| Literature DB >> 26233164 |
Mateusz Chwastyk1, Marek Cieplak1.
Abstract
We study the folding process in the shallowly knotted protein MJ0366 within two variants of a structure-based model. We observe that the resulting topological pathways are much richer than identified in previous studies. In addition to the single knot-loop events, we find novel, and dominant, two-loop mechanisms. We demonstrate that folding takes place in a range of temperatures and the conditions of most successful folding are at temperatures which are higher than those required for the fastest folding. We also demonstrate that nascent conditions are more favorable to knotting than off-ribosome folding.Mesh:
Substances:
Year: 2015 PMID: 26233164 DOI: 10.1063/1.4927153
Source DB: PubMed Journal: J Chem Phys ISSN: 0021-9606 Impact factor: 3.488