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Clark, Jim (August 2007). "an introduction to amino acids". chemguide. Retrieved
2015-07-04.
Jakubke H-D and Sewald N. Amino Acids. In: Peptides from a-z. Darmstadt,
Germany. Wiley-VCH; c2008. p. 20-21.
The amino acids (2-aminocarboxylic acids) fulfill various functions in the organism.
Above all, they serve as the components of peptides and proteins. Only the 20
proteinogenic amino acids are included in the genetic code and therefore regularly
found in proteins. Some of these amino acids undergo further (post-translational)
change following their incorporation into proteins. Amino acids or their derivatives
are also form components of lipidse. g., serine in phospholipids and glycine in bile
salts. Several amino acids function as neurotransmitters themselves, while others
are precursors of neurotransmitters, mediators, or hormones. Amino acids are
important (and sometimes essential) components of food. Specific amino acids form
precursors for other metabolitese. g., for glucose in gluconeogenesis, for purine
and pyrimidine bases, for heme, and for other molecules. Several nonproteinogenic
amino acids function as intermediates in the synthesis and breakdown of
proteinogenic amino acids and in the urea cycle. (2) Figure 1 Common amino acids
have the general structure depicted in Figure 1. They contain in common a central
alpha (a)-carbon atom to which a carboxylic acid group, an amino group, and a
hydrogen atom are covalently bonded. In addition, the a-carbon atom is bound to a
specific chemical group, designated R and called the side chain that uniquely
defines each of the 20 common amino acids. Figure 1 depicts the ionized form of a
common amino acid in solution at pH 7. The a-amino group is protonated and in its
ammonium ion form; the carboxylic acid group is in its unprotonated or carboxylate
ion form.