Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework. - Test2 - elhamkhani - TriplyDB

Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.

Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.

http://www.wikidata.org/entity/Q37389799

about

Radical-mediated enzymatic carbon chain fragmentation-recombination Mechanistic and functional versatility of radical SAM enzymes Catalytic Promiscuity of the Radical S-adenosyl-L-methionine Enzyme NosL Thiopeptide antibiotics: retrospective and recent advances Radical SAM-mediated methylation reactions Radical-mediated enzymatic methylation: a tale of two SAMS ThioFinder: a web-based tool for the identification of thiopeptide gene clusters in DNA sequences Mining of the pyrrolamide antibiotics analogs in Streptomyces netropsis reveals the amidohydrolase-dependent "iterative strategy" underlying the pyrrole polymerization The phosphopantetheinyl transferases: catalysis of a post-translational modification crucial for life Comparative genomics and transcriptomics of Propionibacterium acnes A simple reverse genetics approach to elucidating the biosynthetic pathway of nocathiacin.Identification and analysis of the biosynthetic gene cluster encoding the thiopeptide antibiotic cyclothiazomycin in Streptomyces hygroscopicus 10-22.Emerging themes in radical SAM chemistry Manipulation of thiocillin variants by prepeptide gene replacement: structure, conformation, and activity of heterocycle substitution mutants.Natural products version 2.0: connecting genes to molecules.Genetic interception and structural characterization of thiopeptide cyclization precursors from Bacillus cereus.Thiazolyl peptide antibiotic biosynthesis: a cascade of post-translational modifications on ribosomal nascent proteins.Genome mining for ribosomally synthesized natural products Thiazole/oxazole-modified microcins: complex natural products from ribosomal templates A systematic analysis of biosynthetic gene clusters in the human microbiome reveals a common family of 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.Genome shuffling and ribosome engineering of Streptomyces actuosus for high-yield nosiheptide production.Identification of an Auxiliary Leader Peptide-Binding Protein Required for Azoline Formation in Ribosomal Natural Products.Characterization of NocL involved in thiopeptide nocathiacin I biosynthesis: a [4Fe-4S] cluster and the catalysis of a radical S-adenosylmethionine enzyme.Peptidomimetics via modifications of amino acids and peptide bonds.Identification of the thiazolyl peptide GE37468 gene cluster from Streptomyces ATCC 55365 and heterologous expression in Streptomyces lividans.Complex biotransformations catalyzed by radical S-adenosylmethionine enzymes.Structure-based Mechanistic Insights into Terminal Amide Synthase in Nosiheptide-Represented Thiopeptides Biosynthesis Elucidating and engineering thiopeptide biosynthesis.Microbial and biochemical basis of a Fusarium wilt-suppressive soil New Insights into the Biosynthetic Logic of Ribosomally Synthesized and Post-translationally Modified Peptide Natural Products.Revealing nature's synthetic potential through the study of ribosomal natural product biosynthesis.Follow the leader: the use of leader peptides to guide natural product biosynthesis.Radical new paradigm for heme degradation in Escherichia coli O157:H7.An α/β-hydrolase fold protein in the biosynthesis of thiostrepton exhibits a dual activity for endopeptidyl hydrolysis and epoxide ring opening/macrocyclization.Recent advances in thiopeptide antibiotic biosynthesis.Radical S-adenosylmethionine enzymes.Radical S-adenosylmethionine enzymes: mechanism, control and function.Biosynthesis of thiopeptide antibiotics and their pathway engineering.

P2860

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P2860

Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework.

http://www.wikidata.org/entity/Q37389799

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on October 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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ACS Chemical Biology

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Nosiheptide biosynthesis featu ...... eristic thiopeptide framework.

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Ben Shen

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Evelyn Wendt-Pienkowski

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Gongli Tang

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Qi Zhang

http://www.w3.org/2001/XMLSchema#string

Rijing Liao

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Wen Liu

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Yi Yu

http://www.w3.org/2001/XMLSchema#string

Ying Ding

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P2860

Antimicrobial evaluation of nocathiacins, a thiazole peptide class of antibiotics.

Thiostrepton biosynthesis: prototype for a new family of bacteriocins.

A global assembly line for cyanobactins

Nosiheptide, a sulfur-containing peptide antibiotic isolated from Streptomyces actuosus 40037.

Thiopeptide antibiotics.

Assembly-line enzymology for polyketide and nonribosomal Peptide antibiotics: logic, machinery, and mechanisms.

Thiamine biosynthesis in Escherichia coli: identification of the intermediate and by-product derived from tyrosine.

Discovery of a widely distributed toxin biosynthetic gene cluster.

Thirteen posttranslational modifications convert a 14-residue peptide into the antibiotic thiocillin.

Thiopeptide biosynthesis featuring ribosomally synthesized precursor peptides and conserved posttranslational modifications.

P304

855-864

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scholarly article

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10.1021/CB900133X

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10

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4

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2009-10-01T00:00:00Z

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26740019

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19678698

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P921

3-methylindolyl precursor of nosiheptide

3,4-dimethylindolyl precursor of nosiheptide

3,4-dimethylindole-2-carboxylate

P932

2763056

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