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Membrane Biology
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- Membrane BiologyOpen Access
Conserved cysteines in the finger domain of the epithelial Na+ channel α and γ subunits are proximal to the dynamic finger–thumb domain interface
Journal of Biological ChemistryVol. 293Issue 13p4928–4939Published online: February 7, 2018- Brandon M. Blobner
- Xue-Ping Wang
- Ossama B. Kashlan
Cited in Scopus: 4The epithelial Na+ channel (ENaC) is a member of the ENaC/degenerin family of ion channels. In the structure of a related family member, the “thumb” domain’s base interacts with the pore, and its tip interacts with the divergent “finger” domain. Between the base and tip, the thumb domain is characterized by a conserved five-rung disulfide ladder holding together two anti-parallel α helices. The ENaC α and γ subunits’ finger domains harbor autoinhibitory tracts that can be proteolytically liberated to activate the channel and also host an ENaC-specific pair of cysteines.