Article
Common motifs and topological effects in the protein folding transition state.
Journal of molecular biology - 16 Jun 2006
Hubner Isaac A, Lindberg Magnus, Haglund Ellinor, Oliveberg Mikael, Shakhnovich Eugene I
Abstract excerpt
Through extensive experiment, simulation, and analysis of protein S6 (1RIS), we find that variations in nucleation and folding pathway between circular permutations are determined principally by the restraints of topology and specific nucleation, and affected by changes in chain entropy. Simulations also relate topological features to experimentally measured stabilities. Despite many sizable changes in phi values...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
