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Similar folds with different stabilization mechanisms: the cases of prion and doppel proteins
BACKGROUND: Protein misfolding is the main cause of a group of fatal neurodegenerative diseases in humans and animals. In particular, in Prion-related diseases the normal cellular form of the Prion Protein PrP (PrP(C)) is converted into the infectious PrP(Sc )through a conformational process during...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2006
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1574322/ https://ncbi.nlm.nih.gov/pubmed/16857062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1472-6807-6-17 |
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