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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Bibliografiset tiedot
Päätekijät: Hutzler, Johannes, Schmid, Maria, Bernard, Thomas, Henrissat, Bernard, Strahl, Sabine
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2007
Aiheet:
Biological Sciences
Linkit: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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