Fructose 1,6 Bisphosphate Aldolase
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   Fructose 1,6 Bisphosphate Aldolase


Fructose 1,6 Bisphosphate Aldolase

   An enzyme of the lyase class that catalyzes 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.

RELATED TERMS
--------------------------------------

Enzyme
A cellular protein whose shape allows it to hold together several other molecules in close proximity to each other. In this way, enzymes are able to induce chemical reactions in other substances with little expenditure of energy and without being changed themselves. Basically, an enzyme acts as a catalyst.

Cleavage
The process of cell division in the very early embryo before it becomes a blastocyst.

Fructose
Fruit sugar.

Dihydroxyacetone
Also known as DHA, the active ingredient in most sunless tanning lotions.

Yeast
A single-celled fungus that reproduces by budding and may lead to infections of the skin or other moist areas.

Bacterial
Of or pertaining to bacteria. For example, a bacterial lung infection.

Enzymes
Proteins that act as a catalysts in mediating and speeding a specific chemical reaction.



SIMILAR TERMS
--------------------------------------

Fructans
Polysaccharides composed of D-fructose units.

Fructokinases
A class of enzymes that catalyzes the phosphorylation of fructose in the presence of ATP. EC 2.7.1.-.

Fructosamine
A term referring to the linking of blood sugar onto protein molecules in the bloodstream. The fructosamine value depends upon the average blood sugar level during the past three weeks. The fructosamine test could be viewed as complementary to the glycohemoglobin, as the two tests are different reflections of diabetes control: glycohemoglobin looks back approximately eight to twelve weeks, and the fructosamine test looks back about three weeks. |Note: the term fructosamine has nothing to do with the term fructose.

Fructose
Fruit sugar.

Fructose 1 Phosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructose 1,6 Biphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose 1,6 Bisphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose 1,6 Bisphosphatase 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 hypoglycemia, 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.

Fructose 1,6 Diphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

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 hypoglycemia, 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.

Fructose 1,6-Bisphosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructose 1,6-Bisphosphate Aldolase, Class II
An enzyme of the lyase class that catalyzes 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.

Fructose 1-Phosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructose 2,6-bisphosphatase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose Biphosphatase 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 hypoglycemia, 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.

Fructose Biphosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructose Bisphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose Bisphosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructose Intolerance
An autosomal recessive fructose metabolism disorder due to deficient fructose-1-phosphate aldolase (EC 2.1.2.13) activity, resulting in accumulation of fructose-1-phosphate. The accumulated fructose-1-phosphate inhibits glycogenolysis and gluconeogenesis, causing severe hypoglycemia following ingestion of fructose. Prolonged fructose ingestion in infants leads ultimately to hepatic failure and death. Patients develop a strong distaste for sweet food, and avoid a chronic course of the disease by remaining on a fructose- and sucrose-free diet.

Fructose Intolerances
An autosomal recessive fructose metabolism disorder due to deficient fructose-1-phosphate aldolase (EC 2.1.2.13) activity, resulting in accumulation of fructose-1-phosphate. The accumulated fructose-1-phosphate inhibits glycogenolysis and gluconeogenesis, causing severe hypoglycemia following ingestion of fructose. Prolonged fructose ingestion in infants leads ultimately to hepatic failure and death. Patients develop a strong distaste for sweet food, and avoid a chronic course of the disease by remaining on a fructose- and sucrose-free diet.

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 hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test.

Fructose-1,6-Biphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose-1,6-Bisphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose-1,6-Bisphosphatase Deficiencies
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 hypoglycemia, 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.

Fructose-1,6-Bisphosphatase 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 hypoglycemia, 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.

Fructose-1,6-Diphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose-1,6-Diphosphatase Deficiencies
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 hypoglycemia, 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.

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 hypoglycemia, 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.

Fructose-2,6-bisphosphatase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose-2,6-bisphosphate 2-phosphatase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose-2,6-diphosphatase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose-6-P 1-Kinase
An allosteric enzyme that regulates glycolysis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-1,6-bisphosphate. D-tagatose- 6-phosphate and sedoheptulose-7-phosphate also are acceptors. UTP, CTP, and ITP also are donors. In human phosphofructokinase-1, three types of subunits have been identified. They are muscle type M (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE); liver type L (PHOSPHOFRUCTOKINASE-1, LIVER TYPE); and type C (PHOSPHOFRUCTOKINASE-1, C TYPE) found in platelets, brain, and other tissues.

