Yeast pah1p phosphatidate phosphatase is regulated by proteasome-mediated degradation

Journal of Biological Chemistry

Volumn 289, Issue 14, 2014, Pages 9811-9822

  Pascual, Florencia ^a   Hsieh, Lu Sheng ^a   Soto Cardalda, Aníbal ^a   Carman, George M ^a  

^a the State University of New Jersey   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOLOGY; GLYCEROL; LIPIDS; PHOSPHATASES; YEAST;

DIACYLGLYCEROL KINASE; EXPONENTIAL PHASE; PHOSPHATASE ACTIVITY; RECOMBINANT ENZYMES; STABILIZING EFFECTS; STATIONARY PHASE; TRIACYLGLYCEROLS; UBIQUITINATION;

CELLS;

BENZYLOXYCARBONYLLEUCYLLEUCYLLEUCINAL; CHYMOTRYPSIN; DIACYLGLYCEROL KINASE; PHOSPHATIDATE PHOSPHATASE; PHOSPHATIDIC ACID; PROTEASOME; PROTEIN PAH1P; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME DEGRADATION; ENZYME REGULATION; ENZYME STABILITY; MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; UBIQUITINATION; YEAST;

GLYCEROPHOSPHOLIPID; PHOSPHATIDATE; PHOSPHOLIPID; PHOSPHOLIPID METABOLISM; PROTEASOME; YEAST;

DIGLYCERIDES; ENZYME STABILITY; LEUPEPTINS; MUTATION; PHOSPHATIDATE PHOSPHATASE; PHOSPHOLIPIDS; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEASOME INHIBITORS; PROTEOLYSIS; REPRESSOR PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS;

EID: 84898079090     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.550103     Document Type: Article

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