antiSMASH 8.0: extended gene cluster detection capabilities and analyses of chemistry, enzymology, and regulation

Kai Blin(Novo Nordisk Foundation), Simon J. Shaw(Novo Nordisk Foundation), Lisa Vader(Novo Nordisk Foundation), Judit Szenei(Novo Nordisk Foundation), Zachary L. Reitz(University of California, Santa Barbara), Hannah E. Augustijn(Leiden University), José D D Cediel-Becerra(Florida Museum of Natural History), Valérie de Crécy‐Lagard(Florida Museum of Natural History), Robert A. Koetsier(Wageningen University & Research), Sam E. Williams(Novo Nordisk Foundation), Pablo Cruz‐Morales(Novo Nordisk Foundation), Sopida Wongwas(University of Warwick), Alejandro E Segurado Luchsinger(VIB-KU Leuven Center for Microbiology), Friederike Biermann(Goethe University Frankfurt), Aleksandra Korenskaia(Czech Academy of Sciences, Institute of Microbiology), Mitja M. Zdouc(Wageningen University & Research), David Meijer(Wageningen University & Research), Barbara R. Terlouw(Wageningen University & Research), Justin J. J. van der Hooft(University of Johannesburg), Nadine Ziemert(Czech Academy of Sciences, Institute of Microbiology), Eric J. N. Helfrich(Goethe University Frankfurt), Joleen Masschelein(VIB-KU Leuven Center for Microbiology), Christophe Corre(University of Warwick), Marc G. Chevrette(Florida Museum of Natural History), Gilles P. van Wezel(Leiden University), Marnix H. Medema(Leiden University), Tilmann Weber(Novo Nordisk Foundation)
Nucleic Acids Research
April 25, 2025
Cited by 411Open Access
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Abstract

Microorganisms synthesize small bioactive compounds through their secondary or specialized metabolism. Those compounds play an important role in microbial interactions and soil health, but are also crucial for the development of pharmaceuticals or agrochemicals. Over the past decades, advancements in genome sequencing have enabled the identification of large numbers of biosynthetic gene clusters directly from microbial genomes. Since its inception in 2011, antiSMASH (https://antismash.secondarymetabolites.org/), has become the leading tool for detecting and characterizing these gene clusters in bacteria and fungi. This paper introduces version 8 of antiSMASH, which has increased the number of detectable cluster types from 81 to 101, and has improved analysis support for terpenoids and tailoring enzymes, as well as improvements in the analysis of modular enzymes like polyketide synthases and nonribosomal peptide synthetases. These modifications keep antiSMASH up-to-date with developments in the field and extend its overall predictive capabilities for natural product genome mining.


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