Cellular basis for protein C deficiency caused by a single amino acid substitution at Arg15 in the γ-carboxyglutamic acid domain

Journal of Biochemistry

Volumn 120, Issue 2, 1996, Pages 360-368

  Tokunaga, Fuminori ^a   Tsukamoto, Toshiro ^a   Koide, Takehiko ^a  

^a UNIVERSITY OF HYOGO   (Japan)

Author keywords

Inherited deficiency; Protein C; Secretion; Vitamin K dependent factor; carboxyglutamic acid domain

Indexed keywords

4 CARBOXYGLUTAMIC ACID; ARGININE; GLUTAMINE; GLYCINE; LEUCINE; PROLINE; PROTEIN C; PROTEIN DISULFIDE ISOMERASE; RECOMBINANT PROTEIN; SERINE PROTEINASE; TRYPTOPHAN;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CELL ORGANELLE; CELL STRAIN BHK; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME LINKED IMMUNOSORBENT ASSAY; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; HYDROPHOBICITY; KIDNEY CELL; NONHUMAN; PROTEIN C DEFICIENCY; PROTEIN DOMAIN; PROTEIN SECRETION; RADIOACTIVITY; RISK; VEIN THROMBOSIS;

ANIMALIA;

EID: 0029680791     PISSN: 0021924X     EISSN: None     Source Type: Journal    
DOI: 10.1093/oxfordjournals.jbchem.a021421     Document Type: Article

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