| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| Acsf3 | Mcee | ENSRNOP00000020313 | ENSRNOP00000021884 | Acyl-CoA synthetase family member 3. | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | 0.938 |
| Acsf3 | Mmadhc | ENSRNOP00000020313 | ENSRNOP00000058814 | Acyl-CoA synthetase family member 3. | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.559 |
| Acsf3 | Mmut | ENSRNOP00000020313 | ENSRNOP00000064363 | Acyl-CoA synthetase family member 3. | Methylmalonyl-CoA mutase. | 0.918 |
| Echdc1 | Mcee | ENSRNOP00000015440 | ENSRNOP00000021884 | Ethylmalonyl-CoA decarboxylase; Decarboxylates ethylmalonyl-CoA, a potentially toxic metabolite, to form butyryl-CoA, suggesting it might be involved in metabolite proofreading. Also has methylmalonyl-CoA decarboxylase activity at lower level; Belongs to the enoyl-CoA hydratase/isomerase family. | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | 0.954 |
| Echdc1 | Ndufs8 | ENSRNOP00000015440 | ENSRNOP00000023526 | Ethylmalonyl-CoA decarboxylase; Decarboxylates ethylmalonyl-CoA, a potentially toxic metabolite, to form butyryl-CoA, suggesting it might be involved in metabolite proofreading. Also has methylmalonyl-CoA decarboxylase activity at lower level; Belongs to the enoyl-CoA hydratase/isomerase family. | NADH dehydrogenase (Ubiquinone) Fe-S protein 8 (Predicted), isoform CRA_a. | 0.563 |
| Echdc1 | Pcca | ENSRNOP00000015440 | ENSRNOP00000073510 | Ethylmalonyl-CoA decarboxylase; Decarboxylates ethylmalonyl-CoA, a potentially toxic metabolite, to form butyryl-CoA, suggesting it might be involved in metabolite proofreading. Also has methylmalonyl-CoA decarboxylase activity at lower level; Belongs to the enoyl-CoA hydratase/isomerase family. | Propionyl-CoA carboxylase alpha chain, mitochondrial; This is one of the 2 subunits of the biotin-dependent propionyl-CoA carboxylase (PCC), a mitochondrial enzyme involved in the catabolism of odd chain fatty acids, branched-chain amino acids isoleucine, threonine, methionine, and valine and other metabolites. Propionyl-CoA carboxylase catalyzes the carboxylation of propionyl- CoA/propanoyl-CoA to D-methylmalonyl-CoA/(S)-methylmalonyl-CoA (By similarity). Within the holoenzyme, the alpha subunit catalyzes the ATP-dependent carboxylation of the biotin carried by the biotin carboxyl car [...] | 0.602 |
| Echdc1 | Pccb | ENSRNOP00000015440 | ENSRNOP00000021657 | Ethylmalonyl-CoA decarboxylase; Decarboxylates ethylmalonyl-CoA, a potentially toxic metabolite, to form butyryl-CoA, suggesting it might be involved in metabolite proofreading. Also has methylmalonyl-CoA decarboxylase activity at lower level; Belongs to the enoyl-CoA hydratase/isomerase family. | Propionyl-CoA carboxylase beta chain, mitochondrial; This is one of the 2 subunits of the biotin-dependent propionyl-CoA carboxylase (PCC), a mitochondrial enzyme involved in the catabolism of odd chain fatty acids, branched-chain amino acids isoleucine, threonine, methionine, and valine and other metabolites. Propionyl-CoA carboxylase catalyzes the carboxylation of propionyl- CoA/propanoyl-CoA to D-methylmalonyl-CoA/(S)-methylmalonyl-CoA (By similarity). Within the holoenzyme, the alpha subunit catalyzes the ATP-dependent carboxylation of the biotin carried by the biotin carboxyl carr [...] | 0.954 |
| Mcee | Acsf3 | ENSRNOP00000021884 | ENSRNOP00000020313 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Acyl-CoA synthetase family member 3. | 0.938 |
