EC: 1.3.8.1
short-chain acyl-CoA dehydrogenase (short-chain acyl-CoA:electron-transfer flavoprotein 2,3-oxidoreductase)
Pathways
| pathway id | name |
|---|---|
| BioCyc:HUMAN_LEU-DEG2-PWY | leucine degradation |
| BioCyc:META_PWY-6604 | superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation |
| BioCyc:META_PWY-6594 | superpathway of Clostridium acetobutylicum solventogenic fermentation |
| BioCyc:META_CENTFERM-PWY | pyruvate fermentation to butanoate |
| BioCyc:META_PWY-7003 | glycerol degradation to butanol |
| BioCyc:MTBH37RV_FAO-PWY | fatty acid β-oxidation I |
| BioCyc:MOUSE_PWY3DJ-6 | Leucine Catabolism |
| BioCyc:MOUSE_LEU-DEG2-PWY | leucine degradation I |
| BioCyc:META_PWY-5327 | superpathway of L-lysine degradation |
| BioCyc:META_PWY-6583 | pyruvate fermentation to butanol I |
| BioCyc:META_PWY-6590 | superpathway of Clostridium acetobutylicum acidogenic fermentation |
| Reactome:R-BTA-1430728 | Metabolism |
| Reactome:R-BTA-71291 | Amino acid and derivative metabolism |
| Reactome:R-HSA-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-HSA-70895 | Branched-chain amino acid catabolism |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-556833 | Metabolism of lipids |
| Reactome:R-MMU-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-MMU-70895 | Branched-chain amino acid catabolism |
| Reactome:R-RNO-8978868 | Fatty acid metabolism |
| Reactome:R-RNO-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-RNO-77352 | Beta oxidation of butanoyl-CoA to acetyl-CoA |
| Reactome:R-RNO-70895 | Branched-chain amino acid catabolism |
| Reactome:R-BTA-70895 | Branched-chain amino acid catabolism |
| Reactome:R-HSA-556833 | Metabolism of lipids |
| Reactome:R-HSA-8978868 | Fatty acid metabolism |
| Reactome:R-HSA-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-HSA-77352 | Beta oxidation of butanoyl-CoA to acetyl-CoA |
| Reactome:R-MMU-8978868 | Fatty acid metabolism |
| Reactome:R-MMU-77289 | Mitochondrial Fatty Acid Beta-Oxidation |
| Reactome:R-MMU-77352 | Beta oxidation of butanoyl-CoA to acetyl-CoA |
| Reactome:R-RNO-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-HSA-71291 | Amino acid and derivative metabolism |
| Reactome:R-MMU-71291 | Amino acid and derivative metabolism |
| Reactome:R-RNO-1430728 | Metabolism |
| Reactome:R-RNO-556833 | Metabolism of lipids |
| Reactome:R-RNO-77286 | mitochondrial fatty acid beta-oxidation of saturated fatty acids |
| Reactome:R-RNO-71291 | Amino acid and derivative metabolism |
| Reactome:R-HSA-1430728 | Metabolism |
| Reactome:R-HSA-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| Reactome:R-MMU-77350 | Beta oxidation of hexanoyl-CoA to butanoyl-CoA |
| WikiPathways:WP5123 | Mitochondrial fatty acid oxidation disorders |
| WikiPathways:WP4686 | Leucine, isoleucine and valine metabolism |
| WikiPathways:WP2318 | Fatty acid oxidation |
| PathBank:SMP0120662 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120746 | Saccharopinuria/Hyperlysinemia II |
| PathBank:SMP0120806 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120822 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0120826 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| PathBank:SMP0120854 | Pyridoxine Dependency with Seizures |
| PathBank:SMP0120870 | 2-Aminoadipic 2-Oxoadipic Aciduria |
| PathBank:SMP0120440 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120444 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120476 | Ethylmalonic Encephalopathy |
| PathBank:SMP0120516 | Maple Syrup Urine Disease |
| PathBank:SMP0120520 | Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency) |
| PathBank:SMP0120589 | Isovaleric Acidemia |
| PathBank:SMP0120605 | Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) |
| PathBank:SMP0120609 | Trifunctional Protein Deficiency |
| 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:SMP0000141 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0000524 | Isovaleric Acidemia |
| PathBank:SMP0000540 | Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) |
| PathBank:SMP0000568 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0087185 | Butyrate Metabolism |
| PathBank:SMP0087234 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0087358 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| 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:SMP0120503 | Isovaleric Aciduria |
| PathBank:SMP0120523 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120588 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120604 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0120632 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| 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:SMP0000185 | Glutaric Aciduria Type I |
| PathBank:SMP0000523 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000539 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0087172 | Fatty Acid Metabolism |
| PathBank:SMP0087265 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0063603 | Butyrate Metabolism |
| PathBank:SMP0063641 | Mitochondrial Beta-Oxidation of Short Chain Saturated Fatty Acids |
| PathBank:SMP0063689 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0120660 | 2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0120664 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0120696 | Ethylmalonic Encephalopathy |
| PathBank:SMP0120704 | Glutaric Aciduria Type I |
| PathBank:SMP0120736 | Maple Syrup Urine Disease |
| PathBank:SMP0120740 | Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency) |
| PathBank:SMP0120808 | Isovaleric Acidemia |
| PathBank:SMP0120812 | Hyperlysinemia II or Saccharopinuria |
| 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:SMP0120525 | Methylmalonic Aciduria |
| PathBank:SMP0120537 | Propionic Acidemia |
| PathBank:SMP0120586 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0120606 | Carnitine Palmitoyl Transferase Deficiency II |
| 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:SMP0000541 | Carnitine Palmitoyl Transferase Deficiency II |
| PathBank:SMP0000545 | Trifunctional Protein Deficiency |
| PathBank:SMP0087280 | Fatty Acid Metabolism |
| PathBank:SMP0087300 | Lysine Degradation |
| 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:SMP0120811 | Hyperlysinemia I, Familial |
| PathBank:SMP0120823 | Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD) |
| PathBank:SMP0120851 | Short-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (SCHAD) |
| PathBank:SMP0120442 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120587 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120603 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0120607 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| 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:SMP0000522 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0000538 | Carnitine Palmitoyl Transferase Deficiency I |
| PathBank:SMP0000542 | Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) |
| PathBank:SMP0000635 | Valproic Acid Metabolism Pathway |
| PathBank:SMP0087267 | Mitochondrial Beta-Oxidation of Long Chain Saturated Fatty Acids |
| PathBank:SMP0087287 | Butyrate Metabolism |
| PathBank:SMP0087327 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0063589 | Fatty Acid Metabolism |