| Protein | Synonyms | Taxonomy |
|---|
| Hydroxyacid oxidase 1 | HAOX1; EC 1.1.3.15; Glycolate oxidase; GOX | Homo sapiens (human) |
| Aspartate aminotransferase, mitochondrial | mAspAT; EC 2.6.1.1; EC 2.6.1.7; Fatty acid-binding protein; FABP-1; Glutamate oxaloacetate transaminase 2; Kynurenine aminotransferase 4; Kynurenine aminotransferase IV; Kynurenine--oxoglutarate transaminase 4; Kynurenine--oxoglutarate transaminase IV; Pl | Homo sapiens (human) |
| Serine--pyruvate aminotransferase | SPT; EC 2.6.1.51; Alanine--glyoxylate aminotransferase; AGT; 2.6.1.44 | Homo sapiens (human) |
| Hydroxyproline dehydrogenase | HYPDH; EC 1.5.5.3; Kidney and liver proline oxidase 1; HsPOX1; Probable proline dehydrogenase 2; 1.5.5.2; Probable proline oxidase 2 | Homo sapiens (human) |
| Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial | P5C dehydrogenase; EC 1.2.1.88; Aldehyde dehydrogenase family 4 member A1; L-glutamate gamma-semialdehyde dehydrogenase | Homo sapiens (human) |
| D-amino-acid oxidase | DAAO; DAMOX; DAO; EC 1.4.3.3 | Homo sapiens (human) |
| L-lactate dehydrogenase A chain | LDH-A; EC 1.1.1.27; Cell proliferation-inducing gene 19 protein; LDH muscle subunit; LDH-M; Renal carcinoma antigen NY-REN-59 | Homo sapiens (human) |
| Glyoxylate reductase/hydroxypyruvate reductase | EC 1.1.1.79; EC 1.1.1.81 | Homo sapiens (human) |
| 4-hydroxy-2-oxoglutarate aldolase, mitochondrial | EC 4.1.3.16; Dihydrodipicolinate synthase-like; DHDPS-like protein; Probable 2-keto-4-hydroxyglutarate aldolase; Probable KHG-aldolase; Protein 569272 | Homo sapiens (human) |
| Sulfate anion transporter 1 | SAT-1; Solute carrier family 26 member 1 | Homo sapiens (human) |
| Peroxisomal membrane protein 2 | 22 kDa peroxisomal membrane protein | Homo sapiens (human) |
| Compound | Description |
|---|
| flavin-adenine dinucleotide | A condensation product of riboflavin and adenosine diphosphate. The coenzyme of various aerobic dehydrogenases, e.g., D-amino acid oxidase and L-amino acid oxidase. (Lehninger, Principles of Biochemistry, 1982, p972) |
| Pyruvic Acid | An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed) |
| glyoxylate | |
| 2-keto-4-hydroxyglutarate | RN given refers to parent cpd |
| glycolate | |
| Calcium | A basic element found in nearly all tissues. It is a member of the alkaline earth family of metals with the atomic symbol Ca, atomic number 20, and atomic weight 40. Calcium is the most abundant mineral in the body and combines with phosphorus to form calcium phosphate in the bones and teeth. It is essential for the normal functioning of nerves and muscles and plays a role in blood coagulation (as factor IV) and in many enzymatic processes. |
| hydroxyproline | A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation. |