ABCD3 and ACADM

		ABCD3	ACADM
Description		ATP binding cassette subfamily D member 3	acyl-CoA dehydrogenase medium chain
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Peroxisome Peroxisomal Membrane Peroxisomal Matrix Cytosol Membrane Integral Component Of Membrane Intracellular Membrane-bounded Organelle	Nucleus Mitochondrion Mitochondrial Matrix Axon Mitochondrial Membrane
	Molecular Function	Long-chain Fatty Acid Transporter Activity Protein Binding ATP Binding ATPase Activity ATPase Activity, Coupled To Transmembrane Movement Of Substances Protein Homodimerization Activity Protein Self-association	Acyl-CoA Dehydrogenase Activity Identical Protein Binding Flavin Adenine Dinucleotide Binding Medium-chain-acyl-CoA Dehydrogenase Activity
	Biological Process	Fatty Acid Biosynthetic Process Fatty Acid Beta-oxidation Peroxisome Organization Response To Organic Cyclic Compound Peroxisomal Long-chain Fatty Acid Import Response To Drug Very Long-chain Fatty Acid Catabolic Process Transmembrane Transport	Fatty Acid Beta-oxidation Regulation Of Lipid Metabolic Process Carnitine Metabolic Process, CoA-linked Fatty Acid Beta-oxidation Using Acyl-CoA Dehydrogenase Carnitine Biosynthetic Process Medium-chain Fatty Acid Metabolic Process Medium-chain Fatty Acid Catabolic Process Oxidation-reduction Process
Pathways		ABC transporters in lipid homeostasis Class I peroxisomal membrane protein import	PPARA activates gene expression mitochondrial fatty acid beta-oxidation of unsaturated fatty acids Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA Beta oxidation of octanoyl-CoA to hexanoyl-CoA
Drugs			Octanoyl-Coenzyme A Flavin adenine dinucleotide 3-Thiaoctanoyl-Coenzyme A
Diseases			Disorders of fatty-acid oxidation, including: Medium-chain (MC) acyl-CoA dehydrogenase (AD) deficiency (MCADD); Short-chain AD deficiency (SCADD) ; Short-branched-chain AD deficiency (SBCADD) ; Very long-chain AD deficiency (VLCADD) ; Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency (LCHADD) ; Trifunctional protein deficiency (TFP); Carnitine palmitoyltransferase deficiency (CPT); Carnitine-acylcarnitine translocase deficiency (CACT); Systemic primary carnitine deficiency (CDSP)
GWAS			Acylcarnitine levels ( 26068415) Blood metabolite levels ( 24816252) Blood metabolite ratios ( 24816252) Daytime sleep phenotypes ( 27126917) Glycine levels ( 31070104 30837465) Metabolic traits ( 21886157) Metabolite levels ( 20037589) Serum metabolite concentrations in chronic kidney disease ( 29545352) Serum metabolite levels ( 23093944) Serum metabolite ratios in chronic kidney disease ( 29545352) Urinary metabolite levels in chronic kidney disease ( 31959995) Urinary metabolite modules (eigenmetabolites) in chronic kidney disease ( 31959995)
Interacting Genes		7 interacting genes: ABCD1 ABCD2 ACADM COL6A2 PEX19 PSMA1 TUFT1	7 interacting genes: ABCD3 AGTR1 CALM1 DBT DIRAS3 MSH4 SUMO4
Entrez ID		5825	34
HPRD ID		01368	08447
Ensembl ID		ENSG00000117528	ENSG00000117054
Uniprot IDs		P28288	A0A0S2Z366 B4DJE7 B7Z9I1 P11310 Q5HYG7 Q5T4U5
PDB IDs			1EGC 1EGD 1EGE 1T9G 2A1T 4P13
Enriched GO Terms of Interacting Partners?
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