| Literature DB >> 20888467 |
Matthew L Baker1, Mariah R Baker, Corey F Hryc, Frank Dimaio.
Abstract
Today, electron cryomicroscopy (cryo-EM) can routinely achieve subnanometer resolutions of complex macromolecular assemblies. From a density map, one can extract key structural and functional information using a variety of computational analysis tools. At subnanometer resolution, these tools make it possible to isolate individual subunits, identify secondary structures, and accurately fit atomic models. With several cryo-EM studies achieving resolutions beyond 5Å, computational modeling and feature recognition tools have been employed to construct backbone and atomic models of the protein components directly from a density map. In this chapter, we describe several common classes of computational tools that can be used to analyze and model subnanometer resolution reconstructions from cryo-EM. A general protocol for analyzing subnanometer resolution density maps is presented along with a full description of steps used in analyzing the 4.3Å resolution structure of Mm-cpn.Entities:
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Year: 2010 PMID: 20888467 PMCID: PMC3107677 DOI: 10.1016/S0076-6879(10)83001-0
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600