Phenylalanine is a compound.
Specifically it is 2-amino-3-phenylpropanoic acid.
Phenylalanine is a compound, family of aminoacids.Additional answerYou obviously don't know what an element is. It is a substance that cannot be broken down into another substance by chemical processes. Hydrogen, neon, iron, cobalt, uranium are all examples of elements.
Phenylalanine hydroxylase breaks down phenylalanine.
There are three and they are called aromatic amino acids: tryptophan phenylalanine tyrosine. Proline also contains a ring but is not an aromatic compound
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
how many atoms are in this compound
Phenylalanine is a compound, family of aminoacids.Additional answerYou obviously don't know what an element is. It is a substance that cannot be broken down into another substance by chemical processes. Hydrogen, neon, iron, cobalt, uranium are all examples of elements.
Phenylalanine hydroxylase breaks down phenylalanine.
Phenylalanine is a component in aspartame.
It has 718mg of phenylalanine.
There are three and they are called aromatic amino acids: tryptophan phenylalanine tyrosine. Proline also contains a ring but is not an aromatic compound
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.