On the public citation graph

EPR Spectroscopic and Computational Characterization of the Hydroxyethylidene-Thiamine Pyrophosphate Radical Intermediate of Pyruvate:Ferredoxin Oxidoreductase

0 signed · 102 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9781119951438.eibc0647openalex-snapshot
Pyruvate–Ferredoxin Oxidoreductase
inferredcites →https://doi.org/10.1007/978-94-009-4075-8openalex-snapshot
Electron Spin Resonance
inferredcites →https://doi.org/10.1016/0014-5793(80)80236-5openalex-snapshot
A stable free radical intermediate in the reaction of 2‐oxoacid:ferredoxin oxidoreductases of Halobacterium halobium
inferredcites →https://doi.org/10.1016/0022-2364(81)90067-6openalex-snapshot
Theory and applications of electron spin resonance
inferredcites →https://doi.org/10.1016/0304-4076(94)90038-8openalex-snapshot
Global optimization of statistical functions with simulated annealing
inferredcites →https://doi.org/10.1016/j.bioorg.2005.02.001openalex-snapshot
Experimental observation of thiamin diphosphate-bound intermediates on enzymes and mechanistic information derived from these observations
inferredcites →https://doi.org/10.1016/j.bmcl.2003.07.026openalex-snapshot
An efficient enzymatic synthesis of thiamin pyrophosphate
inferredcites →https://doi.org/10.1016/j.str.2005.10.013openalex-snapshot
Flexibility of Thiamine Diphosphate Revealed by Kinetic Crystallographic Studies of the Reaction of Pyruvate-Ferredoxin Oxidoreductase with Pyruvate
inferredcites →https://doi.org/10.1016/s0005-2728(98)00145-5openalex-snapshot
Purification and characterization of pyruvate oxidoreductase from the photosynthetic bacterium Rhodobacter capsulatus
inferredcites →https://doi.org/10.1016/s0014-5793(97)00998-8openalex-snapshot
The iron‐sulfur centers of the pyruvate:ferredoxin oxidoreductase from Methanosarcina barkeri (Fusaro)
inferredcites →https://doi.org/10.1016/s0014-5793(99)01061-3openalex-snapshot
Interplay of organic and biological chemistry in understanding coenzyme mechanisms: example of thiamin diphosphate‐dependent decarboxylations of 2‐oxo acids
inferredcites →https://doi.org/10.1016/s0065-3233(08)60362-9openalex-snapshot
Oxidoreductase-Type Enzymes and Redox Proteins Involved in Fermentative Metabolisms of Hyperthermophilic Archaea
inferredcites →https://doi.org/10.1016/s0959-440x(99)00027-5openalex-snapshot
Structure and electron transfer mechanism of pyruvate:ferredoxin oxidoreductase
inferredcites →https://doi.org/10.1021/bi00136a004openalex-snapshot
Electron paramagnetic resonance studies of a ras p21-MnIIGDP complex in solution
inferredcites →https://doi.org/10.1021/bi0257641openalex-snapshot
The Roles of Coenzyme A in the Pyruvate:Ferredoxin Oxidoreductase Reaction Mechanism: Rate Enhancement of Electron Transfer from a Radical Intermediate to an Iron−Sulfur Cluster
inferredcites →https://doi.org/10.1021/bi051058zopenalex-snapshot
Radical Phosphate Transfer Mechanism for the Thiamin Diphosphate- and FAD-Dependent Pyruvate Oxidase from Lactobacillus plantarum . Kinetic Coupling of Intercofactor Electron Transfer with Phosphate Transfer to Acetyl-thiamin Diphosphate via a Transient FAD Semiquinone/Hydroxyethyl-ThDP Radical Pair
inferredcites →https://doi.org/10.1021/bi970403kopenalex-snapshot
