PTGIS and PTGS1

Number of citations of the paper that reports this interaction (PMID 21035466)
4

Data Source:
BioGRID (fluorescent resonance energy transfer)

		PTGIS	PTGS1
Gene Name		prostaglandin I2 (prostacyclin) synthase	prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
Image			No pdb structure
Gene Ontology Annotations	Cellular Component	Extracellular Space Nucleus Endoplasmic Reticulum Endoplasmic Reticulum Membrane Caveola Integral Component Of Membrane	Photoreceptor Outer Segment Nucleus Cytoplasm Endoplasmic Reticulum Membrane Intracellular Membrane-bounded Organelle Extracellular Vesicular Exosome
	Molecular Function	Monooxygenase Activity Iron Ion Binding Protein Binding Prostaglandin-I Synthase Activity Oxidoreductase Activity, Acting On Paired Donors, With Incorporation Or Reduction Of Molecular Oxygen Heme Binding	Peroxidase Activity Prostaglandin-endoperoxide Synthase Activity Heme Binding Metal Ion Binding Dioxygenase Activity
	Biological Process	Prostaglandin Biosynthetic Process Icosanoid Metabolic Process Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process Nicotinamide Metabolic Process Xenobiotic Metabolic Process Arachidonic Acid Metabolic Process Cyclooxygenase Pathway NAD Metabolic Process Negative Regulation Of NF-kappaB Transcription Factor Activity Positive Regulation Of Peroxisome Proliferator Activated Receptor Signaling Pathway Small Molecule Metabolic Process Negative Regulation Of Nitric Oxide Biosynthetic Process Positive Regulation Of Angiogenesis Negative Regulation Of Inflammatory Response Oxidation-reduction Process Cellular Response To Interleukin-1 Cellular Response To Interleukin-6 Cellular Response To Hypoxia Apoptotic Signaling Pathway Positive Regulation Of Execution Phase Of Apoptosis	Prostaglandin Biosynthetic Process Lipid Metabolic Process Xenobiotic Metabolic Process Inflammatory Response Response To Oxidative Stress Regulation Of Blood Pressure Arachidonic Acid Metabolic Process Cyclooxygenase Pathway Regulation Of Cell Proliferation Small Molecule Metabolic Process Oxidation-reduction Process
Pathways		Metabolism of vitamins and cofactors Bile acid and bile salt metabolism Defective CD320 causes methylmalonic aciduria Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Metabolism of lipids and lipoproteins Defective BTD causes biotidinase deficiency Metabolic disorders of biological oxidation enzymes Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Arachidonic acid metabolism Defective AMN causes hereditary megaloblastic anemia 1 Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Endogenous sterols Synthesis of bile acids and bile salts Synthesis of bile acids and bile salts via 24-hydroxycholesterol Defective GIF causes intrinsic factor deficiency Defective FMO3 causes Trimethylaminuria (TMAU) Defective HLCS causes multiple carboxylase deficiency Defective MMAB causes methylmalonic aciduria type cblB Eicosanoids Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Defective MMAA causes methylmalonic aciduria type cblA Defective CUBN causes hereditary megaloblastic anemia 1 Synthesis of bile acids and bile salts via 27-hydroxycholesterol Defective MAOA causes Brunner syndrome (BRUNS) Defects in biotin (Btn) metabolism Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3) Defective TCN2 causes hereditary megaloblastic anemia Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Defective MTR causes methylmalonic aciduria and homocystinuria type cblG Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Phase 1 - Functionalization of compounds Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Cytochrome P450 - arranged by substrate type Nicotinamide salvaging Biological oxidations Sterols are 12-hydroxylated