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The structure of monoamine oxidases: past, present, and future

Journal of Neural Transmission, 2018-11, Vol.125 (11), p.1567-1579

2018

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A Novel Mammalian Flavin-dependent Histone Demethylase

The Journal of biological chemistry, 2009-06, Vol.284 (26), p.17775-17782

2009

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Structure-Based Enzyme Tailoring of 5‑Hydroxymethylfurfural Oxidase

ACS catalysis, 2015-03, Vol.5 (3), p.1833-1839

2015

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Monoamine oxidase‐A is a novel driver of stress‐induced premature senescence through inhibition of parkin‐mediated mitophagy

Aging cell, 2018-10, Vol.17 (5), p.e12811-n/a

2018

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Molecular and Mechanistic Properties of the Membrane-Bound Mitochondrial Monoamine Oxidases

Biochemistry (Easton), 2009-05, Vol.48 (20), p.4220-4230

2009

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Structural Basis of LSD1-CoREST Selectivity in Histone H3 Recognition

The Journal of biological chemistry, 2007-07, Vol.282 (28), p.20070-20074

2007

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Biochemical, Structural, and Biological Evaluation of Tranylcypromine Derivatives as Inhibitors of Histone Demethylases LSD1 and LSD2

Journal of the American Chemical Society, 2010-05, Vol.132 (19), p.6827-6833

2010

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The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis

Applied microbiology and biotechnology, 2013-10, Vol.97 (20), p.8841-8848

2013

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LSD1: oxidative chemistry for multifaceted functions in chromatin regulation

Trends in biochemical sciences (Amsterdam. Regular ed.), 2008-04, Vol.33 (4), p.181-189

2008

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Three-Dimensional Structure of Human Monoamine Oxidase A (MAO A): Relation to the Structures of Rat MAO A and Human MAO B

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (36), p.12684-12689

2005

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New roles of flavoproteins in molecular cell biology: Histone demethylase LSD1 and chromatin

The FEBS journal, 2009-08, Vol.276 (16), p.4304-4312

2009

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Alternative Splicing of the Histone Demethylase LSD1/KDM1 Contributes to the Modulation of Neurite Morphogenesis in the Mammalian Nervous System

The Journal of neuroscience, 2010-02, Vol.30 (7), p.2521-2532

2010

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Molecular Mimicry and Ligand Recognition in Binding and Catalysis by the Histone Demethylase LSD1-CoREST Complex

Structure (London), 2011-02, Vol.19 (2), p.212-220

2011

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The ‘gating’ residues Ile199 and Tyr326 in human monoamine oxidase B function in substrate and inhibitor recognition

The FEBS journal, 2011-12, Vol.278 (24), p.4860-4869

2011

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Human Histone Demethylase LSD1 Reads the Histone Code

The Journal of biological chemistry, 2005-12, Vol.280 (50), p.41360-41365

2005

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Diphenylene Iodonium Is a Noncovalent MAO Inhibitor: A Biochemical and Structural Analysis

ChemMedChem, 2020-08, Vol.15 (15), p.1394-1397

2020

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Monoamine Oxidase Inhibitors Prevent Glucose-Dependent Energy Production, Proliferation and Migration of Bladder Carcinoma Cells

International journal of molecular sciences, 2022-10, Vol.23 (19), p.11747

2022

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Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders

Nature structural & molecular biology, 2002-01, Vol.9 (1), p.22-26

2002

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Assessment of Tractable Cysteines for Covalent Targeting by Screening Covalent Fragments

Chembiochem : a European journal of chemical biology, 2021-02, Vol.22 (4), p.743-753

2021

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Insights into the Mode of Inhibition of Human Mitochondrial Monoamine Oxidase B from High-Resolution Crystal Structures

Proceedings of the National Academy of Sciences - PNAS, 2003-08, Vol.100 (17), p.9750-9755

2003

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Potentiation of Ligand Binding through Cooperative Effects in Monoamine Oxidase B

The Journal of biological chemistry, 2010-11, Vol.285 (47), p.36849-36856

2010

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Demonstration of Isoleucine 199 as a Structural Determinant for the Selective Inhibition of Human Monoamine Oxidase B by Specific Reversible Inhibitors

The Journal of biological chemistry, 2005-04, Vol.280 (16), p.15761-15766

2005

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Functional Role of the “Aromatic Cage” in Human Monoamine Oxidase B: Structures and Catalytic Properties of Tyr435 Mutant Proteins

Biochemistry (Easton), 2006-04, Vol.45 (15), p.4775-4784

2006

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A Highly Specific Mechanism of Histone H3-K4 Recognition by Histone Demethylase LSD1

The Journal of biological chemistry, 2006-11, Vol.281 (46), p.35289-35295

2006

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The structure of monoamine oxidases: past, present, and future

A Novel Mammalian Flavin-dependent Histone Demethylase

Structure-Based Enzyme Tailoring of 5‑Hydroxymethylfurfural Oxidase

Monoamine oxidase‐A is a novel driver of stress‐induced premature senescence through inhibition of parkin‐mediated mitophagy

Molecular and Mechanistic Properties of the Membrane-Bound Mitochondrial Monoamine Oxidases

Structural Basis of LSD1-CoREST Selectivity in Histone H3 Recognition

Biochemical, Structural, and Biological Evaluation of Tranylcypromine Derivatives as Inhibitors of Histone Demethylases LSD1 and LSD2

The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis

LSD1: oxidative chemistry for multifaceted functions in chromatin regulation

Three-Dimensional Structure of Human Monoamine Oxidase A (MAO A): Relation to the Structures of Rat MAO A and Human MAO B

New roles of flavoproteins in molecular cell biology: Histone demethylase LSD1 and chromatin

Alternative Splicing of the Histone Demethylase LSD1/KDM1 Contributes to the Modulation of Neurite Morphogenesis in the Mammalian Nervous System

Molecular Mimicry and Ligand Recognition in Binding and Catalysis by the Histone Demethylase LSD1-CoREST Complex

The ‘gating’ residues Ile199 and Tyr326 in human monoamine oxidase B function in substrate and inhibitor recognition

Human Histone Demethylase LSD1 Reads the Histone Code

Diphenylene Iodonium Is a Noncovalent MAO Inhibitor: A Biochemical and Structural Analysis

Monoamine Oxidase Inhibitors Prevent Glucose-Dependent Energy Production, Proliferation and Migration of Bladder Carcinoma Cells

Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders

Assessment of Tractable Cysteines for Covalent Targeting by Screening Covalent Fragments

Insights into the Mode of Inhibition of Human Mitochondrial Monoamine Oxidase B from High-Resolution Crystal Structures

Potentiation of Ligand Binding through Cooperative Effects in Monoamine Oxidase B

Demonstration of Isoleucine 199 as a Structural Determinant for the Selective Inhibition of Human Monoamine Oxidase B by Specific Reversible Inhibitors

Functional Role of the “Aromatic Cage” in Human Monoamine Oxidase B: Structures and Catalytic Properties of Tyr435 Mutant Proteins

Tranylcypromine‐Based LSD1 Inhibitors: Structure‐Activity Relationships, Antiproliferative Effects in Leukemia, and Gene Target Modulation

A Highly Specific Mechanism of Histone H3-K4 Recognition by Histone Demethylase LSD1

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