Evidence map›Paper›PMID 35059023›Full record

ReviewBiophysical reviews2021

Sequence-dependent structural properties of B-DNA: what have we learned in 40 years?

Gabriela da Rosa, Leandro Grille, Victoria Calzada, Katya Ahmad, Juan Pablo Arcon, Federica Battistini, Genís Bayarri, Thomas Bishop, Paolo Carloni, Thomas Cheatham Iii and 16 more

Open access · greenAbstract readReview
In one paragraph

Review in Biophysical reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

19 citing papers in PubMed, 42 citations in OpenAlex.

  1. hexABC seeking the physical code of DNA.Nature communications · 2026
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  16. How acidic amino acid residues facilitate DNA target site selection.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

26 authors at 12 institutions in 9 countries.

Gabriela da Rosa *Computational Biophysics Group, Department of Biological Sciences, CENUR Litoral Norte, Universidad de la República, Salto, Uruguay.
Leandro Grille *Computational Biophysics Group, Department of Biological Sciences, CENUR Litoral Norte, Universidad de la República, Salto, Uruguay.
Victoria Calzada *Radiopharmacy Department, Centro de Investigaciones Nucleares, Universidad de La República, Montevideo, Uruguay.
Katya AhmadComputational Biomedicine, Forschungszentrum Jülich, Jülich, Germany.
Juan Pablo ArconMolecular Modelling and Bioinformatics Group, Institute for Research in Biomedicine, Barcelona, Spain.
Federica BattistiniMolecular Modelling and Bioinformatics Group, Institute for Research in Biomedicine, Barcelona, Spain.
Genís BayarriMolecular Modelling and Bioinformatics Group, Institute for Research in Biomedicine, Barcelona, Spain.
Thomas BishopTheoretical Molecular Biology Lab, Louisiana Tech University, Ruston, LA USA.
Paolo CarloniComputational Biomedicine, Forschungszentrum Jülich, Jülich, Germany.
Thomas Cheatham IiiCollege of Pharmacy, University of Utah, Salt Lake City, UT USA.
Rosana Collepardo-GuevaraComputational Physics of Chromatin, Departments of Chemistry and Genetics, University of Cambridge, Cambridge, UK.
Jacek CzubDeparment of Physical Chemistry, Gdansk University of Technology, Gdansk, Poland.
Jorge R EspinosaComputational Physics of Chromatin, Departments of Chemistry and Genetics, University of Cambridge, Cambridge, UK.
Rodrigo Galindo-MurilloCollege of Pharmacy, University of Utah, Salt Lake City, UT USA.
Sarah A HarrisEngineering and Physical Sciences, University of Leeds, Leeds, UK.
Adam HospitalMolecular Modelling and Bioinformatics Group, Institute for Research in Biomedicine, Barcelona, Spain.
Charles LaughtonSchool of Pharmacy, University of Nottingham, Nottingham, UK.
John H MaddocksLaboratory for Computation and Visualization in Mathematics and Mechanics, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Agnes NoyDeparment of Physics, University of York, York, UK.
Modesto OrozcoMolecular Modelling and Bioinformatics Group, Institute for Research in Biomedicine, Barcelona, Spain.
Marco PasiLaboratory of Biology and Applied Pharmacology, University Paris-Saclay, Cachan, France.
Alberto PérezDepartment of Chemistry, University of Florida, Gainesville, FL USA.
Daiva Petkevičiūtė-GerlachNonlinear Systems Mathematical Research Centre, Kaunas University of Technology, Kaunas, Lithuania.
Rahul SharmaLaboratory for Computation and Visualization in Mathematics and Mechanics, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Ran SunTheoretical Molecular Biology Lab, Louisiana Tech University, Ruston, LA USA.
Pablo D DansComputational Biophysics Group, Department of Biological Sciences, CENUR Litoral Norte, Universidad de la República, Salto, Uruguay.ORCID 0000-0002-5927-372X
Institute for Research in Biomedicine · ESUniversidad de la República de Uruguay · UYÉcole Polytechnique Fédérale de Lausanne · CHForschungszentrum Jülich · DEKaunas University of Technology · LTUniversity of Cambridge · GBUniversity of Nottingham · GBUniversity of Utah · USGdańsk University of Technology · PLLouisiana Tech University · USUniversity of Florida · USUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The structure of B-DNA, the physiological form of the DNA molecule, has been a central topic in biology, chemistry and physics. Far from uniform and rigid, the double helix was revealed as a flexible and structurally polymorphic molecule. Conformational changes that lead to local and global changes in the helix geometry are mediated by a complex choreography of base and backbone rearrangements affecting the ability of the B-DNA to recognize ligands and consequently on its functionality. In this sense, the knowledge obtained from the sequence-dependent structural properties of B-DNA has always been thought crucial to rationalize how ligands and, most notably, proteins recognize B-DNA and modulate its activity, i.e. the structural basis of gene regulation. Honouring the anniversary of the first high-resolution X-ray structure of a B-DNA molecule, in this contribution, we present the most important discoveries of the last 40 years on the sequence-dependent structural and dynamical properties of B-DNA, from the early beginnings to the current frontiers in the field.

Indexed as

Ascona B-DNA ConsortiumDrew-Dickerson dodecamerHelical parametersNearest neighboursStructural polymorphisms

Identifiers

PMID35059023
PMCPMC8724355
OpenAlexW3214018575

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.