Phosphorylation of Argonaute 2 at serine-387 facilitates its localization to processing bodies

Biochemical Journal

Volumn 413, Issue 3, 2008, Pages 429-436

  Zeng, Yan ^a   Sankala, Heidi ^b   Zhang, Xiaoxiao ^a   Graves, Paul R ^b  

^a UNIVERSITY OF MINNESOTA   (United States)

^b VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

Author keywords

Argonaute (Ago); Mitogen activated protein kinase (MAPK); Phosphorylation; Processing body; RNA interference (RNAi)

Indexed keywords

AMINO ACIDS; ANIMAL CELL CULTURE; CHEMICAL REACTIONS; ENZYME ACTIVITY; GENETIC ENGINEERING; MECHANISMS; NUCLEIC ACIDS; PROTEINS; RNA; SODIUM;

ACTIVATED PROTEIN KINASE (AMPK); ANISOMYCIN; C JUN N TERMINAL KINASE (JNK); EXTRACELLULAR SIGNAL REGULATED KINASE (ESRKS); GENE SILENCING; IN-VITRO; IN-VIVO; MITOGEN-ACTIVATED-PROTEIN-KINASE (MAPK); P38 MAPK; PHOSPHORYLATION SITES; REGULATORY MECHANISMS; RNA SILENCING; SODIUM ARSENITE;

PHOSPHORYLATION;

ANISOMYCIN; ARGONAUTE 2 PROTEIN; ARSENITE SODIUM; MITOGEN ACTIVATED PROTEIN KINASE ACTIVATED PROTEIN KINASE 2; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE P38 INHIBITOR; MUTANT PROTEIN; PROTEIN KINASE; STRESS ACTIVATED PROTEIN KINASE INHIBITOR;

ARTICLE; CONTROLLED STUDY; EMBRYO; ENZYME PHOSPHORYLATION; GENE EXPRESSION SYSTEM; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION; REGULATORY MECHANISM;

AMINO ACID SEQUENCE; ANTHRACENES; ARSENITES; BLOTTING, WESTERN; CELL LINE; EUKARYOTIC INITIATION FACTOR-2; FLAVONOIDS; GLUTATHIONE TRANSFERASE; HUMANS; IMIDAZOLES; IMMUNOPRECIPITATION; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; JNK MITOGEN-ACTIVATED PROTEIN KINASES; MASS SPECTROMETRY; MICROSCOPY, CONFOCAL; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; MOLECULAR SEQUENCE DATA; MUTATION; P38 MITOGEN-ACTIVATED PROTEIN KINASES; PHOSPHORYLATION; PROTEIN-SERINE-THREONINE KINASES; PYRIDINES; RECOMBINANT PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; SERINE; SODIUM COMPOUNDS;

EID: 48249114811     PISSN: 02646021     EISSN: None     Source Type: Journal    
DOI: 10.1042/BJ20080599     Document Type: Article

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