Identification of novel in vivo phosphorylation sites of the human proapoptotic protein BAD. Pore-forming activity of bad is regulated by phosphorylation

Journal of Biological Chemistry

Volumn 284, Issue 41, 2009, Pages 28004-28020

  Polzien, Lisa ^a   Baljuls, Angela ^a   Rennefahrt, Ulrike E E ^a   Fischer, Andreas ^a   Schmitz, Werner ^a   Zahedi, Rene P ^a   Sickmann, Albert ^c,d   Metz, Renate ^a   Albert, Stefan ^b   Benz, Roland ^a   Hekman, Mirko ^a   Rapp, Ulf R ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

^c LEIBNIZ INSTITUT FÜR ANALYTISCHE WISSENSCHAFTEN ISAS E V   (Germany)

^d RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

14-3-3 PROTEINS; APOPTOSIS; BAY 43-9006; COLONY FORMATION; CONSTITUTIVELY ACTIVES; CONTROL LEVEL; IN-VITRO; IN-VIVO; PHOSPHORYLATION SITES; PLANAR BILAYERS; PROTEIN FAMILY; PROTEIN KINASE A; SERINE RESIDUES; SURFACE PLASMONS; SURVIVAL FACTOR;

AMINO ACIDS; BINDING ENERGY; BINDING SITES; BIOLOGICAL MEMBRANES; CELL DEATH; MASS SPECTROMETRY; PROTEINS; STEEL METALLOGRAPHY; SURFACE PLASMON RESONANCE;

PHOSPHORYLATION;

CYCLIC AMP DEPENDENT PROTEIN KINASE; PHOSPHOSERINE; PROTEIN 14 3 3; PROTEIN BAD; PROTEIN BCL 2; PROTEIN BCL XL; PROTEIN KINASE B; RAF PROTEIN;

APOPTOSIS; ARTICLE; BINDING SITE; COLONY FORMATION; CONTROLLED STUDY; HUMAN; HUMAN CELL; IN VIVO STUDY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; SURFACE PLASMON RESONANCE;

14-3-3 PROTEINS; AMINO ACID SEQUENCE; ANIMALS; BCL-ASSOCIATED DEATH PROTEIN; BCL-X PROTEIN; CYCLIC AMP-DEPENDENT PROTEIN KINASES; HUMANS; ION CHANNELS; LIPID BILAYERS; MASS SPECTROMETRY; MICE; MOLECULAR SEQUENCE DATA; NIH 3T3 CELLS; P21-ACTIVATED KINASES; PEPTIDES; PHOSPHORYLATION; PROTEIN BINDING; PROTO-ONCOGENE PROTEINS C-AKT; PROTO-ONCOGENE PROTEINS C-BCL-2; RAF KINASES; SEQUENCE ALIGNMENT;

MURINAE;

EID: 70350514520     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.010702     Document Type: Article

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