AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification

Many antibiotics, chemotherapeutics, crop protection agents and food preservatives originate from molecules produced by bacteria, fungi or plants. In recent years, genome mining methodologies have been widely adopted to identify and characterize the biosynthetic gene clusters encoding the production of such compounds. Since 2011, the â € antibiotics and secondary metabolite analysis shell - antiSMASH' has assisted researchers in efficiently performing this, both as a web server and a standalone tool. Here, we present the thoroughly updated antiSMASH version 4, which adds several novel features, including prediction of gene cluster boundaries using the ClusterFinder method or the newly integrated CASSIS algorithm, improved substrate specificity prediction for non-ribosomal peptide synthetase adenylation domains based on the new SANDPUMA algorithm, improved predictions for terpene and ribosomally synthesized and post-translationally modified peptides cluster products, reporting of sequence similarity to proteins encoded in experimentally characterized gene clusters on a per-protein basis and a domain-level alignment tool for comparative analysis of trans-AT polyketide synthase assembly line architectures. Additionally, several usability features have been updated and improved. Together, these improvements make antiSMASH up-to-date with the latest developments in natural product research and will further facilitate computational genome mining for the discovery of novel bioactive molecules.

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Main Authors: Blin, Kai, Wolf, Thomas, Chevrette, Marc G., Lu, Xiaowen, Schwalen, Christopher J., Kautsar, Satria A., Suarez Duran, Hernando G., De Los Santos, Emmanuel L.C., Kim, Hyun Uk, Nave, Mariana, Dickschat, Jeroen S., Mitchell, Douglas A., Shelest, Ekaterina, Breitling, Rainer, Takano, Eriko, Lee, Sang Yup, Weber, Tilmann, Medema, Marnix H.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:Life Science,
Online Access:https://research.wur.nl/en/publications/antismash-40-improvements-in-chemistry-prediction-and-gene-cluste
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spelling dig-wur-nl-wurpubs-5243912024-10-01 Blin, Kai Wolf, Thomas Chevrette, Marc G. Lu, Xiaowen Schwalen, Christopher J. Kautsar, Satria A. Suarez Duran, Hernando G. De Los Santos, Emmanuel L.C. Kim, Hyun Uk Nave, Mariana Dickschat, Jeroen S. Mitchell, Douglas A. Shelest, Ekaterina Breitling, Rainer Takano, Eriko Lee, Sang Yup Weber, Tilmann Medema, Marnix H. Article/Letter to editor Nucleic acids research 45 (2017) W1 ISSN: 0305-1048 AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification 2017 Many antibiotics, chemotherapeutics, crop protection agents and food preservatives originate from molecules produced by bacteria, fungi or plants. In recent years, genome mining methodologies have been widely adopted to identify and characterize the biosynthetic gene clusters encoding the production of such compounds. Since 2011, the â € antibiotics and secondary metabolite analysis shell - antiSMASH' has assisted researchers in efficiently performing this, both as a web server and a standalone tool. Here, we present the thoroughly updated antiSMASH version 4, which adds several novel features, including prediction of gene cluster boundaries using the ClusterFinder method or the newly integrated CASSIS algorithm, improved substrate specificity prediction for non-ribosomal peptide synthetase adenylation domains based on the new SANDPUMA algorithm, improved predictions for terpene and ribosomally synthesized and post-translationally modified peptides cluster products, reporting of sequence similarity to proteins encoded in experimentally characterized gene clusters on a per-protein basis and a domain-level alignment tool for comparative analysis of trans-AT polyketide synthase assembly line architectures. Additionally, several usability features have been updated and improved. Together, these improvements make antiSMASH up-to-date with the latest developments in natural product research and will further facilitate computational genome mining for the discovery of novel bioactive molecules. en application/pdf https://research.wur.nl/en/publications/antismash-40-improvements-in-chemistry-prediction-and-gene-cluste 10.1093/nar/gkx319 https://edepot.wur.nl/420215 Life Science https://creativecommons.org/licenses/by/4.0/ Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic Life Science
Life Science
spellingShingle Life Science
Life Science
Blin, Kai
Wolf, Thomas
Chevrette, Marc G.
Lu, Xiaowen
Schwalen, Christopher J.
Kautsar, Satria A.
Suarez Duran, Hernando G.
De Los Santos, Emmanuel L.C.
Kim, Hyun Uk
Nave, Mariana
Dickschat, Jeroen S.
Mitchell, Douglas A.
Shelest, Ekaterina
Breitling, Rainer
Takano, Eriko
Lee, Sang Yup
Weber, Tilmann
Medema, Marnix H.
AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification
description Many antibiotics, chemotherapeutics, crop protection agents and food preservatives originate from molecules produced by bacteria, fungi or plants. In recent years, genome mining methodologies have been widely adopted to identify and characterize the biosynthetic gene clusters encoding the production of such compounds. Since 2011, the â € antibiotics and secondary metabolite analysis shell - antiSMASH' has assisted researchers in efficiently performing this, both as a web server and a standalone tool. Here, we present the thoroughly updated antiSMASH version 4, which adds several novel features, including prediction of gene cluster boundaries using the ClusterFinder method or the newly integrated CASSIS algorithm, improved substrate specificity prediction for non-ribosomal peptide synthetase adenylation domains based on the new SANDPUMA algorithm, improved predictions for terpene and ribosomally synthesized and post-translationally modified peptides cluster products, reporting of sequence similarity to proteins encoded in experimentally characterized gene clusters on a per-protein basis and a domain-level alignment tool for comparative analysis of trans-AT polyketide synthase assembly line architectures. Additionally, several usability features have been updated and improved. Together, these improvements make antiSMASH up-to-date with the latest developments in natural product research and will further facilitate computational genome mining for the discovery of novel bioactive molecules.
format Article/Letter to editor
topic_facet Life Science
author Blin, Kai
Wolf, Thomas
Chevrette, Marc G.
Lu, Xiaowen
Schwalen, Christopher J.
Kautsar, Satria A.
Suarez Duran, Hernando G.
De Los Santos, Emmanuel L.C.
Kim, Hyun Uk
Nave, Mariana
Dickschat, Jeroen S.
Mitchell, Douglas A.
Shelest, Ekaterina
Breitling, Rainer
Takano, Eriko
Lee, Sang Yup
Weber, Tilmann
Medema, Marnix H.
author_facet Blin, Kai
Wolf, Thomas
Chevrette, Marc G.
Lu, Xiaowen
Schwalen, Christopher J.
Kautsar, Satria A.
Suarez Duran, Hernando G.
De Los Santos, Emmanuel L.C.
Kim, Hyun Uk
Nave, Mariana
Dickschat, Jeroen S.
Mitchell, Douglas A.
Shelest, Ekaterina
Breitling, Rainer
Takano, Eriko
Lee, Sang Yup
Weber, Tilmann
Medema, Marnix H.
author_sort Blin, Kai
title AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification
title_short AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification
title_full AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification
title_fullStr AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification
title_full_unstemmed AntiSMASH 4.0 - improvements in chemistry prediction and gene cluster boundary identification
title_sort antismash 4.0 - improvements in chemistry prediction and gene cluster boundary identification
url https://research.wur.nl/en/publications/antismash-40-improvements-in-chemistry-prediction-and-gene-cluste
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