The Pathogenic Mutation T182A Converts the Prion Protein into a Molten Globule-like Conformation Whose Misfolding to Oligomers but Not to Fibrils Is Drastically Accelerated.
Singh, Jogender
The Pathogenic Mutation T182A Converts the Prion Protein into a Molten Globule-like Conformation Whose Misfolding to Oligomers but Not to Fibrils Is Drastically Accelerated. [electronic resource] - Biochemistry Jan 2016 - 459-69 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1520-4995
10.1021/acs.biochem.5b01266 doi
Amyloid--chemistry
Animals
Hydrogen-Ion Concentration
Mice
Mutation
Prions--chemistry
Protein Folding
Protein Structure, Secondary
Protein Structure, Tertiary
Thermodynamics
The Pathogenic Mutation T182A Converts the Prion Protein into a Molten Globule-like Conformation Whose Misfolding to Oligomers but Not to Fibrils Is Drastically Accelerated. [electronic resource] - Biochemistry Jan 2016 - 459-69 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1520-4995
10.1021/acs.biochem.5b01266 doi
Amyloid--chemistry
Animals
Hydrogen-Ion Concentration
Mice
Mutation
Prions--chemistry
Protein Folding
Protein Structure, Secondary
Protein Structure, Tertiary
Thermodynamics