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Structural basis of LSD1-CoREST selectivity in histone H3 recognitionBinding of rasagiline-related inhibitors to human monoamine oxidases: a kinetic and crystallographic analysisStructural insights into the mechanism of amine oxidation by monoamine oxidases A and BCross-talk and ammonia channeling between active centers in the unexpected domain arrangement of glutamate synthaseStructural bases for inhibitor binding and catalysis in polyamine oxidaseStructure of human monoamine oxidase B, a drug target for the treatment of neurological disordersInsights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structuresStructures of human monoamine oxidase B complexes with selective noncovalent inhibitors: safinamide and coumarin analogsStructural and mechanistic studies of arylalkylhydrazine inhibition of human monoamine oxidases A and BStructural and Mechanistic Studies of Mofegiline Inhibition of Recombinant Human Monoamine Oxidase B ∥Alternative splicing of the histone demethylase LSD1/KDM1 contributes to the modulation of neurite morphogenesis in the mammalian nervous systemBiochemical, structural, and biological evaluation of tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and LSD2Potentiation of Ligand Binding through Cooperative Effects in Monoamine Oxidase BInteractions of Monoamine Oxidases with the Antiepileptic Drug Zonisamide: Specificity of Inhibition and Structure of the Human Monoamine Oxidase B ComplexMolecular Mimicry and Ligand Recognition in Binding and Catalysis by the Histone Demethylase LSD1-CoREST ComplexStructural Basis for Benzothiazinone-Mediated Killing of Mycobacterium tuberculosisThe ‘gating’ residues Ile199 and Tyr326 in human monoamine oxidase B function in substrate and inhibitor recognitionMolecular Insights into Human Monoamine Oxidase B Inhibition by the Glitazone Antidiabetes DrugsKinetic and structural analysis of the irreversible inhibition of human monoamine oxidases by ASS234, a multi-target compound designed for use in Alzheimer's disease2-Carboxyquinoxalines kill mycobacterium tuberculosis through noncovalent inhibition of DprE1Biocatalytic Properties and Structural Analysis of Eugenol Oxidase from Rhodococcus jostii RHA1: A Versatile Oxidative BiocatalystThe FAD binding sites of human monoamine oxidases A and BStructural properties of human monoamine oxidases A and BCrystal structures of monoamine oxidase B in complex with four inhibitors of the N-propargylaminoindan classMolecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidasesA novel mammalian flavin-dependent histone demethylasePolystyrene microbridges used in sitting-drop crystallization release 1,4-diphenyl-2-butene, a novel inhibitor of human MAO B.Three-dimensional structure of human monoamine oxidase A (MAO A): relation to the structures of rat MAO A and human MAO BStructure-function relationships in flavoenzyme-dependent amine oxidations: a comparison of polyamine oxidase and monoamine oxidase.An unprecedented NADPH domain conformation in lysine monooxygenase NbtG provides insights into uncoupling of oxygen consumption from substrate hydroxylationCrystal structure of human monoamine oxidase B, a drug target enzyme monotopically inserted into the mitochondrial outer membrane.LSD1: oxidative chemistry for multifaceted functions in chromatin regulation.New roles of flavoproteins in molecular cell biology: histone demethylase LSD1 and chromatin.Lights and shadows on monoamine oxidase inhibition in neuroprotective pharmacological therapies.The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis.4-aminoquinolone piperidine amides: noncovalent inhibitors of DprE1 with long residence time and potent antimycobacterial activity.A highly specific mechanism of histone H3-K4 recognition by histone demethylase LSD1.Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.Demonstration of isoleucine 199 as a structural determinant for the selective inhibition of human monoamine oxidase B by specific reversible inhibitors.Histone demethylation catalysed by LSD1 is a flavin-dependent oxidative process.
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P50
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hulumtuese
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հետազոտող
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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Claudia Binda
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0000-0003-2038-9845