Flavins
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Subject Areas on Research
- A new purification procedure for bovine milk xanthine oxidase: effect of proteolysis on the subunit structure.
- Atrial shunt device for heart failure with preserved and mildly reduced ejection fraction (REDUCE LAP-HF II): a randomised, multicentre, blinded, sham-controlled trial.
- Balancing iron and calcium: Flavin carrier family proteins in Aspergillus fumigatus virulence.
- Calculating solution redox free energies with ab initio quantum mechanical/molecular mechanical minimum free energy path method.
- Characterisation of PduS, the pdu metabolosome corrin reductase, and evidence of substructural organisation within the bacterial microcompartment.
- Conformational selection or induced fit: a flux description of reaction mechanism.
- Effect of conformation on the binding of flavins to flavoenzymes.
- Flavin-dependent antioxidant properties of a new series of meso-N,N'-dialkyl-imidazolium substituted manganese(III) porphyrins.
- Flavin-dependent thymidylate synthase ThyX activity: implications for the folate cycle in bacteria.
- Nonequivalence of the flavin adenine dinucleotide moieties of chicken liver xanthine dehydrogenase.
- Purification and initial characterization of a putative blue light-regulated phosphodiesterase from Escherichia coli.
- Purification and properties of chicken liver xanthine dehydrogenase.
- Purification and properties of xanthine dehydroganase from Micrococcus lactilyticus.
- Reduced nicotinamide adenine dinucleotide phosphate-sulfite reductase of enterobacteria. V. Studies with the Escherichia coli hemoflavoprotein depleted of flavin mononucleotide: distinct roles for the flavin adenine dinucleotide and flavin mononucleotide prosthetic groups in catalysis.
- STRUCTURE AND FUNCTION OF IRON-FLAVOPROTEINS.
- Studies of aldehyde oxidase by electron paramagnetic resonance spectroscopy. I. Spectra at equilibrium states.
- Studies of aldehyde oxidase by electron paramagnetic resonance spectroscopy. II. Kinetic studies by rapid freezing.
- Thermodynamics of oxidation-reduction reactions in mammalian nitric-oxide synthase isoforms.
- trans-2-Phenylcyclopropylamine is a mechanism-based inactivator of the histone demethylase LSD1.