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A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation
The proton-coupled folate transporter (PCFT, SLC46A1) is required for folate intestinal absorption and transport across the choroid plexus. Recent work has identified a F392V mutation causing hereditary folate malabsorption. However, the residue properties responsible for this loss of function remai...
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| Publicado no: | J Biol Chem |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7667981/ https://ncbi.nlm.nih.gov/pubmed/32893190 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA120.014757 |
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