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Aromatic Amino Acids

Aromatic amino acids are relatively nonpolar. To different degrees, all aromatic amino acids absorb ultraviolet light. Tyrosine and tryptophan absorb more than do phenylalanine; tryptophan is responsible for most of the absorbance of ultraviolet light (ca. 280 nm) by proteins. Tyrosine is the only one of the aromatic amino acids with an ionizable side chain. Tyrosine is one of three hydroxyl containing amino acids.

molecular structure of tyrosine HO-p-Ph-CH2-CH(NH3)-COO molecular structure of tryptophanPh-NH-CH=C-CH2-CH(NH3)-COO Molecular structure of phenylalanine
Least hydrophobic Very hydrophobic

Chemical structure for tyrosine
Chemical structure for tryptophan
chemical structure for phenylalanine

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The Biology Project > Biochemistry > The Chemistry of Amino Acids


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August 25, 2003
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