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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...

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Autores principales: Khater, Shradha, Gupta, Money, Agrawal, Priyesh, Sain, Neetu, Prava, Jyoti, Gupta, Priya, Grover, Mansi, Kumar, Narendra, Mohanty, Debasisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
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.
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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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