Evidence map›Paper›PMID 30674277›Full record

ArticleBMC bioinformatics2019

A deep learning method to more accurately recall known lysine acetylation sites.

Meiqi Wu, Yingxi Yang, Hui Wang, Yan Xu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–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

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3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  10. Post-translational modifications in the Protein Data Bank.Acta crystallographica. Section D, Structural biology · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Meiqi WuDepartment of Information and Computer Science, University of Science and Technology Beijing, Beijing, 100083, China.
Yingxi YangDepartment of Information and Computer Science, University of Science and Technology Beijing, Beijing, 100083, China.
Hui WangInstitute of Computing Technology, Chinese Academy of Sciences, Beijing, 100190, China.
Yan XuDepartment of Information and Computer Science, University of Science and Technology Beijing, Beijing, 100083, China. xuyan@ustb.edu.cn.ORCID http://orcid.org/0000-0001-9462-580X

Funding

Fundamental Research Funds for the Central Universities FRF-TP-17-024A2National Natural Science Foundation of China 11671032
6 · The paper itself

Abstract

backgroundLysine acetylation in protein is one of the most important post-translational modifications (PTMs). It plays an important role in essential biological processes and is related to various diseases. To obtain a comprehensive understanding of regulatory mechanism of lysine acetylation, the key is to identify lysine acetylation sites. Previously, several shallow machine learning algorithms had been applied to predict lysine modification sites in proteins. However, shallow machine learning has some disadvantages. For instance, it is not as effective as deep learning for processing big data.

resultsIn this work, a novel predictor named DeepAcet was developed to predict acetylation sites. Six encoding schemes were adopted, including a one-hot, BLOSUM62 matrix, a composition of K-space amino acid pairs, information gain, physicochemical properties, and a position specific scoring matrix to represent the modified residues. A multilayer perceptron (MLP) was utilized to construct a model to predict lysine acetylation sites in proteins with many different features. We also integrated all features and implemented the feature selection method to select a feature set that contained 2199 features. As a result, the best prediction achieved 84.95% accuracy, 83.45% specificity, 86.44% sensitivity, 0.8540 AUC, and 0.6993 MCC in a 10-fold cross-validation. For an independent test set, the prediction achieved 84.87% accuracy, 83.46% specificity, 86.28% sensitivity, 0.8407 AUC, and 0.6977 MCC.

conclusionThe predictive performance of our DeepAcet is better than that of other existing methods. DeepAcet can be freely downloaded from https://github.com/Sunmile/DeepAcet .

Indexed as

AcetylationDeep LearningLysineProtein Processing, Post-TranslationalLysineDeep learningLysine acetylationPTMs

Identifiers

PMID30674277
PMCPMC6343287

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LicenceCC BY
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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.