PEX5 and PAOX

Number of citations of the paper that reports this interaction (PMID 20178365)
7

Data Source:
BioGRID (unspecified method)

		PEX5	PAOX
Gene Name		peroxisomal biogenesis factor 5	polyamine oxidase (exo-N4-amino)
Image			No pdb structure
Gene Ontology Annotations	Cellular Component	Intracellular Cytoplasm Peroxisome Peroxisomal Membrane Peroxisomal Matrix Golgi Apparatus Cytosol Membrane Protein Complex	Peroxisomal Matrix
	Molecular Function	Peroxisome Targeting Sequence Binding Peroxisome Matrix Targeting Signal-1 Binding Protein Binding Protein C-terminus Binding Enzyme Binding Small GTPase Binding Protein N-terminus Binding	Receptor Binding Polyamine Oxidase Activity N(1),N(12)-diacetylspermine:oxygen Oxidoreductase (3-acetamidopropanal-forming) Activity Spermine:oxygen Oxidoreductase (spermidine-forming) Activity Spermidine:oxygen Oxidoreductase (3-aminopropanal-forming) Activity N1-acetylspermine:oxygen Oxidoreductase (3-acetamidopropanal-forming) Activity N1-acetylspermidine:oxygen Oxidoreductase (3-acetamidopropanal-forming) Activity
	Biological Process	Protein Targeting To Peroxisome Protein Import Into Peroxisome Matrix Protein Import Into Peroxisome Matrix, Docking Protein Import Into Peroxisome Matrix, Translocation Protein Import Into Peroxisome Membrane Protein Tetramerization Negative Regulation Of Protein Homotetramerization	Polyamine Metabolic Process Polyamine Biosynthetic Process Polyamine Catabolic Process Xenobiotic Metabolic Process Putrescine Biosynthetic Process Putrescine Catabolic Process Cellular Nitrogen Compound Metabolic Process Small Molecule Metabolic Process Spermidine Catabolic Process Spermine Catabolic Process Oxidation-reduction Process Positive Regulation Of Spermidine Biosynthetic Process
Pathways			Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Metabolic disorders of biological oxidation enzymes Phase 1 - Functionalization of compounds Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Metabolism of amino acids and derivatives Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Biological oxidations PAOs oxidise polyamines to amines Amine Oxidase reactions Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Defective FMO3 causes Trimethylaminuria (TMAU) Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Defective CYP1B1 causes Glaucoma Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Metabolism of polyamines Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Interconversion of polyamines Defective MAOA causes Brunner syndrome (BRUNS) Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Drugs
Diseases
GWAS		IgG glycosylation ( 23382691)
Protein-Protein Interactions		68 interactors: ACD ACOT2 ACOT4 ACOT8 ACOX2 ACOX3 AGXT AMACR ATM BAAT BRCA1 CAPRIN2 CCDC14 CROT DAO DDO DECR2 DHRS4 ECH1 ECI2 EP400NL EPHX2 FIS1 GDPD5 GNPAT GSTK1 HACL1 HAO1 HAO2 HMGCL HOXA7 HSPA1A IDE IDH1 LDHB LONP2 MKRN3 MLYCD MPV17 NOS2 NUDT19 NUDT3 NUDT7 PAOX PDZK1 PECR PEX10 PEX12 PEX13 PEX14 PEX7 PIPOX POT1 PRDX5 PRR13 RPL14 S100A6 SCARB1 SCP2 SIRT3 SLC27A2 SNUPN SSTR5 TINF2 TM6SF1 TOMM7 USP9X ZNF772	1 interactors: PEX5
Entrez ID		5830	196743
HPRD ID		02684	10136
Ensembl ID		ENSG00000139197	ENSG00000148832
Uniprot IDs		B4DR50 B4E0T2 P50542	Q6QHF9
PDB IDs		1FCH 2C0L 2C0M 2J9Q 2W84 3R9A
Enriched GO Terms of Interacting Partners?		