A subunit of eukaryotic translation initiation factor 2α-phosphatase (CreP/PPP1R15B) regulates membrane

Journal of Biological Chemistry

Volumn 287, Issue 42, 2012, Pages 35299-35317

  Kloft, Nicole ^a   Neukirch, Claudia ^a   Von Hoven, Gisela ^a   Bobkiewicz, Wiesia ^a   Weis, Silvia ^a   Boller, Klaus ^b   Husmann, Matthias ^a  

^a JOHANNES GUTENBERG UNIVERSITY   (Germany)

^b PAUL EHRLICH INSTITUT   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMPHIPATHIC; CATALYTIC SUBUNITS; DEPHOSPHORYLATIONS; ENDOSOMES; EPITHELIAL CELLS; ERYTHROLEUKEMIA CELLS; EUKARYOTIC TRANSLATION; EXOSOMES; INITIATION FACTORS; INTERACTION DOMAIN; INTRACELLULAR VESICLES; LIPID MARKERS; MODE OF ACTION; MULTIVESICULAR BODIES; OVER-EXPRESSION; PHOSPHATIDYLETHANOLAMINE; PROTEIN PHOSPHATASE-1; RHODAMINE B; STAPHYLOCOCCUS AUREUS;

BACTERIA; ENZYME INHIBITION; MACHINERY; MAMMALS; PHOSPHATASES; PHOSPHORYLATION; RHODIUM;

TOXIC MATERIALS;

CONSTITUTIVE REVERTER OF EUKARYOTIC TRANSLATION INITIATION FACTOR 2ALPHA PHOSPHORYLATION; INITIATION FACTOR 2ALPHA; LIPID; N (LISSAMINE RHODAMINE B SULFONYL)PHOSPHATIDYLENOLAMINE; PHOSPHOPROTEIN PHOSPHATASE 1; PHOSPHOPROTEIN PHOSPHATASE 1 CATALYTIC SUBUNIT; PROTEIN KINASE R; REGULATOR PROTEIN; STAPHYLOCOCCUS ALPHA TOXIN; UNCLASSIFIED DRUG;

ALPHA HELIX; ARTICLE; CELL MEMBRANE; CELL VACUOLE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; ENDOSOME; EPITHELIUM CELL; ERYTHROLEUKEMIA CELL; EXOCYTOSIS; HUMAN; HUMAN CELL; INTERNALIZATION; MEMBRANE TRANSPORT; MULTIVESICULAR BODY; PRIORITY JOURNAL; PROTEIN DEPHOSPHORYLATION; PROTEIN DOMAIN; PROTEIN PROTEIN INTERACTION; STAPHYLOCOCCUS AUREUS; TRANSLATION INITIATION;

ANIMALS; BACTERIAL TOXINS; CELL MEMBRANE; ENDOSOMES; EPITHELIAL CELLS; EUKARYOTIC INITIATION FACTOR-2; HUMANS; K562 CELLS; PEPTIDE CHAIN INITIATION, TRANSLATIONAL; PHOSPHORYLATION; PROTEIN PHOSPHATASE 1; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; RABBITS; STAPHYLOCOCCUS AUREUS;

EID: 84867423363     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.379883     Document Type: Article

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