EC: 1.2.1.31
L-aminoadipate-semialdehyde dehydrogenase (L-2-aminoadipate-6-semialdehyde:NAD(P)+ 6-oxidoreductase)
Pathways
| pathway id | name |
|---|---|
| BioCyc:HUMAN_PWY66-414 | superpathway of choline degradation to L-serine |
| BioCyc:META_LYSINE-DEG1-PWY | L-lysine degradation XI (mammalian) |
| BioCyc:HUMAN_LYSINE-DEG1-PWY | lysine degradation I (saccharopine pathway) |
| BioCyc:META_CHOLINE-BETAINE-ANA-PWY | choline degradation I |
| BioCyc:MOUSE_PWY-2501 | fatty acid α-oxidation |
| BioCyc:MOUSE_PWY66-21 | ethanol degradation II (cytosol) |
| BioCyc:META_PWY-5327 | superpathway of L-lysine degradation |
| BioCyc:HUMAN_CHOLINE-BETAINE-ANA-PWY | choline degradation |
| BioCyc:MOUSE_PWY-0 | putrescine degradation III |
| BioCyc:MOUSE_PWY-3981 | β-alanine biosynthesis I |
| Reactome:R-HSA-71064 | Lysine catabolism |
| Reactome:R-HSA-6798163 | Choline catabolism |
| Reactome:R-MMU-1430728 | Metabolism |
| Reactome:R-MMU-71064 | Lysine catabolism |
| Reactome:R-MMU-6798163 | Choline catabolism |
| Reactome:R-RNO-71064 | Lysine catabolism |
| Reactome:R-RNO-6798163 | Choline catabolism |
| 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-71291 | Amino acid and derivative metabolism |
| Reactome:R-HSA-1430728 | Metabolism |
| WikiPathways:WP4288 | MTHFR deficiency |
| PathBank:SMP0120440 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120444 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120516 | Maple Syrup Urine Disease |
| PathBank:SMP0120528 | Methylmalonic Aciduria Due to Cobalamin-Related Disorders |
| PathBank:SMP0120589 | Isovaleric Acidemia |
| PathBank:SMP0000239 | Saccharopinuria/Hyperlysinemia II |
| PathBank:SMP0000528 | Hyperlysinemia II or Saccharopinuria |
| PathBank:SMP0002313 | Sarcosine Oncometabolite Pathway |
| PathBank:SMP0002337 | Lysine Metabolism |
| PathBank:SMP0063656 | Propanoate Metabolism |
| 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:SMP0000186 | Glutaric Aciduria Type I |
| PathBank:SMP0000527 | Hyperlysinemia I, Familial |
| PathBank:SMP0000571 | Pyridoxine Dependency with Seizures |
| PathBank:SMP0063599 | beta-Alanine Metabolism |
| PathBank:SMP0063689 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0120441 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120525 | Methylmalonic Aciduria |
| PathBank:SMP0120537 | Propionic Acidemia |
| PathBank:SMP0120558 | Carnosinuria, Carnosinemia |
| PathBank:SMP0120586 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0000123 | Betaine Metabolism |
| PathBank:SMP0000719 | 2-Aminoadipic 2-Oxoadipic Aciduria |
| PathBank:SMP0087203 | Lysine Degradation |
| PathBank:SMP0120442 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120478 | GABA-Transaminase Deficiency |
| PathBank:SMP0120514 | Malonic Aciduria |
| PathBank:SMP0120567 | Malonyl-CoA Decarboxylase Deficiency |
| PathBank:SMP0120587 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0000037 | Lysine Degradation |
| PathBank:SMP0087182 | Betaine Metabolism |