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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Physiological Society 2010
Gaiak:
Membrane Transporters, Ion Channels and Pumps
Sarrera elektronikoa: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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