MCCC2

Description		methylcrotonoyl-CoA carboxylase 2
Image		No pdb structure
GO Annotations	Cellular Component	3-methylcrotonyl-CoA Carboxylase Complex, Mitochondrial Mitochondrion Mitochondrial Matrix Cytosol Methylcrotonoyl-CoA Carboxylase Complex
	Molecular Function	Methylcrotonoyl-CoA Carboxylase Activity Protein Binding ATP Binding
	Biological Process	Leucine Catabolic Process Biotin Metabolic Process Branched-chain Amino Acid Catabolic Process Coenzyme A Metabolic Process
Pathways		Biotin transport and metabolism Defective HLCS causes multiple carboxylase deficiency Branched-chain amino acid catabolism
Drugs		Biotin
Diseases		3-Methylcrotonylglycinuria; 3-Methylcrotonyl-CoA carboxylase deficiency
GWAS		Chromosomal aberration frequency (chromatid type) ( 31586183) Depressive symptoms x independent stressful life events interaction (2df test) ( 30718454) Metabolite levels ( 23823483)
Interacting Genes		1 interacting genes: HSPB2
Entrez ID		64087
HPRD ID		01952
Ensembl ID		ENSG00000131844
Uniprot IDs		A0A140VK29 Q9HCC0
PDB IDs
Enriched GO Terms of Interacting Partners?
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