Conversion of (2S)-arginine to (2S,3R)-capreomycidine by VioC and VioD from the viomycin biosynthetic pathway of Streptomyces sp. strain ATCC11861.
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Investigations into viomycin biosynthesis by using heterologous production in Streptomyces lividansMuraymycin nucleoside-peptide antibiotics: uridine-derived natural products as lead structures for the development of novel antibacterial agentsStructural basis for the erythro-stereospecificity of the l-arginine oxygenase VioC in viomycin biosynthesisStructural and Functional Characterization of MppR, an Enduracididine Biosynthetic Enzyme from Streptomyces hygroscopicus : Functional Diversity in the Acetoacetate Decarboxylase-like SuperfamilyBiosynthesis of streptolidine involved two unexpected intermediates produced by a dihydroxylase and a cyclase through unusual mechanismsThe biosynthetic gene cluster of zorbamycin, a member of the bleomycin family of antitumor antibiotics, from Streptomyces flavoviridis ATCC 21892.Roles of VioG and VioQ in the incorporation and modification of the Capreomycidine residue in the peptide antibiotic viomycinMechanistically distinct nonribosomal peptide synthetases assemble the structurally related antibiotics viomycin and capreomycin.Characterization of LipL as a non-heme, Fe(II)-dependent α-ketoglutarate:UMP dioxygenase that generates uridine-5'-aldehyde during A-90289 biosynthesis.Nonribosomal peptide synthetases involved in the production of medically relevant natural products.Identification of the biosynthetic gene cluster and an additional gene for resistance to the antituberculosis drug capreomycinNonribosomal Peptide Synthesis-Principles and Prospects.The α-ketoglutarate/Fe(II)-dependent dioxygenase VldW is responsible for the formation of validamycin B.A biomimetic domino reaction for the concise synthesis of capreomycidine and epicapreomycidine.Biosynthesis of natural products containing β-amino acids.Oxidative Cyclization in Natural Product BiosynthesisTargeting Reactive Carbonyls for Identifying Natural Products and Their Biosynthetic Origins.Novel Enzyme Family Found in Filamentous Fungi Catalyzing trans-4-Hydroxylation of L-Pipecolic Acid.Mining of a streptothricin gene cluster from Streptomyces sp. TP-A0356 genome via heterologous expression.Visualizing the Reaction Cycle in an Iron(II)- and 2-(Oxo)-glutarate-Dependent Hydroxylase.Synthesis and Identification of Key Biosynthetic Intermediates for the Formation of the Tricyclic Skeleton of Saxitoxin.
P2860
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P2860
Conversion of (2S)-arginine to (2S,3R)-capreomycidine by VioC and VioD from the viomycin biosynthetic pathway of Streptomyces sp. strain ATCC11861.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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name
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@en
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@nl
type
label
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@en
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@nl
prefLabel
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@en
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@nl
P2093
P2860
P921
P356
P1433
P1476
Conversion of (2S)-arginine to ...... ptomyces sp. strain ATCC11861.
@en
P2093
Jianhua Ju
Michael G Thomas
Sarah G Ozanick
P2860
P304
P356
10.1002/CBIC.200400136
P577
2004-09-01T00:00:00Z