A defect of the vacuolar putative lipase Atg15 accelerates degradation of lipid droplets through lipolysis

Autophagy

Volumn 11, Issue 8, 2015, Pages 1247-1258

  Maeda, Yuichiro ^a   Oku, Masahide ^a   Sakai, Yasuyoshi ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Atg15; Autophagy; Lipid droplet; Lipolysis; Tgl3; Tgl4; Triacylglycerol

Indexed keywords

ATG15 PROTEIN; FAT DROPLET; PROTEIN; TGL3 PROTEIN; TGL4 PROTEIN; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; ATG15 PROTEIN, S CEREVISIAE; AUTOPHAGY RELATED PROTEIN; CARBOXYLESTERASE; LIPID; MEMBRANE PROTEIN; SACCHAROMYCES CEREVISIAE PROTEIN; TGL3 PROTEIN, S CEREVISIAE; TGL4 PROTEIN, S CEREVISIAE;

ARTICLE; AUTOPHAGOSOME; AUTOPHAGY; CELL VACUOLE; DYNAMICS; GENE DELETION; LIPID DEGRADATION; LIPOLYSIS; METABOLITE; MUTANT; NONHUMAN; PHOSPHORYLATION; PROTEIN EXPRESSION; SACCHAROMYCES CEREVISIAE; CELL SURVIVAL; CHEMISTRY; CYTOPLASM; FLUORESCENCE MICROSCOPY; METABOLISM; MUTATION; PHENOTYPE; PHYSIOLOGY; PROTEIN MOTIF;

AMINO ACID MOTIFS; AUTOPHAGY-RELATED PROTEINS; CARBOXYLIC ESTER HYDROLASES; CELL SURVIVAL; CYTOPLASM; GENE DELETION; LIPASE; LIPIDS; LIPOLYSIS; MEMBRANE GLYCOPROTEINS; MICROSCOPY, FLUORESCENCE; MUTATION; PHENOTYPE; PHOSPHORYLATION; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; VACUOLES;

EID: 84943746516     PISSN: 15548627     EISSN: 15548635     Source Type: Journal    
DOI: 10.1080/15548627.2015.1056969     Document Type: Article

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