ArticleBMC bioinformatics2008
Prediction of mucin-type O-glycosylation sites in mammalian proteins using the composition of k-spaced amino acid pairs.
Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.
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Who cites it
58 citing papers in PubMed.
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- Integrating In Silico and In Vitro Approaches to Identify Natural Peptides with Selective Cytotoxicity against Cancer Cells.International journal of molecular sciences · 2024Article
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- BERT-Kgly: A Bidirectional Encoder Representations From Transformers (BERT)-Based Model for Predicting Lysine Glycation Site forFrontiers in bioinformatics · 2022Article
- GlyinsRNA: a webserver for predicting glycosylation sites on small RNAs.RNA biology · 2021Article
- nhKcr: a new bioinformatics tool for predicting crotonylation sites on human nonhistone proteins based on deep learning.Briefings in bioinformatics · 2021Article
- Identification of subtypes of anticancer peptides based on sequential features and physicochemical properties.Scientific reports · 2021Article
- PUP-Fuse: Prediction of Protein Pupylation Sites by Integrating Multiple Sequence Representations.International journal of molecular sciences · 2021Article
- Insights into Bioinformatic Applications for Glycosylation: Instigating an Awakening towards Applying Glycoinformatic Resources for Cancer Diagnosis and Therapy.International journal of molecular sciences · 2020Review
- Predicting mucin-type O-Glycosylation using enhancement value products from derived protein features.Journal of theoretical & computational chemistry · 2020Article
- Deep Structural Analysis and Quantitation of O-Linked Glycans on Cell Membrane Reveal High Abundances and Distinct Glycomic Profiles Associated with Cell Type and Stages of Differentiation.Analytical chemistry · 2020Article
- Succinylation Site Prediction Based on Protein Sequences Using the IFS-LightGBM (BO) Model.Computational and mathematical methods in medicine · 2020Article
- RF-MaloSite and DL-Malosite: Methods based on random forest and deep learning to identify malonylation sites.Computational and structural biotechnology journal · 2020Article
- Identify Lysine Neddylation Sites Using Bi-profile Bayes Feature ExtractionCurrent genomics · 2019Article
- csDMA: an improved bioinformatics tool for identifying DNA 6 mA modifications via Chou's 5-step rule.Scientific reports · 2019Article
- PACES: prediction of N4-acetylcytidine (ac4C) modification sites in mRNA.Scientific reports · 2019Article
- Computational identification of microbial phosphorylation sites by the enhanced characteristics of sequence information.Scientific reports · 2019Article
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4 authors.
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Abstract
backgroundAs one of the most common protein post-translational modifications, glycosylation is involved in a variety of important biological processes. Computational identification of glycosylation sites in protein sequences becomes increasingly important in the post-genomic era. A new encoding scheme was employed to improve the prediction of mucin-type O-glycosylation sites in mammalian proteins.
resultsA new protein bioinformatics tool, CKSAAP_OGlySite, was developed to predict mucin-type O-glycosylation serine/threonine (S/T) sites in mammalian proteins. Using the composition of k-spaced amino acid pairs (CKSAAP) based encoding scheme, the proposed method was trained and tested in a new and stringent O-glycosylation dataset with the assistance of Support Vector Machine (SVM). When the ratio of O-glycosylation to non-glycosylation sites in training datasets was set as 1:1, 10-fold cross-validation tests showed that the proposed method yielded a high accuracy of 83.1% and 81.4% in predicting O-glycosylated S and T sites, respectively. Based on the same datasets, CKSAAP_OGlySite resulted in a higher accuracy than the conventional binary encoding based method (about +5.0%). When trained and tested in 1:5 datasets, the CKSAAP encoding showed a more significant improvement than the binary encoding. We also merged the training datasets of S and T sites and integrated the prediction of S and T sites into one single predictor (i.e. S+T predictor). Either in 1:1 or 1:5 datasets, the performance of this S+T predictor was always slightly better than those predictors where S and T sites were independently predicted, suggesting that the molecular recognition of O-glycosylated S/T sites seems to be similar and the increase of the S+T predictor's accuracy may be a result of expanded training datasets. Moreover, CKSAAP_OGlySite was also shown to have better performance when benchmarked against two existing predictors.
conclusionBecause of CKSAAP encoding's ability of reflecting characteristics of the sequences surrounding mucin-type O-glycosylation sites, CKSAAP_ OGlySite has been proved more powerful than the conventional binary encoding based method. This suggests that it can be used as a competitive mucin-type O-glycosylation site predictor to the biological community. CKSAAP_OGlySite is now available at http://bioinformatics.cau.edu.cn/zzd_lab/CKSAAP_OGlySite/.
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