ACACA and PRKAB1

Number of citations of the paper that reports this interaction (PMID 18480843)
26

Data Source:
BioGRID (enzymatic study)

		ACACA	PRKAB1
Gene Name		acetyl-CoA carboxylase alpha	protein kinase, AMP-activated, beta 1 non-catalytic subunit
Image			No pdb structure
Gene Ontology Annotations	Cellular Component	Nucleolus Cytoplasm Mitochondrion Cytosol Actin Cytoskeleton Extracellular Vesicular Exosome	Nucleus Cytosol AMP-activated Protein Kinase Complex
	Molecular Function	Acetyl-CoA Carboxylase Activity Biotin Carboxylase Activity Protein Binding ATP Binding Metal Ion Binding	Protein Kinase Activity AMP-activated Protein Kinase Activity Protein Binding Protein Kinase Binding
	Biological Process	Tissue Homeostasis Acetyl-CoA Metabolic Process Energy Reserve Metabolic Process Fatty Acid Biosynthetic Process Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process Biotin Metabolic Process Carnitine Shuttle Triglyceride Biosynthetic Process Positive Regulation Of Cellular Metabolic Process Long-chain Fatty-acyl-CoA Biosynthetic Process Cellular Lipid Metabolic Process Multicellular Organismal Protein Metabolic Process Small Molecule Metabolic Process Protein Homotetramerization Lipid Homeostasis Malonyl-CoA Biosynthetic Process	Protein Phosphorylation Fatty Acid Biosynthetic Process Organelle Organization Mitochondrion Organization Cell Cycle Arrest Signal Transduction Insulin Receptor Signaling Pathway Positive Regulation Of Gene Expression Regulation Of Protein Kinase Activity Protein Heterooligomerization Membrane Organization
Pathways		Metabolism of vitamins and cofactors Defective CD320 causes methylmalonic aciduria Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Integration of energy metabolism Metabolism of lipids and lipoproteins ChREBP activates metabolic gene expression Defective BTD causes biotidinase deficiency Import of palmitoyl-CoA into the mitochondrial matrix 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 Regulation of cholesterol biosynthesis by SREBP (SREBF) Fatty Acyl-CoA Biosynthesis Defective AMN causes hereditary megaloblastic anemia 1 Triglyceride Biosynthesis Defects in cobalamin (B12) metabolism Defective GIF causes intrinsic factor deficiency Fatty acid, triacylglycerol, and ketone body metabolism 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 Activation of gene expression by SREBF (SREBP) Defective TCN2 causes hereditary megaloblastic anemia Biotin transport and metabolism Defects in vitamin and cofactor metabolism	Organelle biogenesis and maintenance Insulin receptor signalling cascade Regulation of AMPK activity via LKB1 IRS-mediated signalling Regulation of Rheb GTPase activity by AMPK mTOR signalling Translocation of GLUT4 to the plasma membrane IRS-related events mTOR signalling IGF1R signaling cascade Mitochondrial biogenesis IRS-related events triggered by IGF1R Activation of PPARGC1A (PGC-1alpha) by phosphorylation IRS-mediated signalling Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) Energy dependent regulation of mTOR by LKB1-AMPK PKB-mediated events PI3K Cascade PKB-mediated events PI3K Cascade Signaling by Insulin receptor
Drugs		Biotin	Adenosine monophosphate Metformin
Diseases
GWAS		Ovarian cancer ( 23535730)
Protein-Protein Interactions		9 interactors: ATXN1 BRCA1 CHGB CSNK2A1 CSNK2A2 PRKAA1 PRKAA2 PRKAB1 PRKAG1	13 interactors: ACACA AGL APP F10 GRB2 MAP3K7 MAPK6 NDUFA7 PRKAA1 PRKAA2 PRKAG1 PRKAG2 PRKAG3
Entrez ID		31	5564
HPRD ID		01938	04116
Ensembl ID		ENSG00000132142	ENSG00000111725
Uniprot IDs		B2ZZ90 Q13085 Q7Z5W8	Q9Y478
PDB IDs		2YL2 3COJ 4ASI
