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Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank

As the number of macromolecular structures in the worldwide Protein Data Bank (wwPDB) continues to grow rapidly, more attention is being paid to the quality of its data, especially for use in aggregated structural and dynamics analyses. In this study, we systematically analyzed 3.5 Å regions around...

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Autores principales: Yao, Sen, Moseley, Hunter N.B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751499/
https://www.ncbi.nlm.nih.gov/pubmed/31480623
http://dx.doi.org/10.3390/molecules24173179
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author Yao, Sen
Moseley, Hunter N.B.
author_facet Yao, Sen
Moseley, Hunter N.B.
author_sort Yao, Sen
collection PubMed
description As the number of macromolecular structures in the worldwide Protein Data Bank (wwPDB) continues to grow rapidly, more attention is being paid to the quality of its data, especially for use in aggregated structural and dynamics analyses. In this study, we systematically analyzed 3.5 Å regions around all metal ions across all PDB entries with supporting electron density maps available from the PDB in Europe. All resulting metal ion-centric regions were evaluated with respect to four quality-control criteria involving electron density resolution, atom occupancy, symmetry atom exclusion, and regional electron density discrepancy. The resulting list of metal binding sites passing all four criteria possess high regional structural quality and should be beneficial to a wide variety of downstream analyses. This study demonstrates an approach for the pan-PDB evaluation of metal binding site structural quality with respect to underlying X-ray crystallographic experimental data represented in the available electron density maps of proteins. For non-crystallographers in particular, we hope to change the focus and discussion of structural quality from a global evaluation to a regional evaluation, since all structural entries in the wwPDB appear to have both regions of high and low structural quality.
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spelling pubmed-67514992019-09-27 Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank Yao, Sen Moseley, Hunter N.B. Molecules Article As the number of macromolecular structures in the worldwide Protein Data Bank (wwPDB) continues to grow rapidly, more attention is being paid to the quality of its data, especially for use in aggregated structural and dynamics analyses. In this study, we systematically analyzed 3.5 Å regions around all metal ions across all PDB entries with supporting electron density maps available from the PDB in Europe. All resulting metal ion-centric regions were evaluated with respect to four quality-control criteria involving electron density resolution, atom occupancy, symmetry atom exclusion, and regional electron density discrepancy. The resulting list of metal binding sites passing all four criteria possess high regional structural quality and should be beneficial to a wide variety of downstream analyses. This study demonstrates an approach for the pan-PDB evaluation of metal binding site structural quality with respect to underlying X-ray crystallographic experimental data represented in the available electron density maps of proteins. For non-crystallographers in particular, we hope to change the focus and discussion of structural quality from a global evaluation to a regional evaluation, since all structural entries in the wwPDB appear to have both regions of high and low structural quality. MDPI 2019-09-01 /pmc/articles/PMC6751499/ /pubmed/31480623 http://dx.doi.org/10.3390/molecules24173179 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yao, Sen
Moseley, Hunter N.B.
Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank
title Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank
title_full Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank
title_fullStr Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank
title_full_unstemmed Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank
title_short Finding High-Quality Metal Ion-Centric Regions Across the Worldwide Protein Data Bank
title_sort finding high-quality metal ion-centric regions across the worldwide protein data bank
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751499/
https://www.ncbi.nlm.nih.gov/pubmed/31480623
http://dx.doi.org/10.3390/molecules24173179
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