Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
1.4.3.21
Oxidoreductases;
Acting on the CH-NH2 group of donors;
With oxygen as acceptor;
primary-amine oxidase
1.4.3.4
Oxidoreductases;
Acting on the CH-NH2 group of donors;
With oxygen as acceptor;
monoamine oxidase
PDB | Resolution (Å) | PDB name |
---|---|---|
2BXR | 3.0 | Human Monoamine Oxidase A in complex with Clorgyline, Crystal Form A |
2BXS | 3.15 | Human Monoamine Oxidase A in complex with Clorgyline, Crystal Form B |
2Z5X | 2.2 | Crystal Structure of Human Monoamine Oxidase A with Harmine |
2Z5Y | 2.17 | Crystal Structure of Human Monoamine Oxidase A (G110A) with Harmine |
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0006576 | biogenic amine metabolic process |
Biological Process | GO:0042420 | dopamine catabolic process |
Biological Process | GO:0042135 | neurotransmitter catabolic process |
Biological Process | GO:0009967 | positive regulation of signal transduction |
Molecular Function | GO:0052595 | aliphatic amine oxidase activity |
Molecular Function | GO:0097621 | monoamine oxidase activity |
Molecular Function | GO:0052596 | phenethylamine:oxygen oxidoreductase (deaminating) activity |
Molecular Function | GO:0008131 | primary amine oxidase activity |
Cellular Component | GO:0005829 | cytosol |
Cellular Component | GO:0005741 | mitochondrial outer membrane |
Cellular Component | GO:0005739 | mitochondrion |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-141333 | Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB | Leaf | R-HSA-1430728 | Metabolism |
R-HSA-181430 | Norepinephrine Neurotransmitter Release Cycle | Leaf | R-HSA-112316 | Neuronal System |
R-HSA-379397 | Enzymatic degradation of dopamine by COMT | Leaf | R-HSA-112316 | Neuronal System |
R-HSA-379398 | Enzymatic degradation of Dopamine by monoamine oxidase | Leaf | R-HSA-112316 | Neuronal System |
R-HSA-379401 | Dopamine clearance from the synaptic cleft | Internal node | R-HSA-112316 | Neuronal System |
R-HSA-380612 | Metabolism of serotonin | Leaf | R-HSA-112316 | Neuronal System |
R-HSA-5579012 | Defective MAOA causes BRUNS | Leaf | R-HSA-1643685 | Disease |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | Leaf | R-HSA-168256 | Immune System |
Location | ECO term | Pubmed |
---|---|---|
Mitochondrion outer membrane | ECO:0000250 |
HPO ID | HPO name |
---|---|
HP:0000708 | Atypical behavior |
HP:0000717 | Autism |
HP:0000718 | Aggressive behavior |
HP:0000744 | Low frustration tolerance |
HP:0001249 | Intellectual disability |
HP:0001270 | Motor delay |
HP:0001419 | X-linked recessive inheritance |
HP:0002014 | Diarrhea |
HP:0002315 | Headache |
HP:0030186 | Kinetic tremor |
HP:0031284 | Flushing |
HP:0100543 | Cognitive impairment |
HP:0100710 | Impulsivity |
HP:0100716 | Self-injurious behavior |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
brunner syndrome | MONDO:0010379 | E70 | chapter4, Endocrine, nutritional and metabolic diseases | OMIM:300615 | Orphanet:3057 |