Mechanism of the Clostridium thermoaceticum Pyruvate:Ferredoxin Oxidoreductase: Evidence for the Common Catalytic Intermediacy of the Hydroxyethylthiamine Pyropyrosphate Radical
inferredcites →https://doi.org/10.1021/bi990620gopenalex-snapshot
Hydrazine Cation Radical in the Active Site of Ethanolamine Ammonia-Lyase: Mechanism-Based Inactivation by Hydroxyethylhydrazine
inferredcites →https://doi.org/10.1021/cr020423eopenalex-snapshot
Pyruvate Ferredoxin Oxidoreductase and Its Radical Intermediate
inferredcites →https://doi.org/10.1021/ja00178a044openalex-snapshot
Electrochemical oxidation of enamines related to the key intermediate on thiamin diphosphate dependent enzymic pathways: evidence for one-electron oxidation via a thiazolium cation radical
inferredcites →https://doi.org/10.1021/ja01300a086openalex-snapshot
Studies of Crystalline Vitamin B1. XIV. Sulfite Cleavage. IV. The Thiazole Half
inferredcites →https://doi.org/10.1021/ja984057lopenalex-snapshot
ENDOR Studies of Pyruvate:Ferredoxin Oxidoreductase Reaction Intermediates
inferredcites →https://doi.org/10.1021/jp0466901openalex-snapshot
Density Functional Theory Predictions of Isotropic Hyperfine Coupling Constants
inferredcites →https://doi.org/10.1021/jp0522361openalex-snapshot
Theoretical Isotropic Hyperfine Coupling Constants of Third-Row Nuclei (29Si, 31P, and 33S)
inferredcites →https://doi.org/10.1038/5870openalex-snapshot
Crystal structures of the key anaerobic enzyme pyruvate:ferredoxin oxidoreductase, free and in complex with pyruvate.
inferredcites →https://doi.org/10.1042/bst0130572openalex-snapshot
Electron-spin-resonance/electron-paramagnetic-resonance spectroscopy of iron-sulphur enzymes
inferredcites →https://doi.org/10.1126/science.1066198openalex-snapshot
Crystal Structure of the Free Radical Intermediate of Pyruvate:Ferredoxin Oxidoreductase
inferredcites →https://doi.org/10.1126/science.1067916openalex-snapshot
Coenzymes and Radicals

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4857463openalex-extracted
The Redox Landscape of the 2-Oxoacid:Ferredoxin Oxidoreductase Superfamily Reveals Universally Conserved Fe–S Cluster Potentials
inferred← citeshttps://doi.org/10.1002/0470028637.met220openalex-snapshot
Pyruvate–Ferredoxin Oxidoreductase
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0647openalex-snapshot
Pyruvate–Ferredoxin Oxidoreductase
inferred← citeshttps://doi.org/10.1002/9783527809042.ch7openalex-snapshot
Recent Activation Modes in NHC Organocatalysis
inferred← citeshttps://doi.org/10.1002/ange.200702993openalex-snapshot
The Enamine Intermediate May Not Be Universal to Thiamine Catalysis
inferred← citeshttps://doi.org/10.1002/ange.200802735openalex-snapshot
Biomimetische Carben‐katalysierte Oxidation von Aldehyden mit TEMPO
inferred← citeshttps://doi.org/10.1002/ange.201611692openalex-snapshot
Polyhalides as Efficient and Mild Oxidants for Oxidative Carbene Organocatalysis by Radical Processes
inferred← citeshttps://doi.org/10.1002/anie.200702993openalex-snapshot
The Enamine Intermediate May Not Be Universal to Thiamine Catalysis
inferred← citeshttps://doi.org/10.1002/anie.200802735openalex-snapshot
Biomimetic Carbene‐Catalyzed Oxidations of Aldehydes Using TEMPO
inferred← citeshttps://doi.org/10.1002/anie.201611692openalex-snapshot
Polyhalides as Efficient and Mild Oxidants for Oxidative Carbene Organocatalysis by Radical Processes
