ArticleBiophysical journal2004
Refinement of F-actin model against fiber diffraction data by long-range normal modes.
Article in Biophysical journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Multiple CaMKII Binding Modes to the Actin Cytoskeleton Revealed by Single-Molecule Imaging.Biophysical journal · 2016Article
- Elastic network models capture the motions apparent within ensembles of RNA structures.RNA (New York, N.Y.) · 2014Article
- Article
- Coarse-grained modeling of the actin filament derived from atomistic-scale simulations.Biophysical journal · 2006Article
- A New Method for Coarse-Grained Elastic Normal-Mode Analysis.Journal of chemical theory and computation · 2006Article
- The role of shape in determining molecular motions.Biophysical journal · 2005Article
- How similar are protein folding and protein binding nuclei? Examination of vibrational motions of energy hot spots and conserved residues.Biophysical journal · 2005Article
- Normal mode-based fitting of atomic structure into electron density maps: application to sarcoplasmic reticulum Ca-ATPase.Biophysical journal · 2005Article
- New advances in normal mode analysis of supermolecular complexes and applications to structural refinement.Current protein & peptide science · 2004Review
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
The atomic model of F-actin was refined against fiber diffraction data using long-range normal modes as adjustable parameters to account for the collective long-range filamentous deformations. To determine the effect of long-range deformations on the refinement, each of the four domains of G-actin was treated as a rigid body. It was found that among all modes, the bending modes make the most significant contributions to the improvement of the refinement. Inclusion of only 7-9 bending modes as adjustable parameters yielded a lowest R-factor of 6.3%. These results demonstrate that employing normal modes as refinement parameters has the advantage of using a small number of adjustable parameters to achieve a good fitting efficiency. Such a refinement procedure may therefore prevent the refinement from overfitting the structural model. More importantly, the results of this study demonstrate that, for any fiber diffraction data, a substantial amount of refinement error is due to long-range deformations, especially the bending, of the filaments. The effects of these intrinsic deformations cannot be easily compensated for by adjusting local structural parameters, and must be properly accounted for in the refinement to achieve improved fit of refined models with experimental diffraction data.
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