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Current developments in <i>Coot</i> for macromolecular model building of Electron Cryo‐microscopy and Crystallographic Data

Protein Science · 2019 · Vol. 29(4) · pp. 1055–1064
Ana CasañalBernhard LohkampPaul Emsley

Abstract

Coot is a tool widely used for model building, refinement, and validation of macromolecular structures. It has been extensively used for crystallography and, more recently, improvements have been introduced to aid in cryo-EM model building and refinement, as cryo-EM structures with resolution ranging 2.5-4 A are now routinely available. Model building into these maps can be time-consuming and requires experience in both biochemistry and building into low-resolution maps. To simplify and expedite the model building task, and minimize the needed expertise, new tools are being added in Coot. Some examples include morphing, Geman-McClure restraints, full-chain refinement, and Fourier-model based residue-type-specific Ramachandran restraints. Here, we present the current state-of-the-art in Coot usage.

Enzyme Structure and FunctionAdvanced Electron Microscopy Techniques and ApplicationsProtein Structure and DynamicsMorphingModel buildingComputer scienceCrystallographyArtificial intelligencePhysicsChemistry

MeSH terms

Models, MolecularSoftwareCrystallography, X-RayCryoelectron MicroscopyMacromolecular Substances

Funding

  • European Molecular Biology Organization
  • UK Research and Innovation
  • European Commission
  • Medical Research Council Canada
  • Röntgen-Ångström Cluster
  • Medical Research Council
  • FP7 People: Marie-Curie Actions
Citations
827
FWCI
23.39
field-weighted impact
References
52
Percentile
100%
vs. same field & year
Citations per year
References
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Proteins Structure Function and Bioinformatics · 2003 · 4,581 citations
<i>Phaser</i>crystallographic software
Journal of Applied Crystallography · 2007 · 20,684 citations
DrugBank 5.0: a major update to the DrugBank database for 2018
Nucleic Acids Research · 2017 · 8,622 citations
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