Evidence map›Paper›PMID 24586884›Full record

ArticlePloS one2014

LAceP: lysine acetylation site prediction using logistic regression classifiers.

Ting Hou, Guangyong Zheng, Pingyu Zhang, Jia Jia, Jing Li, Lu Xie, Chaochun Wei, Yixue Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
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

41 citing papers in PubMed, 122 citations in OpenAlex.

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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 at 5 institutions in 1 country.

Ting HouSchool of Biological Engineering, East China University of Science and Technology, Shanghai, China ; Shanghai Center for Bioinformation Technology, Shanghai, China ; Key Laboratory of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Guangyong ZhengCAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Pingyu ZhangKey Laboratory of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Jia JiaShanghai Center for Bioinformation Technology, Shanghai, China.
Jing LiShanghai Center for Bioinformation Technology, Shanghai, China.
Lu XieShanghai Center for Bioinformation Technology, Shanghai, China.
Chaochun WeiShanghai Center for Bioinformation Technology, Shanghai, China ; School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Yixue LiSchool of Biological Engineering, East China University of Science and Technology, Shanghai, China ; Shanghai Center for Bioinformation Technology, Shanghai, China ; Key Laboratory of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Shanghai Center For Bioinformation Technology · CNChinese Academy of Sciences · CNEast China University of Science and Technology · CNShanghai Institutes for Biological Sciences · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLysine acetylation is a crucial type of protein post-translational modification, which is involved in many important cellular processes and serious diseases. However, identification of protein acetylated sites through traditional experiment methods is time-consuming and laborious. Those methods are not suitable to identify a large number of acetylated sites quickly. Therefore, computational methods are still very valuable to accelerate lysine acetylated site finding.

resultIn this study, many biological characteristics of acetylated sites have been investigated, such as the amino acid sequence around the acetylated sites, the physicochemical property of the amino acids and the transition probability of adjacent amino acids. A logistic regression method was then utilized to integrate these information for generating a novel lysine acetylation prediction system named LAceP. When compared with existing methods, LAceP overwhelms most of state-of-the-art methods. Especially, LAceP has a more balanced prediction capability for positive and negative datasets.

conclusionLAceP can integrate different biological features to predict lysine acetylation with high accuracy. An online web server is freely available at http://www.scbit.org/iPTM/.

Indexed as

Computational BiologyProtein Processing, Post-TranslationalSoftwareAcetylationAlgorithmsDatabases, ProteinHumansLogistic ModelsLysineProteinsLysineProteins

Identifiers

PMID24586884
PMCPMC3930742
OpenAlexW1991199546

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.