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Improved Lanthipeptide Detection and Prediction for antiSMASH
Lanthipeptides are a class of ribosomally synthesised and post-translationally modified peptide (RiPP) natural products from the bacterial secondary metabolism. Their name is derived from the characteristic lanthionine or methyl-lanthionine residues contained in the processed peptide. Lanthipeptides...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930743/ https://www.ncbi.nlm.nih.gov/pubmed/24586765 http://dx.doi.org/10.1371/journal.pone.0089420 |
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author | Blin, Kai Kazempour, Daniyal Wohlleben, Wolfgang Weber, Tilmann |
author_facet | Blin, Kai Kazempour, Daniyal Wohlleben, Wolfgang Weber, Tilmann |
author_sort | Blin, Kai |
collection | PubMed |
description | Lanthipeptides are a class of ribosomally synthesised and post-translationally modified peptide (RiPP) natural products from the bacterial secondary metabolism. Their name is derived from the characteristic lanthionine or methyl-lanthionine residues contained in the processed peptide. Lanthipeptides that possess an antibacterial activity are called lantibiotics. Whereas multiple tools exist to identify lanthipeptide gene clusters from genomic data, no programs are available to predict the post-translational modifications of lanthipeptides, such as the proteolytic cleavage of the leader peptide part or tailoring modifications based on the analysis of the gene cluster sequence. antiSMASH is a software pipeline for the identification of secondary metabolite biosynthetic clusters from genomic input and the prediction of products produced by the identified clusters. Here we present a novel antiSMASH module using a rule-based approach to combine signature motifs for biosynthetic enzymes and lanthipeptide-specific cleavage site motifs to identify lanthipeptide clusters in genomic data, assign the specific lanthipeptide class, predict prepeptide cleavage, tailoring reactions, and the processed molecular weight of the mature peptide products. |
format | Online Article Text |
id | pubmed-3930743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39307432014-02-25 Improved Lanthipeptide Detection and Prediction for antiSMASH Blin, Kai Kazempour, Daniyal Wohlleben, Wolfgang Weber, Tilmann PLoS One Research Article Lanthipeptides are a class of ribosomally synthesised and post-translationally modified peptide (RiPP) natural products from the bacterial secondary metabolism. Their name is derived from the characteristic lanthionine or methyl-lanthionine residues contained in the processed peptide. Lanthipeptides that possess an antibacterial activity are called lantibiotics. Whereas multiple tools exist to identify lanthipeptide gene clusters from genomic data, no programs are available to predict the post-translational modifications of lanthipeptides, such as the proteolytic cleavage of the leader peptide part or tailoring modifications based on the analysis of the gene cluster sequence. antiSMASH is a software pipeline for the identification of secondary metabolite biosynthetic clusters from genomic input and the prediction of products produced by the identified clusters. Here we present a novel antiSMASH module using a rule-based approach to combine signature motifs for biosynthetic enzymes and lanthipeptide-specific cleavage site motifs to identify lanthipeptide clusters in genomic data, assign the specific lanthipeptide class, predict prepeptide cleavage, tailoring reactions, and the processed molecular weight of the mature peptide products. Public Library of Science 2014-02-20 /pmc/articles/PMC3930743/ /pubmed/24586765 http://dx.doi.org/10.1371/journal.pone.0089420 Text en © 2014 Blin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Blin, Kai Kazempour, Daniyal Wohlleben, Wolfgang Weber, Tilmann Improved Lanthipeptide Detection and Prediction for antiSMASH |
title | Improved Lanthipeptide Detection and Prediction for antiSMASH |
title_full | Improved Lanthipeptide Detection and Prediction for antiSMASH |
title_fullStr | Improved Lanthipeptide Detection and Prediction for antiSMASH |
title_full_unstemmed | Improved Lanthipeptide Detection and Prediction for antiSMASH |
title_short | Improved Lanthipeptide Detection and Prediction for antiSMASH |
title_sort | improved lanthipeptide detection and prediction for antismash |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930743/ https://www.ncbi.nlm.nih.gov/pubmed/24586765 http://dx.doi.org/10.1371/journal.pone.0089420 |
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