The equivalent of a thallium binding residue from an archeal homolog controls cation interactions in brain glutamate transporters

Proceedings of the National Academy of Sciences of the United States of America

Volumn 106, Issue 34, 2009, Pages 14297-14302

  Teichman, Shlomit ^a   Qu, Shaogang ^a   Kanner, Baruch I ^a  

^a HEBREW UNIVERSITY   (Israel)

Author keywords

Cation binding site; Obligate exchange mutant; Sodium selectivity

Indexed keywords

AMINO ACID; ANION; ASPARAGINE; ASPARTIC ACID; CATION; CYSTEINE; GLUTAMATE TRANSPORTER; LIPOSOME; POTASSIUM; SERINE; SODIUM; THALLIUM; VESICULAR GLUTAMATE TRANSPORTER 1;

AMINO ACID TRANSPORT; ARTICLE; BINDING AFFINITY; BRAIN; CONTROLLED STUDY; CRYSTAL STRUCTURE; EUKARYOTE; EXPERIMENTAL STUDY; FEMALE; HELA CELL; HUMAN; HUMAN CELL; MUTATION; OOCYTE; POTASSIUM CONDUCTANCE; PRIORITY JOURNAL; PROTEIN INTERACTION; PROTEIN TRANSPORT; RADIOACTIVITY; SODIUM TRANSPORT; WILD TYPE;

ANIMALS; ARCHAEAL PROTEINS; ASPARTIC ACID; BINDING SITES; BRAIN; CATIONS; EXCITATORY AMINO ACID TRANSPORTER 2; EXCITATORY AMINO ACID TRANSPORTER 3; FEMALE; HELA CELLS; HUMANS; ION TRANSPORT; LIPOSOMES; LITHIUM; MEMBRANE POTENTIALS; MUTATION; OOCYTES; POTASSIUM; PROTEIN BINDING; RABBITS; RATS; SODIUM; THALLIUM; XENOPUS LAEVIS;

EUKARYOTA;

EID: 70149086286     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0904625106     Document Type: Article

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