Evidence map›Paper›PMID 36632613›Full record

ArticleNAR genomics and bioinformatics2023

Identification and characterization of RNA pentaloop sequence families.

MdSharear Saon, Charles C Kirkpatrick, Brent M Znosko

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

MdSharear SaonDepartment of Chemistry, Saint Louis University, Saint Louis, MO 63103, USA.
Charles C KirkpatrickDepartment of Chemistry, Saint Louis University, Saint Louis, MO 63103, USA.
Brent M ZnoskoDepartment of Chemistry, Saint Louis University, Saint Louis, MO 63103, USA.ORCID https://orcid.org/0000-0002-6823-6218

Funding

Understanding the Thermodynamics and Structure of RNA Secondary Structure MotifsR15GM085699 · NIGMS · SAINT LOUIS UNIVERSITY · PI ZNOSKO, BRENT · 2009 to 2025
$2.0M
NIGMS NIH HHS R15 GM085699
6 · The paper itself

Abstract

One of the current methods for predicting RNA tertiary structure is fragment-based homology, which predicts tertiary structure from secondary structure. For a successful prediction, this method requires a library of the tertiary structures of small motifs clipped from previously solved RNA 3D structures. Because of the limited number of available tertiary structures, it is not practical to find structures for all sequences of all motifs. Identifying sequence families for motifs can fill the gaps because all sequences within a family are expected to have similar structural features. Currently, a collection of well-characterized sequence families has been identified for tetraloops. Because of their prevalence and biological functions, pentaloop structures should also be well-characterized. In this study, 10 pentaloop sequence families are identified. For each family, the common and distinguishing structural features are highlighted. These sequence families can be used to predict the tertiary structure of pentaloop sequences for which a solved structure is not available.

Identifiers

PMID36632613
PMCPMC9830547

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.