Protein phosphatase 2A is regulated by protein kinase Cα (PKCα)-dependent phosphorylation of its targeting subunit B56α at Ser41

Journal of Biological Chemistry

Volumn 289, Issue 1, 2014, Pages 163-176

  Kirchhefer, Uwe ^a   Heinick, Alexander ^a   König, Simone ^b   Kristensen, Torsten ^c   Müller, Frank U ^a   Seidl, Matthias D ^a   Boknik, Peter ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c AARHUS UNIVERSITY   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CELL MEMBRANES; PHOSPHATASES;

CELLULAR FUNCTION; ENDOPLASMIC RETICULUM; ENZYME COMPLEXES; FLUORESCENCE MEASUREMENTS; FUNCTIONAL SPECIFICITY; PHOSPHOAMINO ACIDS; PHOSPHORYLATION SITES; PROTEIN PHOSPHATASE 2A;

PHOSPHORYLATION;

ASPARTIC ACID; PHOSPHOPROTEIN; PHOSPHOPROTEIN PHOSPHATASE 2A; PHOSPHOPROTEIN SUBUNIT B56ALPHA; PROTEIN KINASE C ALPHA; SERINE; UNCLASSIFIED DRUG; ALPHA 1 ADRENERGIC RECEPTOR STIMULATING AGENT; CALCIUM; PHENYLEPHRINE; PHOSPHOPROTEIN PHOSPHATASE 2; PPP2R5A PROTEIN, HUMAN; PRKCA PROTEIN, HUMAN;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CALCIUM HOMEOSTASIS; CALCIUM TRANSPORT; CONTROLLED STUDY; DOWN REGULATION; ENDOPLASMIC RETICULUM; ENZYME ACTIVATION; ENZYME INHIBITION; HEART MUSCLE; HUMAN; HUMAN TISSUE; IN VITRO STUDY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEPHOSPHORYLATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROCESSING; PROTEIN TARGETING; WILD TYPE; AMINO ACID SUBSTITUTION; ANIMAL; CLINICAL TRIAL; DRUG EFFECTS; GENETICS; HEK293 CELL LINE; HOMEOSTASIS; METABOLISM; MISSENSE MUTATION; PHOSPHORYLATION; PHYSIOLOGY; SF9 CELL LINE; SPODOPTERA;

ADRENERGIC ALPHA-1 RECEPTOR AGONISTS; AMINO ACID SUBSTITUTION; ANIMALS; CALCIUM; ENDOPLASMIC RETICULUM; HEK293 CELLS; HOMEOSTASIS; HUMANS; MUTATION, MISSENSE; PHENYLEPHRINE; PHOSPHORYLATION; PROTEIN KINASE C-ALPHA; PROTEIN PHOSPHATASE 2; SERINE; SF9 CELLS; SPODOPTERA;

EID: 84891719063     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.507996     Document Type: Article

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