about
Metal Selectivity of a Cd-, Co-, and Zn-Transporting P1B-type ATPase.Substrate-Dependent Cleavage Site Selection by Unconventional Radical S-Adenosylmethionine Enzymes in Diphthamide Biosynthesis.Monovalent Cation Activation of the Radical SAM Enzyme Pyruvate Formate-Lyase Activating Enzyme.ENDOR characterization of an iron-alkene complex provides insight into a corresponding organometallic intermediate of nitrogenase.Across the tree of life, radiation resistance is governed by antioxidant Mn2+, gauged by paramagnetic resonance.Photoinduced Reductive Elimination of H2 from the Nitrogenase Dihydride (Janus) State Involves a FeMo-cofactor-H2 Intermediate.Mechanism of Nitrogenase H2 Formation by Metal-Hydride Protonation Probed by Mediated Electrocatalysis and H/D Isotope Effects.The Mechanism of N2 Reduction Catalyzed by Fe-Nitrogenase Involves Reductive Elimination of H2.13C ENDOR Spectroscopy of Lipoxygenase-Substrate Complexes Reveals the Structural Basis for C-H Activation by Tunneling.EPR/ENDOR and Theoretical Study of the Jahn-Teller-Active [HIPTN3N]MoVL Complexes (L = N-, NH).Cu+-specific CopB transporter: Revising P1B-type ATPase classification.A structurally-characterized peroxomanganese(iv) porphyrin from reversible O2 binding within a metal-organic framework.Organometallic and radical intermediates reveal mechanism of diphthamide biosynthesis.Hydride Conformers of the Nitrogenase FeMo-cofactor Two-Electron Reduced State E2(2H), Assigned Using Cryogenic Intra Electron Paramagnetic Resonance Cavity Photolysis.Beyond fossil fuel-driven nitrogen transformationsCritical computational analysis illuminates the reductive-elimination mechanism that activates nitrogenase for N reductionMechanism of Radical Initiation in the Radical S-Adenosyl-l-methionine SuperfamilyEnergy Transduction in NitrogenaseParadigm Shift for Radical S-Adenosyl-l-methionine Reactions: The Organometallic Intermediate Ω Is Central to CatalysisThe Soybean Lipoxygenase-Substrate Complex: Correlation between the Properties of Tunneling-Ready States and ENDOR-Detected Structures of Ground StatesPhotoinduced Electron Transfer in a Radical SAM Enzyme Generates an S-Adenosylmethionine Derived Methyl RadicalTime-Resolved EPR Study of H2 Reductive Elimination from the Photoexcited Nitrogenase Janus E4(4H) IntermediateReduction of Substrates by NitrogenasesENDOR Characterization of (N2)FeII(μ-H)2FeI(N2)-: A Spectroscopic Model for N2 Binding by the Di-μ-hydrido Nitrogenase Janus IntermediateThe Elusive 5'-Deoxyadenosyl Radical: Captured and Characterized by Electron Paramagnetic Resonance and Electron Nuclear Double Resonance SpectroscopiesMo-, V-, and Fe-Nitrogenases Use a Universal Eight-Electron Reductive-Elimination Mechanism To Achieve N2 ReductionCorrection to "High-Resolution ENDOR Spectroscopy Combined with Quantum Chemical Calculations Reveals the Structure of Nitrogenase Janus Intermediate E4(4H)"Particulate methane monooxygenase contains only mononuclear copper centersHigh-Resolution ENDOR Spectroscopy Combined with Quantum Chemical Calculations Reveals the Structure of Nitrogenase Janus Intermediate E4(4H)Formation and Electronic Structure of an Atypical CuA SiteSpectroscopic Description of the E1 State of Mo Nitrogenase Based on Mo and Fe X-ray Absorption and Mössbauer Studies
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-3100-0746
@en
name
brian hoffman
@ast
brian hoffman
@en
brian hoffman
@es
brian hoffman
@nl
type
label
brian hoffman
@ast
brian hoffman
@en
brian hoffman
@es
brian hoffman
@nl
prefLabel
brian hoffman
@ast
brian hoffman
@en
brian hoffman
@es
brian hoffman
@nl
P106
P31
P496
0000-0002-3100-0746