Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiency

Biochem Biophys Res Commun. 1991 Mar 29;175(3):1097-103. doi: 10.1016/0006-291x(91)91678-6.

Abstract

The biosynthesis of human alpha-N-acetylgalactosaminidase (alpha-NAGA) was studied in normal fibroblasts and in cells from patients with infantile alpha-NAGA deficiency. Normal alpha-NAGA is synthesized as a 52 kDa precursor which matures to a 49 kDa species through phosphorylation and carbohydrate triming. Fibroblasts from the patients synthesize normal amounts of a 52 kDa precursor, however phosphorylation does not occur and this precursor is subsequently degraded intracellularly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Metabolism, Inborn Errors / enzymology*
  • Carbohydrate Metabolism, Inborn Errors / genetics
  • Cells, Cultured
  • Fibroblasts / enzymology
  • Hexosaminidases / biosynthesis*
  • Hexosaminidases / deficiency
  • Humans
  • Infant
  • Kinetics
  • Phosphorylation
  • Reference Values

Substances

  • Hexosaminidases