A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformation
He-Qin Zhan(Albert Einstein College of Medicine), Rongbao Zhao(Albert Einstein College of Medicine)
Cited by 6
Related Papers
Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues
|Expert Reviews in Molecular Medicine|2009|384
Random Mutagenesis of the Proton-coupled Folate Transporter (SLC46A1), Clustering of Mutations, and the Bases for Associated Losses of Function
|Journal of Biological Chemistry|2011|19