Abnormal glycosylation of procathepsin L due to N-terminal point mutations correlates with failure to sort to lysosomes

Journal of Biological Chemistry

Volumn 272, Issue 13, 1997, Pages 8808-8816

  Chapman, Richard L ^a   Kane, Susan E ^b   Erickson, Ann H ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^b CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; PROCATHEPSIN L; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; ENZYME INHIBITION; HUMAN; HUMAN CELL; LYSOSOME; MOUSE; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN GLYCOSYLATION; PROTEIN STRUCTURE; PROTEIN TARGETING; RECEPTOR BINDING;

3T3 CELLS; ANIMALS; ASPARTIC ACID; CATHEPSINS; ENZYME PRECURSORS; GLYCOSYLATION; HELA CELLS; HUMANS; LYSOSOMES; MANNOSE; MICE; MOLECULAR WEIGHT; OLIGOSACCHARIDES; PHOSPHORYLATION; POINT MUTATION; TUMOR CELLS, CULTURED;

EID: 0030888604     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.272.13.8808     Document Type: Article

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