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 Video

Updated: May 21, 2026

Computational Prediction of Amino Acid Preferences of Potentially Multispecific Peptide-Binding Domains Involved in Protein-Protein Interactions
06:50

Computational Prediction of Amino Acid Preferences of Potentially Multispecific Peptide-Binding Domains Involved in Protein-Protein Interactions

Published on: January 26, 2024

KmalPred: a deep learning framework for lysine malonylation site prediction using protein language model

Shihu Jiao1,2, Chunyan Ao1,2, Quan Zou1,2

  • 1Yangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.

BMC Biology
|May 20, 2026
PubMed
Summary

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

DiffuScope: A diffusion-regularized autoencoder for spatial transcriptomic clustering.

Computational biology and chemistry·2025
Same author

YModPred: an interpretable prediction method for multi-type RNA modification sites in S. cerevisiae based on deep learning.

BMC biology·2025
Same author

Feadm5C: Enhancing prediction of RNA 5-Methylcytosine modification sites with physicochemical molecular graph features.

Genomics·2025
Same author

Elevating VAPB-PTPIP51 integration repairs damaged mitochondria-associated endoplasmic reticulum membranes and inhibits lung fibroblasts activation.

International immunopharmacology·2025
Same author

Biological Sequence Classification: A Review on Data and General Methods.

Research (Washington, D.C.)·2024
Same author

Identification of histone acetylation modification sites in the striatum of subchronically manganese-exposed rats.

Epigenomics·2024
This summary is machine-generated.

KmalPred, a new deep learning tool, accurately predicts lysine malonylation sites by analyzing full protein sequences. This method improves upon existing predictors, aiding research into metabolic regulation and post-translational modifications.

Area of Science:

  • Biochemistry
  • Computational Biology
  • Proteomics

Background:

  • Lysine malonylation (Kmal) is a crucial reversible post-translational modification impacting metabolic regulation.
  • Experimental identification of Kmal sites is challenging due to its labor-intensive and time-consuming nature.
  • Current computational methods often miss long-range protein information.

Purpose of the Study:

  • To develop an advanced computational tool for accurate Kmal site prediction.
  • To overcome limitations of existing predictors by incorporating global protein context.

Main Methods:

  • Developed KmalPred, a deep learning framework utilizing ProtT5-derived residue representations and a bidirectional LSTM.
  • Implemented a sequence-first approach, encoding the entire protein before extracting lysine-centered windows.
Keywords:
Data imbalanceLong short-term memory networkLysine malonylationProtein language modelSequence representation

More Related Videos

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
08:48

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays

Published on: November 29, 2014

Related Experiment Videos

Last Updated: May 21, 2026

Computational Prediction of Amino Acid Preferences of Potentially Multispecific Peptide-Binding Domains Involved in Protein-Protein Interactions
06:50

Computational Prediction of Amino Acid Preferences of Potentially Multispecific Peptide-Binding Domains Involved in Protein-Protein Interactions

Published on: January 26, 2024

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
08:48

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays

Published on: November 29, 2014

  • Leveraged full-sequence encoding to preserve global context and enhance efficiency.
  • Main Results:

    • KmalPred achieved 0.78 accuracy and 0.56 MCC on an independent test set, outperforming existing predictors.
    • The sequence-first strategy demonstrated superior performance compared to conventional segment-first methods.
    • ProtT5 representations proved more informative than other protein language models, with stable performance under class imbalance.

    Conclusions:

    • KmalPred offers an effective and robust solution for large-scale Kmal site prediction.
    • Full-sequence protein language model representations are valuable for predicting post-translational modifications.
    • The KmalPred framework is adaptable for predicting other post-translational modification sites.