EC: 2.6.1.3

cysteine transaminase (L-cysteine:2-oxoglutarate aminotransferase)

enzyme lambda metabolic reaction experiment

Pathways

pathway id name
BioCyc:HUMAN_MALATE-ASPARTATE-SHUTTLE-PWY malate-aspartate shuttle
BioCyc:HUMAN_ASPARAGINE-DEG1-PWY-1 asparagine degradation
BioCyc:HUMAN_PWY-5328 superpathway of methionine degradation
BioCyc:META_ASPARAGINE-DEG1-PWY-1 L-asparagine degradation III (mammalian)
BioCyc:META_ASPARTATE-DEG1-PWY L-aspartate degradation I
BioCyc:META_CYSTEINE-DEG-PWY L-cysteine degradation I
BioCyc:META_PWY-5328 superpathway of L-methionine salvage and degradation
BioCyc:MOUSE_HYDROXYPRODEG-PWY 4-hydroxyproline degradation I
BioCyc:MOUSE_CYSTEINE-DEG-PWY L-cysteine degradation I
BioCyc:MOUSE_PWY-5328 superpathway of methionine degradation
BioCyc:HUMAN_PWY-5329 L-cysteine degradation II
BioCyc:META_ASPARTATESYN-PWY L-aspartate biosynthesis
BioCyc:META_MALATE-ASPARTATE-SHUTTLE-PWY L-aspartate degradation II
BioCyc:META_PWY-5329 L-cysteine degradation III
BioCyc:HUMAN_ASPARTATESYN-PWY aspartate biosynthesis
BioCyc:HUMAN_CYSTEINE-DEG-PWY L-cysteine degradation I
Reactome:R-BTA-8963693 Aspartate and asparagine metabolism
Reactome:R-SSC-8963693 Aspartate and asparagine metabolism
Reactome:R-GGA-8963693 Aspartate and asparagine metabolism
Reactome:R-RNO-8963693 Aspartate and asparagine metabolism
Reactome:R-MMU-8963693 Aspartate and asparagine metabolism
Reactome:R-HSA-8963693 Aspartate and asparagine metabolism
Reactome:R-SSC-9856872 Malate-aspartate shuttle
Reactome:R-HSA-9856872 Malate-aspartate shuttle
Reactome:R-GGA-9856872 Malate-aspartate shuttle
Reactome:R-MMU-9856872 Malate-aspartate shuttle
Reactome:R-RNO-9856872 Malate-aspartate shuttle
Reactome:R-BTA-9856872 Malate-aspartate shuttle
Reactome:R-BTA-1430728 Metabolism
Reactome:R-BTA-1428517 Aerobic respiration and respiratory electron transport
Reactome:R-BTA-71291 Amino acid and derivative metabolism
Reactome:R-GGA-1660598 Metabolism
Reactome:R-GGA-352875 Gluconeogenesis
Reactome:R-HSA-611105 Respiratory electron transport
Reactome:R-MMU-1430728 Metabolism
Reactome:R-MMU-611105 Respiratory electron transport
Reactome:R-RNO-611105 Respiratory electron transport
Reactome:R-BTA-611105 Respiratory electron transport
Reactome:R-GGA-1428517 Aerobic respiration and respiratory electron transport
Reactome:R-GGA-71291 Amino acid and derivative metabolism
Reactome:R-HSA-1237112 Methionine salvage pathway
Reactome:R-SSC-1430728 Metabolism
Reactome:R-GGA-1430728 Metabolism
Reactome:R-GGA-353098 Carbohydrate metabolism
Reactome:R-GGA-372568 Amino acid metabolism
Reactome:R-HSA-1428517 Aerobic respiration and respiratory electron transport
Reactome:R-HSA-71291 Amino acid and derivative metabolism
Reactome:R-MMU-1428517 Aerobic respiration and respiratory electron transport
Reactome:R-MMU-71291 Amino acid and derivative metabolism
Reactome:R-RNO-1430728 Metabolism
Reactome:R-RNO-1428517 Aerobic respiration and respiratory electron transport
Reactome:R-RNO-71291 Amino acid and derivative metabolism
Reactome:R-SSC-611105 Respiratory electron transport
Reactome:R-SSC-71291 Amino acid and derivative metabolism
Reactome:R-GGA-611105 Respiratory electron transport
Reactome:R-HSA-1430728 Metabolism
Reactome:R-HSA-1614635 Sulfur amino acid metabolism
Reactome:R-SSC-1428517 Aerobic respiration and respiratory electron transport
WikiPathways:WP4595 Urea cycle and associated pathways
WikiPathways:WP4583 Biomarkers for urea cycle disorders
WikiPathways:WP5220 Metabolic reprogramming in pancreatic cancer
WikiPathways:WP4504 Cysteine and methionine catabolism
