The C-terminal domain of the neutral amino acid transporter SNAT2 regulates transport activity through voltage-dependent processes

Biochemical Journal

Volumn 434, Issue 2, 2011, Pages 287-296

  Zhang, Zhou ^a   Zander, Catherine B ^b   Grewer, Christof ^b  

^a SHANGHAI NORMAL UNIVERSITY   (China)

^b BINGHAMTON UNIVERSITY   (United States)

Author keywords

Amino acid transport; C terminus; Sodium coupled neutral amino acid transporter (SNAT); Solute carrier 38 (SLC38); Substrate uptake; Transport mechanism

Indexed keywords

AMINO ACID TRANSPORTER; SODIUM COUPLED NEUTRAL AMINO ACID TRANSPORTER 2; UNCLASSIFIED DRUG;

AMINO ACID TRANSPORT; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE POTENTIAL; CELL SURFACE; CONTROLLED STUDY; HUMAN; HUMAN CELL; PH MEASUREMENT; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; WILD TYPE;

AMINO ACID TRANSPORT SYSTEMS; AMINO ACID TRANSPORT SYSTEMS, NEUTRAL; ANIMALS; BIOLOGICAL TRANSPORT, ACTIVE; CELL MEMBRANE; CELLS, CULTURED; HUMANS; HYDROGEN-ION CONCENTRATION; KINETICS; MEMBRANE POTENTIALS; PROTEIN STRUCTURE, TERTIARY; RATS; TRANSFECTION;

EID: 79951548874     PISSN: 02646021     EISSN: 14708728     Source Type: Journal    
DOI: 10.1042/BJ20100507     Document Type: Article

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