Evidence map›Paper›PMID 40138319›Full record

ArticlePloS one2025

PUNCH2: Explore the strategy for intrinsically disordered protein predictor.

Di Meng, Gianluca Pollastri

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Biomolecules · 2025
    Article
  7. Article
  8. Review
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

2 authors.

Di MengSchool of Computer Science, University College Dublin, Dublin, Ireland.ORCID 0009-0003-6063-7951
Gianluca PollastriSchool of Computer Science, University College Dublin, Dublin, Ireland.

Funding

Science Foundation Ireland (SFI: # 1636933 AND # 1920920)
6 · The paper itself

Abstract

Intrinsically disordered proteins (IDPs) and their intrinsically disordered regions (IDRs) lack stable three-dimensional structures, posing significant challenges for computational prediction. This study introduces PUNCH2 and PUNCH2-light, advanced predictors designed to address these challenges through curated datasets, innovative feature extraction, and optimized neural architectures. By integrating experimental datasets from PDB (PDB_missing) and fully disordered sequences from DisProt (DisProt_FD), we enhanced model performance and robustness. Three embedding strategies-One-Hot, MSA-based, and PLM-based embeddings-were evaluated, with ProtTrans emerging as the most effective single embedding and combined embeddings achieving the best results. The predictors employ a 12-layer convolutional network (CNN_L12_narrow), offering a balance between accuracy and computational efficiency. PUNCH2 combines One-Hot, ProtTrans, and MSA-Transformer embeddings, while PUNCH2-light provides a faster alternative excluding MSA-based embeddings. PUNCH2 and its streamlined variant, PUNCH2-light, are competitive with other predictors on the CAID2 benchmark and rank as the top two predictors in the CAID3 competition. These tools provide efficient, accurate solutions to advance IDP research and understanding.

Indexed as

Computational BiologyIntrinsically Disordered ProteinsSoftwareAlgorithmsDatabases, ProteinNeural Networks, ComputerProtein ConformationIntrinsically Disordered Proteins

Identifiers

PMID40138319
PMCPMC11940444

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.