antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences.
antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences.
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Antismash:细菌和真菌基因组序列中继发代谢物生物合成簇的快速鉴定,注释和分析。
DOI:
10.1093/nar/gkr466
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发表时间:
2011-07
影响因子:
14.9
通讯作者:
Breitling R
中科院分区:
文献类型:
--
作者:
Medema MH;Blin K;Cimermancic P;de Jager V;Zakrzewski P;Fischbach MA;Weber T;Takano E;Breitling R
Bacterial and fungal secondary metabolism is a rich source of novel bioactive compounds with potential pharmaceutical applications as antibiotics, anti-tumor drugs or cholesterol-lowering drugs. To find new drug candidates, microbiologists are increasingly relying on sequencing genomes of a wide variety of microbes. However, rapidly and reliably pinpointing all the potential gene clusters for secondary metabolites in dozens of newly sequenced genomes has been extremely challenging, due to their biochemical heterogeneity, the presence of unknown enzymes and the dispersed nature of the necessary specialized bioinformatics tools and resources. Here, we present antiSMASH (antibiotics & Secondary Metabolite Analysis Shell), the first comprehensive pipeline capable of identifying biosynthetic loci covering the whole range of known secondary metabolite compound classes (polyketides, non-ribosomal peptides, terpenes, aminoglycosides, aminocoumarins, indolocarbazoles, lantibiotics, bacteriocins, nucleosides, beta-lactams, butyrolactones, siderophores, melanins and others). It aligns the identified regions at the gene cluster level to their nearest relatives from a database containing all other known gene clusters, and integrates or cross-links all previously available secondary-metabolite specific gene analysis methods in one interactive view. antiSMASH is available at http://antismash.secondarymetabolites.org.
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影响因子:
5.6
作者:
Yadav, G;Gokhale, RS;Mohanty, B
通讯作者:
Mohanty, B
影响因子:
4.1
作者:
Weber, T.;Rausch, C.;Wohlleben, W.
通讯作者:
Wohlleben, W.
影响因子:
14.9
作者:
Letunic I;Doerks T;Bork P
通讯作者:
Bork P
影响因子:
14.9
作者:
Finn RD;Mistry J;Tate J;Coggill P;Heger A;Pollington JE;Gavin OL;Gunasekaran P;Ceric G;Forslund K;Holm L;Sonnhammer EL;Eddy SR;Bateman A
通讯作者:
Bateman A
影响因子:
3
作者:
Camacho C;Coulouris G;Avagyan V;Ma N;Papadopoulos J;Bealer K;Madden TL
通讯作者:
Madden TL