Carboxylic Acid Catabolic Process Monocarboxylic Acid Metabolic Process Fatty Acid Metabolic Process Carboxylic Acid Metabolic Process Organic Acid Metabolic Process Small Molecule Metabolic Process Fatty Acid Oxidation Catabolic Process Lipid Oxidation Fatty Acid Catabolic Process Lipid Metabolic Process Cellular Lipid Metabolic Process Lipid Modification Cellular Lipid Catabolic Process Lipid Catabolic Process Peroxisome Organization Oxidation-reduction Process Fatty Acid Beta-oxidation Fatty Acid Beta-oxidation Using Acyl-CoA Oxidase Protein Import Into Peroxisome Matrix Cellular Metabolic Process Acyl-CoA Metabolic Process Protein Targeting To Peroxisome Establishment Of Protein Localization To Peroxisome Bile Acid Biosynthetic Process Intracellular Protein Transmembrane Transport Cofactor Metabolic Process Protein Transmembrane Transport Lipid Biosynthetic Process Bile Acid Metabolic Process Fatty Acid Alpha-oxidation Sulfur Compound Metabolic Process Glyoxylate Metabolic Process Protein Import Protein Localization To Organelle Establishment Of Protein Localization To Organelle Steroid Biosynthetic Process Protein Targeting Telomere Assembly Metabolic Process Negative Regulation Of Telomere Maintenance Via Telomerase Steroid Metabolic Process Cellular Amino Acid Catabolic Process Long-chain Fatty Acid Metabolic Process Negative Regulation Of Telomere Maintenance Regulation Of Telomere Maintenance Via Telomerase Negative Regulation Of Chromosome Organization Cellular Process Dicarboxylic Acid Catabolic Process Coenzyme A Catabolic Process	Negative Regulation Of Protein Homotetramerization Protein Import Into Peroxisome Matrix, Translocation Protein Import Into Peroxisome Matrix, Docking Negative Regulation Of Protein Homooligomerization Protein Import Into Peroxisome Membrane Protein To Membrane Docking Peroxisomal Membrane Transport Negative Regulation Of Protein Oligomerization Protein Import Into Peroxisome Matrix Protein Targeting To Peroxisome Establishment Of Protein Localization To Peroxisome Very Long-chain Fatty Acid Metabolic Process Cerebral Cortex Neuron Differentiation Regulation Of Protein Oligomerization Endoplasmic Reticulum Organization Fatty Acid Beta-oxidation Peroxisome Organization Positive Regulation Of Multicellular Organism Growth Intracellular Protein Transmembrane Transport Mitochondrial Membrane Organization Protein Transmembrane Transport Fatty Acid Oxidation Lipid Oxidation Fatty Acid Catabolic Process Cerebral Cortex Cell Migration Membrane Docking Regulation Of Multicellular Organism Growth Telencephalon Cell Migration Forebrain Cell Migration Protein Tetramerization Neuromuscular Process Negative Regulation Of Protein Complex Assembly Cellular Lipid Catabolic Process Positive Regulation Of Developmental Growth Cerebral Cortex Development Protein Import Protein Targeting To Membrane Neuron Migration Lipid Modification Carboxylic Acid Catabolic Process Pallium Development Central Nervous System Neuron Differentiation Positive Regulation Of Growth Establishment Of Protein Localization To Membrane Lipid Catabolic Process Telencephalon Development Regulation Of Developmental Growth Fatty Acid Metabolic Process Regulation Of Protein Complex Assembly Establishment Of Protein Localization To Organelle
Tagcloud ?		behave behaves cargo cooperatively couple cytosol deubiquitination differently disuse energetics folded identically import importers importomer lumen organelles peroxisomal peroxisome peroxisomes pexophagy shuttle stochastic traffic translationally translocated translocation ubiquitin uncoupled	acetylpolyamine antizyme az biosynthesis catabolic chemoresistance conversely define degradation dnp73 drugs fosb genotoxic jun junb mechanistic mediator namely np73 overcome overexpressing oxidase polyamine precludes sirna suppressing tap73 upregulates widen
Tagcloud (Difference) ?		behave behaves cargo cooperatively couple cytosol deubiquitination differently disuse energetics folded identically import importers importomer lumen organelles peroxisomal peroxisome peroxisomes pexophagy shuttle stochastic traffic translationally translocated translocation ubiquitin uncoupled	acetylpolyamine antizyme az biosynthesis catabolic chemoresistance conversely define degradation dnp73 drugs fosb genotoxic jun junb mechanistic mediator namely np73 overcome overexpressing oxidase polyamine precludes sirna suppressing tap73 upregulates widen
Tagcloud (Intersection) ?