Evidence map›Paper›PMID 42278389›Full record

ReviewInternational journal of molecular sciences2026

Data Resources and Computational Methods for Lactylation Site Prediction: A Mini-Review.

Cong Wang, Ye Pan, Yunlong Wu, Xiaolin Wu

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. 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
–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

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

4 authors.

Cong WangData and Informatization Department, Jiangsu University, Zhenjiang 212013, China.
Ye PanPublic Experiment & Service Center, Jiangsu University, Zhenjiang 212013, China.
Yunlong WuData and Informatization Department, Jiangsu University, Zhenjiang 212013, China.
Xiaolin WuPublic Experiment & Service Center, Jiangsu University, Zhenjiang 212013, China.

Funding

Jiangsu University No. 2025JGYB038
6 · The paper itself

Abstract

Lysine lactylation (Kla), a novel post-translational modification (PTM) discovered in 2019, establishes a critical link between cellular metabolism and epigenetic regulation. A growing number of studies have reported that it is involved in several physiological and pathological processes. Traditional experimental methods for identifying Kla sites are time-consuming and labor-intensive; in contrast, computational prediction models offer efficient and systematic alternatives for high-throughput screening of potential modification sites. In this review, we summarize computational methods and data resources used for Kla site prediction. The biological roles of Kla in major human diseases, such as cancers, cardiovascular diseases, and neurological diseases, were summarized. Furthermore, a summary and comprehensive overview of seven Kla site prediction models is presented, covering dataset construction, methodological principles, and evaluation methods. Finally, the challenges and future trends in Kla prediction have been discussed.

Indexed as

Computational BiologyLysinePredictive Learning ModelsProtein Processing, Post-TranslationalAnimalsHumansPrediction AlgorithmsLysinecomputational predictiondeep learninglysine lactylationmachine learningpost-translational modification

Identifiers

PMID42278389
PMCPMC13256538

What OpenQuestion 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 OpenQuestion graph.