MemProtMD simulation of NavAb I22V as a basis for the human Nav1.7 Inherited Erythromelalgia I136V mutation in a lipid bilayer at both coarse-grained and atomistic respresentation, including both file download and analysis. Classification based on PDB 8div.
voltage-gated sodium channel ion transport protein, membrane protein, MemProtMD, membrane protein, simulation, coarse-grained, intrinsic membrane, martini, CG
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