טוען...
Functional organization of cytoplasmic portals controlling access to the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel pore
The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl(−) channel that apparently has evolved from an ancestral active transporter. Key to the CFTR's switch from pump to channel function may have been the appearance of one or more “lateral portals.” Such portals connect the cyto...
שמור ב:
| הוצא לאור ב: | J Biol Chem |
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| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Biochemistry and Molecular Biology
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5900759/ https://ncbi.nlm.nih.gov/pubmed/29475947 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA117.001373 |
| תגים: |
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