| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| AADAT | AFMID | ENSPPYP00000016979 | ENSPPYP00000009753 | Aminoadipate aminotransferase. | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. | 0.932 |
| AADAT | ALDH7A1 | ENSPPYP00000016979 | ENSPPYP00000023896 | Aminoadipate aminotransferase. | ALDH7A1 isoform 1; Belongs to the aldehyde dehydrogenase family. | 0.923 |
| AADAT | BCAT1 | ENSPPYP00000016979 | ENSPPYP00000004984 | Aminoadipate aminotransferase. | Branched-chain-amino-acid aminotransferase; Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family. | 0.757 |
| AADAT | BCAT2 | ENSPPYP00000016979 | ENSPPYP00000011426 | Aminoadipate aminotransferase. | Branched-chain-amino-acid aminotransferase, mitochondrial; Catalyzes the first reaction in the catabolism of the essential branched chain amino acids leucine, isoleucine, and valine. May also function as a transporter of branched chain alpha-keto acids (By similarity). | 0.757 |
| AADAT | CR201_G0027561 | ENSPPYP00000016979 | ENSPPYP00000022040 | Aminoadipate aminotransferase. | KYAT1 isoform 2. | 0.962 |
| AADAT | DHTKD1 | ENSPPYP00000016979 | ENSPPYP00000003298 | Aminoadipate aminotransferase. | Probable 2-oxoglutarate dehydrogenase E1 component DHKTD1, mitochondrial; The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components: 2-oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) (By similarity). | 0.938 |
| AADAT | KMO | ENSPPYP00000016979 | ENSPPYP00000000068 | Aminoadipate aminotransferase. | Kynurenine 3-monooxygenase; Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid, a neurotoxic NMDA receptor antagonist and potential endogenous inhibitor of NMDA receptor signaling in axonal targeting, synaptogenesis and apoptosis during brain development. Quinolinic acid may also affect NMDA receptor signaling in pancreatic beta cells, osteoblasts, myocardial cells, and the gastrointestinal tract. | 0.956 |
| AADAT | KYAT3 | ENSPPYP00000016979 | ENSPPYP00000001362 | Aminoadipate aminotransferase. | Kynurenine aminotransferase 3. | 0.942 |
| AADAT | KYNU | ENSPPYP00000016979 | ENSPPYP00000014317 | Aminoadipate aminotransferase. | Kynureninase; Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively. Has a preference for the L-3-hydroxy form. Also has cysteine-conjugate-beta-lyase activity. Belongs to the kynureninase family. | 0.952 |
| AADAT | SHE | ENSPPYP00000016979 | ENSPPYP00000000908 | Aminoadipate aminotransferase. | Src homology 2 domain containing E. | 0.727 |
| AFMID | AADAT | ENSPPYP00000009753 | ENSPPYP00000016979 | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. | Aminoadipate aminotransferase. | 0.932 |
| AFMID | CR201_G0027561 | ENSPPYP00000009753 | ENSPPYP00000022040 | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. | KYAT1 isoform 2. | 0.936 |
| AFMID | KMO | ENSPPYP00000009753 | ENSPPYP00000000068 | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. | Kynurenine 3-monooxygenase; Catalyzes the hydroxylation of L-kynurenine (L-Kyn) to form 3-hydroxy-L-kynurenine (L-3OHKyn). Required for synthesis of quinolinic acid, a neurotoxic NMDA receptor antagonist and potential endogenous inhibitor of NMDA receptor signaling in axonal targeting, synaptogenesis and apoptosis during brain development. Quinolinic acid may also affect NMDA receptor signaling in pancreatic beta cells, osteoblasts, myocardial cells, and the gastrointestinal tract. | 0.970 |
| AFMID | KYAT3 | ENSPPYP00000009753 | ENSPPYP00000001362 | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. | Kynurenine aminotransferase 3. | 0.929 |
| AFMID | KYNU | ENSPPYP00000009753 | ENSPPYP00000014317 | Kynurenine formamidase; Catalyzes the hydrolysis of N-formyl-L-kynurenine to L- kynurenine, the second step in the kynurenine pathway of tryptophan degradation. Kynurenine may be further oxidized to nicotinic acid, NAD(H) and NADP(H). Required for elimination of toxic metabolites. | Kynureninase; Catalyzes the cleavage of L-kynurenine (L-Kyn) and L-3- hydroxykynurenine (L-3OHKyn) into anthranilic acid (AA) and 3- hydroxyanthranilic acid (3-OHAA), respectively. Has a preference for the L-3-hydroxy form. Also has cysteine-conjugate-beta-lyase activity. Belongs to the kynureninase family. | 0.978 |
| ALDH7A1 | AADAT | ENSPPYP00000023896 | ENSPPYP00000016979 | ALDH7A1 isoform 1; Belongs to the aldehyde dehydrogenase family. | Aminoadipate aminotransferase. | 0.923 |
| ALDH7A1 | DHTKD1 | ENSPPYP00000023896 | ENSPPYP00000003298 | ALDH7A1 isoform 1; Belongs to the aldehyde dehydrogenase family. | Probable 2-oxoglutarate dehydrogenase E1 component DHKTD1, mitochondrial; The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components: 2-oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) (By similarity). | 0.410 |
| BCAT1 | AADAT | ENSPPYP00000004984 | ENSPPYP00000016979 | Branched-chain-amino-acid aminotransferase; Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family. | Aminoadipate aminotransferase. | 0.757 |
| BCAT1 | BCAT2 | ENSPPYP00000004984 | ENSPPYP00000011426 | Branched-chain-amino-acid aminotransferase; Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family. | Branched-chain-amino-acid aminotransferase, mitochondrial; Catalyzes the first reaction in the catabolism of the essential branched chain amino acids leucine, isoleucine, and valine. May also function as a transporter of branched chain alpha-keto acids (By similarity). | 0.901 |
| BCAT2 | AADAT | ENSPPYP00000011426 | ENSPPYP00000016979 | Branched-chain-amino-acid aminotransferase, mitochondrial; Catalyzes the first reaction in the catabolism of the essential branched chain amino acids leucine, isoleucine, and valine. May also function as a transporter of branched chain alpha-keto acids (By similarity). | Aminoadipate aminotransferase. | 0.757 |
