8jpr
From Proteopedia
Jump to navigationJump to search
Cryo-EM structure of Y553C human ClC-6
| ||||||||||||
Structural highlights
DiseaseCLCN6_HUMAN CLCN6-related childhood-onset progressive neurodegeneration-peripheral neuropathy syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionCLCN6_HUMAN Voltage-gated channel mediating the exchange of chloride ions against protons. Functions as antiporter and contributes to the acidification of the late endosome lumen. The CLC channel family contains both chloride channels and proton-coupled anion transporters that exchange chloride or another anion for protons. The presence of conserved gating glutamate residues is typical for family members that function as antiporters.[1] References
| ||||||||||||||||||||
This page was last modified 14:46, 20 September 2023.