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1
|
A novel mammalian flavin-dependent histone demethylase.
|
J Biol Chem
|
2009
|
2.25
|
|
2
|
Human histone demethylase LSD1 reads the histone code.
|
J Biol Chem
|
2005
|
2.14
|
|
3
|
Structural basis of LSD1-CoREST selectivity in histone H3 recognition.
|
J Biol Chem
|
2007
|
1.92
|
|
4
|
Histone demethylation catalysed by LSD1 is a flavin-dependent oxidative process.
|
FEBS Lett
|
2005
|
1.82
|
|
5
|
Structural basis for benzothiazinone-mediated killing of Mycobacterium tuberculosis.
|
Sci Transl Med
|
2012
|
1.78
|
|
6
|
Three-dimensional structure of human monoamine oxidase A (MAO A): relation to the structures of rat MAO A and human MAO B.
|
Proc Natl Acad Sci U S A
|
2005
|
1.65
|
|
7
|
LSD1: oxidative chemistry for multifaceted functions in chromatin regulation.
|
Trends Biochem Sci
|
2008
|
1.54
|
|
8
|
A highly specific mechanism of histone H3-K4 recognition by histone demethylase LSD1.
|
J Biol Chem
|
2006
|
1.53
|
|
9
|
Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B.
|
Arch Biochem Biophys
|
2007
|
1.23
|
|
10
|
Alternative splicing of the histone demethylase LSD1/KDM1 contributes to the modulation of neurite morphogenesis in the mammalian nervous system.
|
J Neurosci
|
2010
|
1.22
|
|
11
|
Molecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidases.
|
Biochemistry
|
2009
|
1.21
|
|
12
|
Functional role of the "aromatic cage" in human monoamine oxidase B: structures and catalytic properties of Tyr435 mutant proteins.
|
Biochemistry
|
2006
|
1.21
|
|
13
|
Demonstration of isoleucine 199 as a structural determinant for the selective inhibition of human monoamine oxidase B by specific reversible inhibitors.
|
J Biol Chem
|
2005
|
1.18
|
|
14
|
Molecular mimicry and ligand recognition in binding and catalysis by the histone demethylase LSD1-CoREST complex.
|
Structure
|
2011
|
1.06
|
|
15
|
The DprE1 enzyme, one of the most vulnerable targets of Mycobacterium tuberculosis.
|
Appl Microbiol Biotechnol
|
2013
|
1.04
|
|
16
|
New roles of flavoproteins in molecular cell biology: histone demethylase LSD1 and chromatin.
|
FEBS J
|
2009
|
1.01
|
|
17
|
The FAD binding sites of human monoamine oxidases A and B.
|
Neurotoxicology
|
2004
|
0.91
|
|
18
|
Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues.
|
J Med Chem
|
2004
|
0.88
|
|
19
|
The 'gating' residues Ile199 and Tyr326 in human monoamine oxidase B function in substrate and inhibitor recognition.
|
FEBS J
|
2011
|
0.84
|
|
20
|
4-aminoquinolone piperidine amides: noncovalent inhibitors of DprE1 with long residence time and potent antimycobacterial activity.
|
J Med Chem
|
2014
|
0.82
|
|
21
|
Potentiation of ligand binding through cooperative effects in monoamine oxidase B.
|
J Biol Chem
|
2010
|
0.80
|
|
22
|
Polystyrene microbridges used in sitting-drop crystallization release 1,4-diphenyl-2-butene, a novel inhibitor of human MAO B.
|
Acta Crystallogr D Biol Crystallogr
|
2003
|
0.78
|
|
23
|
Structural and mechanistic studies of mofegiline inhibition of recombinant human monoamine oxidase B.
|
J Med Chem
|
2008
|
0.77
|
|
24
|
Comparative analysis of the neurochemical profile and MAO inhibition properties of N-(furan-2-ylmethyl)-N-methylprop-2-yn-1-amine.
|
ACS Chem Neurosci
|
2016
|
0.75
|