Evidence map›Paper›PMID 36987885›Full record

ArticleNucleic acids research2023

CircularSTAR3D: a stack-based RNA 3D structural alignment tool for circular matching.

Xiaoli Chen, Shaojie Zhang

Abstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

2 authors.

Xiaoli ChenDepartment of Computer Science, University of Central Florida, Orlando, FL 32816, USA.ORCID 0000-0001-9215-6886
Shaojie ZhangDepartment of Computer Science, University of Central Florida, Orlando, FL 32816, USA.ORCID 0000-0002-4051-5549

Funding

RNA Structural Motif Analysis Revisited: Towards a Systematic Understanding of Noncoding RNA as Modular BiomoleculesR01GM102515 · NIGMS · UNIVERSITY OF CENTRAL FLORIDA · PI ZHANG, SHAOJIE, ZHONG, CUNCONG · 2012 to 2025
$2.3M
NIGMS NIH HHS R01 GM102515NIH HHS R01GM102515
6 · The paper itself

Abstract

The functions of non-coding RNAs usually depend on their 3D structures. Therefore, comparing RNA 3D structures is critical in analyzing their functions. We noticed an interesting phenomenon that two non-coding RNAs may share similar substructures when rotating their sequence order. To the best of our knowledge, no existing RNA 3D structural alignment tools can detect this type of matching. In this article, we defined the RNA 3D structure circular matching problem and developed a software tool named CircularSTAR3D to solve this problem. CircularSTAR3D first uses the conserved stacks (consecutive base pairs with similar 3D structures) in the input RNAs to identify the circular matched internal loops and multiloops. Then it performs a local extension iteratively to obtain the whole circular matched substructures. The computational experiments conducted on a non-redundant RNA structure dataset show that circular matching is ubiquitous. Furthermore, we demonstrated the utility of CircularSTAR3D by detecting the conserved substructures missed by regular alignment tools, including structural motifs and conserved structures between riboswitches and ribozymes from different classes. We anticipate CircularSTAR3D to be a valuable supplement to the existing RNA 3D structural analysis techniques.

Indexed as

Nucleic Acid ConformationRNASequence AlignmentSequence Analysis, RNASoftwareAlgorithmsBase PairingRNA

Identifiers

PMID36987885
PMCPMC10201423

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Registered trials

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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.