Evidence map›Paper›PMID 42599970›Full record

ArticlePLoS computational biology2026

CLASPP: A unified model for predicting post-translational modifications.

Nathan Gravel, Zhongliang Zhou, Ruili Fang, Austin Downes, Saber Soleymani, Natarajan Kannan

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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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

5 · Who and what money

Authors and funding

6 authors.

Nathan GravelInstitute of Bioinformatics, University of Georgia, Atlanta, Georgia, United States of America.
Zhongliang ZhouSchool of Computing, University of Georgia, Atlanta, Georgia, United States of America.ORCID 0000-0003-4471-6759
Ruili FangSchool of Computing, University of Georgia, Atlanta, Georgia, United States of America.
Austin DownesSchool of Computing, University of Georgia, Atlanta, Georgia, United States of America.
Saber SoleymaniInstitute for Insight, Georgia State University, Atlanta, Georgia, United States of America.
Natarajan KannanInstitute of Bioinformatics, University of Georgia, Atlanta, Georgia, United States of America.ORCID 0000-0002-2833-8375

Funding

Unlocking sequence-structure-function-disease relationships in large protein super-familiesR35GM139656 · NIGMS · UNIVERSITY OF GEORGIA · PI KANNAN, NATARAJAN · 2021 to 2025
$2.2M
NIGMS NIH HHS R35 GM139656
6 · The paper itself

Abstract

Post-Translational Modifications (PTMs) are a fundamental mechanism for regulating cellular pathways and increasing the functional diversity of the proteome. Accurately predicting the PTM types that are likely to occur at a given site in the primary sequence is a key challenge in functional proteomics. Existing PTM prediction models predominantly focus on either single PTM types or employ ensemble methods that combine multiple models to predict different PTM types. This fragmentation is largely driven by the vast imbalance in data availability across PTM types, making it difficult to predict multiple PTM types with a single model. To address this limitation, we present the Contrastively Learned Attention-based Stratified PTM Predictor (CLASPP), a unified PTM prediction model. CLASPP addresses imbalance challenges by leveraging unsupervised clustering-based undersampling and a novel contrastive learning framework tailored to PTM data. Additionally, our hierarchical data organization and curation are shown to improve CLASPP's performance by balancing the representation of individual PTM types and provides a standardized dataset to train and validate future model designs. Drawing inspiration from advancements in image and natural language processing, the CLASPP model employs a multi-stage training strategy and a high-quality, curated training dataset to improve PTM prediction performance. To uncover what is learned during the contrastive learning stage, the CLASPP model is shown to distinguish known protein kinase substrate specificity profiles as a form of explainability. Finally, we evaluate the application of CLASPP in predicting PTMs in different model organisms and experimentally validated ubiquitination sites in the understudied DCLK3 kinase. Overall, CLASPP represents a unified model for PTM prediction that addresses key bottlenecks in data imbalance and offers new strategies for biological data curation, thereby improving PTM-type prediction performance across diverse organisms.

Indexed as

Computational BiologyProtein Processing, Post-TranslationalAnimalsDatabases, ProteinHumansPrediction AlgorithmsPredictive Learning ModelsProteomeProteomicsProteome

Identifiers

PMID42599970
PMCPMC13475974

What OpenQuestion holds

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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.