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Which enzyme breaks down phenylalanine?
The enzyme phenylalanine hydroxylase breaks down phenylalanine into tyrosine. This enzyme is essential for the conversion of phenylalanine to tyrosine in the body. Deficiency in this enzyme can lead to a build-up of phenylalanine, which can result in a condition called phenylketonuria (PKU).
Does Phenylalanine have the same effect as Apartame does?
Phenylalanine is a component in aspartame.
How much phenylalanine does Dr Pepper 10 have?
It has 718mg of phenylalanine.
Is phenylalanine a compound?
Phenylalanine is a compound. Specifically it is 2-amino-3-phenylpropanoic acid.
What is the molecular formula for Phenylalanine?
The molecular formula for phenylalanine is C9H11NO2.
What are the DNA codons for phenylalanine?
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
What codon codes for amino acids phenylalanine did scientist find?
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
Is phenylalanine alchohol?
yup!
Phenylalanine C9H11NO2 is an amino acid used to make proteins It has a molar mass of 165.19 g mol What is the mass percent of oxygen in phenylalanine?
The molar mass of oxygen in phenylalanine is 16.00 g/mol. To calculate the mass percent of oxygen in phenylalanine, divide the molar mass of oxygen by the molar mass of phenylalanine, then multiply by 100. (16.00 g/mol / 165.19 g/mol) * 100 = 9.68% Therefore, the mass percent of oxygen in phenylalanine is approximately 9.68%.
Why is phenylalanine observed in the urine of a classical PKU patient?
PKU stands for phenylketonuria, the classic symptom of which (and the diagnostic test for the disease) is phenylalanine in the urine. This is a genetic disorder in which the body is unable to process phenylalalanine, so it is excreted in the urine.
What is a genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing is known as?
A genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing is known as Phenylketonuria (PKU). This leads to a buildup of phenylalanine in the body, which can be toxic to the brain if not managed properly through a restricted diet low in phenylalanine.
Is phenylalanine an abnormal substance created by the babys altered genes If so how is it made If not where does it come from?
Its an excessive accumulation of phenylalanine in the blood
