| NAGO | neuraminidase and galactose oxidase |
|---|---|
| AMI | acquired monosaccharide intolerance; acute myocardial infarction; amitriptyline; anterior myocardial... |
| ASA | acetylsalicylic acid; active systemic anaphylaxis; Adams-Stokes attack; American Society of Anesthes... |
| FCI | fixed-cell immunofluorescence; food chemical intolerance |
| FI | fasciculus intrafascicularis; fever caused by infection; fibrinogen; fixed interval; flame ionizatio... |
familial leiomyomatosis cutis et uteri (가족성 피부 자궁 근종증
acute angle
| fructose 1,6-bisphosphate | <biochemistry> This key intermediate in glycolysis and gluconeogenesis (a hexose diphosphate) was discovered by Arthur Harden and William Young in 1905. In the third step of glycolysis, fructose 6-phosphate and ATP are converted to fructose 1,6-bisphosphate and ADP with the aid of phosphofructokinase. In step 4, fructose 1,6 bisphosphate (with the aid of aldolase) is cleaved into duhydroxyacetone phosphate and glyceraldehyde 3-phosphate. Synonym: hexosebisphosphatase, hexosediphosphatase. (08 Mar 2000) |
|---|---|
| fructose-1,6-diphosphatase deficiency | An autosomal recessive fructose metabolism disorder due to absent or deficient fructose-1,6-diphosphatase activity. Gluconeogenesis is impaired, resulting in accumulation of gluconeogenic precursors (e.g., amino acids, lactate, ketones) and manifested as hypoglycaemia, ketosis, and lactic acidosis. Episodes in the newborn infant are often lethal. Later episodes are often brought on by fasting and febrile infections. As patients age through early childhood, tolerance to fasting improves and development becomes normal. (12 Dec 1998) |
| fructose-1,6-diphosphate reductase | <enzyme> From bovine lens; reduces fructose-1,6-diphosphate to sorbitol-1,6-diphosphate in presence of NADH; 3 isoenzymes which copurify with lactate dehydrogenase isoenzymes Registry number: EC 1.1.1.- Synonym: fdp reductase (26 Jun 1999) |
| fructose 1-phosphate | A fructose derivative that accumulates in individuals with hereditary fructose intolerance. (05 Mar 2000) |
| fructose 2,6-bisphosphate | An analog of fructose 1,6-bisphosphate that plays a key role in the regulation of glycolysis and gluconeogenesis; activates phosphofructokinase and inhibits fructose 1,6-bisphosphatase. (05 Mar 2000) |
| fructose-2,6-bisphosphate 2-phosphatase | <enzyme> Copurifies with 6-phosphofructo-2-kinase; probably is a single protein with both activities; do not confuse with EC 3.1.3.54, fructose-2,6-bisphosphate 6-phosphatase Registry number: EC 3.1.3.46 Synonym: fructose-2,6-diphosphatase, fructose 2,6-bisphosphatase, fructose-2,6-bisphosphatase (26 Jun 1999) |
| fructose-2,6-bisphosphate 6-phosphatase | <enzyme> Do not confuse with fructose-2,6-bisphosphate 2-phosphatase (EC 3.1.3.46) Registry number: EC 3.1.3.54 Synonym: fdp 6-phosphatase, fru(2,6)p2 6-phosphatase (26 Jun 1999) |
| fructose 6-phosphate | <biochemistry> A phosphorylated six-carbon sugar formed in the second step of glycolysis by the action of phosphoglucose isomerase on glucose-6-phosphate. In the third step, fructose 6-phospate and ATP are used to create fructose 1,6-biphosphate, ADP and a free hydrogen with the aid of phosphofructokinase. (08 Mar 2000) |
| fructose-6-phosphate phosphoketolase | <enzyme> Catalyses the conversion of d-fructose 6-phosphate and orthophosphate to acetylphosphate and d-erythrose 4-phosphate and water Registry number: EC 4.1.2.22 Synonym: f6p phosphoketolase (26 Jun 1999) |
| fructose-bisphosphatase | <enzyme> An enzyme that catalyses the conversion of d-fructose 1,6-bisphosphate and water to d-fructose 6-phosphate and orthophosphate. Chemical name: D-Fructose-1,6-bisphosphate 1-phosphohydrolase Registry number: EC 3.1.3.11 (12 Dec 1998) |
| fructose-bisphosphate aldolase | <enzyme> An enzyme of the lyase class that catalyses the cleavage of fructose 1,6-biphosphate to form dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. The enzyme also acts on (3s,4r)-ketose 1-phosphates. The yeast and bacterial enzymes are zinc proteins. (enzyme nomenclature, 1992) e.c. 4.1.2.13. Chemical name: D-Fructose-1,6-biphosphate D-glyceraldehyde-3-phosphate-lyase Registry number: EC 4.1.2.13 (12 Dec 1998) |
| fructose-diphosphate aldolase | <enzyme> An enzyme of the lyase class that catalyses the cleavage of fructose 1,6-biphosphate to form dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. The enzyme also acts on (3s,4r)-ketose 1-phosphates. The yeast and bacterial enzymes are zinc proteins. (enzyme nomenclature, 1992) e.c. 4.1.2.13. Chemical name: D-Fructose-1,6-biphosphate D-glyceraldehyde-3-phosphate-lyase Registry number: EC 4.1.2.13 (12 Dec 1998) |
| fructose metabolism, inborn errors | Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosaemia, but with no clinical dysfunction; may produce a false-positive diabetes test. (12 Dec 1998) |
| fructose permease | <chemical> Fructose-specific enzyme II of phosphoenolpyruvate-dependent phosphotransferase system in e. Coli (26 Jun 1999) |
| galactose | <biochemistry> Hexose identical to glucose except that orientation of H and OH on carbon 4 are exchanged. A component of cerebrosides and gangliosides, glycoproteins. Lactose, the disaccharide of milk, consists of galactose joined to glucose by a _(1-4) glycosidic link. (18 Nov 1997) |