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Phenylalanine (symbol Phe or F) [3] is an essential α-amino acid with the formula C 9 H 11 NO 2.It can be viewed as a benzyl group substituted for the methyl group of alanine, or a phenyl group in place of a terminal hydrogen of alanine.
In plants, the shikimate pathway first leads to the formation of chorismate, which is the precursor of phenylalanine, tyrosine, and tryptophan. These aromatic amino acids are the precursors of many secondary metabolites , all essential to a plant's biological functions, such as the hormones salicylate and auxin .
Nonpolar amino acid interactions are the primary driving force behind the processes that fold proteins into their functional three dimensional structures. [32] None of these amino acids' side chains ionize easily, and therefore do not have pK a s, with the exception of tyrosine (Tyr, Y).
Most common among natural products is the amino acid phenylalanine, which contains a phenyl group. A major product of the petrochemical industry is " BTX " consisting of benzene, toluene, and xylene - all of which are building blocks for phenyl compounds.
Phenylalanine: F Phe Essential for humans, phenylalanine, tyrosine, and tryptophan contain a large, rigid aromatic group on the side chain. These are the biggest amino acids. Like isoleucine, leucine, and valine, these are hydrophobic and tend to orient towards the interior of the folded protein molecule. Phenylalanine can be converted into ...
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Vapor phases represent the simplest non polar phases, because it has no interaction with the solute. [18] The hydration potential and its correlation to the appearance of amino acids on the surface of proteins was studied by Wolfenden. Aqueous and polymer phases were used in the development of a novel partitioning scale. [19]
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