EC: 2.6.1.22
(S)-3-amino-2-methylpropionate transaminase ((S)-3-amino-2-methylpropanoate:2-oxoglutarate aminotransferase)
Pathways
| pathway id | name |
|---|---|
| BioCyc:HUMAN_PWY-6535 | 4-aminobutyrate degradation |
| BioCyc:META_PWY-6535 | 4-aminobutanoate degradation I |
| BioCyc:MTBH37RV_PWY-6537 | 4-aminobutanoate degradation II |
| BioCyc:MTBCDC1551_PWY-6535 | 4-aminobutanoate degradation I |
| BioCyc:HUMAN_GLUDEG-I-PWY | GABA shunt |
| BioCyc:META_GLUDEG-I-PWY | GABA shunt |
| BioCyc:META_VALDEG-PWY | L-valine degradation I |
| BioCyc:MTBCDC1551_PWY-6536 | 4-aminobutanoate degradation III |
| BioCyc:MOUSE_PWY-6535 | 4-aminobutyrate degradation I |
| BioCyc:HUMAN_VALDEG-PWY | valine degradation |
| BioCyc:HUMAN_BETA-ALA-DEGRADATION-I-PWY | β-alanine degradation |
| BioCyc:MTBH37RV_PWY-6536 | 4-aminobutanoate degradation III |
| BioCyc:MOUSE_BETA-ALA-DEGRADATION-I-PWY | β-alanine degradation I |
| BioCyc:MOUSE_VALDEG-PWY | valine degradation I |
| BioCyc:MOUSE_GLUDEG-I-PWY | glutamate degradation III (via 4-aminobutyrate) |
| BioCyc:BSUB_PWY-6536 | 4-aminobutanoate degradation III |
| BioCyc:MTBCDC1551_GLUDEG-I-PWY | GABA shunt |
| BioCyc:MTBCDC1551_PWY-6537 | 4-aminobutanoate degradation II |
| BioCyc:MOUSE_PWY-6473 | 4-aminobutyrate degradation IV |
| BioCyc:MOUSE_PWY-4321 | glutamate degradation IV |
| Reactome:R-CEL-112315 | Transmission across Chemical Synapses |
| Reactome:R-HSA-112315 | Transmission across Chemical Synapses |
| Reactome:R-HSA-888590 | GABA synthesis, release, reuptake and degradation |
| Reactome:R-MMU-916853 | Degradation of GABA |
| Reactome:R-RNO-112316 | Neuronal System |
| Reactome:R-SSC-112315 | Transmission across Chemical Synapses |
| Reactome:R-SSC-888590 | GABA synthesis, release, reuptake and degradation |
| Reactome:R-CEL-112316 | Neuronal System |
| Reactome:R-CEL-888590 | GABA synthesis, release, reuptake and degradation |
| Reactome:R-HSA-916853 | Degradation of GABA |
| Reactome:R-MMU-112310 | Neurotransmitter release cycle |
| Reactome:R-RNO-112315 | Transmission across Chemical Synapses |
| Reactome:R-RNO-888590 | GABA synthesis, release, reuptake and degradation |
| Reactome:R-SSC-916853 | Degradation of GABA |
| Reactome:R-CEL-112310 | Neurotransmitter release cycle |
| Reactome:R-HSA-112316 | Neuronal System |
| Reactome:R-MMU-112315 | Transmission across Chemical Synapses |
| Reactome:R-MMU-888590 | GABA synthesis, release, reuptake and degradation |
| Reactome:R-RNO-112310 | Neurotransmitter release cycle |
| Reactome:R-SSC-112316 | Neuronal System |
| Reactome:R-CEL-916853 | Degradation of GABA |
| Reactome:R-HSA-112310 | Neurotransmitter release cycle |
| Reactome:R-MMU-112316 | Neuronal System |
| Reactome:R-RNO-916853 | Degradation of GABA |
| Reactome:R-SSC-112310 | Neurotransmitter release cycle |
| WikiPathways:WP4159 | GABA receptor signaling |
| WikiPathways:WP4225 | Pyrimidine metabolism and related diseases |
| WikiPathways:WP4157 | GABA metabolism (aka GHB) |
| PathBank:SMP0120662 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120666 | 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120698 | GABA-Transaminase Deficiency |
| PathBank:SMP0120714 | Homocarnosinosis |
| PathBank:SMP0120722 | Hypoacetylaspartia |
| PathBank:SMP0120734 | Malonic Aciduria |
| PathBank:SMP0120778 | Carnosinuria, Carnosinemia |
| PathBank:SMP0120786 | Malonyl-CoA Decarboxylase Deficiency |
| PathBank:SMP0120806 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120850 | Succinic Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120440 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120444 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120496 | Hyperinsulinism-Hyperammonemia Syndrome |
| PathBank:SMP0120516 | Maple Syrup Urine Disease |
| PathBank:SMP0120528 | Methylmalonic Aciduria Due to Cobalamin-Related Disorders |
| PathBank:SMP0120589 | Isovaleric Acidemia |
| PathBank:SMP0000032 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0000016 | Propanoate Metabolism |
| PathBank:SMP0000173 | beta-Ketothiolase Deficiency |
| PathBank:SMP0000199 | Maple Syrup Urine Disease |
| PathBank:SMP0000384 | Methylmalonate Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0000339 | Hyperinsulinism-Hyperammonemia Syndrome |
