No, because phenylalanine does not react with the nitric acid in this test.
Phenylalanine hydroxylase breaks down phenylalanine.
Phenylalanine is a compound. Specifically it is 2-amino-3-phenylpropanoic acid.
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.
phenylalanine
No, because phenylalanine does not react with the nitric acid in this test.
Phenylalanine hydroxylase breaks down phenylalanine.
Phenylalanine is a component in aspartame.
It has 718mg of phenylalanine.
a tripeptide
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.
Glutathione is a tripeptide composed of a cysteine, glutamate, and glycine.
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