Target of rapamycin complex 2 regulates actin polarization and endocytosis via multiple pathways

Journal of Biological Chemistry

Volumn 290, Issue 24, 2015, Pages 14963-14978

  Rispal, Delphine ^a   Eltschinger, Sandra ^a   Stahl, Michael ^a   Vaga, Stefania ^b   Bodenmiller, Bernd ^c   Abraham, Yann ^d   Filipuzzi, Ireos ^d   Movva, N Rao ^d   Aebersold, Ruedi ^b,c   Helliwell, Stephen B ^d   Loewith, Robbie ^a,e  

^a UNIVERSITY OF GENEVA   (Switzerland)

^b ETH ZURICH   (Switzerland)

^c UNIVERSITY OF ZURICH   (Switzerland)

^d NOVARTIS PHARMA AG   (Switzerland)

^e National Centre for Competence in Research Chemical Biology   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CELL MEMBRANES; CYTOLOGY; ENZYMES; MOLECULAR BIOLOGY; PHOSPHOLIPIDS; PHYSIOLOGY; POLARIZATION;

FUNCTIONAL CHARACTERIZATION; MEMBRANE TENSION; MULTI-PROTEIN COMPLEX; MULTIPLE PATHWAYS; PHOSPHOPROTEOMICS; PROTEIN PHOSPHORYLATION; SIGNALING PATHWAYS; TARGET OF RAPAMYCIN;

PROTEINS;

COAT PROTEIN; FPK1 PROTEIN; FPK2 PROTEIN; IMIDAZOQUINOLINE DERIVATIVE; MAMMALIAN TARGET OF RAPAMYCIN COMPLEX 2; MAMMALIAN TARGET OF RAPAMYCIN INHIBITOR; PAN1 PROTEIN; PROTEIN KINASE; SPHINGOLIPID; UNCLASSIFIED DRUG; ACTIN; FPK1 PROTEIN, S CEREVISIAE; FPK2 PROTEIN, S CEREVISIAE; FUNGAL PROTEIN; MULTIPROTEIN COMPLEX; SACCHAROMYCES CEREVISIAE PROTEIN; TARGET OF RAPAMYCIN KINASE; TOR COMPLEX 2;

ACTIN FILAMENT; ACTIN POLARIZATION; ARTICLE; CELL MEMBRANE; CONTROLLED STUDY; ENDOCYTOSIS; MASS SPECTROMETRY; NONHUMAN; PRIORITY JOURNAL; PROTEIN MODIFICATION; PROTEIN PHOSPHORYLATION; PROTEOMICS; SIGNAL TRANSDUCTION; YEAST; METABOLISM; PHOSPHORYLATION; PHYSIOLOGY; PRINCIPAL COMPONENT ANALYSIS; SACCHAROMYCES CEREVISIAE;

EUKARYOTA;

ACTINS; ENDOCYTOSIS; FUNGAL PROTEINS; MULTIPROTEIN COMPLEXES; PHOSPHORYLATION; PRINCIPAL COMPONENT ANALYSIS; PROTEIN KINASES; PROTEOMICS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SIGNAL TRANSDUCTION; TOR SERINE-THREONINE KINASES;

EID: 84931281895     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.627794     Document Type: Article

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