| PDHB | pyruvate dehydrogenase beta |
|---|---|
| PDHC | pyruvate dehydrogenase complex |
| GPD | glucose-6-phosphate dehydrogenase; glycerol-phosphate dehydrogenase |
| LAD | lactic acid dehydrogenase; left anterior descending [artery]; left axis deviation; leukocyte adhesio... |
| LADH | lactic acid dehydrogenase; liver alcohol dehydrogenase |
| pyruvate kinase phosphatase | <enzyme> Reactivates pyruvate kinase Registry number: EC 3.1.3.- (26 Jun 1999) |
|---|---|
| pyruvate metabolism, inborn errors | Hereditary disorders of pyruvate metabolism. They are difficult to diagnose and describe because pyruvate is a key intermediate in glycolysis, gluconeogenesis, and the tricarboxylic acid cycle. Some inherited metabolic disorders may alter pyruvate metabolism indirectly. Disorders in pyruvate metabolism appear to lead to deficiencies in neurotransmitter synthesis and, consequently, to nervous system disorders. (12 Dec 1998) |
| pyruvate, orthophosphate dikinase | <enzyme> An enzyme that catalyses the reaction of ATP, pyruvate, and orthophosphate to form AMP plus phosphoenolpyruvate plus pyrophosphate. Chemical name: ATP:pyruvate, orthophosphate phosphotransferase Registry number: EC 2.7.9.1 (12 Dec 1998) |
| pyruvate oxidase | <enzyme> Registry number: EC 1.2.3.3 (12 Dec 1998) |
| pyruvate oxidation factor | <biochemistry> 1,2 dithiolane 3 valeric acid. Regarded as a coenzyme in the oxoglutarate dehydrogenase complex of the citric acid cycle. Involved generally in oxidative decarboxylations of _ keto acids. A growth factor for some organisms. (18 Nov 1997) |
| enol pyruvate | CH2==C(OH)-COO-un, the form of pyruvate encountered in the biologically important phosphoenolpyruvate (enol pyruvate phosphate), not in the free form. (05 Mar 2000) |
| ketal pyruvate transferase | <enzyme> Involves the transfer of the pyruvyl residue from phosphoenolpyruvate to the external mannose of pentasaccharide diphosphate lipid Registry number: EC 2.3.1.- (26 Jun 1999) |
| kynurenine-pyruvate aminotransferase | <enzyme> Found in rat kidney and brain; forms kynurenic acid from kynurenine; pyruvate, 2-keto-n-valerate, 2-keto-n-caproate, 2-keto-isocaproate and oxaloacetate are good acceptors Registry number: EC 2.6.1.- (26 Jun 1999) |
| acetaldehyde dehydrogenase | <enzyme> Works with both nad and nadp Registry number: EC 1.2.1.5 Synonym: aldehyde dehydrogenase (NADP+), naho gene product (26 Jun 1999) |
| acetoin dehydrogenase | <enzyme> An enzyme that catalyses the conversion of acetoin to diacetyl in the presence of NAD. Chemical name: Acetoin:NAD+ oxidoreductase Registry number: EC 1.1.1.5 (12 Dec 1998) |
| acetol dehydrogenase | <enzyme> Forms methylglyoxal; uses nad+ Registry number: EC 1.1.1.- Synonym: 1-hydroxyacetone dehydrogenase (26 Jun 1999) |
| acyl-ACP dehydrogenase | enoyl-ACP reductase (NADPH) |
| acyl-CoA dehydrogenase | <enzyme> See also records for specific fatty acyl groups which have full EC nomenclature number; electron-transferring flavoprotein system reducing ubiquinone and other acceptors; formerly EC 1.3.2.2 Registry number: EC 1.3.99.3 Synonym: fatty-acyl CoA dehydrogenase, palmitoyl-CoA dehydrogenase, short-chain acyl-CoA dehydrogenase, acyl-coenzyme a dehydrogenase, lauroyl-CoA oxidase (26 Jun 1999) |
| acyl-CoA dehydrogenase (NADPH+) | Enzyme catalyzing the reversible reduction of enoyl-CoA derivatives of chain length 4 to 16, with NADPH as the hydrogen donor, forming acyl-CoA and NADP+. Synonym: enoyl-CoA reductase. (05 Mar 2000) |
| alanopine dehydrogenase | <enzyme> Catalyses reductive elimination between pyruvate and alanine, or glycine, utilizing NADH as coenzyme, producing 2,2'-iminodipropionic acid (alanopine) Registry number: EC 1.5.1.- (26 Jun 1999) |