EMD-3214

Electron Crystallography
5.0 Å
EMD-3214 Deposition: 26/10/2015
Map released: 30/12/2015
Last modified: 13/04/2016
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-3214

crystal structure of AQP4 bound to AZA

EMD-3214

Electron Crystallography
5.0 Å
EMD-3214 Deposition: 26/10/2015
Map released: 30/12/2015
Last modified: 13/04/2016
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Rattus norvegicus
Sample: Aquaporin-4 bound to acetazolamide

Deposition Authors: Kamegawa A, Hiroaki Y, Tani K, Fujiyoshi Y
Two-dimensional crystal structure of aquaporin-4 bound to the inhibitor acetazolamide
Kamegawa A, Hiroaki Y, Tani K , Fujiyoshi Y
(2016) Microscopy , 65 , 177 - 184
Abstract:
Acetazolamide (AZA) reduces the water permeability of aquaporin-4, the predominant water channel in the brain. We determined the structure of aquaporin-4 in the presence of AZA using electron crystallography. Most of the features of the 5-Å density map were consistent with those of the previously determined atomic model. The map showed a protruding density from near the extracellular pore entrance, which most likely represents the bound AZA. Molecular docking simulations supported the location of the protrusion as the likely AZA-binding site. These findings suggest that AZA reduces water conduction by obstructing the pathway at the extracellular entrance without inducing a large conformational change in the protein.