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- W2418270349 abstract "In many mammalian cells, the transport of newly synthesized or externally added lysosomal enzymes to lysosomes is depend on their specific recognition by receptors for mannose 6-phosphate (Man-6-P). The physiological importance of this pathway was confirmed by the finding that fibroblasts from patients with mucolipidosis type II (ML-II ; I - cell disease) fail to phosphorylate mannose residues on their newly synthesized lysosomal enzymes, which results in the secretion of a large percentage of their acid hydrolases into the culture medium. However, lysosomal enzymes themselves do not contain the any consensus amino acid sequences for acquiring the Man-6-P recognition marker. Kornfeld et al revealed using cathepsin D-pepsinogen chimera proteins that UDP-N-acetylglucosamine: lysosomal enzyme N-acetylglucosamine-1-phosphotransferase recognizes not only oligosaccharides but also the three-dimensional structure of the lysosomal enzymes when transfers N-acetylglucosamine-1-phosphate to lysosomal acid hydrolases." @default.
- W2418270349 created "2016-06-24" @default.
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- W2418270349 date "1995-12-01" @default.
- W2418270349 modified "2023-09-25" @default.
- W2418270349 title "[Lysosomal hydrolases have specific conformational domains for acquisition of mannose-6-phosphate]." @default.
- W2418270349 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8577031" @default.
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