PathBank:SMP0120654 Cystinosis, Ocular Nonnephropathic
PathBank:SMP0120666 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency
PathBank:SMP0120682 Carbamoyl Phosphate Synthetase Deficiency
PathBank:SMP0120686 Citrullinemia Type I
PathBank:SMP0120714 Homocarnosinosis
PathBank:SMP0120762 Ornithine Transcarbamylase Deficiency (OTC Deficiency)
PathBank:SMP0120850 Succinic Semialdehyde Dehydrogenase Deficiency
PathBank:SMP0120540 Phenylketonuria
PathBank:SMP0120569 Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency
PathBank:SMP0000020 Arginine and Proline Metabolism
PathBank:SMP0000362 Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
PathBank:SMP0000188 Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
PathBank:SMP0000369 Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
PathBank:SMP0000190 Hawkinsinuria
PathBank:SMP0000504 Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency
PathBank:SMP0000722 Cystinosis, Ocular Nonnephropathic
PathBank:SMP0087278 Glutamate Metabolism
PathBank:SMP0063596 Arginine and Proline Metabolism
PathBank:SMP0120677 Argininosuccinic Aciduria
PathBank:SMP0120491 Hawkinsinuria
PathBank:SMP0120499 Hyperprolinemia Type I
PathBank:SMP0120511 Tyrosinemia Type 3 (TYRO3)
PathBank:SMP0120539 Prolinemia Type II
PathBank:SMP0120564 beta-Mercaptolactate-Cysteine Disulfiduria
PathBank:SMP0120572 L-Arginine:Glycine Amidinotransferase Deficiency
PathBank:SMP0000207 Prolidase Deficiency (PD)
PathBank:SMP0000208 Prolinemia Type II
PathBank:SMP0000206 Phenylketonuria
PathBank:SMP0000169 Alkaptonuria
PathBank:SMP0000429 Disulfiram Action Pathway
PathBank:SMP0000499 beta-Mercaptolactate-Cysteine Disulfiduria
PathBank:SMP0000507 L-Arginine:Glycine Amidinotransferase Deficiency
PathBank:SMP0087301 Malate-Aspartate Shuttle
PathBank:SMP0063607 Cysteine Metabolism
PathBank:SMP0063684 Tyrosine Metabolism
PathBank:SMP0120676 Argininemia
PathBank:SMP0120716 Hyperinsulinism-Hyperammonemia Syndrome
PathBank:SMP0108773 Glutaminolysis and Cancer
PathBank:SMP0120453 Alkaptonuria
PathBank:SMP0120501 Hyperprolinemia Type II
PathBank:SMP0120509 Tyrosinemia Type I
PathBank:SMP0120513 Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
PathBank:SMP0120541 Prolidase Deficiency (PD)
PathBank:SMP0120570 Hyperornithinemia with Gyrate Atrophy (HOGA)
PathBank:SMP0120598 Monoamine Oxidase-A Deficiency (MAO-A)
PathBank:SMP0000013 Cysteine Metabolism
PathBank:SMP0000360 Hyperprolinemia Type II
PathBank:SMP0000363 Ornithine Aminotransferase Deficiency (OAT Deficiency)
PathBank:SMP0000370 Tyrosinemia Type 3 (TYRO3)
PathBank:SMP0000218 Tyrosinemia Type I
PathBank:SMP0000505 Hyperornithinemia with Gyrate Atrophy (HOGA)
PathBank:SMP0000533 Monoamine Oxidase-A Deficiency (MAO-A)
PathBank:SMP0120659 2-Hydroxyglutric Aciduria (D and L Form)
PathBank:SMP0120454 Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
PathBank:SMP0120490 Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
PathBank:SMP0120538 Ornithine Aminotransferase Deficiency (OAT Deficiency)
PathBank:SMP0120559 Tyrosinemia, Transient, of the Newborn
PathBank:SMP0120563 Dopamine beta-Hydroxylase Deficiency
PathBank:SMP0120571 Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]
PathBank:SMP0000006 Tyrosine Metabolism
PathBank:SMP0000008 Phenylalanine and Tyrosine Metabolism
PathBank:SMP0000361 Hyperprolinemia Type I
PathBank:SMP0000494 Tyrosinemia, Transient, of the Newborn
PathBank:SMP0000498 Dopamine beta-Hydroxylase Deficiency
PathBank:SMP0000506 Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]
PathBank:SMP0087319 Urea Cycle
PathBank:SMP0063649 Phenylalanine and Tyrosine Metabolism