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Membrane association is a determinant for substrate recognition by PMT4 protein O-mannosyltransferases
Protein O-mannosylation represents an evolutionarily conserved, essential posttranslational modification with immense impact on a variety of cellular processes. In humans, O-mannosylation defects result in Walker–Warburg syndrome, a severe recessive congenital muscular dystrophy associated with defe...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1876532/ https://ncbi.nlm.nih.gov/pubmed/17470820 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0700374104 |
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