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  2. Glucose-6-phosphate dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Glucose-6-phosphate...

    G6PD converts G6P into 6-phosphoglucono-δ-lactone and is the rate-limiting enzyme of the pentose phosphate pathway. Thus, regulation of G6PD has downstream consequences for the activity of the rest of the pentose phosphate pathway. Glucose-6-phosphate dehydrogenase is stimulated by its substrate G6P.

  3. Glucose-6-phosphate dehydrogenase deficiency - Wikipedia

    en.wikipedia.org/wiki/Glucose-6-phosphate...

    Glucose-6-phosphate dehydrogenase (G6PD) is an enzyme in the pentose phosphate pathway (see image, also known as the HMP shunt pathway). G6PD converts glucose-6-phosphate into 6-phosphoglucono-δ-lactone and is the rate-limiting enzyme of this metabolic pathway that supplies reducing energy to cells by maintaining the level of the reduced form ...

  4. Heinz body - Wikipedia

    en.wikipedia.org/wiki/Heinz_body

    G6PD deficient red cells in combination with high levels of oxidants causes a cross-linking of sulfhydryl groups on globin chains which causes a denaturing and formation of Heinz body precipitates. [8] Heinz bodies can also be found in chronic liver disease. [9] Alpha-thalassemia. Normal adult hemoglobin is composed of two alpha and two beta ...

  5. 6-phosphogluconate dehydrogenase deficiency - Wikipedia

    en.wikipedia.org/wiki/6-phosphogluconate...

    6-Phosphogluconate dehydrogenase (6PGD) is an enzyme in the pentose phosphate pathway (see image). 6PGD catalyzes the reaction of 6-phosphogluconate to an unstable form of 3-keto-6-phosphogluconate, and yields a co-enzyme nicotinamide adenine dinucleotide phosphate (NADPH) as a byproduct.

  6. 6-Phosphogluconate dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/6-phosphogluconate...

    6-Phosphogluconate dehydrogenase (6PGD) is an enzyme in the pentose phosphate pathway. It forms ribulose 5-phosphate from 6-phosphogluconate:

  7. Sweat test - Wikipedia

    en.wikipedia.org/wiki/Sweat_test

    Positive test results may also be caused by malnutrition, adrenal insufficiency, glycogen storage diseases, hypothyroidism, hypoparathyroidism, nephrogenic diabetes insipidus, G6PD deficiency or ectodermal dysplasia.

  8. Acetogenin - Wikipedia

    en.wikipedia.org/wiki/Acetogenin

    Acetogenin core unit (mono-THF) Acetogenin terminal lactone ring core unit (unsaturated) Structurally, acetogenins are a series of C-35/C-37 compounds usually characterized by a long aliphatic chain bearing a terminal methyl-substituted α,β-unsaturated γ-lactone ring, as well as one to three tetrahydrofuran rings. [4]

  9. Tagaturonate reductase - Wikipedia

    en.wikipedia.org/wiki/Tagaturonate_reductase

    Tagaturonate reductase (EC 1.1.1.58) is an enzyme that catalyzes the chemical reaction. D-altronate + NAD + D-tagaturonate + NADH + H +. Thus, the two substrates of this enzyme are D-altronate and NAD +, whereas its 3 products are D-tagaturonate, NADH, and H +.