EC: 4.1.3.4
hydroxymethylglutaryl-CoA lyase ((S)-3-hydroxy-3-methylglutaryl-CoA acetoacetate-lyase (acetyl-CoA-forming))
Pathways
| pathway id | name |
|---|---|
| BioCyc:HUMAN_PWY66-367 | ketogenesis |
| BioCyc:META_PWY-6672 | cis-genanyl-CoA degradation |
| BioCyc:MOUSE_PWY66-367 | ketogenesis |
| BioCyc:HUMAN_LEU-DEG2-PWY | leucine degradation |
| BioCyc:META_PWY-5074 | mevalonate degradation |
| BioCyc:ARA_LEU-DEG2-PWY | L-leucine degradation I |
| BioCyc:MOUSE_PWY3DJ-6 | Leucine Catabolism |
| BioCyc:MOUSE_LEU-DEG2-PWY | leucine degradation I |
| BioCyc:META_LEU-DEG2-PWY | L-leucine degradation I |
| BioCyc:META_PWY66-367 | ketogenesis |
| BioCyc:MOUSE_PWY3FA-941 | ketogenesis |
| PlantCyc:ARA_LEU-DEG2-PWY | L-leucine degradation I |
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-556833 | Metabolism of lipids |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-556833 | Metabolism of lipids |
| Reactome:R-MMU-77111 | Synthesis of Ketone Bodies |
| Reactome:R-RNO-74182 | Ketone body metabolism |
| Reactome:R-BTA-77111 | Synthesis of Ketone Bodies |
| Reactome:R-HSA-556833 | Metabolism of lipids |
| Reactome:R-HSA-77111 | Synthesis of Ketone Bodies |
| Reactome:R-MMU-74182 | Ketone body metabolism |
| Reactome:R-RNO-1430728 | Metabolism |
| Reactome:R-RNO-556833 | Metabolism of lipids |
| Reactome:R-RNO-77111 | Synthesis of Ketone Bodies |
| Reactome:R-BTA-74182 | Ketone body metabolism |
| Reactome:R-HSA-1430728 | Metabolism |
| Reactome:R-HSA-74182 | Ketone body metabolism |
| WikiPathways:WP4686 | Leucine, isoleucine and valine metabolism |
| WikiPathways:WP4190 | Mevalonate arm of cholesterol biosynthesis pathway |
| PathBank:SMP0120662 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120806 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120440 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120444 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120516 | Maple Syrup Urine Disease |
| PathBank:SMP0120589 | Isovaleric Acidemia |
| PathBank:SMP0120633 | Succinyl CoA: 3-Ketoacid CoA Transferase Deficiency |
| PathBank:SMP0000032 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0000173 | beta-Ketothiolase Deficiency |
| PathBank:SMP0000199 | Maple Syrup Urine Disease |
| PathBank:SMP0000384 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0000141 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0000524 | Isovaleric Acidemia |
| PathBank:SMP0002433 | Leucine Degradation |
| 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:SMP0120439 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120443 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120459 | beta-Ketothiolase Deficiency |
| PathBank:SMP0120503 | Isovaleric Aciduria |
| PathBank:SMP0120523 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120588 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000071 | Ketone Body Metabolism |
| PathBank:SMP0000073 | Butyrate Metabolism |
| PathBank:SMP0000138 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0000140 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0000238 | Isovaleric Aciduria |
| PathBank:SMP0000523 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0063603 | Butyrate Metabolism |
| PathBank:SMP0063689 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0120660 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120664 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120736 | Maple Syrup Urine Disease |
| PathBank:SMP0120808 | Isovaleric Acidemia |
| PathBank:SMP0120852 | Succinyl CoA: 3-Ketoacid CoA Transferase Deficiency |
| PathBank:SMP0120441 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| 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:SMP0000521 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0000569 | Succinyl CoA: 3-Ketoacid CoA Transferase Deficiency |
| 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:SMP0120442 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120587 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0000236 | Propionic Acidemia |
| PathBank:SMP0000139 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0000522 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0087287 | Butyrate Metabolism |
| PathBank:SMP0087299 | Ketone Body Metabolism |
| PathBank:SMP0087327 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0012467 | Butanoate Metabolism |
| PathBank:SMP0063631 | Ketone Body Metabolism |