Retromer function in endosome-to-Golgi retrograde transport is regulated by the yeast Vps34 Ptdlns 3-kinase

Journal of Cell Science

Volumn 115, Issue 20, 2002, Pages 3889-3900

  Burda, Patricie ^a   Padilla, Steven M ^a   Sarkar, Srimonti ^a   Emr, Scott D ^a  

^a HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

Endosome to Golgi retrograde transport; Phosphatidylinositol 3 phosphate; PX domain; Saccharomyces cerevisiae; Vesicular transport

Indexed keywords

FUNGAL ENZYME; PHOSPHATIDYLINOSITIDE; PHOSPHATIDYLINOSITOL 3 KINASE; PHOSPHOTRANSFERASE; POLYPHOSPHOINOSITIDE; PROTEIN SUBUNIT; PROTEINASE; CARBOXYPEPTIDASE; CARRIER PROTEIN; HYBRID PROTEIN; MEMBRANE PROTEIN; PHOSPHATIDYLINOSITOL 3 PHOSPHATE; PROTEIN SERINE THREONINE KINASE; SACCHAROMYCES CEREVISIAE PROTEIN;

ARTICLE; CELL LEVEL; CELL VACUOLE; COMPLEX FORMATION; CONTROLLED STUDY; CYTOPLASM; ENDOSOME; ENZYME BINDING; ENZYME LOCALIZATION; ENZYME SYNTHESIS; FUNGAL STRAIN; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; GOLGI COMPLEX; IN VITRO STUDY; IN VIVO STUDY; INTRACELLULAR TRANSPORT; LIPOGENESIS; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; PROTEIN PROCESSING; SACCHAROMYCES CEREVISIAE; SEQUENCE HOMOLOGY; YEAST; BIOSYNTHESIS; CELL COMPARTMENTALIZATION; CHEMISTRY; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; POINT MUTATION; PROTEIN BINDING; PROTEIN MOTIF; PROTEIN TERTIARY STRUCTURE; PROTEIN TRANSPORT; SITE DIRECTED MUTAGENESIS;

1-PHOSPHATIDYLINOSITOL 3-KINASE; AMINO ACID MOTIFS; CARBOXYPEPTIDASES; CARRIER PROTEINS; CELL COMPARTMENTATION; CYTOPLASM; ENDOSOMES; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GENE EXPRESSION REGULATION, FUNGAL; GOLGI APPARATUS; MEMBRANE PROTEINS; MUTAGENESIS, SITE-DIRECTED; PHENOTYPE; PHOSPHATIDYLINOSITOL PHOSPHATES; POINT MUTATION; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; PROTEIN-SERINE-THREONINE KINASES; RECOMBINANT FUSION PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0037107491     PISSN: 00219533     EISSN: None     Source Type: Journal    
DOI: 10.1242/jcs.00090     Document Type: Article

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