antiSMASH 7.0: new and improved predictions for detection, regulation, chemical structures and visualisation.
antiSMASH 7.0: new and improved predictions for detection, regulation, chemical structures and visualisation.
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DOI:
10.1093/nar/gkad344
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发表时间:
2023-07-05
影响因子:
14.9
通讯作者:
Weber, Tilmann
中科院分区:
文献类型:
--
作者:
Blin, Kai;Shaw, Simon;Augustijn, Hannah E.;Reitz, Zachary L.;Biermann, Friederike;Alanjary, Mohammad;Fetter, Artem;Terlouw, Barbara R.;Metcalf, William W.;Helfrich, Eric J. N.;van Wezel, Gilles P.;Medema, Marnix H.;Weber, Tilmann
Microorganisms produce small bioactive compounds as part of their secondary or specialised metabolism. Often, such metabolites have antimicrobial, anticancer, antifungal, antiviral or other bio-activities and thus play an important role for applications in medicine and agriculture. In the past decade, genome mining has become a widely-used method to explore, access, and analyse the available biodiversity of these compounds. Since 2011, the ‘antibiotics and secondary metabolite analysis shell—antiSMASH’ (https://antismash.secondarymetabolites.org/) has supported researchers in their microbial genome mining tasks, both as a free to use web server and as a standalone tool under an OSI-approved open source licence. It is currently the most widely used tool for detecting and characterising biosynthetic gene clusters (BGCs) in archaea, bacteria, and fungi. Here, we present the updated version 7 of antiSMASH. antiSMASH 7 increases the number of supported cluster types from 71 to 81, as well as containing improvements in the areas of chemical structure prediction, enzymatic assembly-line visualisation and gene cluster regulation. antiSMASH 7 increases the number of supported cluster types from 71 to 81, as well as containing improvements in the areas of chemical structure prediction, enzymatic assembly-line visualisation and gene cluster regulation.
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影响因子:
14.9
作者:
Mistry J;Chuguransky S;Williams L;Qureshi M;Salazar GA;Sonnhammer ELL;Tosatto SCE;Paladin L;Raj S;Richardson LJ;Finn RD;Bateman A
通讯作者:
Bateman A
影响因子:
9.2
作者:
Kautsar SA;van der Hooft JJJ;de Ridder D;Medema MH
通讯作者:
Medema MH
影响因子:
14.9
作者:
Haft DH;Selengut JD;Richter RA;Harkins D;Basu MK;Beck E
通讯作者:
Beck E
影响因子:
9.5
作者:
Blin K;Kim HU;Medema MH;Weber T
通讯作者:
Weber T
影响因子:
14.8
作者:
Medema, Marnix H.;Fischbach, Michael A.
通讯作者:
Fischbach, Michael A.