Gln3 mutations dissociate responses to nitrogen limitation (nitrogen catabolite repression) and rapamycin inhibition of TorC1

Journal of Biological Chemistry

Volumn 288, Issue 4, 2013, Pages 2789-2804

  Rai, Rajendra ^a   Tate, Jennifer J ^a   Nelson, David R ^a   Cooper, Terrance G ^a  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; C-TERMINAL TRUNCATION; ENVIRONMENTAL RESOURCES; INTERACTING SITES; NITROGEN CATABOLITE REPRESSION; NITROGEN LIMITATION; NITROGEN REQUIREMENTS; NITROGEN SOURCES; PHYSIOLOGICAL RESPONSE; RAPAMYCIN; RAPAMYCIN TREATMENT; REGULATORY PATHWAY; REGULATORY SYSTEMS; TRANSCRIPTION ACTIVATORS; WILD-TYPE CONTROLS;

AMINO ACIDS; CELLS; CYTOLOGY; PHYSIOLOGICAL MODELS; TRANSCRIPTION;

NITROGEN;

BACTERIAL PROTEIN; MAMMALIAN TARGET OF RAPAMYCIN COMPLEX 1; PROTEIN GLN3; UNCLASSIFIED DRUG;

ALPHA HELIX; AMINO ACID SUBSTITUTION; ARTICLE; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; CYTOPLASM; GENE MUTATION; NITROGEN CATABOLITE REPRESSION; NITROGEN METABOLISM; NONHUMAN; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN SYNTHESIS INHIBITION; SIGNAL TRANSDUCTION;

CYTOPLASM; FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT; GATA TRANSCRIPTION FACTORS; GENE DELETION; GLUTAMINE; MODELS, GENETIC; MULTIPROTEIN COMPLEXES; MUTATION; NITROGEN; PLASMIDS; PROTEIN INTERACTION MAPPING; PROTEIN STRUCTURE, SECONDARY; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SIROLIMUS; TOR SERINE-THREONINE KINASES; TRANSCRIPTION FACTORS; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 84873880352     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.421826     Document Type: Article

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