Atg18 regulates organelle morphology and Fab1 kinase activity independent of its membrane recruitment by phosphatidylinositol 3,5-bisphosphate

Molecular Biology of the Cell

Volumn 18, Issue 11, 2007, Pages 4232-4244

  Efe, Jem A ^a   Botelho, Roberto J ^b,c   Emr, Scott D ^a,b,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c Department of Obstetrics Gynecology   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADAPTOR PROTEIN; CELL PROTEIN; MYOSIN V; PHOSPHATIDYLINOSITOL 3 PHOSPHATE; PHOSPHATIDYLINOSITOL 3,5 BISPHOSPHATE; PHOSPHOLIPID; PROTEIN ATG18; PROTEIN FAB1; PROTEIN KINASE; PROTEIN VAC14; PROTEIN VAC7; UNCLASSIFIED DRUG;

ARTICLE; BINDING SITE; CELL ORGANELLE; CELL VACUOLE; CONTROLLED STUDY; CYTOSKELETON; ENDOSOME; ENZYME ACTIVITY; FEEDBACK SYSTEM; HOMEOSTASIS; MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; TONOPLAST;

BINDING SITES; CELL MEMBRANE; CYTOSOL; ENZYME ACTIVATION; FLAVOPROTEINS; GENE DELETION; GENES, REPORTER; MEMBRANE PROTEINS; MUTATION; ORGANELLES; PHOSPHATIDYLINOSITOL PHOSPHATES; PHOSPHORIC MONOESTER HYDROLASES; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PROTEIN BINDING; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; VACUOLES;

EID: 35848929068     PISSN: 10591524     EISSN: None     Source Type: Journal    
DOI: 10.1091/mbc.E07-04-0301     Document Type: Article

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