The titration curve of phenylanaline is around pk value 6.89 which neutral pH. It has a two buffer one in the acidic portion and the neutral one.
Phenylalanine exist in eggs, soybeans, milk, chicken, beef, etc.
Peptide bonds.
19.37 g/mol
It's just made up of hydrogens and carbons. There isn't a big energy difference in electronegativity anywhere on the phenylalanine sidechain, so it's considered nonpolar.
Phenylalanine hydroxylase breaks down phenylalanine.
The titration curve of phenylanaline is around pk value 6.89 which neutral pH. It has a two buffer one in the acidic portion and the neutral one.
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.