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 Experiment Videos

DPP-PseAAC: A DNA-binding protein prediction model using Chou's general PseAAC.

M Saifur Rahman1, Swakkhar Shatabda2, Sanjay Saha3

  • 1Department of CSE, BUET, ECE Building, West Palasi, Dhaka 1205, Bangladesh.

Journal of Theoretical Biology
|May 14, 2018
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Trainable clustering framework for spatial transcriptomics.

Bioinformatics advances·2026
Same author

TextEconomizer: Enhancing lossy text compression with denoising transformers and entropy coding.

Neural networks : the official journal of the International Neural Network Society·2026
Same author

Protocol for spatially resolved pathology scores using optimal transport on spatial transcriptomics data.

STAR protocols·2026
Same author

Validation of remote multimodal AI screening for Parkinson disease across diverse settings.

Communications medicine·2026
Same author

The good, the bad, and the ugly: opportunities, challenges, and pitfalls in spatial proteomics modeling.

Briefings in bioinformatics·2026
Same author

ORANGE: a machine learning approach for modeling tissue-specific aging from transcriptomic data.

Briefings in bioinformatics·2026

A new computational model, DPP-PseAAC, accurately predicts DNA-binding proteins (DNA-BPs) directly from protein sequences. This method offers an efficient alternative to costly experimental identification, improving prediction accuracy significantly.

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Molecular Biology

Background:

  • Experimental identification of DNA-binding proteins (DNA-BPs) is costly and time-consuming.
  • There is a need for fast and accurate computational methods to predict DNA-BP interactions.
  • Protein sequences contain inherent information for predicting DNA-binding capabilities.

Purpose of the Study:

  • To develop an efficient and accurate computational model for identifying DNA-binding proteins.
  • To extract predictive features directly from protein sequences, avoiding reliance on structural or domain information.
  • To establish a novel predictor named DNA-binding Protein Prediction model using Chou's general PseAAC (DPP-PseAAC).

Main Methods:

  • Feature extraction directly from protein sequences.
Keywords:
ClassificationDNA bindingPredictionPseAACRandom ForestSupport Vector Machine

Related Experiment Videos

  • Utilized Random Forest (RF) for feature ranking.
  • Employed Recursive Feature Elimination (RFE) for optimal feature selection.
  • Trained a Support Vector Machine (SVM) with a linear kernel for prediction.
  • Main Results:

    • The proposed DPP-PseAAC model demonstrated superior performance over existing state-of-the-art predictors.
    • Achieved high accuracy rates: 93.21% (10-fold cross-validation), 95.91% (jackknife test), and 77.42% (independent test).
    • The model effectively identifies DNA-binding proteins based solely on sequence information.

    Conclusions:

    • DPP-PseAAC provides a highly accurate and efficient computational approach for DNA-BP identification.
    • The method's reliance on sequence data makes it broadly applicable.
    • Source code and a web interface are available for public use, facilitating further research and application.