One of the important and essential amino acids that the body needs daily through our diets or supplements.
Phenylalanine hydroxylase breaks down phenylalanine.
Phenylalanine is a component in aspartame.
It has 718mg of phenylalanine.
Phenylalanine is a compound. Specifically it is 2-amino-3-phenylpropanoic acid.
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
Phenylalanine exist in eggs, soybeans, milk, chicken, beef, etc.
yup!
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
Its an excessive accumulation of phenylalanine in the blood
Phenylketonuria (PKU) is a condition that makes it impossible to metabolize the amino acid phenylalanine. People with PKU lack an enzyme called phenylalanine hydroxylase, which is required to break down phenylalanine. If left untreated, the buildup of phenylalanine can lead to brain damage and other neurological problems, so individuals with PKU must follow a strict low-phenylalanine diet.
Yes
Yes.