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  2. Ribulose 1,5-bisphosphate - Wikipedia

    en.wikipedia.org/wiki/Ribulose_1,5-bisphosphate

    Ribulose 1,5-bisphosphate (RuBP) is an organic substance that is involved in photosynthesis, notably as the principal CO 2 acceptor in plants. [ 1 ] : 2 It is a colourless anion, a double phosphate ester of the ketopentose ( ketone -containing sugar with five carbon atoms) called ribulose .

  3. Ribulose - Wikipedia

    en.wikipedia.org/wiki/Ribulose

    For example, d-ribulose is an intermediate in the fungal pathway for d-arabitol production. Also, as the 1,5-bisphosphate, d-ribulose combines with carbon dioxide at the start of the photosynthesis process in green plants (carbon dioxide trap). [2] Ribulose has the same stereochemistry at carbons 3 and 4 as the five-carbon aldoses ribose and ...

  4. 2-Carboxy-D-arabitinol 1-phosphate - Wikipedia

    en.wikipedia.org/wiki/2-Carboxy-D-arabitinol_1...

    2-Carboxy-D-arabitinol 1-phosphate (CA1P) is a molecule produced in plants that inhibits RuBisCO, a key enzyme in the Calvin cycle and carbon fixation.In dark conditions, this molecule binds to RuBisCO, preventing it from participating in chemical reactions.

  5. Phosphogluconate dehydrogenase (decarboxylating) - Wikipedia

    en.wikipedia.org/wiki/Phosphogluconate_de...

    Then, the intermediate is decarboxylated, yielding a 1,2-enediol of ribulose 5-phosphate, which tautomerizes to form ribulose 5-phosphate. [3] High levels of NADPH are believed to inhibit the enzyme, while 6-phosphogluconate acts to activate the enzyme.

  6. Congenital hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Congenital_hemolytic_anemia

    Pyruvate kinase deficiency is the second most common cause of enzyme-deficient hemolytic anemia, following G6PD deficiency. [13] The symptoms of pyruvate kinase deficiency are mild to severe hemolytic Anemia, cholecystolithiasis, tachycardia, hemochromatosis, icteric sclera, splenomegaly, leg ulcers, jaundice, fatigue, and shortness of breath. [14]

  7. Beta-ketothiolase deficiency - Wikipedia

    en.wikipedia.org/wiki/Beta-ketothiolase_deficiency

    Beta-ketothiolase deficiency is a rare, autosomal recessive metabolic disorder in which the body cannot properly process the amino acid isoleucine or the products of lipid breakdown. [ 1 ] [ 2 ] Along with SCOT deficiency , it belongs to a group of disorders called ketone utilisation disorders.

  8. Isomerase - Wikipedia

    en.wikipedia.org/wiki/Isomerase

    Phosphohexose Isomerase Deficiency (PHI) is also known as phosphoglucose isomerase deficiency or Glucose-6-phosphate isomerase deficiency, and is a hereditary enzyme deficiency. PHI is the second most frequent erthoenzyopathy in glycolysis besides pyruvate kinase deficiency , and is associated with non-spherocytic haemolytic anaemia of variable ...

  9. Reference ranges for blood tests - Wikipedia

    en.wikipedia.org/wiki/Reference_ranges_for_blood...

    Enzyme activity is commonly used for e.g. liver function tests like AST, ALT, LD and γ-GT in Sweden. [ 5 ] Percentages and time-dependent units (mol/s) are used for calculated derived parameters, e.g. for beta cell function in homeostasis model assessment or thyroid's secretory capacity .