Loading...
On the Mechanism of MgATP-dependent Gating of CFTR Cl(−) Channels
CFTR, the product of the gene mutated in cystic fibrosis, is an ATPase that functions as a Cl(−) channel in which bursts of openings separate relatively long interburst closed times (τib). Channel gating is controlled by phosphorylation and MgATP, but the underlying molecular mechanisms remain contr...
Na minha lista:
| Main Authors: | , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The Rockefeller University Press
2003
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2217317/ https://ncbi.nlm.nih.gov/pubmed/12508051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.20028673 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|