| L-dopa peroxidase | <enzyme> Found in human erythrocytes associated with catalase Registry number: EC 1.11.- (26 Jun 1999) |
|---|---|
| L-erythro-3,5-diaminohexanoate dehydrogenase | <enzyme> Possible reaction mechanism given Registry number: EC 1.4.1.11 Synonym: 3,5-diaminohexanoate dehydrogenase (26 Jun 1999) |
| L-fucose permease | <chemical> Synonym: fucose permease (26 Jun 1999) |
| L-fuculokinase | <enzyme> Reaction: ATP + l-fuculose = ADP + l-fuculose 1-phosphate; from escherichia coli; has been sequenced Registry number: EC 2.7.1.51 Synonym: fuck gene product (26 Jun 1999) |
| L-galactitol-1-phosphate dehydrogenase | <enzyme> Nad-specific; forms d-tagatose-6-phosphate Registry number: EC 1.1.1.- Synonym: d-galactitol-6-phosphate dehydrogenase, galactitol-p-dhgase (26 Jun 1999) |
| L-galactonolactone oxidase | <enzyme> Flavin-containing enzyme from yeast which utilises oxygen as electron acceptor; forms ascorbic acid Registry number: EC 1.3.3.24 Synonym: galactono-gamma-lactone oxidase, l-galactono-1,4-lactone-oxygen 3-oxidoreductase (26 Jun 1999) |
| L-glyceraldehyde 3-phosphate-NADPH-dependent oxidoreductase | <enzyme> Converts l-glyceraldehyde 3-phosphate to sn-glycerol 3-phosphate; does not act on d-glyceraldehyde 3-phosphate or dihydroxyacetone phosphate Registry number: EC 1.1.1.- Synonym: l-gap oxidoreductase (26 Jun 1999) |
| l-glyceric aciduria | Excretion of l-glyceric acid in the urine; a primary metabolic error due to deficiency of d-glyceric dehydrogenase resulting in excretion of l-glyceric and oxalic acids, leading to the clinical syndrome of oxalosis with frequent formation of oxalate renal calculi. (05 Mar 2000) |
| L-glycol dehydrogenase | <enzyme> Catalyses NADPH linked reversible reduction of uncharged vicinal dicarbonyls and alpha-hydroxycarbonyls to l-(+)-glycols Registry number: EC 1.1.1.185 Synonym: l-(+)-glycol-NADP oxidoreductase, alpha-dicarbonyl reductase, l-(+)-alpha-hydroxycarbonyl-NADP oxidoreductase (26 Jun 1999) |
| l-gulonic acid | Reduction product of glucuronic acid (-CHO → -CH2OH); oxidation product of l-gulose (-CHO → -COOH); a precursor (except in primates, guinea pigs, certain fishes, and the Indian fruit bat) of ascorbic acid via l-gulonolactone. (05 Mar 2000) |
| l-gulono-gamma-lactone | The immediate precursor of ascorbic acid in those animals capable of ascorbic acid biosynthesis. Synonym: dihydroascorbic acid, l-gulono-gamma-lactone. L-gulonolactone oxidase, the enzyme catalyzing the conversion of l-gulonolactone and O2 to H2O2 and l-xylo-hexulonolactone, a precursor of ascorbic acid; absent in primates. (05 Mar 2000) |
| l-gulonolactone | The immediate precursor of ascorbic acid in those animals capable of ascorbic acid biosynthesis. Synonym: dihydroascorbic acid, l-gulono-gamma-lactone. L-gulonolactone oxidase, the enzyme catalyzing the conversion of l-gulonolactone and O2 to H2O2 and l-xylo-hexulonolactone, a precursor of ascorbic acid; absent in primates. (05 Mar 2000) |
| L-gulonolactone oxidase | <enzyme> Forms ascorbic acid Registry number: EC 1.1.3.8 Synonym: l-gulonooxidase, l-gulono-gamma-lactone dehydrogenase, l-gulono-gamma-lactone oxidase (26 Jun 1999) |
| L-L factor | <chemical> Fibrin stabilizing factor. It is a glycoprotein activated by thrombin in the presence of calcium to form factor xiiia. Factor xiii is found evenly distributed between plasma and platelets. Its function is to stabilise the formation of the fibrin polymer (clot) which culminates the coagulation cascade. Chemical name: Blood-coagulation factor XIII (12 Dec 1998) |
| L-lysine oxidase | <enzyme> Converts l-lysine to 2-oxo-6-aminohexanoate Registry number: EC 1.4.3.14 Synonym: l-lysine-alpha oxidase (26 Jun 1999) |