Evidence map›Paper›PMID 40601258›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

CNN-Meth: A Tool to Accurately Predict Lysine Methylation Sites Using Evolutionary Information-Based Protein Modeling.

Austin Spadaro, Alok Sharma, Iman Dehzangi

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Austin SpadaroCenter for Computational and Integrative Biology, Rutgers University, Camden, NJ, USA.
Alok SharmaInstitute for Integrated and Intelligent Systems, Griffith University, Brisbane, Australia.
Iman DehzangiCenter for Computational and Integrative Biology, Rutgers University, Camden, NJ, USA. i.dehzangi@rutgers.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lysine methylation is a crucial posttranslational modification influencing both histone and nonhistone protein functions. Disruptions in lysine methyltransferase activity are linked to numerous diseases, including various cancers and developmental disorders. Accurate identification of lysine methylation sites is essential for early diagnosis and therapeutic development. Here, we present CNN-Meth, a newly developed Web-based utility that employs a convolutional neural network (CNN) to predict lysine methylation sites. CNN-Meth leverages evolutionary, structural, and physicochemical data alongside binary encoding for its training process. Evolutionary and structural features used to build CNN-Meth are extracted using protein modeling, which works similarly to using Protein Language Models (PLM). Unlike traditional approaches that rely on manually extracted features, CNN-Meth uses CNNs for automated feature extraction, ensuring minimal information loss. This novel methodology enhances prediction accuracy, achieving 96.0% Accuracy, 85.1% Sensitivity, 96.4% Specificity, and a Matthew's Correlation Coefficient (MCC) of 0.65. This demonstrates the possible effectiveness of using PLM to predict Methylation sites as a future direction. The CNN-Meth tool and its source code are readily accessible at https://github.com/MLBC-lab/CNN-Meth , providing a robust resource for researchers and clinicians.

Indexed as

Computational BiologyLysineNeural Networks, ComputerProteinsSoftwareEvolution, MolecularHumansMethylationModels, MolecularProtein Processing, Post-TranslationalLysineProteinsAutomated feature extractionConvolutional neural networkEvolutionary featuresMethylationPhysicochemical featuresPosttranslational modificationStructural features

Identifiers

What OpenQuestion holds

Textmetadata
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.