Four-electron oxidation of p-hydroxylaminobenzoate to p-nitrobenzoate by a peroxodiferric complex in AurF from Streptomyces thioluteus.
about
Detection of formate, rather than carbon monoxide, as the stoichiometric coproduct in conversion of fatty aldehydes to alkanes by a cyanobacterial aldehyde decarbonylase.Conversion of fatty aldehydes to alka(e)nes and formate by a cyanobacterial aldehyde decarbonylase: cryptic redox by an unusual dimetal oxygenase.Cyanobacterial alkane biosynthesis further expands the catalytic repertoire of the ferritin-like 'di-iron-carboxylate' proteins.Mechanistic studies of reactions of peroxodiiron(III) intermediates in T201 variants of toluene/o-xylene monooxygenase hydroxylaseCombining Mass Spectrometric Metabolic Profiling with Genomic Analysis: A Powerful Approach for Discovering Natural Products from Cyanobacteria.CmlI is an N-oxygenase in the biosynthesis of chloramphenicolSubstrate-triggered addition of dioxygen to the diferrous cofactor of aldehyde-deformylating oxygenase to form a diferric-peroxide intermediate.Novel Approaches for the Accumulation of Oxygenated Intermediates to Multi-Millimolar Concentrations.Naturally-occurring nitro compounds.Structure/function correlations over binuclear non-heme iron active sitesDivergent mechanisms of iron-containing enzymes for hydrocarbon biosynthesis.Heteroatom-Heteroatom Bond Formation in Natural Product Biosynthesis.Alteration of the oxygen-dependent reactivity of de novo Due Ferri proteins.Molecular-Level Insight into the Differential Oxidase and Oxygenase Reactivities of de Novo Due Ferri Proteins.Crystal structure of CmlI, the arylamine oxygenase from the chloramphenicol biosynthetic pathway.Mechanism for Six-Electron Aryl-N-Oxygenation by the Non-Heme Diiron Enzyme CmlI.An unusual peroxo intermediate of the arylamine oxygenase of the chloramphenicol biosynthetic pathway.Biosynthesis-assisted structural elucidation of the bartolosides, chlorinated aromatic glycolipids from cyanobacteria.CmlI N-Oxygenase Catalyzes the Final Three Steps in Chloramphenicol Biosynthesis without Dissociation of Intermediates.Peroxide Activation for Electrophilic Reactivity by the Binuclear Non-heme Iron Enzyme AurF.A nitrous acid biosynthetic pathway for diazo group formation in bacteria.Diiron monooxygenases in natural product biosynthesis.A ribonucleotide reductase-like electron transfer system in the nitroaryl-forming N-oxygenase AurF.
P2860
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P2860
Four-electron oxidation of p-hydroxylaminobenzoate to p-nitrobenzoate by a peroxodiferric complex in AurF from Streptomyces thioluteus.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@ast
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@en
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@nl
type
label
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@ast
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@en
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@nl
prefLabel
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@ast
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@en
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@nl
P2093
P2860
P356
P1476
Four-electron oxidation of p-h ...... from Streptomyces thioluteus.
@en
P2093
J Martin Bollinger
Victoria Korneeva Korboukh
P2860
P304
15722-15727
P356
10.1073/PNAS.1002785107
P407
P577
2010-08-23T00:00:00Z