Accounting for large amplitude protein deformation during in silico macromolecular docking

TitleAccounting for large amplitude protein deformation during in silico macromolecular docking
Publication TypeJournal Article
Year of Publication2011
AuthorsBastard K, Saladin A, Prévost C
JournalInt. J. Mol. Sci.
Volume12
Pagination1316–33
Keywordsflexibility, macromolecular docking, protein loops and domains
Abstract

Rapid progress of theoretical methods and computer calculation resources has turned in silico methods into a conceivable tool to predict the 3D structure of macromolecular assemblages, starting from the structure of their separate elements. Still, some classes of complexes represent a real challenge for macromolecular docking methods. In these complexes, protein parts like loops or domains undergo large amplitude deformations upon association, thus remodeling the surface accessible to the partner protein or DNA. We discuss the problems linked with managing such rearrangements in docking methods and we review strategies that are presently being explored, as well as their limitations and success.

DOI10.3390/ijms12021316
Citation Key2011|1654