Evidence map›Paper›PMID 40563483›Full record

ArticleBiomolecules2025

MTPrompt-PTM: A Multi-Task Method for Post-Translational Modification Prediction Using Prompt Tuning on a Structure-Aware Protein Language Model.

Ye Han, Fei He, Qing Shao, Duolin Wang, Dong Xu

Abstract read
In one paragraph

Article in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

6 citing papers in PubMed.

  1. Article
  2. CLASPP: A unified model for predicting post-translational modifications.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
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

5 authors.

Ye HanDepartment of Electrical Engineering and Computer Science, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0001-9704-0284
Fei HeDepartment of Electrical Engineering and Computer Science, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-3284-9506
Qing ShaoChemical & Materials Engineering, University of Kentucky, Lexington, KY 40506, USA.
Duolin WangDepartment of Electrical Engineering and Computer Science, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Dong XuDepartment of Electrical Engineering and Computer Science, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-4809-0514

Funding

Multi-view self-supervised deep learning for biological sequences and beyondR35GM126985 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI DONG XU · 2018 to 2026
$3.8M
Structure-Function-Aware Large Protein Language Models for Enhanced Biomedical ApplicationsR01LM014510 · NLM · UNIVERSITY OF KENTUCKY · PI Qing Shao · 2024 to 2026
$994k
NIGMS NIH HHS R35 GM126985NIH HHS R01LM014510-01NIH HHS R35GM126985-04S1NLM NIH HHS R01 LM014510
6 · The paper itself

Abstract

Post-translational modifications (PTMs) regulate protein function, stability, and interactions, playing essential roles in cellular signaling, localization, and disease mechanisms. Computational approaches enable scalable PTM site prediction; however, traditional models focus only on local sequence features from fragments around potential modification sites, limiting the scope of their predictions. Recently, pre-trained protein language models (PLMs) have improved PTM prediction by leveraging biological knowledge derived from extensive protein databases. However, most PLMs used for PTM site prediction are pre-trained solely on amino acid sequences, limiting their ability to capture the structural context necessary for accurate PTM site prediction. Moreover, these methods typically train separate single-task models for each PTM type, which hinders the sharing of common features and limits potential knowledge transfer across tasks. To overcome these limitations, we introduce MTPrompt-PTM, a multi-task PTM prediction framework developed by applying prompt tuning to a structure-aware protein language model (S-PLM). Instead of training several single-task models, MTPrompt-PTM trains one multi-task model to predict multiple types of PTM sites using shared feature extraction layers and task-specific classification heads. Additionally, we incorporate a knowledge distillation strategy to enhance the efficiency and generalizability of multi-task training. Experimental results demonstrate that MTPrompt-PTM outperforms state-of-the-art PTM prediction tools on 13 types of PTM sites, highlighting the advantages of multi-task learning and structural integration.

Indexed as

Computational BiologyProtein Processing, Post-TranslationalProteinsDatabases, ProteinHumansProteinsknowledge distillationmulti-task predictionpost-translational modification predictionprompt tuningstructure-aware protein language model (S-PLM)

Identifiers

PMID40563483
PMCPMC12190693

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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.