node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
AGXT | AGXT2 | ENSP00000302620 | ENSP00000231420 | alanine-glyoxylate aminotransferase | alanine--glyoxylate aminotransferase 2; Can metabolize asymmetric dimethylarginine (ADMA) via transamination to alpha-keto-delta-(NN-dimethylguanidino) valeric acid (DMGV). ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure | 0.988 |
AGXT | DMGDH | ENSP00000302620 | ENSP00000255189 | alanine-glyoxylate aminotransferase | dimethylglycine dehydrogenase | 0.415 |
AGXT | GCSH | ENSP00000302620 | ENSP00000319531 | alanine-glyoxylate aminotransferase | glycine cleavage system protein H (aminomethyl carrier); The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | 0.913 |
AGXT | GLDC | ENSP00000302620 | ENSP00000370737 | alanine-glyoxylate aminotransferase | glycine dehydrogenase (decarboxylating); The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein | 0.965 |
AGXT | SARDH | ENSP00000302620 | ENSP00000360938 | alanine-glyoxylate aminotransferase | sarcosine dehydrogenase | 0.929 |
AGXT | SHMT1 | ENSP00000302620 | ENSP00000318868 | alanine-glyoxylate aminotransferase | serine hydroxymethyltransferase 1 (soluble); Interconversion of serine and glycine (By similarity) | 0.963 |
AGXT | SHMT2 | ENSP00000302620 | ENSP00000333667 | alanine-glyoxylate aminotransferase | serine hydroxymethyltransferase 2 (mitochondrial); Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Required to prevent uracil accumulation in mtDNA. Interconversion of serine and glycine. Associates with mitochondrial DNA | 0.961 |
AGXT2 | AGXT | ENSP00000231420 | ENSP00000302620 | alanine--glyoxylate aminotransferase 2; Can metabolize asymmetric dimethylarginine (ADMA) via transamination to alpha-keto-delta-(NN-dimethylguanidino) valeric acid (DMGV). ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure | alanine-glyoxylate aminotransferase | 0.988 |
AGXT2 | GLDC | ENSP00000231420 | ENSP00000370737 | alanine--glyoxylate aminotransferase 2; Can metabolize asymmetric dimethylarginine (ADMA) via transamination to alpha-keto-delta-(NN-dimethylguanidino) valeric acid (DMGV). ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure | glycine dehydrogenase (decarboxylating); The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein | 0.953 |
AGXT2 | SARDH | ENSP00000231420 | ENSP00000360938 | alanine--glyoxylate aminotransferase 2; Can metabolize asymmetric dimethylarginine (ADMA) via transamination to alpha-keto-delta-(NN-dimethylguanidino) valeric acid (DMGV). ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure | sarcosine dehydrogenase | 0.909 |
AGXT2 | SHMT1 | ENSP00000231420 | ENSP00000318868 | alanine--glyoxylate aminotransferase 2; Can metabolize asymmetric dimethylarginine (ADMA) via transamination to alpha-keto-delta-(NN-dimethylguanidino) valeric acid (DMGV). ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure | serine hydroxymethyltransferase 1 (soluble); Interconversion of serine and glycine (By similarity) | 0.900 |
AGXT2 | SHMT2 | ENSP00000231420 | ENSP00000333667 | alanine--glyoxylate aminotransferase 2; Can metabolize asymmetric dimethylarginine (ADMA) via transamination to alpha-keto-delta-(NN-dimethylguanidino) valeric acid (DMGV). ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure | serine hydroxymethyltransferase 2 (mitochondrial); Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Required to prevent uracil accumulation in mtDNA. Interconversion of serine and glycine. Associates with mitochondrial DNA | 0.913 |
AMT | DLD | ENSP00000273588 | ENSP00000205402 | aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine (By similarity) | dihydrolipoamide dehydrogenase; Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes. Involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction | 0.990 |
AMT | GCSH | ENSP00000273588 | ENSP00000319531 | aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine (By similarity) | glycine cleavage system protein H (aminomethyl carrier); The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | 0.999 |
AMT | GLDC | ENSP00000273588 | ENSP00000370737 | aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine (By similarity) | glycine dehydrogenase (decarboxylating); The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein | 0.999 |
AMT | SHMT1 | ENSP00000273588 | ENSP00000318868 | aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine (By similarity) | serine hydroxymethyltransferase 1 (soluble); Interconversion of serine and glycine (By similarity) | 0.985 |
AMT | SHMT2 | ENSP00000273588 | ENSP00000333667 | aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine (By similarity) | serine hydroxymethyltransferase 2 (mitochondrial); Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Required to prevent uracil accumulation in mtDNA. Interconversion of serine and glycine. Associates with mitochondrial DNA | 0.988 |
DLD | AMT | ENSP00000205402 | ENSP00000273588 | dihydrolipoamide dehydrogenase; Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes. Involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction | aminomethyltransferase; The glycine cleavage system catalyzes the degradation of glycine (By similarity) | 0.990 |
DLD | DMGDH | ENSP00000205402 | ENSP00000255189 | dihydrolipoamide dehydrogenase; Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes. Involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction | dimethylglycine dehydrogenase | 0.493 |
DLD | GCSH | ENSP00000205402 | ENSP00000319531 | dihydrolipoamide dehydrogenase; Lipoamide dehydrogenase is a component of the glycine cleavage system as well as of the alpha-ketoacid dehydrogenase complexes. Involved in the hyperactivation of spermatazoa during capacitation and in the spermatazoal acrosome reaction | glycine cleavage system protein H (aminomethyl carrier); The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | 0.901 |