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).
Phenylalanine is a component in aspartame.
It has 718mg of phenylalanine.
Yes, phenylalanine is an amino acid and is considered as a compound.
The molecular formula for phenylalanine is C9H11NO2.
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
Scientists found that the codon UUC codes for the amino acid phenylalanine.
yup!
It is halal if from halal meat.
no, it is not halal
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%.
Phenylalanine is observed in the urine of a classical PKU (phenylketonuria) patient because they lack an enzyme called phenylalanine hydroxylase, which is needed to convert phenylalanine into tyrosine. As a result, phenylalanine accumulates in the body and is excreted in the urine. This buildup can lead to various health issues if not managed properly.