NDRG1 and MAOA

Number of citations of the paper that reports this interaction (PubMedID 17220478)
24

Data Source:
HPRD (in vivo)

		NDRG1	MAOA
Description		N-myc downstream regulated 1	monoamine oxidase A
Image		No pdb structure
GO Annotations	Cellular Component	Nucleus Cytoplasm Centrosome Cytosol Microtubule Plasma Membrane Adherens Junction Microtubule Cytoskeleton Perinuclear Region Of Cytoplasm Recycling Endosome Membrane Extracellular Exosome Glutamatergic Synapse	Mitochondrion Mitochondrial Outer Membrane Cytosol Integral Component Of Membrane
	Molecular Function	Protein Binding Microtubule Binding Rab GTPase Binding Gamma-tubulin Binding Cadherin Binding	Protein Binding Primary Amine Oxidase Activity
	Biological Process	Signal Transduction Negative Regulation Of Cell Proliferation Response To Metal Ion DNA Damage Response, Signal Transduction By P53 Class Mediator Peripheral Nervous System Myelin Maintenance Regulation Of Apoptotic Process Mast Cell Activation Cellular Response To Hypoxia Postsynapse Organization	Cellular Biogenic Amine Metabolic Process Positive Regulation Of Signal Transduction Cytokine-mediated Signaling Pathway Neurotransmitter Metabolic Process Neurotransmitter Catabolic Process Dopamine Catabolic Process Oxidation-reduction Process
Pathways		TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain	Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB Norepinephrine Neurotransmitter Release Cycle Enzymatic degradation of dopamine by COMT Enzymatic degradation of Dopamine by monoamine oxidase Metabolism of serotonin Defective MAOA causes Brunner syndrome (BRUNS) Interleukin-4 and Interleukin-13 signaling
Drugs			Amphetamine Phentermine Procaine Tranylcypromine Phenelzine Minaprine Zonisamide Selegiline Procarbazine Moclobemide Isocarboxazid Ephedra MMDA 4-Methoxyamphetamine Methamphetamine Pargyline Flavin adenine dinucleotide N-Methyl-N-Propargyl-3-(2,4-Dichlorophenoxy)Propylamine Nialamide Nomifensine Zimelidine Posizolid CX157 DECYL(DIMETHYL)PHOSPHINE OXIDE 7-METHOXY-1-METHYL-9H-BETA-CARBOLINE Brofaromine
Diseases		Charcot-Marie-Tooth disease (CMT); Hereditary motor and sensory neuropathy; Peroneal muscular atrophy	Brunner syndrome; MAOA deficiency
GWAS		Estimated glomerular filtration rate ( 31015462) Nontyphoidal Salmonella bacteraemia ( 29523850) Post-traumatic stress disorder (asjusted for relatedness) ( 23726511)	Smoking behavior ( 19247474)
Interacting Genes		71 interacting genes: ACSL3 ACTG1 AP1M2 AP2M1 APOA1 APOA2 ARL4D ATP1A1 CANX CDH1 CLTC CNDP2 COPB2 CTNNB1 DDX1 DDX5 DLST EEF1G EEF2 EIF2S3 EIF3E EWSR1 FASN GPAA1 GSK3B HNRNPF HNRNPH1 HNRNPU HSD17B4 HSP90AA1 HSPA5 ILF3 KIF5B LDHA MAOA MLH1 MME MYC NCL NR4A1 PABPC1 PHYHIP PKM PPP2R2A PRKACA PSMC2 PSMC3 PSMD2 RPL24 RPL3 RPL4 RPN2 RPS16 RPS20 RPS26 RPS3 RPS6 RPS8 RTN1 RUVBL2 S100B SEC23A SGK1 SHMT2 TAF9 TARS1 TLE3 UPF1 VCP XRCC5 ZNF155	1 interacting genes: NDRG1
Entrez ID		10397	4128
HPRD ID		05586	02400
Ensembl ID		ENSG00000104419	ENSG00000189221
Uniprot IDs		B3KWB2 Q8N959 Q92597	P21397 Q49A63 Q53YE7
PDB IDs			1H8Q 2BXR 2BXS 2Z5X 2Z5Y
Enriched GO Terms of Interacting Partners?
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