EC: 6.2.1.7
cholate-CoA ligase (cholate:CoA ligase (AMP-forming))
Pathways
| pathway id | name |
|---|---|
| BioCyc:HUMAN_PWY-7592 | arachidonate biosynthesis III (metazoa) |
| BioCyc:META_PWY-7592 | arachidonate biosynthesis III (6-desaturase, mammals) |
| BioCyc:META_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:HUMAN_PWY-5143 | fatty acid activation |
| BioCyc:HUMAN_PWY66-387 | fatty acid α-oxidation |
| BioCyc:META_PWY66-387 | fatty acid α-oxidation II |
| BioCyc:HUMAN_PWY-6000 | γ-linolenate biosynthesis |
| BioCyc:HUMAN_PWY-5972 | stearate biosynthesis |
| BioCyc:HUMAN_FAO-PWY | fatty acid β-oxidation |
| BioCyc:HUMAN_PWY66-391 | fatty acid β-oxidation (peroxisome) |
| BioCyc:META_PWY-6000 | γ-linolenate biosynthesis II (animals) |
| BioCyc:META_PWY66-391 | fatty acid β-oxidation VI (peroxisome) |
| BioCyc:META_PWY-7754 | bile acids degradation |
| BioCyc:META_PWY-5972 | stearate biosynthesis I (animals and fungi) |
| BioCyc:MOUSE_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:MOUSE_PWY-6000 | γ-linolenate biosynthesis II (animals) |
| BioCyc:MOUSE_PWY-5136 | fatty acid β-oxidation II (core pathway) |
| Reactome:R-HSA-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-HSA-194068 | Bile acid and bile salt metabolism |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-556833 | Metabolism of lipids |
| Reactome:R-MMU-75105 | Fatty acyl-CoA biosynthesis |
| Reactome:R-MMU-8957322 | Metabolism of steroids |
| Reactome:R-MMU-193775 | Synthesis of bile acids and bile salts via 24-hydroxycholesterol |
| Reactome:R-RNO-8978868 | Fatty acid metabolism |
| Reactome:R-RNO-389599 | Alpha-oxidation of phytanate |
| Reactome:R-RNO-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-HSA-556833 | Metabolism of lipids |
| Reactome:R-HSA-8978868 | Fatty acid metabolism |
| Reactome:R-HSA-389599 | Alpha-oxidation of phytanate |
| Reactome:R-HSA-193775 | Synthesis of bile acids and bile salts via 24-hydroxycholesterol |
| Reactome:R-MMU-8978868 | Fatty acid metabolism |
| Reactome:R-MMU-389599 | Alpha-oxidation of phytanate |
| 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-HSA-390247 | Beta-oxidation of very long chain fatty acids |
| Reactome:R-HSA-192105 | Synthesis of bile acids and bile salts |
| Reactome:R-HSA-159418 | Recycling of bile acids and salts |
| Reactome:R-MMU-390247 | Beta-oxidation of very long chain fatty acids |
| 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-8957322 | Metabolism of steroids |
| Reactome:R-RNO-193775 | Synthesis of bile acids and bile salts via 24-hydroxycholesterol |
| Reactome:R-HSA-1430728 | Metabolism |
| Reactome:R-HSA-390918 | Peroxisomal lipid metabolism |
| Reactome:R-HSA-8957322 | Metabolism of steroids |
| Reactome:R-HSA-193368 | Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| 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-390247 | Beta-oxidation of very long chain fatty acids |
| Reactome:R-RNO-194068 | Bile acid and bile salt metabolism |
| WikiPathways:WP5176 | Disorders of bile acid synthesis and biliary transport |
| PathBank:SMP0120468 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0000318 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0120697 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0120749 | Refsum Disease |
| PathBank:SMP0120463 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120467 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0120495 | Zellweger Syndrome |
| PathBank:SMP0000035 | Bile Acid Biosynthesis |
| PathBank:SMP0000314 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0000315 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0087329 | Bile Acid Biosynthesis |
| PathBank:SMP0120652 | 27-Hydroxylase Deficiency |
| PathBank:SMP0120688 | Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0120477 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000450 | Phytanic Acid Peroxisomal Oxidation |
| PathBank:SMP0000317 | Familial Hypercholanemia (FHCA) |
| PathBank:SMP0087312 | Phytanic Acid Peroxisomal Oxidation |
| PathBank:SMP0120683 | Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120687 | Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0120715 | Zellweger Syndrome |
| PathBank:SMP0120871 | 27-Hydroxylase Deficiency |
| PathBank:SMP0000451 | Refsum Disease |
| PathBank:SMP0000316 | Zellweger Syndrome |
| PathBank:SMP0000720 | 27-Hydroxylase Deficiency |
| PathBank:SMP0063601 | Bile Acid Biosynthesis |