Evidence map›Paper›PMID 39941016›Full record

ArticleInternational journal of molecular sciences2025

Small Disulfide Proteins with Antifungal Impact: NMR Experimental Structures as Compared to Models of Alphafold Versions.

Jiawei Gai, Márk File, Réka Erdei, András Czajlik, Florentine Marx, László Galgóczy, Györgyi Váradi, Gyula Batta

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Characterization of a novel glycocin from a thermophile.bioRxiv : the preprint server for biology · 2025
    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

8 authors.

Jiawei GaiDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0009-0005-2563-6472
Márk FileDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Réka ErdeiDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
András CzajlikDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Florentine MarxInstitute of Molecular Biology, Biocenter, Medical University of Innsbruck, Innrain 80-82, A-6020 Innsbruck, Austria.ORCID 0000-0002-8408-1842
László GalgóczyDepartment of Biotechnology and Microbiology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, H-6726 Szeged, Hungary.ORCID 0000-0002-6976-8910
Györgyi VáradiDepartment of Medical Chemistry, Albert Szent-Györgyi Medical School, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary.ORCID 0000-0001-7907-8908
Gyula BattaDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-0442-1828

Funding

Austrian Science Fund (FWF) DOI 10.55776/I3132; DOI 10.55776/W1253European Regional Development Fund GINOP-2.3.2-15-2016-00008, GINOP-2.3.3-15-2016-00004Hungarian National Research, Development and Innovation Office FK 134343 and K 146131University of Debrecen, Scientific Research Bridging Fund DETKA
6 · The paper itself

Abstract

In response to the growth of emerging resistance to conventional antifungal drugs, antifungal proteins (AFPs) of filamentous Ascomycetes origin have been discovered in recent years. Understanding the structure of AFPs is crucial for elucidating their antifungal mechanisms and developing new therapeutic agents. While nuclear magnetic resonance (NMR) has proven effective in determining the structures of small proteins, some AFP structures remain unresolved, necessitating the use of alternative prediction methods. Through bioinformatics analysis and heatmaps of amino acid sequence identity and similarity matrix, we categorized AFPs into three major classes and six subcategories, revealing structural and bioactivity differences. We employed AlphaFold (AF) to predict the 3D structures of six different AFPs, with predictions compared to NMR-derived structures. The results demonstrated a high degree of consistency between AF and NMR structures, with AF excelling in structural quality assessment and accurately capturing complex disulfide bond patterns. Both AF2 and AF3 models outperform the NMR model in overall structural quality and coherence, with AF3 showing the best performance. However, the limitations of AF should be considered, including its reduced accuracy in predicting multi-metal ion complexes, suboptimal performance in highly flexible or disordered regions, and its inability to account for multiple conformers, as it generates only a single dominant structure. Moreover, while AF3 accurately predicts all disulfide bond patterns, AF2 falls short in this regard. This study verifies the reliability of AF in the structural prediction of cysteine-rich AFPs while highlighting these constraints, offering important support for the rational design of new protein-based antifungal drugs.

Indexed as

Antifungal AgentsDisulfidesFungal ProteinsAmino Acid SequenceAscomycotaComputational BiologyMagnetic Resonance SpectroscopyModels, MolecularProtein ConformationProtein FoldingAntifungal AgentsDisulfidesFungal ProteinsAlphaFoldantifungal proteinsdisulfide proteinsmini-proteinNMR

Identifiers

PMID39941016
PMCPMC11818080

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Registered trials

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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.