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Carbamoyl phosphate synthetase I deficiency has an autosomal recessive pattern of inheritance.. CPS I deficiency is inherited in an autosomal recessive manner. [1] This means the defective gene responsible for the disorder is located on an autosome, and two copies of the defective gene (one inherited from each parent) are required in order to be born with the disorder.
Carbamoyl phosphate synthetase I (CPS I) is a ligase enzyme located in the mitochondria involved in the production of urea.Carbamoyl phosphate synthetase I (CPS1 or CPSI) transfers an ammonia molecule to a molecule of bicarbonate that has been phosphorylated by a molecule of ATP.
Carbamoyl phosphate synthetase catalyzes the ATP-dependent synthesis of carbamoyl phosphate from glutamine (EC 6.3.5.5) or ammonia (EC 6.3.4.16) and bicarbonate. [1] This ATP-grasp enzyme catalyzes the reaction of ATP and bicarbonate to produce carboxy phosphate and ADP. Carboxy phosphate reacts with ammonia to give carbamic acid.
Counts per second (abbreviated to cps) is used for measurements when higher count rates are being encountered, or if hand held radiation survey instruments are being used which can be subject to rapid changes of count rate when the instrument is moved over a source of radiation in a survey area.
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Carbamoyl phosphate synthetase (glutamine-hydrolysing) (EC 6.3.5.5) is an enzyme that catalyzes the reactions that produce carbamoyl phosphate in the cytosol (as opposed to type I, which functions in the mitochondria).
On the other hand, if you are over the age of 50 and cannot perform this 10-second balance test, you could be at a higher risk of dying within a decade compared to your peers, according to 2022 ...
Centipoise, a viscosity subunit, cP, but cps or cPs also used; CERN Proton Synchrotron, a particle accelerator; Counts per second (cps), detected by a radiation monitoring instrument; Cycle per second (c.p.s.), now Hertz