inferred← citeshttps://doi.org/10.1002/cben.201800003openalex-snapshot
Anaerobic Radical Enzymes for Biotechnology
inferred← citeshttps://doi.org/10.1002/cctc.202201320openalex-snapshot
Merging N‐Heterocyclic Carbene Organocatalysis with Hydrogen Atom Transfer Strategy
inferred← citeshttps://doi.org/10.1002/chem.201203707openalex-snapshot
Catalysis with N‐Heterocyclic Carbenes under Oxidative Conditions
inferred← citeshttps://doi.org/10.1002/chem.202004059openalex-snapshot
Single‐Electron Transfer Reactions Enabled by N‐Heterocyclic Carbene Organocatalysis
inferred← citeshttps://doi.org/10.1002/cjoc.202000107openalex-snapshot
N‐Heterocyclic Carbene Organocatalysis: Activation Modes and Typical Reactive Intermediates
inferred← citeshttps://doi.org/10.1002/cjoc.70689openalex-snapshot
Recent Advances in Visible‐Light‐Mediated Acylation of Unsaturated Hydrocarbons
inferred← citeshttps://doi.org/10.1002/qua.23089openalex-snapshot
Evaluation of DFT methods to study reactions of benzene with OH radical
inferred← citeshttps://doi.org/10.1007/bf03166606openalex-snapshot
A CW and pulse EPR spectrometer operating at 122 and 244 GHz using a quasi-optical bridge and a cryogen-free 12 T superconducting magnet
inferred← citeshttps://doi.org/10.1007/s00018-007-6423-5openalex-snapshot
Structure, mechanism and catalytic duality of thiamine-dependent enzymes
inferred← citeshttps://doi.org/10.1007/s11064-019-02765-wopenalex-snapshot
Human 2-Oxoglutarate Dehydrogenase and 2-Oxoadipate Dehydrogenase Both Generate Superoxide/H2O2 in a Side Reaction and Each Could Contribute to Oxidative Stress in Mitochondria
inferred← citeshttps://doi.org/10.1007/s11426-020-9851-8openalex-snapshot
N-heterocyclic carbene-catalyzed radical reactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14833-4openalex-snapshot
An Update on Developments in the Field of Thiamin Diphosphate-Dependent Enzymes
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00141-6openalex-snapshot
Coenzyme A Biosynthesis and Enzymology
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00148-9openalex-snapshot
Thiamin Biosynthesis
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00149-0openalex-snapshot
Thiamin Enzymology
inferred← citeshttps://doi.org/10.1016/bs.mie.2015.06.009openalex-snapshot
Fourier Deconvolution Methods for Resolution Enhancement in Continuous-Wave EPR Spectroscopy
inferred← citeshttps://doi.org/10.1016/j.bbapap.2008.08.012openalex-snapshot
Acetogenesis and the Wood–Ljungdahl pathway of CO2 fixation
inferred← citeshttps://doi.org/10.1016/j.bbapap.2011.11.010openalex-snapshot
Radical reactions of thiamin pyrophosphate in 2-oxoacid oxidoreductases
inferred← citeshttps://doi.org/10.1016/j.bbapap.2014.01.015openalex-snapshot
Four Cys residues in heterodimeric 2-oxoacid:ferredoxin oxidoreductase are required for CoA-dependent oxidative decarboxylation but not for a non-oxidative decarboxylation
inferred← citeshttps://doi.org/10.1016/j.bioorg.2005.02.001openalex-snapshot
Experimental observation of thiamin diphosphate-bound intermediates on enzymes and mechanistic information derived from these observations
inferred← citeshttps://doi.org/10.1016/j.bioorg.2006.08.002openalex-snapshot
Protein-enhanced decarboxylation of the covalent intermediate in benzoylformate decarboxylase—Desolvation or acid catalysis?
