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  2. Urea cycle - Wikipedia

    en.wikipedia.org/wiki/Urea_cycle

    Urea cycle. The urea cycle (also known as the ornithine cycle) is a cycle of biochemical reactions that produces urea (NH 2) 2 CO from ammonia (NH 3). Animals that use this cycle, mainly amphibians and mammals, are called ureotelic. The urea cycle converts highly toxic ammonia to urea for excretion. [1] This cycle was the first metabolic cycle ...

  3. Hyperammonemia - Wikipedia

    en.wikipedia.org/wiki/Hyperammonemia

    Hyperammonemia, or high ammonia levels, is a metabolic disturbance characterised by an excess of ammonia in the blood. It is a dangerous condition that may lead to brain injury and death. It may be primary or secondary. Ammonia is a substance that contains nitrogen. It is a product of the catabolism of protein.

  4. Purine nucleotide cycle - Wikipedia

    en.wikipedia.org/wiki/Purine_nucleotide_cycle

    Contents. Purine nucleotide cycle. The Purine Nucleotide Cycle is a metabolic pathway in protein metabolism requiring the amino acids aspartate and glutamate. The cycle is used to regulate the levels of adenine nucleotides, in which ammonia and fumarate are generated. [ 2 ] AMP converts into IMP and the byproduct ammonia.

  5. Ammonia monooxygenase - Wikipedia

    en.wikipedia.org/wiki/Ammonia_monooxygenase

    Ammonia monooxygenase. Ammonia monooxygenase (EC 1.14.99.39, AMO) is an enzyme, [1][2][3][4][5][6][7][8][9] which catalyses the following chemical reaction. Ammonia monooxygenase contains copper and possibly nonheme iron. AMO is the first enzyme in ammonia oxidation. Aerobic oxidation of ammonia to hydroxylamine via AMO is an endergonic ...

  6. Citrullinemia - Wikipedia

    en.wikipedia.org/wiki/Citrullinemia

    Citrullinemia belongs to a class of genetic diseases called urea cycle disorders. The urea cycle is a sequence of chemical reactions taking place in the liver. These reactions process excess nitrogen, generated when protein is used for energy by the body, to make urea, which is excreted by the kidneys.

  7. Ornithine transcarbamylase - Wikipedia

    en.wikipedia.org/wiki/Ornithine_transcarbamylase

    Mutations in the OTC gene can cause Ornithine Transcarbamylase deficiency. It is classified as a urea cycle disorder due to the fact that without proper OTC function ammonia starts to accumulate in the blood. Accumulation of ammonia in the blood is known as hyperammonemia. Although toxic in excess, ammonia is a nitrogen source for the body.

  8. Urea - Wikipedia

    en.wikipedia.org/wiki/Urea

    The structure of the molecule of urea is O=C(−NH 2) 2.The urea molecule is planar when in a solid crystal because of sp 2 hybridization of the N orbitals. [8] [9] It is non-planar with C 2 symmetry when in the gas phase [10] or in aqueous solution, [9] with C–N–H and H–N–H bond angles that are intermediate between the trigonal planar angle of 120° and the tetrahedral angle of 109.5°.

  9. Ammonia - Wikipedia

    en.wikipedia.org/wiki/Ammonia

    Ammonia forms 1:1 adducts with a variety of Lewis acids such as I 2, phenol, and Al(CH 3) 3. Ammonia is a hard base (HSAB theory) and its E & C parameters are E B = 2.31 and C B = 2.04. Its relative donor strength toward a series of acids, versus other Lewis bases, can be illustrated by C-B plots.