Comparisons of experimental and computed protein anisotropic temperature factors
- 18 November 2008
- journal article
- research article
- Published by Wiley in Proteins-Structure Function and Bioinformatics
- Vol. 76 (1), 164-175
- https://doi.org/10.1002/prot.22328
Abstract
Because of its appealing simplicity, the anisotropic network model (ANM) has been widely accepted and applied to study many molecular motion problems: such as ribosome motions, the molecular mechanisms of GroEL‐GroES function, allosteric changes in hemoglobin, motor‐protein motions, and conformational changes in general. However, the validity of the ANM has not been closely examined. In this work, we use ANM to predict the anisotropic temperature factors of proteins obtained from X‐ray and NMR data. The rich, directional anisotropic temperature factor data available for hundreds of proteins in the protein data bank are used as validation data to closely test the ANM model. The significance of this work is that it presents a timely, important evaluation of the model, shows the extent of its accuracy in reproducing experimental anisotropic temperature factors, and suggests ways to improve the model. An improved model will help us better understand the internal dynamics of proteins, which in turn can greatly expand the usefulness of the models, which has already been demonstrated in many applications. Proteins 2009.Keywords
Funding Information
- NIH (1R01GM072014)
- NSF (CNS-0521568)
This publication has 35 references indexed in Scilit:
- Close Correspondence between the Motions from Principal Component Analysis of Multiple HIV-1 Protease Structures and Elastic Network ModesStructure, 2008
- Ensemble Refinement of Protein Crystal Structures: Validation and ApplicationStructure, 2007
- Normal-Mode Refinement of Anisotropic Thermal Parameters for Potassium Channel KcsA at 3.2 Å Crystallographic ResolutionStructure, 2007
- vGNM: A Better Model for Understanding the Dynamics of Proteins in CrystalsJournal of Molecular Biology, 2007
- Insights into Equilibrium Dynamics of Proteins from Comparison of NMR and X-Ray Data with Computational PredictionsStructure, 2007
- Normal mode refinement of anisotropic thermal parameters for a supramolecular complex at 3.42-Å crystallographic resolutionProceedings of the National Academy of Sciences, 2007
- Protein Structural Variation in Computational Models and Crystallographic DataStructure, 2007
- The Extent of Cooperativity of Protein Motions Observed with Elastic Network Models Is Similar for Atomic and Coarser-Grained ModelsJournal of Chemical Theory and Computation, 2006
- The Protein Data BankNucleic Acids Research, 2000
- On the rigid-body motion of molecules in crystalsActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1968