Evidence map›Paper›PMID 40452145›Full record

ArticleBriefings in bioinformatics2025

EDS-Kcr: deep supervision based on large language model for identifying protein lysine crotonylation sites across multiple species.

Hong-Qi Zhang, Xin-Ran Lin, Yan-Ting Wang, Wen-Fang Pei, Guang-Ji Ma, Ze-Xu Zhou, Ke-Jun Deng, Dan Yan, Tian-Yuan Liu

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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

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

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

9 authors.

Hong-Qi ZhangSchool of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Xin-Ran LinSchool of Medicine, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Yan-Ting WangSchool of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Wen-Fang PeiSchool of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Guang-Ji MaSchool of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Ze-Xu ZhouSchool of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Ke-Jun DengSchool of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, No. 2006 Xiyuan Avenue, West Hi-Tech Zone, Chengdu 610054, China.
Dan YanBeijing Institute of Clinical Pharmacy, Beijing Friendship Hospital, Capital Medical University, No. 13 Shuiche Hutong, Xicheng District, Beijing 100050, China.
Tian-Yuan LiuTsukuba Life Science Innovation Program, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 3058577, Japan.

Funding

Key Discipline of the National Administration of Traditional Chinese Medicine zyyzdxk-2023003National Natural Science Foundation of China 62372090National Natural Science Foundation of China 82130112Youth Beijing Scholar 2022-051
6 · The paper itself

Abstract

With the rapid advancement of proteomics, post-translational modifications, particularly lysine crotonylation (Kcr), have gained significant attention in basic research, drug development, and disease treatment. However, current methods for identifying these modifications are often complex, costly, and time-consuming. To address these challenges, we have proposed EDS-Kcr, a novel bioinformatics tool that integrates the state-of-the-art protein language model ESM2 with deep supervision to improve the efficiency and accuracy of Kcr site prediction. EDS-Kcr demonstrated outstanding performance across various species datasets, proving its applicability to a wide range of proteins, including those from humans, plants, animals, and microbes. Compared to existing Kcr site prediction models, our model excelled in multiple key performance indicators, showcasing superior predictive power and robustness. Furthermore, we enhanced the transparency and interpretability of EDS-Kcr through visualization techniques and attention mechanisms. In conclusion, the EDS-Kcr model provides an efficient and reliable predictive tool suitable for disease diagnosis and drug development. We have also established a freely accessible web server for EDS-Kcr at http://eds-kcr.lin-group.cn/.

Indexed as

Computational BiologyLysineProtein Processing, Post-TranslationalProteinsSoftwareAnimalsDatabases, ProteinHumansLarge Language ModelsLysineProteinsdeep learning modellysine crotonylationpost-translational modificationsprotein language modelweb server

Identifiers

PMID40452145
PMCPMC12127148

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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.