EC: 3.1.2.2
palmitoyl-CoA hydrolase (palmitoyl-CoA hydrolase)
Pathways
| pathway id | name |
|---|---|
| BioCyc:HUMAN_PWY-5996 | oleate biosynthesis |
| BioCyc:HUMAN_PWY-5148 | acyl-CoA hydrolysis |
| BioCyc:META_PWY-7741 | phthiocerol biosynthesis |
| BioCyc:META_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:META_PWY-5996 | oleate biosynthesis II (animals and fungi) |
| BioCyc:MOUSE_PWY-6061 | bile acid biosynthesis, neutral pathway |
| BioCyc:MTBH37RV_PWY-7741 | phthiocerol biosynthesis |
| BioCyc:META_PWY-5148 | acyl-CoA hydrolysis |
| BioCyc:META_PWY-7292 | oleate β-oxidation (thioesterase-dependent, yeast) |
| BioCyc:MTBH37RV_PWY-7742 | phenolphthiocerol biosynthesis |
| BioCyc:HUMAN_LIPASYN-PWY | phospholipases |
| BioCyc:HUMAN_PWY-5972 | stearate biosynthesis |
| BioCyc:HUMAN_FAO-PWY | fatty acid β-oxidation |
| BioCyc:META_PWY-5972 | stearate biosynthesis I (animals and fungi) |
| BioCyc:YEAST_PWY-7292 | oleate β-oxidation (thioesterase-dependent) |
| BioCyc:MOUSE_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:MOUSE_LIPASYN-PWY | phospholipases |
| BioCyc:MOUSE_PWY-5148 | acyl-CoA hydrolysis |
| BioCyc:MOUSE_PWY-5136 | fatty acid β-oxidation II (core pathway) |
| BioCyc:ECOL316407_PWY-5148 | acyl-CoA hydrolysis |
| PathBank:SMP0000817 | Fatty Acid Metabolism |
| Reactome:R-HSA-9824446 | Viral Infection Pathways |
| Reactome:R-HSA-9918432 | Maturation of DENV proteins |
| Reactome:R-HSA-9918487 | Dengue Virus Genome Translation and Replication |
| Reactome:R-HSA-9839923 | Dengue Virus Infection |
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-556833 | Metabolism of lipids |
| Reactome:R-BTA-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-HSA-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-HSA-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-HSA-389887 | Beta-oxidation of pristanoyl-CoA |
| Reactome:R-HSA-194068 | Bile acid and bile salt metabolism |
| Reactome:R-HSA-1643685 | Disease |
| Reactome:R-HSA-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis |
| Reactome:R-MMU-168256 | Immune System |
| Reactome:R-MMU-168249 | Innate Immune System |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-556833 | Metabolism of lipids |
| Reactome:R-MMU-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-MMU-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-MMU-389887 | Beta-oxidation of pristanoyl-CoA |
| Reactome:R-MMU-8957322 | Metabolism of steroids |
| Reactome:R-RNO-8978868 | Fatty acid metabolism |
| Reactome:R-RNO-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-RNO-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-RNO-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-RNO-2029485 | Role of phospholipids in phagocytosis |
| Reactome:R-SCE-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-SCE-8957322 | Metabolism of steroids |
| Reactome:R-SCE-194068 | Bile acid and bile salt metabolism |
| Reactome:R-BTA-8978868 | Fatty acid metabolism |
| Reactome:R-BTA-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-DME-1430728 | Metabolism |
| Reactome:R-HSA-556833 | Metabolism of lipids |
| Reactome:R-HSA-8978868 | Fatty acid metabolism |
| Reactome:R-HSA-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-HSA-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-HSA-1482798 | Acyl chain remodeling of CL |
| Reactome:R-HSA-2029485 | Role of phospholipids in phagocytosis |
| Reactome:R-MMU-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis |
| Reactome:R-MMU-8978868 | Fatty acid metabolism |
| Reactome:R-MMU-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-MMU-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-MMU-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-RNO-390918 | Peroxisomal lipid metabolism |
| Reactome:R-RNO-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-RNO-159418 | Recycling of bile acids and salts |
| Reactome:R-RNO-168256 | Immune System |
| Reactome:R-RNO-168249 | Innate Immune System |
| Reactome:R-SCE-1430728 | Metabolism |
| Reactome:R-SCE-8978868 | Fatty acid metabolism |
| Reactome:R-SCE-2046104 | alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
| Reactome:R-SCE-390918 | Peroxisomal lipid metabolism |
| Reactome:R-DME-8978868 | Fatty acid metabolism |
| Reactome:R-HSA-1483257 | Phospholipid metabolism |
| Reactome:R-HSA-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-HSA-159418 | Recycling of bile acids and salts |
| Reactome:R-HSA-168256 | Immune System |
| Reactome:R-HSA-168249 | Innate Immune System |
| Reactome:R-MMU-194068 | Bile acid and bile salt metabolism |
| Reactome:R-RNO-1430728 | Metabolism |
| Reactome:R-RNO-556833 | Metabolism of lipids |
| Reactome:R-RNO-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-RNO-2046106 | alpha-linolenic acid (ALA) metabolism |
| Reactome:R-RNO-389887 | Beta-oxidation of pristanoyl-CoA |
| Reactome:R-RNO-8957322 | Metabolism of steroids |
| Reactome:R-RNO-2029480 | Fcgamma receptor (FCGR) dependent phagocytosis |
| Reactome:R-SCE-556833 | Metabolism of lipids |
| Reactome:R-SCE-389887 | Beta-oxidation of pristanoyl-CoA |
| Reactome:R-SCE-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-DME-556833 | Metabolism of lipids |
| Reactome:R-DME-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-HSA-1430728 | Metabolism |
| Reactome:R-HSA-390918 | Peroxisomal lipid metabolism |
| Reactome:R-HSA-1483206 | Glycerophospholipid biosynthesis |
| Reactome:R-HSA-8957322 | Metabolism of steroids |
| Reactome:R-HSA-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-HSA-5663205 | Infectious disease |
| Reactome:R-MMU-2029485 | Role of phospholipids in phagocytosis |
| Reactome:R-MMU-390918 | Peroxisomal lipid metabolism |
| Reactome:R-MMU-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-MMU-159418 | Recycling of bile acids and salts |
| Reactome:R-RNO-194068 | Bile acid and bile salt metabolism |
| Reactome:R-SCE-390247 | Beta-oxidation of very long chain fatty acids |
| Reactome:R-SCE-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| WikiPathways:WP5064 | 7-oxo-C and 7-beta-HC pathways |
| WikiPathways:WP4545 | Oxysterols derived from cholesterol |
| WikiPathways:WP5176 | Disorders of bile acid synthesis and biliary transport |
| WikiPathways:WP2318 | Fatty acid oxidation |