by CYP8B1 Defects in cobalamin (B12) metabolism Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Defective CYP1B1 causes Glaucoma Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol Defective MUT causes methylmalonic aciduria mut type Metabolism of water-soluble vitamins and cofactors Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Synthesis of Prostaglandins (PG) and Thromboxanes (TX) Nicotinate metabolism Defects in vitamin and cofactor metabolism	Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Metabolism of lipids and lipoproteins COX reactions Metabolic disorders of biological oxidation enzymes Phase 1 - Functionalization of compounds Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Arachidonic acid metabolism Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Biological oxidations Defective FMO3 causes Trimethylaminuria (TMAU) Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Defective CYP1B1 causes Glaucoma Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Defective MAOA causes Brunner syndrome (BRUNS) Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3) Synthesis of Prostaglandins (PG) and Thromboxanes (TX)
Drugs		Phenylbutazone Epoprostenol (6E)-7-{6-[(1E)-OCT-1-ENYL]-2,3-DIAZABICYCLO[2.2.1]HEPT-2-EN-5-YL}HEPT-6-ENOIC ACID	gamma-Homolinolenic acid Icosapent Mesalazine Acetaminophen Indomethacin Minoxidil Nabumetone Ketorolac Tenoxicam Tolmetin Piroxicam Fenoprofen Diclofenac Sulindac Diethylcarbamazine Flurbiprofen Etodolac Mefenamic acid Naproxen Sulfasalazine Phenylbutazone Meloxicam Carprofen Diflunisal Suprofen Salicyclic acid Meclofenamic acid Acetylsalicylic acid Bromfenac Oxaprozin Ketoprofen Balsalazide Ibuprofen Lumiracoxib Magnesium salicylate Salicylate-sodium Salsalate Trisalicylate-choline Antrafenine Antipyrine Tiaprofenic acid O-Acetylserine Hyperforin 2-(1,1\'-Biphenyl-4-Yl)Propanoic Acid Protoporphyrin Ix Containing Co 2-Bromoacetyl Group Flufenamic Acid Beta-D-Glucose Beta-D-Mannose Resveratrol (3-Chloro-4-Propoxy-Phenyl)-Acetic Acid Alpha-D-Mannose Heme Acetic Acid Salicyloyl-Amino-Ester P-(2\'-Iodo-5\'-Thenoyl)Hydrotropic Acid Flurbiprofen Methyl Ester Phenacetin Niflumic Acid Arachidonic Acid Dipyrone Lornoxicam Nepafenac 2-[1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOL-3-YL]-N-[(1R)-1-(HYDROXYMETHYL)PROPYL]ACETAMIDE 1-(4-IODOBENZOYL)-5-METHOXY-2-METHYL INDOLE-3-ACETIC ACID 2-[1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOL-3-YL]-N-[(1S)-1-(HYDROXYMETHYL)PROPYL]ACETAMIDE Triflusal
Diseases
GWAS
Protein-Protein Interactions		3 interactors: APP PTGS1 PTGS2	3 interactors: NCL NUCB1 PTGIS
Entrez ID		5740	5742
HPRD ID		09046	07518
Ensembl ID		ENSG00000124212	ENSG00000095303
Uniprot IDs		Q16647	B4E2S5 P23219
PDB IDs		2IAG 3B6H
Enriched GO Terms of Interacting Partners?		Cyclooxygenase Pathway Prostaglandin Biosynthetic Process Prostaglandin Metabolic Process Response To Oxidative Stress Icosanoid Biosynthetic Process Unsaturated Fatty Acid Biosynthetic Process Arachidonic Acid Metabolic Process Icosanoid Metabolic Process Unsaturated Fatty Acid Metabolic Process Long-chain Fatty Acid Metabolic Process Fatty Acid Biosynthetic Process Learning Maintenance Of Blood-brain Barrier Lipid Metabolic Process Regulation Of Blood Pressure Defense Response Synaptic Growth At Neuromuscular Junction Positive Regulation Of Fibroblast Growth Factor Production Collateral Sprouting In Absence Of Injury Learning Or Memory Cognition Positive Regulation Of Platelet-derived Growth Factor Production Negative Regulation Of Synaptic Transmission, Dopaminergic Nicotinamide Metabolic Process Blood Circulation Fatty Acid Metabolic Process Collateral Sprouting Axon Midline Choice Point Recognition Response To Light Stimulus