New targets and procedures for validating the valence geometry of nucleic acid structures

A Working Group consisting of the co-authors of this paper was established in 2020 to re-evaluate the standard valence geometry used for the validation of nucleic acid structure models in the Protein Data Bank (PDB). This Working Group re-examined the dependence of Cambridge Structural Database (CSD) derived targets on base and sugar type, sugar pucker, and phosphate and glycosidic conformation, before comparing those targets with the geometry of a quality-filtered reference set of nucleic acid crystal structural models held in the PDB. This revealed that the valence bond and angle mean values are close to the CSD targets, but many parameters have highly non-Gaussian or even multimodal distributions. One explanation is the inconsistency of restraints used over time and by different refinement programs. The Working Group recommends a new validation scheme for use by the PDB. For this purpose, we have developed a new three-tier scale for outlier detection-graded as Preferred, Allowed, and Of Concern intervals-based on a combination of quality-curated reference data from the CSD and the PDB. The proposed approach to validation should lead to improved nucleic acid models in (future) PDB-deposited macromolecular structures.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-11-13
DOI
https://doi.org/10.1093/nar/gkaf1335
Citations
1
Primary Topic
Enzyme Structure and Function
Type
article
Field-Weighted Citation Impact
0.52

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New targets and procedures for validating the valence geometry of nucleic acid structures

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New targets and procedures for validating the valence geometry of nucleic acid structures

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article en
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Abstract

A Working Group consisting of the co-authors of this paper was established in 2020 to re-evaluate the standard valence geometry used for the validation of nucleic acid structure models in the Protein Data Bank (PDB). This Working Group re-examined the dependence of Cambridge Structural Database (CSD) derived targets on base and sugar type, sugar pucker, and phosphate and glycosidic conformation, before comparing those targets with the geometry of a quality-filtered reference set of nucleic acid crystal structural models held in the PDB. This revealed that the valence bond and angle mean values are close to the CSD targets, but many parameters have highly non-Gaussian or even multimodal distributions. One explanation is the inconsistency of restraints used over time and by different refinement programs. The Working Group recommends a new validation scheme for use by the PDB. For this purpose, we have developed a new three-tier scale for outlier detection-graded as Preferred, Allowed, and Of Concern intervals-based on a combination of quality-curated reference data from the CSD and the PDB. The proposed approach to validation should lead to improved nucleic acid models in (future) PDB-deposited macromolecular structures.

Nucleic Acids ResearchVol. 54(1)
Rutgers, The State University of New Jersey (US), University of Southern California (US), Lawrence Berkeley National Laboratory (US), Science and Technology Facilities Council (GB), Duke University (US), Vanderbilt University (US), University of Agriculture in Krakow (PL), Czech Academy of Sciences, Institute of Biotechnology (CZ), Oncode Institute (NL), Global Phasing (United Kingdom) (GB), Institute of Bioorganic Chemistry, Polish Academy of Sciences (PL), Poznań University of Technology (PL), Adam Mickiewicz University in Poznań (PL)
UK Research and Innovation, Ministerstvo Školství, Mládeže a Tělovýchovy, Ministerie van Volksgezondheid, Welzijn en Sport, Akademie Věd České Republiky, National Institutes of Health, Biotechnology and Biological Sciences Research Council, Science and Technology Facilities Council
Partnerships for the goals
Openalex Percentile: Top 29%
Enzyme Structure and Function
0.52
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