Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption

The proton-coupled folate transporter (PCFT-SLC46A1) is required for intestinal folate absorption and is mutated in the autosomal recessive disorder, hereditary folate malabsorption (HFM). This report characterizes properties and requirements of the R376 residue in PCFT function, including a R376Q m...

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Autores principales: Mahadeo, Kris, Diop-Bove, Ndeye, Shin, Daniel, Unal, Ersin Selcuk, Teo, Juliana, Zhao, Rongbao, Chang, Min-Hwang, Fulterer, Andreas, Romero, Michael F., Goldman, I. David
Formato: Artigo
Lenguaje:Inglês
Publicado: American Physiological Society 2010
Materias:
Membrane Transporters, Ion Channels and Pumps
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2980313/
https://ncbi.nlm.nih.gov/pubmed/20686069
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00113.2010
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