Phenylalanine exist in eggs, soybeans, milk, chicken, beef, etc.
For strong teeth and bones- they need calcium.
tacos
Peptide bonds.
19.37 g/mol
Phenylalanine has a net 0 charge at pH 7.0 as the carboxy end has been deprotonated and the amino end still contains it's proton (hydrogen).
PKU or phenylketonuria is caused by mutations in the gene that helps make an enzyme called phenylalanine hydroxylase or PAH. This enzyme is needed to convert the amino acid phenylalanine into other forms that the body uses and needs. When this gene is mutated the body can't break down foods that are high in protein such as milk, cheese, nuts, or meat.
No, but you can control it. I think it is a disease that is developmentally dependent with adulthood superseding the disease. In any case, in infants and toddlers one can control the disease by excluding foods containing, or rich in phenylalanine. Google this.
Phenylalanine hydroxylase breaks down phenylalanine.
He probably has pheylketonuria, commonly referred to as PKU.
Phenylalanine is a component in aspartame.
It has 718mg of phenylalanine.
Foods that are high in fat will be sweets and processed foods that are high in calories and have very little nutritional value. This is also foods that are very tasty and appealing.
Phenylalanine is not used in soda pop.However, diet soda pop may contain the artificial sweetener aspartame . This compound, sold under the trade names "Equal" and "NutraSweet", is metabolized by the body into several chemical byproducts including phenylalanine.The breakdown problems phenylketonurics have with protein and the attendant build up of phenylalanine in the body also occurs with the ingestion of aspartame, although to a lesser degree. Accordingly, all products in Australia, the U.S. and Canada that contain aspartame must be labeled: "Phenylketonurics: Contains phenylalanine." In the UK, foods containing aspartame must carry ingredient panels that refer to the presence of "aspartame or E951" and they must be labeled with a warning "Contains a source of phenylalanine." These warnings are specifically placed to aid individuals who suffer from PKU so that they can avoid such foods.
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.
don't have children. It's a genetic disorder.
yup!