Evidence map›Paper›PMID 26184874›Full record

ArticleNucleic acids research2015

DSSR: an integrated software tool for dissecting the spatial structure of RNA.

Xiang-Jun Lu, Harmen J Bussemaker, Wilma K Olson

Abstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 218 papers.

0numbers the graph read from it
0cells of the map it votes in
218citing 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

218 citing papers in PubMed.

  1. Article
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  5. Crystal Structure of Trabectedin-DNA Complex.Journal of molecular biology · 2026
    Article
  6. Article
  7. RNAViruses · 2026
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  9. Article
  10. Article
  11. Article
  12. De novo design of RNA pseudoknots with deep learning.bioRxiv : the preprint server for biology · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

158 more citing papers are in PubMed but not listed here.

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.

Xiang-Jun LuDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA xiangjun@x3dna.org.
Harmen J BussemakerDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA Department of Systems Biology, Columbia University, New York, NY 10032, USA.
Wilma K OlsonDepartment of Chemistry and Chemical Biology, Rutgers - The State University of New Jersey, Piscataway, NJ 08854, USA.

Funding

Inferring regulatory circuitry from microarray dataR01HG003008 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BUSSEMAKER, HARMEN J · 2004 to 2020
$7.0M
THEORETICFAL ASPECTS OF DNA SUPERCOILINGR01GM034809 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI OLSON, WILMA K · 1985 to 2019
$4.6M
Continued Development and Maintenance of the 3DNA Suite of ProgramsR01GM096889 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI LU, XIANG-JUN · 2011 to 2019
$2.2M
NHGRI NIH HHS R01HG003008NIGMS NIH HHS R01 GM034809NIGMS NIH HHS R01GM034809NIGMS NIH HHS R01 GM096889NIGMS NIH HHS R01GM096889
6 · The paper itself

Abstract

Insight into the three-dimensional architecture of RNA is essential for understanding its cellular functions. However, even the classic transfer RNA structure contains features that are overlooked by existing bioinformatics tools. Here we present DSSR (Dissecting the Spatial Structure of RNA), an integrated and automated tool for analyzing and annotating RNA tertiary structures. The software identifies canonical and noncanonical base pairs, including those with modified nucleotides, in any tautomeric or protonation state. DSSR detects higher-order coplanar base associations, termed multiplets. It finds arrays of stacked pairs, classifies them by base-pair identity and backbone connectivity, and distinguishes a stem of covalently connected canonical pairs from a helix of stacked pairs of arbitrary type/linkage. DSSR identifies coaxial stacking of multiple stems within a single helix and lists isolated canonical pairs that lie outside of a stem. The program characterizes 'closed' loops of various types (hairpin, bulge, internal, and junction loops) and pseudoknots of arbitrary complexity. Notably, DSSR employs isolated pairs and the ends of stems, whether pseudoknotted or not, to define junction loops. This new, inclusive definition provides a novel perspective on the spatial organization of RNA. Tests on all nucleic acid structures in the Protein Data Bank confirm the efficiency and robustness of the software, and applications to representative RNA molecules illustrate its unique features. DSSR and related materials are freely available at http://x3dna.org/.

Indexed as

SoftwareCRISPR-Associated ProteinsDatabases, ProteinDNAMolecular Sequence AnnotationNucleic Acid ConformationRiboswitchRNARNA, CatalyticRNA, FungalRNA, Transfer, PheRNA, ViralCRISPR-Associated ProteinsDNARiboswitchRNARNA, CatalyticRNA, FungalRNA, Transfer, PheRNA, Viral

Identifiers

PMID26184874
PMCPMC4666379

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.