Mutation of light-dependent phosphorylation sites of the Drosophila transient receptor potential-like (TRPL) ion channel affects its subcellular localization and stability

Journal of Biological Chemistry

Volumn 288, Issue 22, 2013, Pages 15600-15613

  Cerny, Alexander C ^a   Oberacker, Tina ^a   Pfannstiel, Jens ^a   Weigold, Sebastian ^a   Will, Carina ^a   Huber, Armin ^a  

^a UNIVERSITY OF HOHENHEIM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROPHYSIOLOGICAL RESPONSE; PHOSPHORYLATION SITES; PHOTOTRANSDUCTION; QUANTITATIVE MASS SPECTROMETRIES; STABLE EXPRESSION; SUBCELLULAR LOCALIZATIONS; SUBCELLULAR TRAFFICKING; TRANSIENT RECEPTOR POTENTIALS;

ELECTROPHYSIOLOGY; MASS SPECTROMETRY;

PHOSPHORYLATION;

TRANSIENT RECEPTOR POTENTIAL CHANNEL;

ARTICLE; CARBOXY TERMINAL SEQUENCE; DARK ADAPTATION; DROSOPHILA; IN VIVO STUDY; LIGHT; MASS SPECTROMETRY; MEMBRANE ELECTROPHYSIOLOGY; MUTATION; NONHUMAN; PHOTORECEPTOR CELL; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN MODIFICATION; PROTEIN MULTIMERIZATION; PROTEIN PHOSPHORYLATION; PROTEIN STABILITY; TRANSGENIC ANIMAL;

DROSOPHILA; PROTEIN PHOSPHORYLATION; TRAFFICKING; TRP CHANNELS; VISION;

ANIMALS; DARK ADAPTATION; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; LIGHT; MUTATION; PHOSPHORYLATION; PROTEIN STABILITY; PROTEIN TRANSPORT; TRANSIENT RECEPTOR POTENTIAL CHANNELS;

EID: 84878411233     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.426981     Document Type: Article

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