Fructose-6-P,2-kinase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose-6-phosphate 1-Phosphotransferase
An allosteric enzyme that regulates glycolysis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-1,6-bisphosphate. D-tagatose- 6-phosphate and sedoheptulose-7-phosphate also are acceptors. UTP, CTP, and ITP also are donors. In human phosphofructokinase-1, three types of subunits have been identified. They are muscle type M (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE); liver type L (PHOSPHOFRUCTOKINASE-1, LIVER TYPE); and type C (PHOSPHOFRUCTOKINASE-1, C TYPE) found in platelets, brain, and other tissues.

Fructose-6-phosphate,2-kinase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose-6-phosphate,2-kinase-fructose-2,6-bisphosphatase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

Fructose-Biphosphatase Deficiencies
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 hypoglycemia, 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.

Fructose-Biphosphatase 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 hypoglycemia, 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.

Fructose-Bisphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructose-Bisphosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructosediphosphatase
An enzyme that catalyzes the conversion of D-fructose 1,6-bisphosphate and water to D-fructose 6-phosphate and orthophosphate. EC 3.1.3.11.

Fructosediphosphatase Deficiencies
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 hypoglycemia, 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.

Fructosediphosphatase 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 hypoglycemia, 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.

Fructosediphosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructosediphosphates
Diphosphoric acid esters of fructose. The fructose-1,6- diphosphate isomer is most prevalent. It is an important intermediate in the glycolysis process.

Fructosemonophosphate Aldolase
An enzyme of the lyase class that catalyzes 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.

Fructuronate Reductase
An enzyme that catalyzes the reversible oxidation of mannonate to fructuronate in the presence of NAD. Also reduces D-tagaturonate to D-altronate. EC 1.1.1.57.



PREVIOUS AND NEXT TERMS
--------------------------------------

FRP 1 protein
A heterodimeric protein that is a cell surface antigen associated with lymphocyte activation. The initial characterization of this protein revealed one identifiable heavy chain (CD98 HEAVY CHAIN) and an indeterminate smaller light chain. It is now known that a variety of light chain subunits (CD98 LIGHT CHAINS) can dimerize with the heavy chain. Depending upon its light chain composition a diverse array of functions can be found for this protein. Functions include: type L amino acid transport, type y+L amino acid transport and regulation of cellular fusion.

FRP 1 Heavy Chain
A transmembrane glycoprotein subunit that can dimerize with a variety of light chain subunits (ANTIGENS CD98, LIGHT CHAINS). This protein subunit serves a diverse array of functions including amino acid transport and cell fusion. Its function is altered depending which of the light chain subunits it interacts with.

Frozen Semen
The process by which semen is kept viable outside of the organism from which it was derived (i.e., kept from decay by means of a chemical agent, cooling, or a fluid substitute that mimics the natural state within the organism).

Frozen Sections
Thinly cut sections of frozen tissue specimens prepared with a cryostat or freezing microtome.

Frostbites
Damage to tissues as the result of low environmental temperatures.

Fructose 1,6 Bisphosphate Aldolase

Fructokinases
A class of enzymes that catalyzes the phosphorylation of fructose in the presence of ATP. EC 2.7.1.-.

Fructans
Polysaccharides composed of D-fructose units.

Fru-kinase-Fru-bisphosphatase
An allosteric enzyme that regulates glycolysis and gluconeogenesis by catalyzing the transfer of a phosphate group from ATP to fructose-6-phosphate to yield fructose-2,6-bisphosphate, an allosteric effector for the other 6-phosphofructokinase, PHOSPHOFRUCTOKINASE-1. Phosphofructokinase-2 is bifunctional: the dephosphorylated form is a kinase and the phosphorylated form is a phosphatase that breaks down fructose-2,6-bisphosphate to yield fructose-6-phosphate.

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 hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test.

Fructose Intolerances
An autosomal recessive fructose metabolism disorder due to deficient fructose-1-phosphate aldolase (EC 2.1.2.13) activity, resulting in accumulation of fructose-1-phosphate. The accumulated fructose-1-phosphate inhibits glycogenolysis and gluconeogenesis, causing severe hypoglycemia following ingestion of fructose. Prolonged fructose ingestion in infants leads ultimately to hepatic failure and death. Patients develop a strong distaste for sweet food, and avoid a chronic course of the disease by remaining on a fructose- and sucrose-free diet.

