/pnas.2109083119 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.5 Å) |
Structure validation
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