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SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases
Genome guided discovery of novel natural products has been a promising approach for identification of new bioactive compounds. SBSPKS web-server has been a valuable resource for analysis of polyketide synthase (PKS) and non-ribosomal peptide synthetase (NRPS) gene clusters. We have developed an upda...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570206/ https://www.ncbi.nlm.nih.gov/pubmed/28460065 http://dx.doi.org/10.1093/nar/gkx344 |
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author | Khater, Shradha Gupta, Money Agrawal, Priyesh Sain, Neetu Prava, Jyoti Gupta, Priya Grover, Mansi Kumar, Narendra Mohanty, Debasisa |
author_facet | Khater, Shradha Gupta, Money Agrawal, Priyesh Sain, Neetu Prava, Jyoti Gupta, Priya Grover, Mansi Kumar, Narendra Mohanty, Debasisa |
author_sort | Khater, Shradha |
collection | PubMed |
description | Genome guided discovery of novel natural products has been a promising approach for identification of new bioactive compounds. SBSPKS web-server has been a valuable resource for analysis of polyketide synthase (PKS) and non-ribosomal peptide synthetase (NRPS) gene clusters. We have developed an updated version - SBSPKSv2 which is based on comprehensive analysis of sequence, structure and secondary metabolite chemical structure data from 311 experimentally characterized PKS/NRPS gene clusters with known biosynthetic products. A completely new feature of SBSPKSv2 is the inclusion of features for search in chemical space. It allows the user to compare the chemical structure of a given secondary metabolite to the chemical structures of biosynthetic intermediates and final products. For identification of catalytic domains, SBSPKS now uses profile based searches, which are computationally faster and have high sensitivity. HMM profiles have also been added for a number of new domains and motif information has been used for distinguishing condensation (C), epimerization (E) and cyclization (Cy) domains of NRPS. In summary, the new and updated SBSPKSv2 is a versatile tool for genome mining and analysis of polyketide and non-ribosomal peptide biosynthetic pathways in chemical space. The server is available at: http://www.nii.ac.in/sbspks2.html. |
format | Online Article Text |
id | pubmed-5570206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55702062017-08-29 SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases Khater, Shradha Gupta, Money Agrawal, Priyesh Sain, Neetu Prava, Jyoti Gupta, Priya Grover, Mansi Kumar, Narendra Mohanty, Debasisa Nucleic Acids Res Web Server Issue Genome guided discovery of novel natural products has been a promising approach for identification of new bioactive compounds. SBSPKS web-server has been a valuable resource for analysis of polyketide synthase (PKS) and non-ribosomal peptide synthetase (NRPS) gene clusters. We have developed an updated version - SBSPKSv2 which is based on comprehensive analysis of sequence, structure and secondary metabolite chemical structure data from 311 experimentally characterized PKS/NRPS gene clusters with known biosynthetic products. A completely new feature of SBSPKSv2 is the inclusion of features for search in chemical space. It allows the user to compare the chemical structure of a given secondary metabolite to the chemical structures of biosynthetic intermediates and final products. For identification of catalytic domains, SBSPKS now uses profile based searches, which are computationally faster and have high sensitivity. HMM profiles have also been added for a number of new domains and motif information has been used for distinguishing condensation (C), epimerization (E) and cyclization (Cy) domains of NRPS. In summary, the new and updated SBSPKSv2 is a versatile tool for genome mining and analysis of polyketide and non-ribosomal peptide biosynthetic pathways in chemical space. The server is available at: http://www.nii.ac.in/sbspks2.html. Oxford University Press 2017-07-03 2017-04-29 /pmc/articles/PMC5570206/ /pubmed/28460065 http://dx.doi.org/10.1093/nar/gkx344 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Web Server Issue Khater, Shradha Gupta, Money Agrawal, Priyesh Sain, Neetu Prava, Jyoti Gupta, Priya Grover, Mansi Kumar, Narendra Mohanty, Debasisa SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
title | SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
title_full | SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
title_fullStr | SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
title_full_unstemmed | SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
title_short | SBSPKSv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
title_sort | sbspksv2: structure-based sequence analysis of polyketide synthases and non-ribosomal peptide synthetases |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570206/ https://www.ncbi.nlm.nih.gov/pubmed/28460065 http://dx.doi.org/10.1093/nar/gkx344 |
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