Analysis of domain motions by approximate normal mode calculations

Konrad Hinsen 1
1 LDM - Laboratoire de Dynamique Moléculaire
IBS - UMR 5075 - Institut de biologie structurale
Abstract : The identification of dynamical domains in proteins and the description of the low‐frequency domain motions are one of the important applications of numerical simulation techniques. The application of these techniques to large proteins requires a substantial computational effort and therefore cannot be performed routinely, if at all. This article shows how physically motivated approximations permit the calculation of low‐frequency normal modes in a few minutes on standard desktop computers. The technique is based on the observation that the low‐frequency modes, which describe domain motions, are independent of force field details and can be obtained with simplified mechanical models. These models also provide a useful measure for rigidity in proteins, allowing the identification of quasi‐rigid domains. The methods are validated by application to three well‐studied proteins, crambin, lysozyme, and ATCase. In addition to being useful techniques for studying domain motions, the success of the approximations provides new insight into the relevance of normal mode calculations and the nature of the potential energy surface of proteins. Proteins 33:417–429, 1998. © 1998 Wiley‐Liss, Inc.
Document type :
Journal articles
Complete list of metadatas
Contributor : Laëtitia Legoupil <>
Submitted on : Wednesday, June 19, 2019 - 8:39:54 AM
Last modification on : Saturday, June 22, 2019 - 1:45:14 AM

Links full text




Konrad Hinsen. Analysis of domain motions by approximate normal mode calculations. Proteins: Structure, Function, and Genetics, Wiley, 1998, 33 (3), pp.417-429. ⟨10.1002/(SICI)1097-0134(19981115)33:3<417::AID-PROT10>3.0.CO;2-8⟩. ⟨hal-02159766⟩



Record views