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Hydrocarbon hydroxylation by cytochrome P450 enzymesStabilization and characterization of a heme-oxy reaction intermediate in inducible nitric-oxide synthaseStructure of Cytochrome P450 PimD Suggests Epoxidation of the Polyene Macrolide Pimaricin Occurs via a Hydroperoxoferric IntermediateVariations on a (t)heme--novel mechanisms, redox partners and catalytic functions in the cytochrome P450 superfamilyMechanisms of peroxynitrite interactions with heme proteinsF429 Regulation of Tunnels in Cytochrome P450 2B4: A Top Down Study of Multiple Molecular Dynamics SimulationsPhotochemical production of a highly reactive porphyrin-iron-oxo species.Spectra and kinetic studies of the compound I derivative of cytochrome P450 119.Highly reactive porphyrin-iron-oxo derivatives produced by photolyses of metastable porphyrin-iron(IV) diperchloratesKinetics of oxidation of benzphetamine by compounds I of cytochrome P450 2B4 and its mutants.Quantitative production of compound I from a cytochrome P450 enzyme at low temperatures. Kinetics, activation parameters, and kinetic isotope effects for oxidation of benzyl alcohol.Reaction of N-hydroxyguanidine with the ferrous-oxy state of a heme peroxidase cavity mutant: a model for the reactions of nitric oxide synthase.Low temperature photo-oxidation of chloroperoxidase Compound II.Reactive intermediates in cytochrome p450 catalysis.A novel intermediate in the reaction of seleno CYP119 with m-chloroperbenzoic acidPhotochemical generation and kinetic studies of a putative porphyrin-ruthenium(V)-oxo species.Computational explanation for bioactivation mechanism of targeted anticancer agents mediated by cytochrome P450s: A case of ErlotinibX-ray absorption spectroscopic characterization of a cytochrome P450 compound II derivative.Reactivity patterns of cytochrome P450 enzymes: multifunctionality of the active species, and the two states-two oxidants conundrum.Kinetics of two-electron oxidations by the compound I derivative of chloroperoxidase, a model for cytochrome P450 oxidants.A ligand field chemistry of oxygen generation by the oxygen-evolving complex and synthetic active sites.Cytochrome P450/redox partner fusion enzymes: biotechnological and toxicological prospects.Cytochrome P450 compound I in the plane wave pseudopotential framework: GGA electronic and geometric structure of thiolate-ligated iron(IV)-oxo porphyrin.Kinetic isotope effects in hydroxylation reactions effected by cytochrome P450 compounds I implicate multiple electrophilic oxidants for P450-catalyzed oxidations.Formation of stable and metastable porphyrin- and corrole-iron(IV) complexes and isomerizations to iron(III) macrocycle radical cations.Oxygen activation by cytochrome P450 monooxygenaseCatalytic intermediates of inducible nitric-oxide synthase stabilized by the W188H mutationKinetics and activation parameters for oxidations of styrene by Compounds I from the cytochrome P450(BM-3) (CYP102A1) heme domain and from CYP119.Lessons from Nature: A Bio-Inspired Approach to Molecular Design.Cytochrome P450 119 Compounds I Formed by Chemical Oxidation and Photooxidation Are the Same Species.Tubular membrane bioreactors for biotechnological processes.Fractional transfer of a free unpaired electron to overcome energy barriers in the formation of Fe(4+) from Fe(3+) during the core contraction of macrocycles: implication for heme distortion.Anilinic N-oxides support cytochrome P450-mediated N-dealkylation through hydrogen-atom transfer.Density Functional Theory Calculations on Fe-O and O-O Cleavage of Ferric Hydroperoxide Species: Role of axial ligand and spin state.Remarkable solvent, porphyrin ligand, and substrate effects on participation of multiple active oxidants in manganese(III) porphyrin catalyzed oxidation reactions.Reaction Intermediates and Molecular Mechanism of Peroxynitrite Activation by NO Synthases.Olefin-Supported Rhenium(III) Terminal Oxo Complexes Generated by Nucleophilic Addition to a Cyclopentadienyl Ligand.Characterization of Paramagnetic Reactive Intermediates: Predicting the NMR Spectra of Iron(IV)-Oxo Complexes by DFT.Spectroscopic characterization of a phenolate bound Fe(II)-O2 adduct: gauging the relative "push" effect of a phenolate axial ligand.Ligand control in the photochemical generation of high-valent porphyrin-iron-oxo derivatives.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Cytochrome p450 compound I.
@ast
Cytochrome p450 compound I.
@en
type
label
Cytochrome p450 compound I.
@ast
Cytochrome p450 compound I.
@en
prefLabel
Cytochrome p450 compound I.
@ast
Cytochrome p450 compound I.
@en
P2093
P2860
P356
P1476
Cytochrome p450 compound I.
@en
P2093
James A Halgrimson
John H Horner
Martin Newcomb
R Esala P Chandrasena
Stephen G Sligar
P2860
P304
P356
10.1021/JA060048Y
P407
P577
2006-04-01T00:00:00Z