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CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates.
The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is regulated by phosphorylation of the R domain and ATP hydrolysis at two nucleotide-binding domains (NBDs). It is controversial whether CFTR conducts ATP or whether CFTR might be closely associated with a sepa...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
1998
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1170439/ https://ncbi.nlm.nih.gov/pubmed/9463368 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/emboj/17.4.898 |
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