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Crystallogr Rev. 2018;24(4):236-262. doi: 10.1080/0889311X.2018.1521805. Epub 2018 Sep 21.

Refining the macromolecular model - achieving the best agreement with the data from X-ray diffraction experiment.

Author information

1
Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22908, United States.
2
Center for Structural Genomics of Infectious Diseases (CSGID), Charlottesville, VA, 22908, United States.

Abstract

Refinement of macromolecular X-ray crystal structures involves using complex software with hundreds of different settings. The complexity of underlying concepts and the sheer amount sof instructions may make it difficult for less experienced crystallographers to achieve optimal results in their refinements. This tutorial review offers guidelines for choosing the best settings for the reciprocal-space refinement of macromolecular models and provides practical tips for manual model correction. To help aspiring crystallographers navigate the process, some of the most practically important concepts of protein structure refinement are described. Among the topics covered are the use and purpose of R-free, geometrical restraints, restraints on atomic displacement parameters (ADPs), refinement weights, various parametrizations of ADPs (full anisotropic refinement and TLS), and omit maps. We also give practical tips for manual model correction in Coot, modelling of side-chains with poor or missing density, and ligand identification, fitting, and refinement.

KEYWORDS:

X-ray crystallography; ligands; protein crystal structure; refinement; reproducibility; structural biology

PMID:
30416256
PMCID:
PMC6219471
[Available on 2019-09-21]
DOI:
10.1080/0889311X.2018.1521805

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