Enriched GO Terms of Interacting Partners?		Negative Regulation Of Cell Cycle Fatty Acid Biosynthetic Process Regulation Of Cell Cycle Cell Cycle Process Cell Cycle Fatty Acid Metabolic Process Regulation Of Glycolytic Process Cell Cycle Arrest Insulin Receptor Signaling Pathway Cellular Response To Organonitrogen Compound Lipid Biosynthetic Process Monocarboxylic Acid Metabolic Process Cellular Response To Insulin Stimulus Protein Phosphorylation Wnt Signaling Pathway Response To Insulin Regulation Of Generation Of Precursor Metabolites And Energy Cellular Response To Peptide Hormone Stimulus Cellular Response To Peptide Negative Regulation Of Chromosome Organization Response To Organonitrogen Compound Biosynthetic Process Regulation Of Gene Expression Response To Hormone Cellular Lipid Metabolic Process Phosphorylation Cellular Protein Modification Process Regulation Of Energy Homeostasis Positive Regulation Of Glycolytic Process Carboxylic Acid Metabolic Process Regulation Of Cellular Protein Metabolic Process Response To Peptide Hormone Fatty Acid Homeostasis Protein Heterooligomerization Positive Regulation Of Metabolic Process Regulation Of Lipid Biosynthetic Process Signaling Response To Peptide Cell Communication Organic Acid Metabolic Process Regulation Of Carbohydrate Metabolic Process Regulation Of Protein Metabolic Process Histone-serine Phosphorylation Lipid Metabolic Process Cellular Response To Hormone Stimulus Cellular Response To Glucose Starvation Regulation Of Chromosome Organization Transmembrane Receptor Protein Tyrosine Kinase Signaling Pathway Cellular Protein Metabolic Process Cell Cycle Checkpoint	Fatty Acid Biosynthetic Process Insulin Receptor Signaling Pathway Cellular Response To Insulin Stimulus Regulation Of Glycolytic Process Response To Insulin Energy Derivation By Oxidation Of Organic Compounds Energy Reserve Metabolic Process Cellular Response To Peptide Hormone Stimulus Carnitine Shuttle Fatty Acid Metabolic Process Cellular Response To Peptide Cell Cycle Arrest Carnitine Transmembrane Transport Carnitine Transport Generation Of Precursor Metabolites And Energy Phosphorylation Regulation Of Generation Of Precursor Metabolites And Energy Response To Peptide Hormone Cellular Response To Organonitrogen Compound Protein Phosphorylation Response To Peptide Quaternary Ammonium Group Transport Phosphate-containing Compound Metabolic Process Enzyme Linked Receptor Protein Signaling Pathway Response To Hormone Lipid Biosynthetic Process Monocarboxylic Acid Metabolic Process Cellular Response To Hormone Stimulus Small Molecule Metabolic Process Sterol Metabolic Process Transmembrane Receptor Protein Tyrosine Kinase Signaling Pathway Regulation Of Carbohydrate Metabolic Process Long-chain Fatty Acid Transport Ammonium Transmembrane Transport Sterol Biosynthetic Process Lipid Metabolic Process Response To Organonitrogen Compound Negative Regulation Of Cell Cycle Glycogen Metabolic Process Fatty Acid Transport Regulation Of Cell Cycle Oxidation-reduction Process Cellular Lipid Metabolic Process Cellular Protein Modification Process Ammonium Transport Steroid Metabolic Process Carboxylic Acid Metabolic Process Polysaccharide Metabolic Process Response To Organic Substance Positive Regulation Of Cellular Metabolic Process
Tagcloud ?		aldehyde aldh antifungal biosynthesis capability carboxylase catalyzed coa committed csc impeded intermediates lipogenesis mammosphere mcf novo oleic overexpress participates polyketide renewal silenced siphoning soraphen supraphysiological unrecognized warburg	adipor1 alter amp bdkrb2 changed differential discordant epigenome exercise fh hoxc6 mapk1 mef2a methylation modifies monozygotic muscle myo18b ndufc2 pairs predispose retinol runx1 skeletal t2d thada trib1 twin twins
Tagcloud (Difference) ?		aldehyde aldh antifungal biosynthesis capability carboxylase catalyzed coa committed csc impeded intermediates lipogenesis mammosphere mcf novo oleic overexpress participates polyketide renewal silenced siphoning soraphen supraphysiological unrecognized warburg	adipor1 alter amp bdkrb2 changed differential discordant epigenome exercise fh hoxc6 mapk1 mef2a methylation modifies monozygotic muscle myo18b ndufc2 pairs predispose retinol runx1 skeletal t2d thada trib1 twin twins
Tagcloud (Intersection) ?