Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption

American Journal of Physiology - Cell Physiology

Volumn 303, Issue 8, 2012, Pages

  Shin, Daniel Sanghoon ^a   Zhao, Rongbao ^a   Fiser, Andras ^a   Goldman, I David ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Cerebral folate deficiency; CFD; Folates; HCP1; Hereditary folate malabsorption; HFM; Intestinal folate transport; PCFT; PCFT HCP1 heme carrier protein1; Proton coupled folate transporter; Proton coupled transport

Indexed keywords

AMINO ACID; ARGININE; CYSTEINE; FOLIC ACID; GLYCINE; METHOTREXATE; MUTANT PROTEIN; PEMETREXED; PROTON COUPLED FOLATE TRANSPORTER;

ARTICLE; CONTROLLED STUDY; HEREDITARY FOLATE MALABSORPTION; HUMAN; HUMAN CELL; MALABSORPTION; OSCILLATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; SODIUM TRANSPORT; WILD TYPE;

AMINO ACID SUBSTITUTION; FOLIC ACID; FOLIC ACID DEFICIENCY; HELA CELLS; HUMANS; INTESTINAL ABSORPTION; MALABSORPTION SYNDROMES; MODELS, MOLECULAR; POINT MUTATION; PROTEIN CONFORMATION; PROTEIN TRANSPORT; PROTON-COUPLED FOLATE TRANSPORTER;

EID: 84867623729     PISSN: 03636143     EISSN: 15221563     Source Type: Journal    
DOI: 10.1152/ajpcell.00171.2012     Document Type: Article

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