Autophosphorylation of the C2 domain inhibits translocation of the novel protein kinase C (nPKC) Apl II

Journal of Neurochemistry

Volumn 123, Issue 3, 2012, Pages 360-372

  Farah, Carole A ^a   Lindeman, Amanda A ^a   Siu, Vincent ^a   Gupta, Micaela Das ^a   Sossin, Wayne S ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

Aplysia; lipid binding; novel protein kinase C; phosphatidic acid; phosphorylation; translocation

Indexed keywords

ALANINE; BISINDOLYLMALEIMIDE; BISINDOLYLMALEIMIDE 1; CALCIUM; GLUTAMIC ACID; PHOSPHATASE; PROTEIN KINASE C; SERINE; SEROTONIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; APLYSIA; ARTICLE; AUTOPHOSPHORYLATION; BLOCKING FACTOR; CELL MEMBRANE; CONTROLLED STUDY; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME INHIBITION; ENZYME REGULATION; IN VIVO STUDY; MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN LIPID INTERACTION; PROTEIN PHOSPHORYLATION; PROTEIN PROCESSING; PROTEIN TRANSPORT; REGULATORY MECHANISM; SENSORY NERVE CELL; SENSORY STIMULATION; SIGNAL TRANSDUCTION;

ANIMALS; APLYSIA; MUTAGENESIS; OXAZOLES; PHOSPHATIDIC ACIDS; PHOSPHORYLATION; PROTEIN KINASE C; PROTEIN KINASE INHIBITORS; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN STRUCTURE, TERTIARY; SENSORY RECEPTOR CELLS; SF9 CELLS;

APLYSIA;

EID: 84867332863     PISSN: 00223042     EISSN: 14714159     Source Type: Journal    
DOI: 10.1111/j.1471-4159.2012.07930.x     Document Type: Article

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