Ontology highlight
ABSTRACT:
SUBMITTER: Kachlishvili K
PROVIDER: S-EPMC4060689 | biostudies-literature | 2014 Jun
REPOSITORIES: biostudies-literature
Kachlishvili Khatuna K Maisuradze Gia G GG Martin Osvaldo A OA Liwo Adam A Vila Jorge A JA Scheraga Harold A HA
Proceedings of the National Academy of Sciences of the United States of America 20140527 23
By using local (free-energy profiles along the amino acid sequence and (13)C(α) chemical shifts) and global (principal component) analyses to examine the molecular dynamics of protein-folding trajectories, generated with the coarse-grained united-residue force field, for the B domain of staphylococcal protein A, we are able to (i) provide the main reason for formation of the mirror-image conformation of this protein, namely, a slow formation of the second loop and part of the third helix (Asp29- ...[more]