arXiv · cond-mat/0107624
Conformations of Proteins in Equilibrium
Abstract
We introduce a simple theoretical approach for an equilibrium study of proteins with known native state structures. We test our approach with results on well-studied globular proteins, Chymotrypsin Inhibitor (2ci2), Barnase and the alpha spectrin SH3 domain and present evidence for a hierarchical onset of order on lowering the temperature with significant organization at the local level even at high temperatures. A further application to the folding process of HIV-1 protease shows that the model can be reliably used to identify key folding sites that are responsible for the development of drug resistance .
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Cristian Micheletti, Jayanth Banavar, Amos Maritan. 2001-07-31. Conformations of Proteins in Equilibrium. https://doi.org/10.1103/physrevlett.87.088102
Cite the original work for its findings. Save a collection to share your selection of sources.