| Mcee | Echdc1 | ENSRNOP00000021884 | ENSRNOP00000015440 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Ethylmalonyl-CoA decarboxylase; Decarboxylates ethylmalonyl-CoA, a potentially toxic metabolite, to form butyryl-CoA, suggesting it might be involved in metabolite proofreading. Also has methylmalonyl-CoA decarboxylase activity at lower level; Belongs to the enoyl-CoA hydratase/isomerase family. | 0.954 |
| Mcee | Mmaa | ENSRNOP00000021884 | ENSRNOP00000015508 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | 0.823 |
| Mcee | Mmadhc | ENSRNOP00000021884 | ENSRNOP00000058814 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.772 |
| Mcee | Mmut | ENSRNOP00000021884 | ENSRNOP00000064363 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Methylmalonyl-CoA mutase. | 0.990 |
| Mcee | Ndufs8 | ENSRNOP00000021884 | ENSRNOP00000023526 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | NADH dehydrogenase (Ubiquinone) Fe-S protein 8 (Predicted), isoform CRA_a. | 0.807 |
| Mcee | Pcca | ENSRNOP00000021884 | ENSRNOP00000073510 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Propionyl-CoA carboxylase alpha chain, mitochondrial; This is one of the 2 subunits of the biotin-dependent propionyl-CoA carboxylase (PCC), a mitochondrial enzyme involved in the catabolism of odd chain fatty acids, branched-chain amino acids isoleucine, threonine, methionine, and valine and other metabolites. Propionyl-CoA carboxylase catalyzes the carboxylation of propionyl- CoA/propanoyl-CoA to D-methylmalonyl-CoA/(S)-methylmalonyl-CoA (By similarity). Within the holoenzyme, the alpha subunit catalyzes the ATP-dependent carboxylation of the biotin carried by the biotin carboxyl car [...] | 0.825 |
| Mcee | Pccb | ENSRNOP00000021884 | ENSRNOP00000021657 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Propionyl-CoA carboxylase beta chain, mitochondrial; This is one of the 2 subunits of the biotin-dependent propionyl-CoA carboxylase (PCC), a mitochondrial enzyme involved in the catabolism of odd chain fatty acids, branched-chain amino acids isoleucine, threonine, methionine, and valine and other metabolites. Propionyl-CoA carboxylase catalyzes the carboxylation of propionyl- CoA/propanoyl-CoA to D-methylmalonyl-CoA/(S)-methylmalonyl-CoA (By similarity). Within the holoenzyme, the alpha subunit catalyzes the ATP-dependent carboxylation of the biotin carried by the biotin carboxyl carr [...] | 0.989 |
| Mcee | Sdhc | ENSRNOP00000021884 | ENSRNOP00000004228 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Succinate dehydrogenase complex, subunit C, integral membrane protein, isoform CRA_b. | 0.766 |
| Mcee | Sdhd | ENSRNOP00000021884 | ENSRNOP00000055942 | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial; Membrane-anchoring subunit of succinate dehydrogenase (SDH) that is involved in complex II of the mitochondrial electron transport chain and is responsible for transferring electrons from succinate to ubiquinone (coenzyme Q); Belongs to the CybS family. | 0.763 |
| Mmaa | Mcee | ENSRNOP00000015508 | ENSRNOP00000021884 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Methylmalonyl CoA epimerase (Predicted), isoform CRA_d. | 0.823 |
| Mmaa | Mmadhc | ENSRNOP00000015508 | ENSRNOP00000058814 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Involved in cobalamin metabolism. Plays a role in regulating the biosynthesis of two coenzymes, methylcobalamin and adenosylcobalamin. Plays a role in regulating the proportion of methylcobalamin and adenosylcobalamin. Promotes oxidation of cob(II)alamin bound to MMACHC. | 0.831 |
| Mmaa | Mmut | ENSRNOP00000015508 | ENSRNOP00000064363 | Methylmalonic aciduria (Cobalamin deficiency) cblA type (Predicted), isoform CRA_a. | Methylmalonyl-CoA mutase. | 0.954 |