hydratases oor Spaans
hydratases
en
Plural form of hydratase.
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Citrate Δ Aconitase (Aconitate hydratase) 3.
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Water is added to saturate the double bond and form 3-hydroxyacylCoA, catalyzed by Δ2-enoyl-CoA hydratase.
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Activity of the enzyme 3-methylglutaconyl CoA hydratase is normal.
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Fumarase (fumarate hydratase) catalyzes the addition of water across the double bond of fumarate, yielding malate.
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Other names in common use include epoxide hydratase (ambiguous), microsomal epoxide hydratase (ambiguous), epoxide hydrase, microsomal epoxide hydrase, arene-oxide hydratase (ambiguous), benzopyrene-4,5-oxide hydratase, benzo(a)pyrene-4,5-epoxide hydratase, aryl epoxide hydrase (ambiguous), cis-epoxide hydrolase, and mEH.
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Also called fumarate hydratase.
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Deficiency of 3methylglutaconylCoA hydratase (3MGA)
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Mutated (changed) forms of the fumarate hydratase gene may cause cells to lose the ability to use oxygen.
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The FH gene provides instructions for making an enzyme called fumarase (also known as fumarate hydratase). This enzyme participates in an important series of reactions known as the citric acid cycle or Krebs cycle, which allows cells to use oxygen and generate energy.
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Mutations (changes) in the gene that makes fumarate hydratase may cause cells to lose the ability to use oxygen, which may increase the growth of some cells, including abnormal cells and cancer cells.
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They are inactivated form of PHOSPHOPYRUVATE HYDRATASE.
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(Chapter 4) • Using the same approach, calculations were carried out for the in silico design of hydratases, but in this case based on the inclusion of a novel unnatural amino acid.
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Atypical leiomyoma is a rare tumor that usually presents as a single lesion and is exceptional in patients with cutaneous leiomyomatosis. The relation between fumarate hydratase enzyme mutations with multiple leiomyomas, uterine leiomyomatosis and an increased risk of developing kidney cancer is widely known.
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When your baby has 3MGA type I, their body does not make enough or makes non-working 3-methylglutaconyl-CoA hydratase.
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These were a copper-Phenanthroline containing hydratase based on the Lactococcus Multidrug Resistance Regulator (LmrR) and a variety of novel mutants based on Streptavidine-Noyori complexes for cyclic imine reduction reaction.
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The mutated fumarate hydratase gene has been found in patients with an inherited condition called hereditary leiomyomatosis and renal cell cancer (HLRCC).
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The relation between fumarate hydratase enzyme mutations with multiple leiomyomas, uterine leiomyomatosis and an increased risk of developing kidney cancer is widely known.
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17 sinne gevind in 7 ms. Hulle kom uit baie bronne en word nie nagegaan nie.