inferred← citeshttps://doi.org/10.1016/j.bioorg.2012.03.001openalex-snapshot
Decarboxylation mechanisms in biological system
inferred← citeshttps://doi.org/10.1016/j.bioorg.2014.08.002openalex-snapshot
Progress in the experimental observation of thiamin diphosphate-bound intermediates on enzymes and mechanistic information derived from these observations
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.08.027openalex-snapshot
Recent advances in N-heterocyclic carbene-catalyzed radical reactions
inferred← citeshttps://doi.org/10.1016/j.envres.2026.124326openalex-snapshot
Removal of trace 17α-ethinylestradiol by microalgal-bacterial granular sludge: The overlooked role of extracellular photosensitization
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.11.018openalex-snapshot
The mitochondrial 2-oxoadipate and 2-oxoglutarate dehydrogenase complexes share their E2 and E3 components for their function and both generate reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.jmr.2011.08.030openalex-snapshot
Investigating the intermediates in the reaction of ribonucleoside triphosphate reductase from Lactobacillus leichmannii: An application of HF EPR–RFQ technology
inferred← citeshttps://doi.org/10.1016/j.sbi.2016.05.011openalex-snapshot
A structural phylogeny for understanding 2-oxoacid oxidoreductase function
inferred← citeshttps://doi.org/10.1016/j.str.2024.08.011openalex-snapshot
Structural organization of pyruvate: ferredoxin oxidoreductase from the methanogenic archaeon Methanosarcina acetivorans
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132212openalex-snapshot
Radical N-heterocyclic carbene catalysis for β-ketocarbonyl synthesis
inferred← citeshttps://doi.org/10.1021/acs.biochem.7b00222openalex-snapshot
Properties of Intermediates in the Catalytic Cycle of Oxalate Oxidoreductase and Its Suicide Inactivation by Pyruvate
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02778openalex-snapshot
Effect of Solvents on Proline Modified at the Secondary Sphere: A Multivariate Exploration
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02483openalex-snapshot
Can the Radical Channel Contribute to the Catalytic Cycle of N-Heterocyclic Carbene in Benzoin Condensation?
inferred← citeshttps://doi.org/10.1021/acscatal.0c01795openalex-snapshot
N-Heterocyclic Carbene-Based Catalysis Enabling Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/acschembio.5c00025openalex-snapshot
Trihydroxybenzaldoximes are Redox Cycling Inhibitors of ThDP-Dependent DXP Synthase
inferred← citeshttps://doi.org/10.1021/cr050292sopenalex-snapshot
Free Radical Mechanisms in Enzymology
inferred← citeshttps://doi.org/10.1021/cr0503153openalex-snapshot
Metals and Their Scaffolds To Promote Difficult Enzymatic Reactions
inferred← citeshttps://doi.org/10.1021/cr068444mopenalex-snapshot
Thiamin Diphosphate Catalysis: Enzymic and Nonenzymic Covalent Intermediates
inferred← citeshttps://doi.org/10.1021/ja076468kopenalex-snapshot
Off-Pathway, Oxygen-Dependent Thiamine Radical in the Krebs Cycle
inferred← citeshttps://doi.org/10.1021/ja105204vopenalex-snapshot
Analysis of the Reactivities of Protein C−H Bonds to H Atom Abstraction by OH Radical
inferred← citeshttps://doi.org/10.1021/ja808573fopenalex-snapshot
Structure of the Biliverdin Radical Intermediate in Phycocyanobilin:Ferredoxin Oxidoreductase Identified by High-Field EPR and DFT
inferred← citeshttps://doi.org/10.1021/jacs.6c04025openalex-snapshot
Engineering a Thiamine-Dependent Benzoylformate Decarboxylase for Stereodivergent Radical C(sp 3 )–C(sp 3 ) Bond Formation
inferred← citeshttps://doi.org/10.1021/jacs.8b11824openalex-snapshot
What Are the Radical Intermediates in Oxidative N-Heterocyclic Carbene Organocatalysis?
