PC

Gene Name		pyruvate carboxylase
Image
Gene Ontology Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Mitochondrial Matrix Cytosol
	Molecular Function	DNA Binding Biotin Carboxylase Activity Pyruvate Carboxylase Activity Protein Binding ATP Binding Biotin Binding Metal Ion Binding
	Biological Process	Carbohydrate Metabolic Process Glucose Metabolic Process Pyruvate Metabolic Process Gluconeogenesis Oxaloacetate Metabolic Process Lipid Metabolic Process Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process Biotin Metabolic Process Pathogenesis Small Molecule Metabolic Process
Pathways		Metabolism of vitamins and cofactors Defective CD320 causes methylmalonic aciduria Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Defective BTD causes biotidinase deficiency Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Defective MTR causes methylmalonic aciduria and homocystinuria type cblG Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Gluconeogenesis Glucose metabolism Defective AMN causes hereditary megaloblastic anemia 1 Myoclonic epilepsy of Lafora Glycogen storage diseases Defects in cobalamin (B12) metabolism Defective GIF causes intrinsic factor deficiency Defective HLCS causes multiple carboxylase deficiency Defective MMAB causes methylmalonic aciduria type cblB Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Defective MMAA causes methylmalonic aciduria type cblA Defective CUBN causes hereditary megaloblastic anemia 1 Metabolism of water-soluble vitamins and cofactors Defective MUT causes methylmalonic aciduria mut type Defects in biotin (Btn) metabolism Defective TCN2 causes hereditary megaloblastic anemia Metabolism of carbohydrates Biotin transport and metabolism Defects in vitamin and cofactor metabolism
Drugs		Pyruvic acid Biotin 5-(HEXAHYDRO-2-OXO-1H-THIENO[3,4-D]IMIDAZOL-6-YL)PENTANAL
Diseases
GWAS		Bipolar disorder ( 21926972) HIV-1 susceptibility ( 22174851)
Protein-protein Interactions		3 interactors: GOT1 GOT2 MDH2
Entrez ID		5091
HPRD ID		02032
Ensembl ID		ENSG00000173599
Uniprot IDs		P11498
PDB IDs		3BG3 3BG9
Enriched GO Terms of Interacting Partners?		Oxaloacetate Metabolic Process Glutamate Catabolic Process To 2-oxoglutarate Glutamate Catabolic Process To Aspartate Aspartate Biosynthetic Process Gluconeogenesis Hexose Biosynthetic Process Fumarate Metabolic Process Aspartate Catabolic Process Dicarboxylic Acid Metabolic Process Glutamate Catabolic Process Glucose Metabolic Process Aspartate Metabolic Process Carbohydrate Biosynthetic Process Pathogenesis Hexose Metabolic Process Dicarboxylic Acid Catabolic Process Monosaccharide Metabolic Process 2-oxoglutarate Metabolic Process Glutamate Metabolic Process Cellular Amino Acid Catabolic Process Carboxylic Acid Metabolic Process Carbohydrate Metabolic Process Cellular Amino Acid Biosynthetic Process Organic Acid Metabolic Process Carboxylic Acid Catabolic Process Cellular Carbohydrate Metabolic Process Glycerol Biosynthetic Process Alpha-amino Acid Metabolic Process 4-hydroxyproline Catabolic Process L-kynurenine Metabolic Process Small Molecule Metabolic Process L-methionine Biosynthetic Process From Methylthioadenosine Cellular Amino Acid Metabolic Process L-methionine Salvage Kynurenine Metabolic Process Fatty Acid Homeostasis NADH Metabolic Process Malate Metabolic Process Methionine Biosynthetic Process Methionine Metabolic Process 4-hydroxyproline Metabolic Process Cellular Modified Amino Acid Catabolic Process Sulfur Amino Acid Biosynthetic Process Polyamine Metabolic Process Glycerol Metabolic Process Tricarboxylic Acid Cycle Sulfur Amino Acid Metabolic Process Citrate Metabolic Process Anion Homeostasis NAD Metabolic Process
Tagcloud ?		47d accordance acetyltransferase ar ara70 bridging caf classic cloning coactivator coactivators coordinate cos deduced differs du ele1 ele1alpha ele1beta glucocorticoid gr hela isoform leucine lncap nonallelic rfg steroid testis tfiib