Simple synthesis of a 4a-hydroperoxy adduct of a 1,5-dihydroflavine: preliminary studies of a model for bacterial luciferase.
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Revealing the moonlighting role of NADP in the structure of a flavin-containing monooxygenaseBacterial bioluminescence light emission in the mixed function oxidation of reduced flavin and fatty aldehydeCatalytic mechanism of 2-hydroxybiphenyl 3-monooxygenase, a flavoprotein from Pseudomonas azelaica HBP1Ammosamide D, an oxidatively ring opened ammosamide analog from a marine-derived Streptomyces variabilis.An overview of the mechanism, substrate specificities, and structure of FMOs.Bacterial bioluminescence: Spectral study of the emitters in the in vitro reactionCatalytic Amine Oxidation under Ambient Aerobic Conditions: Mimicry of Monoamine Oxidase BTheoretical investigation of the [1,2]-sigmatropic hydrogen migration in the mechanism of oxidation of 2-aminobenzoyl-CoA by 2-aminobenzoyl-CoA monooxygenase/reductase.Chemiluminescent reactions and electrophilic oxygen donating ability of 4a-hydroperoxyflavins: general synthetic method for the preparation of N5-alkyl-1,5-dihydroflavins.Structure of the oxygen adduct intermediate in the bacterial luciferase reaction: C nuclear magnetic resonance determinationOverexpression of the FAD-binding domain of the sulphite reductase flavoprotein component from Escherichia coli and its inhibition by iodonium diphenyl chloride.Biomimetic flavin-catalysed reactions for organic synthesis.Perspectives on Bioluminescence Mechanisms.Bioluminescence and chemiluminescence.Biochemistry of bacterial bioluminescence.5-Ethyl-4a-meth-oxy-1,3-dimethyl-4a,5-dihydro-benzo[g]pteridine-2,4(1H,3H)dione.Studies on the inhibitory mechanism of iodonium compounds with special reference to neutrophil NADPH oxidase.A novel two-protein component flavoprotein hydroxylase.Electrochemical luminescence with N(5)-ethyl-4a-hydroxy-3-methyl-4a, 5-dihydrolumiflavin. The mechanism of bacterial luciferase.Bioluminophore and Flavin Mononucleotide Fluorescence Quenching of Bacterial Bioluminescence-A Theoretical Study.Modelling flavoenzymatic charge transfer events: development of catalytic indole deuteration strategies.Absolute stereochemistry of a 4 a-hydroxyriboflavin analogue of the key intermediate of the FAD-monooxygenase cycle.
P2860
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P2860
Simple synthesis of a 4a-hydroperoxy adduct of a 1,5-dihydroflavine: preliminary studies of a model for bacterial luciferase.
description
1976 nî lūn-bûn
@nan
1976 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1976 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@ast
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@en
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@nl
type
label
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@ast
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@en
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@nl
prefLabel
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@ast
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@en
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@nl
P2860
P356
P1476
Simple synthesis of a 4a-hydro ...... odel for bacterial luciferase.
@en
P2093
P2860
P304
P356
10.1073/PNAS.73.4.995
P407
P577
1976-04-01T00:00:00Z