ATE1 and ACADSB

		ATE1	ACADSB
Description		arginyltransferase 1	acyl-CoA dehydrogenase short/branched chain
Image		No pdb structure
GO Annotations	Cellular Component	Nucleus Cytoplasm	Mitochondrion Mitochondrial Matrix
	Molecular Function	Arginyltransferase Activity Protein Binding	Acyl-CoA Dehydrogenase Activity Flavin Adenine Dinucleotide Binding
	Biological Process	Proteasomal Protein Catabolic Process Protein Arginylation	Fatty Acid Metabolic Process Branched-chain Amino Acid Catabolic Process Oxidation-reduction Process
Pathways			Branched-chain amino acid catabolism
Drugs			L-Isoleucine Valproic Acid
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		Chronotype ( 30696823)	Antidepressant treatment resistance (> 2 drugs prescribed) ( 30700811) Antidepressant treatment resistance (number of drugs prescribed) ( 30700811) Lower body strength ( 27325353)
Interacting Genes		13 interacting genes: ABRAXAS2 ACADSB ALCAM CTBP2 FAM53B INTS8 NEDD8 NSMCE4A NUP188 PLEKHA1 RBM10 SUV39H1 TIMM17B	1 interacting genes: ATE1
Entrez ID		11101	36
HPRD ID		06979	02626
Ensembl ID		ENSG00000107669	ENSG00000196177
Uniprot IDs		B3KWA3 B4DK25 B4E107 F5GXE4 O95260	A0A0S2Z3P9 P45954
PDB IDs			2JIF
Enriched GO Terms of Interacting Partners?
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