| Literature DB >> 21875597 |
Abstract
Cofilin is a key actin-binding protein that is critical for controlling the assembly of actin within the cell. Here, we present the results of molecular docking and dynamics studies using a muscle actin filament and human cofilin I. Guided by extensive mutagenesis results and other biophysical and structural studies, we arrive at a model for cofilin bound to the actin filament. This predicted structure agrees very well with electron microscopy results for cofilin-decorated filaments, provides molecular insight into how the known F- and G-actin sites on cofilin interact with the filament, and also suggests new interaction sites that may play a role in cofilin binding. The resulting atomic-scale model also helps us understand the molecular function and regulation of cofilin and provides testable data for future experimental and simulation work.Entities:
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Year: 2011 PMID: 21875597 PMCID: PMC3184344 DOI: 10.1016/j.jmb.2011.08.039
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469