Evidence map›Paper›PMID 33225896›Full record

ArticleBMC genomics2020

Mal-Prec: computational prediction of protein Malonylation sites via machine learning based feature integration : Malonylation site prediction.

Xin Liu, Liang Wang, Jian Li, Junfeng Hu, Xiao Zhang

Abstract read
In one paragraph

Article in BMC genomics, 2020. 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
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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xin LiuDepartment of Bioinformatics, School of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, 221004, Jiangsu, China. flyinsky6@gmail.com.
Liang WangDepartment of Bioinformatics, School of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, 221004, Jiangsu, China.ORCID http://orcid.org/0000-0001-5339-7484
Jian LiSchool of Public Health and Tropical Medicine, Tulane University, New Orleans, LA, 70118, USA.
Junfeng HuDepartment of Bioinformatics, School of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, 221004, Jiangsu, China.
Xiao ZhangDepartment of Bioinformatics, School of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, 221004, Jiangsu, China. changshui@hotmail.com.

Funding

Jiangsu Postdoctoral Science Foundation 1601080CJiangsu Postdoctoral Science Foundation 1701062BJiangsu University Natural Science Foundation 17KJB310015Research Foundation for Talented Scholars in Xuzhou Medical University D2015001Xuzhou Science and Technology Project KC17123
6 · The paper itself

Abstract

backgroundMalonylation is a recently discovered post-translational modification that is associated with a variety of diseases such as Type 2 Diabetes Mellitus and different types of cancers. Compared with experimental identification of malonylation sites, computational method is a time-effective process with comparatively low costs.

resultsIn this study, we proposed a novel computational model called Mal-Prec (Malonylation Prediction) for malonylation site prediction through the combination of Principal Component Analysis and Support Vector Machine. One-hot encoding, physio-chemical properties, and composition of k-spaced acid pairs were initially performed to extract sequence features. PCA was then applied to select optimal feature subsets while SVM was adopted to predict malonylation sites. Five-fold cross-validation results showed that Mal-Prec can achieve better prediction performance compared with other approaches. AUC (area under the receiver operating characteristic curves) analysis achieved 96.47 and 90.72% on 5-fold cross-validation of independent data sets, respectively.

conclusionMal-Prec is a computationally reliable method for identifying malonylation sites in protein sequences. It outperforms existing prediction tools and can serve as a useful tool for identifying and discovering novel malonylation sites in human proteins. Mal-Prec is coded in MATLAB and is publicly available at https://github.com/flyinsky6/Mal-Prec , together with the data sets used in this study.

Indexed as

Diabetes Mellitus, Type 2LysineAmino Acid SequenceComputational BiologyHumansMachine LearningProtein Processing, Post-TranslationalSupport Vector MachineLysineMachine learningMalonylationPost-translational modificationPrincipal component analysisSupport vector machine

Identifiers

PMID33225896
PMCPMC7682087

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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.