Conversion of cysteine to formylglycine: A protein modification in the endoplasmic reticulum
In sulfatases a C(α)-formylglycine residue is found at a position where their cDNA sequences predict a cysteine residue. In multiple sulfatase deficiency, an inherited lysosomal storage disorder, catalytically inactive sulfatases are synthesized which retain the cysteine residue, indicating that the...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1997
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC23670/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9342345/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.22.11963 |
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