PCCA

Description		propionyl-CoA carboxylase subunit alpha
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GO Annotations	Cellular Component	Mitochondrion Mitochondrial Matrix Cytosol
	Molecular Function	Propionyl-CoA Carboxylase Activity Protein Binding ATP Binding Biotin Binding Enzyme Binding Metal Ion Binding
	Biological Process	Short-chain Fatty Acid Catabolic Process
Pathways		Biotin transport and metabolism Defective HLCS causes multiple carboxylase deficiency Propionyl-CoA catabolism
Drugs		Biotin
Diseases
GWAS		Chromosomal aberration frequency (chromatid type) in genotoxic compound exposure ( 31586183) Corpus callosum anterior volume ( 31530798) Metabolite levels ( 23823483) Myopia ( 27182965) Refractive error ( 23396134 32231278) Risk-taking tendency (4-domain principal component model) ( 30643258) Smoking initiation (ever regular vs never regular) ( 30679032) Spherical equivalent or myopia (age of diagnosis) ( 29808027)
Interacting Genes		4 interacting genes: ERRFI1 MCC PCCB PJA1
Entrez ID		5095
HPRD ID		01981
Ensembl ID		ENSG00000175198
Uniprot IDs		P05165
PDB IDs		2CQY 2JKU
Enriched GO Terms of Interacting Partners?
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