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Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus
BACKGROUND: The influenza A virus (IAV) is a constant threat for humans worldwide. The understanding of motif-domain protein participation is essential to combat the pathogen. RESULTS: In this study, a data mining approach was employed to extract influenza-human Protein-Protein interactions (PPI) fr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019528/ https://www.ncbi.nlm.nih.gov/pubmed/29940841 http://dx.doi.org/10.1186/s12859-018-2237-8 |
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author | García-Pérez, Carlos A. Guo, Xianwu Navarro, Juan García Aguilar, Diego Alonso Gómez Lara-Ramírez, Edgar E. |
author_facet | García-Pérez, Carlos A. Guo, Xianwu Navarro, Juan García Aguilar, Diego Alonso Gómez Lara-Ramírez, Edgar E. |
author_sort | García-Pérez, Carlos A. |
collection | PubMed |
description | BACKGROUND: The influenza A virus (IAV) is a constant threat for humans worldwide. The understanding of motif-domain protein participation is essential to combat the pathogen. RESULTS: In this study, a data mining approach was employed to extract influenza-human Protein-Protein interactions (PPI) from VirusMentha,Virus MINT, IntAct, and Pfam databases, to mine motif-domain interactions (MDIs) stored as Regular Expressions (RegExp) in 3DID database. A total of 107 RegExp related to human MDIs were searched on 51,242 protein fragments from H1N1, H1N2, H2N2, H3N2 and H5N1 strains obtained from Virus Variation database. A total 46 MDIs were frequently mapped on the IAV proteins and shared between the different strains. IAV kept host-like MDIs that were associated with the virus survival, which could be related to essential biological process such as microtubule-based processes, regulation of cell cycle check point, regulation of replication and transcription of DNA, etc. in human cells. The amino acid motifs were searched for matches in the immune epitope database and it was found that some motifs are part of experimentally determined epitopes on IAV, implying that such interactions exist. CONCLUSION: The directed data-mining method employed could be used to identify functional motifs in other viruses for envisioning new therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2237-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6019528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60195282018-07-06 Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus García-Pérez, Carlos A. Guo, Xianwu Navarro, Juan García Aguilar, Diego Alonso Gómez Lara-Ramírez, Edgar E. BMC Bioinformatics Research Article BACKGROUND: The influenza A virus (IAV) is a constant threat for humans worldwide. The understanding of motif-domain protein participation is essential to combat the pathogen. RESULTS: In this study, a data mining approach was employed to extract influenza-human Protein-Protein interactions (PPI) from VirusMentha,Virus MINT, IntAct, and Pfam databases, to mine motif-domain interactions (MDIs) stored as Regular Expressions (RegExp) in 3DID database. A total of 107 RegExp related to human MDIs were searched on 51,242 protein fragments from H1N1, H1N2, H2N2, H3N2 and H5N1 strains obtained from Virus Variation database. A total 46 MDIs were frequently mapped on the IAV proteins and shared between the different strains. IAV kept host-like MDIs that were associated with the virus survival, which could be related to essential biological process such as microtubule-based processes, regulation of cell cycle check point, regulation of replication and transcription of DNA, etc. in human cells. The amino acid motifs were searched for matches in the immune epitope database and it was found that some motifs are part of experimentally determined epitopes on IAV, implying that such interactions exist. CONCLUSION: The directed data-mining method employed could be used to identify functional motifs in other viruses for envisioning new therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2237-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-25 /pmc/articles/PMC6019528/ /pubmed/29940841 http://dx.doi.org/10.1186/s12859-018-2237-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article García-Pérez, Carlos A. Guo, Xianwu Navarro, Juan García Aguilar, Diego Alonso Gómez Lara-Ramírez, Edgar E. Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
title | Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
title_full | Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
title_fullStr | Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
title_full_unstemmed | Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
title_short | Proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
title_sort | proteome-wide analysis of human motif-domain interactions mapped on influenza a virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019528/ https://www.ncbi.nlm.nih.gov/pubmed/29940841 http://dx.doi.org/10.1186/s12859-018-2237-8 |
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