Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Improving Translational Accuracy02:07

Improving Translational Accuracy

14.0K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
14.0K
Transfer RNA Synthesis02:36

Transfer RNA Synthesis

13.1K
One of the unique features of tRNA is the presence of modified bases. In some tRNAs, modified bases account for nearly 20% of the total bases in the molecule. Altogether, these unusual bases protect the tRNA from enzymatic degradation by RNases.
Each of these chemical modifications is carried by a specific enzyme, post-transcription. All of these enzymes have unique base and site-specificity. Methylation, the most common chemical modification, is carried by at least nine different enzymes, with...
13.1K
Nucleic Acid Structure01:25

Nucleic Acid Structure

8.4K
The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
DNA Structure
DNA...
8.4K
RNA-seq03:21

RNA-seq

11.7K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
11.7K
DNA Base Pairing02:27

DNA Base Pairing

32.8K
Erwin Chargaff’s rules on DNA equivalence paved the way for the discovery of base pairing in DNA. Chargaff’s rules state that in a double-stranded DNA molecule,
32.8K
DNA Base Pairing02:27

DNA Base Pairing

31.4K
31.4K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

ORIGAMI: Orientation-Aware Graph Neural Network for Assessing Multimeric Interfaces of Protein Complex Structures.

Journal of chemical information and modeling·2026
Same author

RNAbpFlow: base pair-augmented SE(3) flow matching for conditional RNA 3D structure generation.

Nature methods·2026
Same author

ORIGAMI: Orientation-Aware Graph Neural Network for Assessing Multimeric Interfaces of Protein Complex Structures.

bioRxiv : the preprint server for biology·2026
Same author

xBind: an integrated webserver for large language model-enabled cross-molecular protein binding site prediction.

Nucleic acids research·2026
Same author

PARSEbp: pairwise agreement-based RNA scoring with emphasis on base pairings.

Bioinformatics advances·2026
Same author

A protocol for single-sequence protein-RNA complex structure prediction using ProRNA3D-single.

STAR protocols·2026

Related Experiment Video

Updated: Jan 10, 2026

A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA
13:00

A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA

Published on: December 2, 2009

12.2K

PARSEbp: Pairwise Agreement-based RNA Scoring with Emphasis on Base Pairings.

Sumit Tarafder1, Debswapna Bhattacharya1

  • 1Department of Computer Science, Virginia Tech, Blacksburg, Virginia, 24061, USA.

Biorxiv : the Preprint Server for Biology
|November 24, 2025
PubMed
Summary

PARSEbp is a new multi-model RNA scoring method that improves RNA 3D structure prediction by considering both 3D structural agreement and 2D base pairing consistency. It outperforms existing methods in ranking RNA conformational ensembles.

Keywords:
RNA 3D structure predictionRNA scoring functionbase pairingstructural ensemble

More Related Videos

RNA Secondary Structure Prediction Using High-throughput SHAPE
13:42

RNA Secondary Structure Prediction Using High-throughput SHAPE

Published on: May 31, 2013

32.1K
Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen
11:32

Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen

Published on: May 24, 2017

12.6K

Related Experiment Videos

Last Updated: Jan 10, 2026

A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA
13:00

A Rapid High-throughput Method for Mapping Ribonucleoproteins RNPs on Human pre-mRNA

Published on: December 2, 2009

12.2K
RNA Secondary Structure Prediction Using High-throughput SHAPE
13:42

RNA Secondary Structure Prediction Using High-throughput SHAPE

Published on: May 31, 2013

32.1K
Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen
11:32

Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen

Published on: May 24, 2017

12.6K

Area of Science:

  • Computational Biology
  • Structural Biology
  • Bioinformatics

Background:

  • Accurate scoring of RNA 3D structures is crucial for RNA structure prediction and conformational sampling.
  • Existing single-model scoring methods struggle to capture the consensus within an ensemble, hindering model selection.
  • There is a need for advanced multi-model scoring approaches to enhance RNA structure prediction fidelity.

Purpose of the Study:

  • To introduce PARSEbp, a novel multi-model RNA scoring method designed for high-fidelity RNA 3D structure evaluation.
  • To address the limitations of single-model scoring by integrating ensemble-level structural information.
  • To improve the accuracy and efficiency of RNA conformational sampling and model selection.

Main Methods:

  • PARSEbp integrates pairwise structural agreement across a conformational ensemble with base pairing consistency.
  • It leverages alignment-based global 3D structural agreement and 2D base pairing information.
  • A consensus similarity matrix is constructed to compute per-structure accuracy scores.

Main Results:

  • PARSEbp significantly outperforms existing single- and multi-model RNA scoring functions on CASP16 RNA targets.
  • The method demonstrates superior performance compared to traditional statistical potentials, deep learning methods, and consensus approaches.
  • Evaluation across diverse metrics confirms the effectiveness of PARSEbp in RNA structure scoring.

Conclusions:

  • PARSEbp offers a fast and effective solution for multi-model RNA scoring, enhancing RNA structure prediction.
  • The integration of 3D and 2D structural information provides a more comprehensive scoring mechanism.
  • PARSEbp represents a significant advancement in computational approaches for RNA structural analysis.