Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
about
Cyclisation mechanisms in the biosynthesis of ribosomally synthesised and post-translationally modified peptidesHUMAN MICROBIOTA. Small molecules from the human microbiotaLessons learned from the transformation of natural product discovery to a genome-driven endeavorStructural and functional insight into an unexpectedly selective N-methyltransferase involved in plantazolicin biosynthesisBacteriocins of lactic acid bacteria: extending the familyRibosomal route to small-molecule diversityStructural investigation of ribosomally synthesized natural products by hypothetical structure enumeration and evaluation using tandem MS.Selectivity, directionality, and promiscuity in peptide processing from a Bacillus sp. Al Hakam cyclodehydratase.Discovery of a new ATP-binding motif involved in peptidic azoline biosynthesis.Nucleophilic 1,4-additions for natural product discovery.Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.YcaO domains use ATP to activate amide backbones during peptide cyclodehydrations.Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature.HIV protease inhibitors block streptolysin S productionIdentification of an Auxiliary Leader Peptide-Binding Protein Required for Azoline Formation in Ribosomal Natural Products.Codon randomization for rapid exploration of chemical space in thiopeptide antibiotic variants.High divergence of the precursor peptides in combinatorial lanthipeptide biosynthesis.Cross-species comparison of the Burkholderia pseudomallei, Burkholderia thailandensis, and Burkholderia mallei quorum-sensing regulons.Complete genome sequence of producer of the glycopeptide antibiotic Aculeximycin Kutzneria albida DSM 43870T, a representative of minor genus of PseudonocardiaceaeIdentification of the minimal cytolytic unit for streptolysin S and an expansion of the toxin family.Expanded natural product diversity revealed by analysis of lanthipeptide-like gene clusters in actinobacteriaThe genomic landscape of ribosomal peptides containing thiazole and oxazole heterocycles.A prevalent peptide-binding domain guides ribosomal natural product biosynthesis.Insights into methyltransferase specificity and bioactivity of derivatives of the antibiotic plantazolicinIdentification and classification of known and putative antimicrobial compounds produced by a wide variety of Bacillales species.Revealing nature's synthetic potential through the study of ribosomal natural product biosynthesis.In Vitro Biosynthesis of the Core Scaffold of the Thiopeptide ThiomuracinMethanobactin and the Link between Copper and Bacterial Methane OxidationSynthesis of plantazolicin analogues enables dissection of ligand binding interactions of a highly selective methyltransferaseRibosomally synthesized and post-translationally modified peptide natural products: new insights into the role of leader and core peptides during biosynthesis.An α/β-hydrolase fold protein in the biosynthesis of thiostrepton exhibits a dual activity for endopeptidyl hydrolysis and epoxide ring opening/macrocyclization.Streptolysin S-like virulence factors: the continuing sagA.Orchestration of enzymatic processing by thiazole/oxazole-modified microcin dehydrogenases.Biosynthesis of thiopeptide antibiotics and their pathway engineering.The structural biology of patellamide biosynthesisStreptococcal toxins: role in pathogenesis and disease.YcaO-Dependent Posttranslational Amide Activation: Biosynthesis, Structure, and Function.The C-terminal part of microcin B is crucial for DNA gyrase inhibition and antibiotic uptake by sensitive cells.Oxidative Cyclization in Natural Product BiosynthesisPost-translational modifications involved in the biosynthesis of thiopeptide antibiotics.
P2860
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P2860
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@ast
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@en
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@nl
type
label
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@ast
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@en
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@nl
prefLabel
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@ast
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@en
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@nl
P2860
P1476
Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates
@en
P2093
Joel O Melby
Nathan J Nard
P2860
P304
P356
10.1016/J.CBPA.2011.02.027
P577
2011-03-21T00:00:00Z