Cellular and Molecular Life Sciences CMLS

, Volume 63, Issue 2, pp 207–219

Protein flexibility: its role in structure and mechanism revealed by molecular simulations


DOI: 10.1007/s00018-005-5236-7

Cite this article as:
Dodson, G. & Verma, C.S. Cell. Mol. Life Sci. (2006) 63: 207. doi:10.1007/s00018-005-5236-7


Computer simulations at the atomic level have arrived at a stage where they provide realistic modeling of flexibility in proteins (and the mobility of their associated solvent) that is important in understanding the nature of molecular motions. This can now be extended to the molecular and atomic motions that are associated with protein mechanisms. Moreover, the derived data agree reasonably accurately with experimental measurements of several kinetic and thermodynamic parameters. Fundamental insights emerge on the roles that this intrinsic flexibility plays in the thermodynamic characteristics of macromolecules in solution; these equip the investigator to probe the consequences of cognate interactions and ligand binding on entropy and enthalpy. Thus simulations can now provide a powerful tool for investigating protein mechanisms that complements the existing and the emerging experimental techniques.

Key words.

Protein structure-function mechanismflexibilityatomistic simulationburied waterlipasechaperoneprion

Copyright information

© Birkhäuser Verlag, Basel 2006

Authors and Affiliations

  1. 1.Division of Protein StructureNational Institute for Medical ResearchLondonUnited Kingdom
  2. 2.York Structural Biology LaboratoryUniversity of YorkYorkUnited Kingdom
  3. 3.Bioinformatics InstituteSingaporeSingapore