| PathBank:SMP0000141 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0000492 | Ureidopropionase Deficiency |
| PathBank:SMP0000524 | Isovaleric Acidemia |
| PathBank:SMP0087165 | Aspartate Metabolism |
| PathBank:SMP0087169 | Glutamate Metabolism |
| PathBank:SMP0087234 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0087278 | Glutamate Metabolism |
| PathBank:SMP0087426 | Aspartate Metabolism |
| PathBank:SMP0063656 | Propanoate Metabolism |
| PathBank:SMP0120661 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0120665 | 3-Methylglutaconic Aciduria Type IV |
| PathBank:SMP0120681 | Canavan Disease |
| PathBank:SMP0120745 | Methylmalonic Aciduria |
| PathBank:SMP0120757 | Propionic Acidemia |
| PathBank:SMP0120777 | Ureidopropionase Deficiency |
| 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:SMP0000138 | 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency |
| PathBank:SMP0000140 | 3-Methylglutaconic Aciduria Type III |
| PathBank:SMP0000385 | Homocarnosinosis |
| PathBank:SMP0000238 | Isovaleric Aciduria |
| PathBank:SMP0000201 | Methylmalonic Aciduria Due to Cobalamin-Related Disorders |
| PathBank:SMP0000136 | 2-Hydroxyglutric Aciduria (D and L Form) |
| PathBank:SMP0000523 | Isobutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000567 | Succinic Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0087180 | beta-Alanine Metabolism |
| PathBank:SMP0087341 | Propanoate Metabolism |
| PathBank:SMP0063599 | beta-Alanine 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:SMP0120716 | Hyperinsulinism-Hyperammonemia Syndrome |
| PathBank:SMP0120736 | Maple Syrup Urine Disease |
| PathBank:SMP0120748 | Methylmalonic Aciduria Due to Cobalamin-Related Disorders |
| PathBank:SMP0120808 | Isovaleric Acidemia |
| PathBank:SMP0120441 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0120445 | 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0120461 | Canavan Disease |
| PathBank:SMP0120525 | Methylmalonic Aciduria |
| PathBank:SMP0120537 | Propionic Acidemia |
| PathBank:SMP0120558 | Carnosinuria, Carnosinemia |
| PathBank:SMP0120586 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0000067 | Aspartate Metabolism |
| PathBank:SMP0000137 | 2-Methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency |
| PathBank:SMP0000237 | 3-Methylcrotonyl-CoA Carboxylase Deficiency Type I |
| PathBank:SMP0000200 | Methylmalonic Aciduria |
| PathBank:SMP0000175 | Canavan Disease |
| PathBank:SMP0000351 | GABA-Transaminase Deficiency |
| PathBank:SMP0000493 | Carnosinuria, Carnosinemia |
| PathBank:SMP0000521 | 3-Hydroxyisobutyric Acid Dehydrogenase Deficiency |
| PathBank:SMP0087248 | Propanoate Metabolism |
| PathBank:SMP0087276 | Aspartate Metabolism |
| PathBank:SMP0087284 | beta-Alanine Metabolism |
| PathBank:SMP0087428 | Glutamate Metabolism |
| PathBank:SMP0087432 | beta-Alanine Metabolism |
| PathBank:SMP0087480 | Propanoate Metabolism |
| PathBank:SMP0063590 | Glutamate Metabolism |
| PathBank:SMP0120659 | 2-Hydroxyglutric Aciduria (D and L Form) |
| 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:SMP0120438 | 2-Hydroxyglutric Aciduria (D and L Form) |
| PathBank:SMP0120442 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0120478 | GABA-Transaminase Deficiency |
| PathBank:SMP0120494 | Homocarnosinosis |
| PathBank:SMP0120502 | Hypoacetylaspartia |
| PathBank:SMP0120514 | Malonic Aciduria |
| PathBank:SMP0120567 | Malonyl-CoA Decarboxylase Deficiency |
| PathBank:SMP0120587 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0120631 | Succinic Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0000007 | beta-Alanine Metabolism |
| PathBank:SMP0000072 | Glutamate Metabolism |
| PathBank:SMP0000236 | Propionic Acidemia |
| PathBank:SMP0000139 | 3-Methylglutaconic Aciduria Type I |
| PathBank:SMP0000243 | 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency |
| PathBank:SMP0000192 | Hypoacetylaspartia |
| PathBank:SMP0000198 | Malonic Aciduria |
| PathBank:SMP0000502 | Malonyl-CoA Decarboxylase Deficiency |
| PathBank:SMP0000522 | 3-Hydroxyisobutyric Aciduria |
| PathBank:SMP0087327 | Valine, Leucine, and Isoleucine Degradation |
| PathBank:SMP0063597 | Aspartate Metabolism |