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Identifying SNARE Proteins Using an Alignment-Free Method Based on Multiscan Convolutional Neural Network and PSSM Profiles
[Image: see text] Background: SNARE proteins play a vital role in membrane fusion and cellular physiology and pathological processes. Many potential therapeutics for mental diseases or even cancer based on SNAREs are also developed. Therefore, there is a dire need to predict the SNAREs for further m...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554904/ https://www.ncbi.nlm.nih.gov/pubmed/36166351 http://dx.doi.org/10.1021/acs.jcim.2c01034 |
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author | Kha, Quang-Hien Ho, Quang-Thai Le, Nguyen Quoc Khanh |
author_facet | Kha, Quang-Hien Ho, Quang-Thai Le, Nguyen Quoc Khanh |
author_sort | Kha, Quang-Hien |
collection | PubMed |
description | [Image: see text] Background: SNARE proteins play a vital role in membrane fusion and cellular physiology and pathological processes. Many potential therapeutics for mental diseases or even cancer based on SNAREs are also developed. Therefore, there is a dire need to predict the SNAREs for further manipulation of these essential proteins, which demands new and efficient approaches. Methods: Some computational frameworks were proposed to tackle the hurdles of biological methods, which take plenty of time and budget to conduct the identification of SNAREs. However, the performances of existing frameworks were insufficiently satisfied, as they failed to retain the SNARE sequence order and capture the mass hidden features from SNAREs. This paper proposed a novel model constructed on the multiscan convolutional neural network (CNN) and position-specific scoring matrix (PSSM) profiles to address these limitations. We employed and trained our model on the benchmark dataset with fivefold cross-validation and two different independent datasets. Results: Overall, the multiscan CNN was cross-validated on the training set and excelled in the SNARE classification reaching 0.963 in AUC and 0.955 in AUPRC. On top of that, with the sensitivity, specificity, accuracy, and MCC of 0.842, 0.968, 0.955, and 0.767, respectively, our proposed framework outperformed previous models in the SNARE recognition task. Conclusions: It is truly believed that our model can contribute to the discrimination of SNARE proteins and general proteins. |
format | Online Article Text |
id | pubmed-9554904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95549042022-10-13 Identifying SNARE Proteins Using an Alignment-Free Method Based on Multiscan Convolutional Neural Network and PSSM Profiles Kha, Quang-Hien Ho, Quang-Thai Le, Nguyen Quoc Khanh J Chem Inf Model [Image: see text] Background: SNARE proteins play a vital role in membrane fusion and cellular physiology and pathological processes. Many potential therapeutics for mental diseases or even cancer based on SNAREs are also developed. Therefore, there is a dire need to predict the SNAREs for further manipulation of these essential proteins, which demands new and efficient approaches. Methods: Some computational frameworks were proposed to tackle the hurdles of biological methods, which take plenty of time and budget to conduct the identification of SNAREs. However, the performances of existing frameworks were insufficiently satisfied, as they failed to retain the SNARE sequence order and capture the mass hidden features from SNAREs. This paper proposed a novel model constructed on the multiscan convolutional neural network (CNN) and position-specific scoring matrix (PSSM) profiles to address these limitations. We employed and trained our model on the benchmark dataset with fivefold cross-validation and two different independent datasets. Results: Overall, the multiscan CNN was cross-validated on the training set and excelled in the SNARE classification reaching 0.963 in AUC and 0.955 in AUPRC. On top of that, with the sensitivity, specificity, accuracy, and MCC of 0.842, 0.968, 0.955, and 0.767, respectively, our proposed framework outperformed previous models in the SNARE recognition task. Conclusions: It is truly believed that our model can contribute to the discrimination of SNARE proteins and general proteins. American Chemical Society 2022-09-27 2022-10-10 /pmc/articles/PMC9554904/ /pubmed/36166351 http://dx.doi.org/10.1021/acs.jcim.2c01034 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Kha, Quang-Hien Ho, Quang-Thai Le, Nguyen Quoc Khanh Identifying SNARE Proteins Using an Alignment-Free Method Based on Multiscan Convolutional Neural Network and PSSM Profiles |
title | Identifying SNARE
Proteins Using an Alignment-Free
Method Based on Multiscan Convolutional Neural Network and PSSM Profiles |
title_full | Identifying SNARE
Proteins Using an Alignment-Free
Method Based on Multiscan Convolutional Neural Network and PSSM Profiles |
title_fullStr | Identifying SNARE
Proteins Using an Alignment-Free
Method Based on Multiscan Convolutional Neural Network and PSSM Profiles |
title_full_unstemmed | Identifying SNARE
Proteins Using an Alignment-Free
Method Based on Multiscan Convolutional Neural Network and PSSM Profiles |
title_short | Identifying SNARE
Proteins Using an Alignment-Free
Method Based on Multiscan Convolutional Neural Network and PSSM Profiles |
title_sort | identifying snare
proteins using an alignment-free
method based on multiscan convolutional neural network and pssm profiles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554904/ https://www.ncbi.nlm.nih.gov/pubmed/36166351 http://dx.doi.org/10.1021/acs.jcim.2c01034 |
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