Evidence map›Paper›PMID 27125735›Full record

ReviewMethods (San Diego, Calif.)2016

The RNA 3D Motif Atlas: Computational methods for extraction, organization and evaluation of RNA motifs.

Lorena G Parlea, Blake A Sweeney, Maryam Hosseini-Asanjan, Craig L Zirbel, Neocles B Leontis

Abstract readReview
In one paragraph

Review in Methods (San Diego, Calif.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. RNA Structure and Its Function.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  3. Article
  4. Article
  5. RNA Structure: Past, Future, and Gene Therapy Applications.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Automated 3D Design and Evaluation of RNA Nanostructures with RNAMake.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  10. RNAloops: a database of RNA multiloops.Bioinformatics (Oxford, England) · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Alternate RNA Structures.Cold Spring Harbor perspectives in biology · 2020
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

5 authors.

Lorena G ParleaDepartment of Biological Sciences, Bowling Green State University, Bowling Green, OH 43403, USA. Electronic address: lorenan@bgsu.edu.
Blake A SweeneyDepartment of Biological Sciences, Bowling Green State University, Bowling Green, OH 43403, USA. Electronic address: bsweene@bgsu.edu.
Maryam Hosseini-AsanjanDepartment of Chemistry, Bowling Green State University, Bowling Green, OH 43403, USA.
Craig L ZirbelDepartment of Mathematics and Statistics, Bowling Green State University, Bowling Green, OH 43403, USA. Electronic address: zirbel@bgsu.edu.
Neocles B LeontisDepartment of Chemistry, Bowling Green State University, Bowling Green, OH 43403, USA. Electronic address: leontis@bgsu.edu.

Funding

RNA 3D Motif Search, Atlas, and Prediction from SequenceR01GM085328 · NIGMS · BOWLING GREEN STATE UNIVERSITY · PI ZIRBEL, CRAIG L · 2010 to 2023
$4.0M
NIGMS NIH HHS R01 GM085328
6 · The paper itself

Abstract

RNA 3D motifs occupy places in structured RNA molecules that correspond to the hairpin, internal and multi-helix junction "loops" of their secondary structure representations. As many as 40% of the nucleotides of an RNA molecule can belong to these structural elements, which are distinct from the regular double helical regions formed by contiguous AU, GC, and GU Watson-Crick basepairs. With the large number of atomic- or near atomic-resolution 3D structures appearing in a steady stream in the PDB/NDB structure databases, the automated identification, extraction, comparison, clustering and visualization of these structural elements presents an opportunity to enhance RNA science. Three broad applications are: (1) identification of modular, autonomous structural units for RNA nanotechnology, nanobiology and synthetic biology applications; (2) bioinformatic analysis to improve RNA 3D structure prediction from sequence; and (3) creation of searchable databases for exploring the binding specificities, structural flexibility, and dynamics of these RNA elements. In this contribution, we review methods developed for computational extraction of hairpin and internal loop motifs from a non-redundant set of high-quality RNA 3D structures. We provide a statistical summary of the extracted hairpin and internal loop motifs in the most recent version of the RNA 3D Motif Atlas. We also explore the reliability and accuracy of the extraction process by examining its performance in clustering recurrent motifs from homologous ribosomal RNA (rRNA) structures. We conclude with a summary of remaining challenges, especially with regard to extraction of multi-helix junction motifs.

Indexed as

AnimalsBase PairingComputer SimulationDatabases, Nucleic AcidHumansModels, MolecularNucleic Acid ConformationNucleotide MotifsRNASoftwareRNAHairpin loopInternal loopMulti-helix junction loopNon-Watson-Crick basepairRNA 3D MotifStructured RNA molecules

Identifiers

PMID27125735
PMCPMC4921307

What OpenQuestion holds

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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.