inferred← citeshttps://doi.org/10.1021/jacs.9b00880openalex-snapshot
N-Heterocyclic Carbene-Catalyzed Decarboxylative Alkylation of Aldehydes
inferred← citeshttps://doi.org/10.1021/ol5027415openalex-snapshot
N-Heterocyclic Carbene Organocatalytic Reductive β,β-Coupling Reactions of Nitroalkenes via Radical Intermediates
inferred← citeshttps://doi.org/10.1038/s41467-020-14798-9openalex-snapshot
Engineering stable radicals using photochromic triggers
inferred← citeshttps://doi.org/10.1038/srep33061openalex-snapshot
Crystal structures of archaeal 2-oxoacid:ferredoxin oxidoreductases from Sulfolobus tokodaii
inferred← citeshttps://doi.org/10.1039/c1mt00042jopenalex-snapshot
Metal centers in the anaerobic microbial metabolism of CO and CO2
inferred← citeshttps://doi.org/10.1039/c3sc51174jopenalex-snapshot
Carbene-stabilized main group radicals and radical ions
inferred← citeshttps://doi.org/10.1039/c5sc02186copenalex-snapshot
NHC-catalysed benzoin condensation – is it all down to the Breslow intermediate?
inferred← citeshttps://doi.org/10.1039/c8qo01420eopenalex-snapshot
Carbene-catalyzed oxidative acylation promoted by an unprecedented oxidant CCl 3 CN
inferred← citeshttps://doi.org/10.1039/d0cc00293copenalex-snapshot
Modular synthesis of α-aryl β-perfluoroalkyl ketones via N-heterocyclic carbene catalysis
inferred← citeshttps://doi.org/10.1039/d0sc01538eopenalex-snapshot
Recent advances in N-heterocyclic carbene-based radical catalysis
inferred← citeshttps://doi.org/10.1039/d5sc09978aopenalex-snapshot
Lewis acid/NHC dual catalysis for regioselective vicinal decarboxylative carbonylation–acylation of alkenes
inferred← citeshttps://doi.org/10.1073/pnas.0609973104openalex-snapshot
The 1′,4′-iminopyrimidine tautomer of thiamin diphosphate is poised for catalysis in asymmetric active centers on enzymes
inferred← citeshttps://doi.org/10.1073/pnas.1201280109openalex-snapshot
Unexpected tautomeric equilibria of the carbanion-enamine intermediate in pyruvate oxidase highlight unrecognized chemical versatility of thiamin
inferred← citeshttps://doi.org/10.1073/pnas.1518537113openalex-snapshot
One-carbon chemistry of oxalate oxidoreductase captured by X-ray crystallography
inferred← citeshttps://doi.org/10.1073/pnas.1722329115openalex-snapshot
Binding site for coenzyme A revealed in the structure of pyruvate:ferredoxin oxidoreductase from Moorella thermoacetica
inferred← citeshttps://doi.org/10.1074/jbc.m114.591073openalex-snapshot
Human 2-Oxoglutarate Dehydrogenase Complex E1 Component Forms a Thiamin-derived Radical by Aerobic Oxidation of the Enamine Intermediate
inferred← citeshttps://doi.org/10.1074/jbc.ra118.001980openalex-snapshot
Oxidative decarboxylation of pyruvate by 1-deoxy-d-xyulose 5-phosphate synthase, a central metabolic enzyme in bacteria
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2009.06966.xopenalex-snapshot
Reaction mechanisms of thiamin diphosphate enzymes: redox reactions
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2009.07506.xopenalex-snapshot
Enzymatic and electron paramagnetic resonance studies of anabolic pyruvate synthesis by pyruvate: ferredoxin oxidoreductase from Hydrogenobacter thermophilus
inferred← citeshttps://doi.org/10.1196/annals.1419.015openalex-snapshot
Enzymology of the Wood–Ljungdahl Pathway of Acetogenesis
inferred← citeshttps://doi.org/10.3390/molecules30224427openalex-snapshot
Covalent Docking to the Active Sites of Thiamine Diphosphate-Dependent Enzymes
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.