Positive Regulation Of Brown Fat Cell Differentiation Smooth Endoplasmic Reticulum Calcium Ion Homeostasis Regulation Of Brown Fat Cell Differentiation Positive Regulation Of Cell Migration Involved In Sprouting Angiogenesis Axon Choice Point Recognition Positive Regulation Of Prostaglandin Biosynthetic Process Inflammatory Response Small Molecule Metabolic Process Positive Regulation Of Sprouting Angiogenesis Positive Regulation Of Synaptic Plasticity Response To Radiation Single-organism Behavior Neuron Remodeling Cellular Response To ATP Response To Fructose Positive Regulation Of Fever Generation Regulation Of Cellular Ketone Metabolic Process Alkaloid Metabolic Process Regulation Of Fever Generation Positive Regulation Of Heat Generation Lipoxygenase Pathway	Positive Regulation Of Transcription Of Nuclear Large RRNA Transcript From RNA Polymerase I Promoter Nicotinamide Metabolic Process Positive Regulation Of Peroxisome Proliferator Activated Receptor Signaling Pathway Alkaloid Metabolic Process Positive Regulation Of Transcription From RNA Polymerase I Promoter Positive Regulation Of Execution Phase Of Apoptosis Regulation Of Peroxisome Proliferator Activated Receptor Signaling Pathway Negative Regulation Of Nitric Oxide Biosynthetic Process Cyclooxygenase Pathway Negative Regulation Of Reactive Oxygen Species Biosynthetic Process Regulation Of Transcription From RNA Polymerase I Promoter Prostaglandin Biosynthetic Process Regulation Of Execution Phase Of Apoptosis Cellular Response To Interleukin-6 Prostaglandin Metabolic Process Response To Interleukin-6 Negative Regulation Of Reactive Oxygen Species Metabolic Process Icosanoid Biosynthetic Process NAD Metabolic Process Unsaturated Fatty Acid Biosynthetic Process Cellular Response To Interleukin-1 Regulation Of Nitric Oxide Biosynthetic Process Regulation Of Reactive Oxygen Species Biosynthetic Process Negative Regulation Of NF-kappaB Transcription Factor Activity Arachidonic Acid Metabolic Process Response To Interleukin-1 Nicotinamide Nucleotide Metabolic Process Water-soluble Vitamin Metabolic Process Icosanoid Metabolic Process Cellular Response To Hypoxia Cellular Response To Decreased Oxygen Levels Unsaturated Fatty Acid Metabolic Process Negative Regulation Of Inflammatory Response Cellular Response To Oxygen Levels Vitamin Metabolic Process Negative Regulation Of Sequence-specific DNA Binding Transcription Factor Activity Long-chain Fatty Acid Metabolic Process Positive Regulation Of Angiogenesis Fatty Acid Biosynthetic Process Xenobiotic Metabolic Process Cellular Response To Xenobiotic Stimulus Response To Xenobiotic Stimulus Regulation Of Reactive Oxygen Species Metabolic Process
Tagcloud ?		amputation boosting candidates computational concordant cryoinjury datasets failing fate heart hearts highlights integrative periostin players promises property qpcr ranked regeneration remarkable reproducible specification top unbiased usp2a validations verified zebrafish	5p blockade centres coincided dendritic fdc fl follicles follicular gc germinal il6 ltbetar lymphoid lymphotoxin micrornas mir mmu nucleotides plausible repressing retain rnas select spleen stromal surfaces tlr4 yb
Tagcloud (Difference) ?		amputation boosting candidates computational concordant cryoinjury datasets failing fate heart hearts highlights integrative periostin players promises property qpcr ranked regeneration remarkable reproducible specification top unbiased usp2a validations verified zebrafish	5p blockade centres coincided dendritic fdc fl follicles follicular gc germinal il6 ltbetar lymphoid lymphotoxin micrornas mir mmu nucleotides plausible repressing retain rnas select spleen stromal surfaces tlr4 yb
Tagcloud (Intersection) ?