Cofactor requirements and reconstitution of microcin B17 synthetase: a multienzyme complex that catalyzes the formation of oxazoles and thiazoles in the antibiotic microcin B17.
about
Patellamide A and C biosynthesis by a microcin-like pathway in Prochloron didemni, the cyanobacterial symbiont of Lissoclinum patellaCyclisation mechanisms in the biosynthesis of ribosomally synthesised and post-translationally modified peptidesStructural and functional insight into an unexpectedly selective N-methyltransferase involved in plantazolicin biosynthesisThermolysin-linearized microcin J25 retains the structured core of the native macrocyclic peptide and displays antimicrobial activity.Genome mining demonstrates the widespread occurrence of gene clusters encoding bacteriocins in cyanobacteria.Identification of a streptolysin S-associated gene cluster and its role in the pathogenesis of Streptococcus iniae disease.Characterization of the interaction between DNA gyrase inhibitor and DNA gyrase of Escherichia coli.Listeriolysin S, a novel peptide haemolysin associated with a subset of lineage I Listeria monocytogenesExpansion of ribosomally produced natural products: a nitrile hydratase- and Nif11-related precursor familyIdentification and analysis of the biosynthetic gene cluster encoding the thiopeptide antibiotic cyclothiazomycin in Streptomyces hygroscopicus 10-22.Manipulation of thiocillin variants by prepeptide gene replacement: structure, conformation, and activity of heterocycle substitution mutants.Thiazolyl peptide antibiotic biosynthesis: a cascade of post-translational modifications on ribosomal nascent proteins.Thiazole/oxazole-modified microcins: complex natural products from ribosomal templatesSelectivity, 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.Structure determination and interception of biosynthetic intermediates for the plantazolicin class of highly discriminating antibiotics.Dissecting the maturation steps of the lasso peptide microcin J25 in vitro.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.Discovery of a widely distributed toxin biosynthetic gene cluster.Structure of microcin B-like compounds produced by Pseudomonas syringae and species specificity of their antibacterial action.Thirteen posttranslational modifications convert a 14-residue peptide into the antibiotic thiocillin.The highly modified microcin peptide plantazolicin is associated with nematicidal activity of Bacillus amyloliquefaciens FZB42.Insights into methyltransferase specificity and bioactivity of derivatives of the antibiotic plantazolicinMorphing peptide backbones into heterocycles.Revealing nature's synthetic potential through the study of ribosomal natural product biosynthesis.Low-molecular-weight post-translationally modified microcins.Insights into the mechanism of peptide cyclodehydrations achieved through the chemoenzymatic generation of amide derivatives.Follow the leader: the use of leader peptides to guide natural product biosynthesis.Ribosomally synthesized and post-translationally modified peptide natural products: new insights into the role of leader and core peptides during biosynthesis.How nature morphs peptide scaffolds into antibioticsCapture of micrococcin biosynthetic intermediates reveals C-terminal processing as an obligatory step for in vivo maturation.Ribosomal peptide natural products: bridging the ribosomal and nonribosomal worlds.Streptolysin S-like virulence factors: the continuing sagA.Orchestration of enzymatic processing by thiazole/oxazole-modified microcin dehydrogenases.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.Structural and functional dissection of the heterocyclic peptide cytotoxin streptolysin S.Insights into heterocyclization from two highly similar enzymes.In Vitro Biosynthesis and Substrate Tolerance of the Plantazolicin Family of Natural Products.
P2860
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P2860
Cofactor requirements and reconstitution of microcin B17 synthetase: a multienzyme complex that catalyzes the formation of oxazoles and thiazoles in the antibiotic microcin B17.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Cofactor requirements and reco ...... n the antibiotic microcin B17.
@en
type
label
Cofactor requirements and reco ...... n the antibiotic microcin B17.
@en
prefLabel
Cofactor requirements and reco ...... n the antibiotic microcin B17.
@en
P2093
P356
P1433
P1476
Cofactor requirements and reco ...... n the antibiotic microcin B17.
@en
P2093
Kelleher NL
P304
P356
10.1021/BI982975Q
P407
P577
1999-04-01T00:00:00Z