| PathBank:SMP0120662 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120806 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120822 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0120826 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| PathBank:SMP0120440 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120444 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120468 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0120516 | Maple Syrup Urine Disease |
| PathBank:SMP0120589 | Isovaleric Acidemia |
| PathBank:SMP0000032 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0000051 | Fatty Acid Metabolism |
| PathBank:SMP0000173 | beta-Ketothiolase Deficiency |
| PathBank:SMP0000199 | Maple Syrup Urine Disease |
| PathBank:SMP0000384 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0000235 | Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency) |
| PathBank:SMP0000482 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |
| PathBank:SMP0000318 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0000141 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0000524 | Isovaleric Acidemia |
| PathBank:SMP0000540 | Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) |
| PathBank:SMP0000544 | Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) |
| PathBank:SMP0000568 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0002324 | Biosynthesis of Unsaturated Fatty Acids |
| PathBank:SMP0002346 | Biosynthesis of Unsaturated Fatty Acids (Icosanoyl-CoA) |
| PathBank:SMP0087294 | Fatty Acid Elongation in Mitochondria |
| PathBank:SMP0087358 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0063612 | Fatty Acid Elongation In Mitochondria |
| PathBank:SMP0120661 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120665 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120745 | Methylmalonic Aciduria |
| PathBank:SMP0120757 | Propionic Acidemia |
| PathBank:SMP0120805 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0120825 | Carnitine Palmitoyl Transferase Deficiency II |
| PathBank:SMP0120439 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120443 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120459 | beta-Ketothiolase Deficiency |
| PathBank:SMP0120463 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120467 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0120495 | Zellweger Syndrome |
| PathBank:SMP0120503 | Isovaleric Aciduria |
| PathBank:SMP0120523 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120588 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120608 | Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) |
| PathBank:SMP0120632 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0000054 | Fatty Acid Elongation in Mitochondria |
| PathBank:SMP0000035 | Bile Acid Biosynthesis |
| PathBank:SMP0000138 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0000140 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0000238 | Isovaleric Aciduria |
| PathBank:SMP0000185 | Glutaric Aciduria Type I |
| PathBank:SMP0000481 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0000314 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0000315 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0000523 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000539 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0002329 | Biosynthesis of Unsaturated Fatty Acids (Docosanoyl-CoA) |
| PathBank:SMP0063641 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0063689 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0120652 | 27-Hydroxylase Deficiency |
| PathBank:SMP0120660 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120664 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120696 | Ethylmalonic Encephalopathy |
| PathBank:SMP0120736 | Maple Syrup Urine Disease |
| PathBank:SMP0120740 | Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency) |
| PathBank:SMP0120808 | Isovaleric Acidemia |
| PathBank:SMP0120824 | Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) |
| PathBank:SMP0120828 | Trifunctional Protein Deficiency |
| PathBank:SMP0120441 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120477 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0120525 | Methylmalonic Aciduria |
| PathBank:SMP0120537 | Propionic Acidemia |
| PathBank:SMP0120586 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0000137 | 2-Methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000237 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0000200 | Methylmalonic Aciduria |
| PathBank:SMP0000317 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000521 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0000541 | Carnitine Palmitoyl Transferase Deficiency II |
| PathBank:SMP0000545 | Trifunctional Protein Deficiency |
| PathBank:SMP0002325 | Biosynthesis of Unsaturated Fatty Acids (Tetracosanoyl-CoA) |
| PathBank:SMP0087280 | Fatty Acid Metabolism |
| PathBank:SMP0087360 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |
| PathBank:SMP0063640 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0120663 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120679 | beta-Ketothiolase Deficiency |
| PathBank:SMP0120723 | Isovaleric Aciduria |
| PathBank:SMP0120743 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120807 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120823 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0120827 | Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD) |
| PathBank:SMP0120851 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0120442 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120587 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0000236 | Propionic Acidemia |
| PathBank:SMP0000139 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0000181 | Ethylmalonic Encephalopathy |
| PathBank:SMP0000480 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0000316 | Zellweger Syndrome |
| PathBank:SMP0000522 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0000538 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0000542 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| PathBank:SMP0000720 | 27-Hydroxylase Deficiency |
| PathBank:SMP0087327 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0087359 | Mitochondrial Beta-Oxidation of Medium Chain Saturated Fatty Acids |
| PathBank:SMP0063601 | Bile Acid Biosynthesis |
| PathBank:SMP0063639 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |