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iPTM-mLys: identifying multiple lysine PTM sites and their different types
Open accessAbstract
Motivation: Post-translational modification, abbreviated as PTM, refers to the change of the amino acid side chains of a protein after its biosynthesis. Owing to its significance for in-depth understanding various biological processes and developing effective drugs, prediction of PTM sites in proteins have currently become a hot topic in bioinformatics. Although many computational methods were established to identify various single-label PTM types and their occurrence sites in proteins, no method has ever been developed for multi-label PTM types. As one of the most frequently observed PTMs, the K-PTM, namely, the modification occurring at lysine (K), can be usually accommodated with many different types, such as ‘acetylation’, ‘crotonylation’, ‘methylation’ and ‘succinylation’. Now we are facing an interesting challenge: given an uncharacterized protein sequence containing many K residues, which ones can accommodate two or more types of PTM, which ones only one, and which ones none? Results: To address this problem, a multi-label predictor called iPTM-mLys has been developed. It represents the first multi-label PTM predictor ever established. The novel predictor is featured by incorporating the sequence-coupled effects into the general PseAAC, and by fusing an array of basic random forest classifiers into an ensemble system. Rigorous cross-validations via a set of multi-label metrics indicate that the first multi-label PTM predictor is very promising and encouraging. Availability and Implementation: For the convenience of most experimental scientists, a user-friendly web-server for iPTM-mLys has been established at http://www.jci-bioinfo.cn/iPTM-mLys, by which users can easily obtain their desired results without the need to go through the complicated mathematical equations involved. Contact: wqiu@gordonlifescience.org, xxiao@gordonlifescience.org, kcchou@gordonlifescience.org Supplementary information: Supplementary data are available at Bioinformatics online.
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Some remarks on protein attribute prediction and pseudo amino acid composition
Chou, K.-C. (2011) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2010.12.024 · Cited by 1,225
Self-citationLin, H., Deng, E.-Z., Ding, H., Chen, W., & Chou, K.-C. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1019 · Cited by 508
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Meher, P. K., Sahu, T. K., Saini, V., & Rao, A. R. (2017) · Scientific Reports · doi:10.1038/srep42362 · Cited by 516
Liu, B., Yang, F., Huang, D.-S., & Chou, K.-C. (2018) · Bioinformatics · doi:10.1093/bioinformatics/btx579 · Cited by 331
Self-citationiRSpot-EL: identify recombination spots with an ensemble learning approach
Liu, B., Wang, S., Long, R., & Chou, K.-C. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btw539 · Cited by 295
Self-citationSu, Z.-D., Huang, Y., Zhang, Z.-Y., Zhao, Y.-W., Wang, D., Chen, W., Chou, K.-C., & Lin, H. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty508 · Cited by 294
Self-citationFeng, P., Ding, H., Yang, H., Chen, W., Lin, H., & Chou, K.-C. (2017) · Molecular Therapy - Nucleic Acids · doi:10.1016/j.omtn.2017.03.006 · Cited by 288
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Metadata
- Authors
- Qiu, W.-R., Sun, B.-Q., Xiao, X., Xu, Z.-C., & Chou, K.-C.
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2016-06-22
- Volume
- 32
- Issue
- 20
- Pages
- 3116-3123
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- OpenAlex
- W2472513547
- Cited by
- 260
- References
- 2
- FWCI
- 28.29
- Type
- journal article
- Language
- en
- Open access
- hybrid
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