Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect.
Saposins are small, heat-stable glycoproteins required for the hydrolysis of sphingolipids by specific lysosomal hydrolases. Saposins A, B, C, and D are derived by proteolytic processing from a single precursor protein named prosaposin. Saposin B, previously known as SAP-1 and sulfatide activator, s...
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| 出版年: | Proc Natl Acad Sci U S A |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
1990
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC53725/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2320574/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.7.2541 |
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