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Updated: Sep 26, 2026

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues
Published on: July 14, 2015
Theoretical approaches to tracing conformational polymorphism of proteins
Miłosz Wieczór1, Gerard Carol2, Pablo Navarro3
1Institute for Research in Biomedicine (IRB Barcelona), Baldiri Reixac 10, Barcelona 08028, Spain; Department of Physical Chemistry, Gdańsk University of Technology, Narutowicza 11/12, Gdańsk 80-233, Poland.
Abstract:
Proteins are not the rigid, static entities as once suggested by early structural biology studies. Instead, they are highly dynamic molecules that are better represented not by a single reference structure, but by a Boltzmann ensemble of conformations. In this article, we review theoretical approaches to reproducing such structural ensembles, with particular emphasis on methods designed to identify major conformational states and the transition pathways connecting them.
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