Evidence map›Paper›PMID 25004957›Full record

ArticleActa crystallographica. Section D, Biological crystallography2014

Phosphates in the Z-DNA dodecamer are flexible, but their P-SAD signal is sufficient for structure solution.

Zhipu Luo, Miroslawa Dauter, Zbigniew Dauter

Abstract read
In one paragraph

Article in Acta crystallographica. Section D, Biological crystallography, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Review
  2. Crystal structure of a tRNA acceptor-stem mimic at 1.94 Å resolution.Acta crystallographica. Section F, Structural biology communications · 2026
    Article
  3. Extracellular DNA-protein interactions.Current opinion in structural biology · 2024
    Review
  4. Structure and Formation of Z-DNA and Z-RNA.Molecules (Basel, Switzerland) · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Phosphorus and sulfur SAD phasing of the nucleic acid-bound DNA-binding domain of interferon regulatory factor 4.Acta crystallographica. Section F, Structural biology communications · 2021
    Article
  9. Article
  10. Article
  11. Accurate geometrical restraints for Watson-Crick base pairs.Acta crystallographica Section B, Structural science, crystal engineering and materials · 2019
    Article
  12. Review
  13. Four highly pseudosymmetric and/or twinned structures of d(CGCGCG)Acta crystallographica. Section D, Structural biology · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. High-resolution crystal structure of Z-DNA in complex with Cr(3+) cations.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2015
    Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Zhipu LuoSynchrotron Radiation Research Section, Macromolecular Crystallography Laboratory, National Cancer Institute, Argonne National Laboratory, Argonne, IL 60439, USA.
Miroslawa DauterLeidos Biomedical Research Inc., Basic Research Program, Argonne National Laboratory, Argonne, IL 60439, USA.
Zbigniew DauterSynchrotron Radiation Research Section, Macromolecular Crystallography Laboratory, National Cancer Institute, Argonne National Laboratory, Argonne, IL 60439, USA.

Funding

Intramural NIH HHSNCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400
6 · The paper itself

Abstract

A large number of Z-DNA hexamer duplex structures and a few oligomers of different lengths are available, but here the first crystal structure of the d(CGCGCGCGCGCG)2 dodecameric duplex is presented. Two synchrotron data sets were collected; one was used to solve the structure by the single-wavelength anomalous dispersion (SAD) approach based on the anomalous signal of P atoms, the other set, extending to an ultrahigh resolution of 0.75 Å, served to refine the atomic model to an R factor of 12.2% and an R(free) of 13.4%. The structure consists of parallel duplexes arranged into practically infinitely long helices packed in a hexagonal fashion, analogous to all other known structures of Z-DNA oligomers. However, the dodecamer molecule shows a high level of flexibility, especially of the backbone phosphate groups, with six out of 11 phosphates modeled in double orientations corresponding to the two previously observed Z-DNA conformations: Z(I), with the phosphate groups inclined towards the inside of the helix, and Z(II), with the phosphate groups rotated towards the outside of the helix.

Indexed as

Nucleic Acid ConformationBiopolymersCrystallography, X-RayDNA, Z-FormModels, MolecularPhosphatesBiopolymersDNA, Z-FormPhosphatesflexibility of phosphate groupsphosphorus SAD phasingultrahigh resolutionZ-DNA dodecamerZ-DNA structure

Identifiers

PMID25004957
PMCPMC4089481

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.