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ffuctose 1,6 bisphosphate aldolase / fductose 1,6 bisphosphate aldolase / feuctose 1,6 bisphosphate aldolase / f3uctose 1,6 bisphosphate aldolase / fr7ctose 1,6 bisphosphate aldolase / fr8ctose 1,6 bisphosphate aldolase / frictose 1,6 bisphosphate aldolase / frkctose 1,6 bisphosphate aldolase / frjctose 1,6 bisphosphate aldolase / frhctose 1,6 bisphosphate aldolase / fryctose 1,6 bisphosphate aldolase / fr6ctose 1,6 bisphosphate aldolase / fruxtose 1,6 bisphosphate aldolase / frustose 1,6 bisphosphate aldolase / frudtose 1,6 bisphosphate aldolase / fruftose 1,6 bisphosphate aldolase / fruvtose 1,6 bisphosphate aldolase / fru tose 1,6 bisphosphate aldolase / fruc5ose 1,6 bisphosphate aldolase / fruc6ose 1,6 bisphosphate aldolase / frucyose 1,6 bisphosphate aldolase / fruchose 1,6 bisphosphate aldolase / frucgose 1,6 bisphosphate aldolase / frucfose 1,6 bisphosphate aldolase / frucrose 1,6 bisphosphate aldolase / fruc4ose 1,6 bisphosphate aldolase / fruct9se 1,6 bisphosphate aldolase / fruct0se 1,6 bisphosphate aldolase / fructpse 1,6 bisphosphate aldolase / fructlse 1,6 bisphosphate aldolase / fructkse 1,6 bisphosphate aldolase / fructise 1,6 bisphosphate aldolase / fruct8se 1,6 bisphosphate aldolase / fructowe 1,6 bisphosphate aldolase / fructoee 1,6 bisphosphate aldolase / fructode 1,6 bisphosphate aldolase / fructoxe 1,6 bisphosphate aldolase / fructoze 1,6 bisphosphate aldolase / fructoae 1,6 bisphosphate aldolase / fructoqe 1,6 bisphosphate aldolase / fructos3 1,6 bisphosphate aldolase / fructos4 1,6 bisphosphate aldolase / fructosr 1,6 bisphosphate aldolase / fructosf 1,6 bisphosphate aldolase / fructosd 1,6 bisphosphate aldolase / fructoss 1,6 bisphosphate aldolase / fructosw 1,6 bisphosphate aldolase / fructose 2,6 bisphosphate aldolase / fructose w,6 bisphosphate aldolase / fructose q,6 bisphosphate aldolase / fructose `,6 bisphosphate aldolase / fructose 1,7 bisphosphate aldolase / fructose 1,u bisphosphate aldolase / fructose 1,y bisphosphate aldolase / fructose 1,t bisphosphate aldolase / fructose 1,5 bisphosphate aldolase / fructose 1,6 visphosphate aldolase / fructose 1,6 fisphosphate aldolase / fructose 1,6 gisphosphate aldolase / fructose 1,6 hisphosphate aldolase / fructose 1,6 nisphosphate aldolase / fructose 1,6 isphosphate aldolase / fructose 1,6 bsphosphate aldolase / fructose 1,6 biwphosphate aldolase / fructose 1,6 biephosphate aldolase / fructose 1,6 bidphosphate aldolase / fructose 1,6 bixphosphate aldolase / fructose 1,6 bizphosphate aldolase / fructose 1,6 biaphosphate aldolase / fructose 1,6 biqphosphate aldolase / fructose 1,6 bis0hosphate aldolase / fructose 1,6 bis-hosphate aldolase / fructose 1,6 bis[hosphate aldolase / fructose 1,6 bis;hosphate aldolase / fructose 1,6 bislhosphate aldolase / fructose 1,6 bisohosphate aldolase / fructose 1,6 bis9hosphate aldolase / fructose 1,6 bispyosphate aldolase / fructose 1,6 bispuosphate aldolase / fructose 1,6 bispjosphate aldolase / fructose 1,6 bispnosphate aldolase / fructose 1,6 bispbosphate aldolase / fructose 1,6 bispgosphate aldolase / fructose 1,6 bisptosphate aldolase / fructose 1,6 bisph9sphate aldolase / fructose 1,6 bisph0sphate aldolase / fructose 1,6 bisphpsphate aldolase / fructose 1,6 bisphlsphate aldolase / fructose 1,6 bisphksphate aldolase / fructose 1,6 bisphisphate aldolase / fructose 1,6 bisph8sphate aldolase / fructose 1,6 bisphowphate