Works matching DE "THIOPEPTIDES"
Results: 26
Ynamide‐Mediated Thiopeptide Synthesis.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1396, doi. 10.1002/ange.201811586
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- Article
Synthetic studies on heterocyclic natural products.
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- Canadian Journal of Chemistry, 2014, v. 92, n. 3, p. 186, doi. 10.1139/cjc-2013-0543
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- Article
Genome Mining‐Mediated Discovery of a New Avermipeptin Analogue in Streptomyces actuosus ATCC 25421.
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- ChemistryOpen, 2018, v. 7, n. 7, p. 558, doi. 10.1002/open.201800130
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Genome Shuffling and Ribosome Engineering of Streptomyces actuosus for High-Yield Nosiheptide Production.
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- Applied Biochemistry & Biotechnology, 2014, v. 173, n. 6, p. 1553, doi. 10.1007/s12010-014-0948-5
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Microbiology: Vaginal microbe makes drug.
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- Nature, 2014, v. 513, n. 7518, p. 283, doi. 10.1038/513283d
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- Article
Structure-activity relationships of thiostrepton derivatives: implications for rational drug design.
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- Journal of Computer-Aided Molecular Design, 2014, v. 28, n. 12, p. 1205, doi. 10.1007/s10822-014-9797-0
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Identification and Functional Analysis of the Nocardithiocin Gene Cluster in Nocardia pseudobrasiliensis.
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- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0143264
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Thiopeptide Antibiotics: Retrospective and Recent Advances.
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- Marine Drugs, 2014, v. 12, n. 1, p. 317, doi. 10.3390/md12010317
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Microbiome: Commensally sourced antibiotics.
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- Nature Reviews Microbiology, 2014, v. 12, n. 11, p. 726, doi. 10.1038/nrmicro3363
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Structure-based Mechanistic Insights into Terminal Amide Synthase in Nosiheptide-Represented Thiopeptides Biosynthesis.
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- Scientific Reports, 2015, p. 12744, doi. 10.1038/srep12744
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Effect Analysis of Mineral Salt Concentrations on Nosiheptide Production by Streptomyces actuosus Z-10 Using Response Surface Methodology.
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- Molecules, 2014, v. 19, n. 10, p. 15507, doi. 10.3390/molecules191015507
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Biosynthesis of the Central Piperidine Nitrogen Heterocycle in Series a Thiopeptides.
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- Chinese Journal of Chemistry, 2019, v. 37, n. 1, p. 35, doi. 10.1002/cjoc.201800497
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A prevalent peptide-binding domain guides ribosomal natural product biosynthesis.
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- Nature Chemical Biology, 2015, v. 11, n. 8, p. 564, doi. 10.1038/nchembio.1856
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Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C−H Arylation/Ring-Transformation Strategy.
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- Chemistry - A European Journal, 2016, v. 22, n. 13, p. 4384, doi. 10.1002/chem.201600351
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- Article
The Catalytic Mechanism of the Class C Radical S-Adenosylmethionine Methyltransferase NosN.
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- Angewandte Chemie, 2017, v. 129, n. 14, p. 3915, doi. 10.1002/ange.201609948
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Totalsynthese von Nosiheptid.
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- Angewandte Chemie, 2016, v. 128, n. 33, p. 9924, doi. 10.1002/ange.201603140
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Total Synthesis and Stereochemical Assignment of Baringolin.
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- Angewandte Chemie, 2013, v. 125, n. 30, p. 7972, doi. 10.1002/ange.201302372
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Crystallographic analysis of NosA, which catalyzes terminal amide formation in the biosynthesis of nosiheptide.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2015, v. 71, n. 8, p. 1033, doi. 10.1107/S2053230X15011085
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Structure, function, and biosynthesis of thiazole/oxazole-modified microcins.
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- Molecular Biology, 2014, v. 48, n. 1, p. 29, doi. 10.1134/S0026893314010105
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Heterologous Expression of the Thiopeptide Antibiotic GE2270 from <i>Planobispora rosea</i> ATCC 53733 in <i>Streptomyces coelicolor</i> Requires Deletion of Ribosomal Genes from the Expression Construct.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090499
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ThioFinder: A Web-Based Tool for the Identification of Thiopeptide Gene Clusters in DNA Sequences.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045878
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From 2,6-Dichloronicotinic Acid to Thiopeptide Cores.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 28, p. 6404, doi. 10.1002/ejoc.201300877
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Total Synthesis of Nosiheptide.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 33, p. 9772, doi. 10.1002/anie.201603140
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- Article
Mechanistic Insights into the Radical S-adenosyl- l-methionine Enzyme NosL From a Substrate Analogue and the Shunt Products.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 10, p. 3334, doi. 10.1002/anie.201509900
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Thiopeptide Engineering: A Multidisciplinary Effort towards Future Drugs.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 26, p. 6602, doi. 10.1002/anie.201307288
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- Article
Total Synthesis and Stereochemical Assignment of Baringolin.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 30, p. 7818, doi. 10.1002/anie.201302372
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- Article