In vivo phosphorylation of Ser21 and Ser83 during nutrient-induced activation of the yeast protein kinase A (PKA) target trehalase

Journal of Biological Chemistry

Volumn 287, Issue 53, 2012, Pages 44130-44142

  Schepers, Wim ^a,b   Van Zeebroeck, Griet ^a,b   Pinkse, Martijn ^c   Verhaert, Peter ^a,b,c   Thevelein, Johan M ^a,b  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c DELFT UNIVERSITY OF TECHNOLOGY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL ACTIVATION; ENZYMES; NUTRIENTS; YEAST;

ESSENTIAL NUTRIENTS; FERMENTING CELLS; IN-VITRO; IN-VIVO; PROTEIN KINASE A; RAPID ACTIVATION; TREHALASE; VIVO PHOSPHORYLATION; YEAST PROTEINS; YEAST SACCHAROMYCES CEREVISIAE;

PHOSPHORYLATION;

BMH1 PROTEIN; BMH2 PROTEIN; CYCLIC AMP DEPENDENT PROTEIN KINASE; DCS1 PROTEIN; FUNGAL PROTEIN; GLUCOSE; NITROGEN; PHOSPHOPROTEIN PHOSPHATASE 2A; PROTEIN 14 3 3; SERINE; TREHALASE; UNCLASSIFIED DRUG; CYCLIC AMP DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT; DCS1 PROTEIN, S CEREVISIAE; GLYCOSIDASE; SACCHAROMYCES CEREVISIAE PROTEIN; TPK1 PROTEIN, S CEREVISIAE; TPK2 PROTEIN, S CEREVISIAE; TPK3 PROTEIN, S CEREVISIAE;

ARTICLE; DEPHOSPHORYLATION; ENZYME ACTIVATION; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME BINDING; ENZYME INHIBITION; FUNGAL STRAIN; IN VIVO STUDY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; PROTEIN TARGETING; SACCHAROMYCES CEREVISIAE; SIGNAL TRANSDUCTION; CHEMISTRY; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; PHOSPHORYLATION; PROTEIN MOTIF;

SACCHAROMYCES CEREVISIAE;

14-3-3 PROTEINS; AMINO ACID MOTIFS; CYCLIC AMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNITS; CYCLIC AMP-DEPENDENT PROTEIN KINASES; ENZYME ACTIVATION; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GLUCOSE; N-GLYCOSYL HYDROLASES; NITROGEN; PHOSPHORYLATION; PROTEIN BINDING; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; TREHALASE;

EID: 84871796376     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.421503     Document Type: Article

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