The N-terminal domain modulates α-Amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid (AMPA) receptor desensitization

Journal of Biological Chemistry

Volumn 289, Issue 19, 2014, Pages 13197-13205

  Möykkynen, Tommi ^a   Coleman, Sarah K ^a   Semenov, Artur ^a   Keinänen, Kari ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

CELL MEMBRANES; MAMMALS;

AMPA-RECEPTOR; CURRENT RATIOS; DESENSITIZED STATE; EXTRACELLULAR; GLUTAMATE TOXICITY; MAMMALIAN BRAIN; N-TERMINAL DOMAINS; NMDA RECEPTOR;

CELL CULTURE;

AMPA RECEPTOR; GLUTAMIC ACID;

AMINO TERMINAL SEQUENCE; ARTICLE; CELL CULTURE; CELL MEMBRANE; CONTROLLED STUDY; CYTOTOXICITY; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN PROCESSING; PROTEIN STABILITY; RECEPTOR DOWN REGULATION; STEADY STATE;

ALLOSTERIC REGULATION; ION CHANNELS; IONOTROPIC GLUTAMATE RECEPTORS (AMPA, NMDA); PROTEIN DOMAINS; RECEPTOR DESENSITIZATION; RECEPTOR STRUCTURE-FUNCTION;

ALLOSTERIC REGULATION; ALPHA-AMINO-3-HYDROXY-5-METHYL-4-ISOXAZOLEPROPIONIC ACID; ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; EXCITATORY AMINO ACID AGONISTS; HEK293 CELLS; HUMANS; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, AMPA;

EID: 84900387298     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.526301     Document Type: Article

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