aldolase / fructose 1,6 bisphoephate aldolase / fructose 1,6 bisphodphate aldolase / fructose 1,6 bisphoxphate aldolase / fructose 1,6 bisphozphate aldolase / fructose 1,6 bisphoaphate aldolase / fructose 1,6 bisphoqphate aldolase / fructose 1,6 bisphos0hate aldolase / fructose 1,6 bisphos-hate aldolase / fructose 1,6 bisphos[hate aldolase / fructose 1,6 bisphos;hate aldolase / fructose 1,6 bisphoslhate aldolase / fructose 1,6 bisphosohate aldolase / fructose 1,6 bisphos9hate aldolase / fructose 1,6 bisphospyate aldolase / fructose 1,6 bisphospuate aldolase / fructose 1,6 bisphospjate aldolase / fructose 1,6 bisphospnate aldolase / fructose 1,6 bisphospbate aldolase / fructose 1,6 bisphospgate aldolase / fructose 1,6 bisphosptate aldolase / fructose 1,6 bisphosphqte aldolase / fructose 1,6 bisphosphwte aldolase / fructose 1,6 bisphosphste aldolase / fructose 1,6 bisphosphxte aldolase / fructose 1,6 bisphosphzte aldolase / fructose 1,6 bisphospha5e aldolase / fructose 1,6 bisphospha6e aldolase / fructose 1,6 bisphosphaye aldolase / fructose 1,6 bisphosphahe aldolase / fructose 1,6 bisphosphage aldolase / fructose 1,6 bisphosphafe aldolase / fructose 1,6 bisphosphare aldolase / fructose 1,6 bisphospha4e aldolase / fructose 1,6 bisphosphat3 aldolase / fructose 1,6 bisphosphat4 aldolase / fructose 1,6 bisphosphatr aldolase / fructose 1,6 bisphosphatf aldolase / fructose 1,6 bisphosphatd aldolase / fructose 1,6 bisphosphats aldolase / fructose 1,6 bisphosphatw aldolase / fructose 1,6 bisphosphate qldolase / fructose 1,6 bisphosphate wldolase / fructose 1,6 bisphosphate sldolase / fructose 1,6 bisphosphate xldolase / fructose 1,6 bisphosphate zldolase / fructose 1,6 bisphosphate aodolase / fructose 1,6 bisphosphate apdolase / fructose 1,6 bisphosphate a;dolase / fructose 1,6 bisphosphate a.dolase / fructose 1,6 bisphosphate a,dolase / fructose 1,6 bisphosphate akdolase / fructose 1,6 bisphosphate aidolase / fructose 1,6 bisphosphate aleolase / fructose 1,6 bisphosphate alrolase / fructose 1,6 bisphosphate alfolase / fructose 1,6 bisphosphate alvolase / fructose 1,6 bisphosphate alcolase / fructose 1,6 bisphosphate alxolase / fructose 1,6 bisphosphate alsolase / fructose 1,6 bisphosphate alwolase / fructose 1,6 bisphosphate ald9lase / fructose 1,6 bisphosphate ald0lase / fructose 1,6 bisphosphate aldplase / fructose 1,6 bisphosphate aldllase / fructose 1,6 bisphosphate aldklase / fructose 1,6 bisphosphate aldilase / fructose 1,6 bisphosphate ald8lase / fructose 1,6 bisphosphate aldooase / fructose 1,6 bisphosphate aldopase / fructose 1,6 bisphosphate aldo;ase / fructose 1,6 bisphosphate aldo.ase / fructose 1,6 bisphosphate aldo,ase / fructose 1,6 bisphosphate aldokase / fructose 1,6 bisphosphate aldoiase / fructose 1,6 bisphosphate aldolqse / fructose 1,6 bisphosphate aldolwse / fructose 1,6 bisphosphate aldolsse / fructose 1,6 bisphosphate aldolxse / fructose 1,6 bisphosphate aldolzse / fructose 1,6 bisphosphate aldolawe / fructose 1,6 bisphosphate aldolaee / fructose 1,6 bisphosphate aldolade / fructose 1,6 bisphosphate aldolaxe / fructose 1,6 bisphosphate aldolaze / fructose 1,6 bisphosphate aldolaae / fructose 1,6 bisphosphate aldolaqe / fructose 1,6 bisphosphate aldolas3 / fructose 1,6 bisphosphate aldolas4 / fructose 1,6 bisphosphate aldolasr / fructose 1,6 bisphosphate aldolasf / fructose 1,6 bisphosphate aldolasd / fructose 1,6 bisphosphate aldolass / fructose 1,6 bisphosphate aldolasw /