ArticleBMC genomics2014
Predicting sumoylation sites using support vector machines based on various sequence features, conformational flexibility and disorder.
Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- SumoPred-PLM: human SUMOylation and SUMO2/3 sites Prediction using Pre-trained Protein Language Model.NAR genomics and bioinformatics · 2024Article
- Paradoxes of Cellular SUMOylation Regulation: A Role of Biomolecular Condensates?Pharmacological reviews · 2023Review
- Systematic Characterization of Lysine Post-translational Modification Sites Using MUscADEL.Methods in molecular biology (Clifton, N.J.) · 2022Article
- Large-scale comparative assessment of computational predictors for lysine post-translational modification sites.Briefings in bioinformatics · 2019Review
- HseSUMO: Sumoylation site prediction using half-sphere exposures of amino acids residues.BMC genomics · 2019Article
- The Impact of the C-Terminal Region on the Interaction of Topoisomerase II Alpha with Mitotic Chromatin.International journal of molecular sciences · 2019Article
- SumSec: Accurate Prediction of Sumoylation Sites Using Predicted Secondary Structure.Molecules (Basel, Switzerland) · 2018Article
- SUMOgo: Prediction of sumoylation sites on lysines by motif screening models and the effects of various post-translational modifications.Scientific reports · 2018Article
- SVM-SulfoSite: A support vector machine based predictor for sulfenylation sites.Scientific reports · 2018Article
- Prediction of neddylation sites from protein sequences and sequence-derived properties.BMC bioinformatics · 2015Article
- InCoB2014: mining biological data from genomics for transforming industry and health.BMC genomics · 2014Article
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Authors and funding
2 authors.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundSumoylation, which is a reversible and dynamic post-translational modification, is one of the vital processes in a cell. Before a protein matures to perform its function, sumoylation may alter its localization, interactions, and possibly structural conformation. Abberations in protein sumoylation has been linked with a variety of disorders and developmental anomalies. Experimental approaches to identification of sumoylation sites may not be effective due to the dynamic nature of sumoylation, laborsome experiments and their cost. Therefore, computational approaches may guide experimental identification of sumoylation sites and provide insights for further understanding sumoylation mechanism.
resultsIn this paper, the effectiveness of using various sequence properties in predicting sumoylation sites was investigated with statistical analyses and machine learning approach employing support vector machines. These sequence properties were derived from windows of size 7 including position-specific amino acid composition, hydrophobicity, estimated sub-window volumes, predicted disorder, and conformational flexibility. 5-fold cross-validation results on experimentally identified sumoylation sites revealed that our method successfully predicts sumoylation sites with a Matthew's correlation coefficient, sensitivity, specificity, and accuracy equal to 0.66, 73%, 98%, and 97%, respectively. Additionally, we have showed that our method compares favorably to the existing prediction methods and basic regular expressions scanner.
conclusionsBy using support vector machines, a new, robust method for sumoylation site prediction was introduced. Besides, the possible effects of predicted conformational flexibility and disorder on sumoylation site recognition were explored computationally for the first time to our knowledge as an additional parameter that could aid in sumoylation site prediction.
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