issue contents

Journal logoSTRUCTURAL
ISSN: 2059-7983

March 2018 issue

From crystal to structure with CCP4 (Part 2)

Proceedings of the CCP4 Study Weekend edited by Charles Ballard, Mike Hough and Keith Wilson

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research papers

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The ARCIMBOLDO method of phasing through the location of small fragments combined with density modification and autotracing is particularly suited to helical structures, but coiled coils remain challenging. Features designed for solving coiled coils at resolutions of up to 3 Å were tested on a pool of 150 structures.

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A new pipeline to solve structures by molecular replacement with ideal protein fragments is described and benchmarked against two test sets of mixed α/β and all-β folds at relatively high resolution.

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Here, a macromolecule-centred approach to three-dimensional structure determination as implemented in REFMAC5 is considered. The use of restraints to transfer chemical and structural information during macromolecular refinement, and how different sources of information can be combined in order to achieve models that are more consistent with data derived from a variety of experimental techniques, including macromolecular crystallography, cryo-EM and NMR spectroscopy, are discussed.

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Better metrics are required to be able to assess small-molecule ligands in macromolecular structures in Worldwide Protein Data Bank validation reports. The local ligand density fit (LLDF) score currently used to assess ligand electron-density fit outliers produces a substantial number of false positives and false negatives.

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The use of validation metrics to rank macromolecular structures, as well as a web tool to investigate trends in and correlations between different properties and validation metrics, are described.
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