Mutation in a valine residue induces drastic changes in 3D structure of human prion protein
Author:
Publisher
Informa UK Limited
Subject
General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://www.tandfonline.com/doi/pdf/10.1080/21553769.2013.775078
Reference29 articles.
1. Prevalent Mutations of Human Prion Protein: A Molecular Modeling and Molecular Dynamics Study
2. Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation
3. Transmissible spongiform encephalopathies
4. High hydrophobic amino acid exposure is responsible of the neurotoxic effects induced by E200K or D202N disease-related mutations of the human prion protein
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