dc.contributor.author | Pakhrin, Subash C. | |
dc.contributor.author | Aoki-Kinoshita, Kiyoko Flora | |
dc.contributor.author | Caragea, Doina | |
dc.contributor.author | KC, Dukka B. | |
dc.date.accessioned | 2022-01-07T14:56:53Z | |
dc.date.available | 2022-01-07T14:56:53Z | |
dc.date.issued | 2021-12-02 | |
dc.identifier.citation | Pakhrin, S. C., Aoki-Kinoshita, K. F., Caragea, D., & Kc, D. B. (2021). DeepNgGlypred: A deep neural network-based approach for human N-linked glycosylation site prediction. Molecules, 26(23) doi:10.3390/molecules26237314 | en_US |
dc.identifier.issn | 1420-3049 | |
dc.identifier.uri | https://doi.org/10.3390/molecules26237314 | |
dc.identifier.uri | https://soar.wichita.edu/handle/10057/22420 | |
dc.description | This article is an open access article
distributed under the terms and
conditions of the Creative Commons
Attribution (CC BY) license (https://
creativecommons.org/licenses/by/
4.0/). | en_US |
dc.description.abstract | Protein N-linked glycosylation is a post-translational modification that plays an importantrole in a myriad of biological processes. Computational prediction approaches serve as comple-mentary methods for the characterization of glycosylation sites. Most of the existing predictors forN-linked glycosylation utilize the information that the glycosylation site occurs at the N-X-[S/T] se-quon, where X is any amino acid except proline. Not all N-X-[S/T] sequons are glycosylated, thus theN-X-[S/T] sequon is a necessary but not sufficient determinant for protein glycosylation. In thatregard, computational prediction of N-linked glycosylation sites confined to N-X-[S/T] sequons is animportant problem. Here, we report DeepNGlyPred a deep learning-based approach that encodes thepositive and negative sequences in the human proteome dataset (extracted from N-GlycositeAtlas)using sequence-based features (gapped-dipeptide), predicted structural features, and evolutionaryinformation. DeepNGlyPred produces SN, SP, MCC, and ACC of 88.62%, 73.92%, 60%, and 79.41%,respectively on N-GlyDE independent test set, which is better than the compared approaches. Theseresults demonstrate that DeepNGlyPred is a robust computational technique to predict N-Linkedglycosylation sites confined to N-X-[S/T] sequon. DeepNGlyPred will be a useful resource for theglycobiology community | en_US |
dc.description.sponsorship | This work was supported by National Science Foundation (NSF) grant nos. 1901793,
2003019, and 2021734 (to D.B.K.). | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | MDPI | en_US |
dc.relation.ispartofseries | Molecules;Vol. 26, Iss. 23 | |
dc.subject | Post-translation modification | en_US |
dc.subject | Sequon | en_US |
dc.subject | Deep neural network | en_US |
dc.subject | N-linked glycosylation | en_US |
dc.title | DeepNGlypred: A deep neural network-based approach for human N-linked glycosylation site prediction | en_US |
dc.type | Article | en_US |
dc.rights.holder | Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). | en_US |