| BioCyc:META_PWY-5328 |
superpathway of L-methionine salvage and degradation |
| BioCyc:META_PWY66-426 |
hydrogen sulfide biosynthesis II (mammalian) |
| BioCyc:MOUSE_PWY-5328 |
superpathway of methionine degradation |
| BioCyc:MOUSE_PWY-6292 |
cysteine biosynthesis III (mammalia) |
| BioCyc:HUMAN_PWY66-426 |
hydrogen sulfide biosynthesis II (mammalian) |
| BioCyc:META_PWY-6292 |
superpathway of L-cysteine biosynthesis (mammalian) |
| BioCyc:MOUSE_HOMOCYSDEGR-PWY |
cysteine biosynthesis/homocysteine degradation |
| BioCyc:META_HOMOCYSDEGR-PWY |
L-cysteine biosynthesis III (from L-homocysteine) |
| BioCyc:META_PWY-701 |
L-methionine degradation II |
| BioCyc:MOUSE_CYSTEINE-SYN2-PWY |
cysteine biosynthesis II |
| Reactome:R-HSA-1614558 |
Degradation of cysteine and homocysteine |
| Reactome:R-MMU-1430728 |
Metabolism |
| Reactome:R-MMU-1614558 |
Degradation of cysteine and homocysteine |
| Reactome:R-RNO-1614558 |
Degradation of cysteine and homocysteine |
| Reactome:R-DDI-71291 |
Amino acid and derivative metabolism |
| Reactome:R-DDI-1614558 |
Degradation of cysteine and homocysteine |
| Reactome:R-HSA-1614603 |
Cysteine formation from homocysteine |
| Reactome:R-HSA-2408508 |
Metabolism of ingested SeMet, Sec, MeSec into H2Se |
| Reactome:R-MMU-1614603 |
Cysteine formation from homocysteine |
| Reactome:R-RNO-1614603 |
Cysteine formation from homocysteine |
| Reactome:R-DDI-1614635 |
Sulfur amino acid metabolism |
| 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-DDI-1430728 |
Metabolism |
| Reactome:R-DDI-1614603 |
Cysteine formation from homocysteine |
| Reactome:R-HSA-1430728 |
Metabolism |
| Reactome:R-HSA-1614635 |
Sulfur amino acid metabolism |
| Reactome:R-HSA-2408522 |
Selenoamino acid metabolism |
| Reactome:R-MMU-1614635 |
Sulfur amino acid metabolism |
| Reactome:R-RNO-1614635 |
Sulfur amino acid metabolism |
| WikiPathways:WP5355 |
Metabolic Epileptic Disorders |
| WikiPathways:WP4504 |
Cysteine and methionine catabolism |
| PathBank:SMP0120654 |
Cystinosis, Ocular Nonnephropathic |
| PathBank:SMP0120694 |
Dihydropyrimidine Dehydrogenase Deficiency (DHPD) |
| PathBank:SMP0120718 |
Hypermethioninemia |
| PathBank:SMP0120754 |
Non-Ketotic Hyperglycinemia |
| PathBank:SMP0120770 |
Hyperglycinemia, Non-Ketotic |
| PathBank:SMP0120798 |
gamma-Cystathionase Deficiency (CTH) |
| PathBank:SMP0000177 |
Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0000340 |
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD) |
| PathBank:SMP0000242 |
Dimethylglycine Dehydrogenase Deficiency |
| PathBank:SMP0000223 |
Non-Ketotic Hyperglycinemia |
| PathBank:SMP0000484 |
Dimethylglycine Dehydrogenase Deficiency |
| PathBank:SMP0000722 |
Cystinosis, Ocular Nonnephropathic |
| PathBank:SMP0087290 |
Cysteine Metabolism |
| PathBank:SMP0087298 |
Homocysteine Degradation |
| PathBank:SMP0087338 |
Glycine and Serine Metabolism |
| PathBank:SMP0087342 |
Methionine Metabolism |
| PathBank:SMP0120653 |
3-Phosphoglycerate Dehydrogenase Deficiency |
| PathBank:SMP0120741 |
Sarcosinemia |
| PathBank:SMP0120853 |
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type |
| PathBank:SMP0120873 |
Cystinosis, Ocular Nonnephropathic |
| PathBank:SMP0120471 |
Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0120475 |
Dimethylglycine Dehydrogenase Deficiency |
| PathBank:SMP0120487 |
Glycine N-Methyltransferase Deficiency |
| PathBank:SMP0120519 |
Methionine Adenosyltransferase Deficiency |
| PathBank:SMP0120527 |
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency |
| PathBank:SMP0120564 |
beta-Mercaptolactate-Cysteine Disulfiduria |
| PathBank:SMP0120580 |
Homocystinuria, Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0000004 |
Glycine and Serine Metabolism |
| PathBank:SMP0000033 |
Methionine Metabolism |
| PathBank:SMP0000455 |
Homocysteine Degradation |
| PathBank:SMP0000222 |
Glycine N-Methyltransferase Deficiency |
| PathBank:SMP0000499 |
beta-Mercaptolactate-Cysteine Disulfiduria |
| PathBank:SMP0000515 |
Homocystinuria, Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0000721 |
3-Phosphoglycerate Dehydrogenase Deficiency |
| PathBank:SMP0087273 |
Selenoamino Acid Metabolism |
| PathBank:SMP0063587 |
Selenoamino Acid Metabolism |
| PathBank:SMP0063607 |
Cysteine Metabolism |
| PathBank:SMP0063637 |
Methionine Metabolism |
| PathBank:SMP0120872 |
3-Phosphoglycerate Dehydrogenase Deficiency |
| PathBank:SMP0120521 |
Sarcosinemia |
| PathBank:SMP0120634 |
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type |
| PathBank:SMP0000013 |
Cysteine Metabolism |
| PathBank:SMP0000341 |
Hypermethioninemia |
| PathBank:SMP0000221 |
Methionine Adenosyltransferase Deficiency |
| PathBank:SMP0000179 |
Dihydropyrimidine Dehydrogenase Deficiency (DHPD) |
| PathBank:SMP0000485 |
Hyperglycinemia, Non-Ketotic |
| PathBank:SMP0063628 |
Homocysteine Degradation |
| PathBank:SMP0120691 |
Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0120695 |
Dimethylglycine Dehydrogenase Deficiency |
| PathBank:SMP0120707 |
Glycine N-Methyltransferase Deficiency |
| PathBank:SMP0120739 |
Methionine Adenosyltransferase Deficiency |
| PathBank:SMP0120747 |
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency |
| PathBank:SMP0120783 |
beta-Mercaptolactate-Cysteine Disulfiduria |
| PathBank:SMP0120799 |
Homocystinuria, Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0120474 |
Dihydropyrimidine Dehydrogenase Deficiency (DHPD) |
| PathBank:SMP0120498 |
Hypermethioninemia |
| PathBank:SMP0120534 |
Non-Ketotic Hyperglycinemia |
| PathBank:SMP0120550 |
Hyperglycinemia, Non-Ketotic |
| PathBank:SMP0120579 |
gamma-Cystathionase Deficiency (CTH) |
| PathBank:SMP0000029 |
Selenoamino Acid Metabolism |
| PathBank:SMP0000214 |
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency |
| PathBank:SMP0000244 |
Sarcosinemia |
| PathBank:SMP0000514 |
gamma-Cystathionase Deficiency (CTH) |
| PathBank:SMP0000570 |
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type |
| PathBank:SMP0063626 |
Glycine and Serine Metabolism |