Efficient glycosylation site utilization by intracellular apolipoprotein B: Implications for proteasomal degradation

Journal of Lipid Research

Volumn 40, Issue 12, 1999, Pages 2212-2222

  Huang, Xue F ^a,b   Shelness, Gregory S ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Dislocation; Endoplasmic reticulum; HepG2 cells; Lipoprotein assembly; Protein turnover; Proteolysis; Quality control; Retrograde translocation; Translocation; Very low density lipoprotein

Indexed keywords

APOLIPOPROTEIN B; PROTEASOME; VERY LOW DENSITY LIPOPROTEIN;

AMINO TERMINAL SEQUENCE; ARTICLE; CHROMOSOME TRANSLOCATION; ENDOPLASMIC RETICULUM; GLYCOSYLATION; HUMAN; HUMAN CELL; LIPOPROTEIN METABOLISM; PEPTIDE MAPPING; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN DEGRADATION; PROTEIN METABOLISM; QUALITY CONTROL; RECEPTOR AFFINITY; TRANSLATION REGULATION;

ANIMALS; APOLIPOPROTEIN B-100; APOLIPOPROTEINS B; BINDING SITES; BIOLOGICAL TRANSPORT; COS CELLS; CYSTEINE ENDOPEPTIDASES; CYSTEINE PROTEINASE INHIBITORS; DETERGENTS; ENDOPEPTIDASES; ENDOPLASMIC RETICULUM; GLYCOSYLATION; HUMANS; LIVER; MOLECULAR PROBES; MULTIENZYME COMPLEXES; PROTEASOME ENDOPEPTIDASE COMPLEX; RECOMBINANT PROTEINS; SOLUBILITY; TRANSFECTION; TUMOR CELLS, CULTURED;

EID: 0033398544     PISSN: 00222275     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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