amino acid, Any of a class of organic compounds in which a carbon atom has bonds to an amino group (―NH2), a carboxyl group (―COOH), a hydrogen atom (―H), and an organic side group (called ―R). They are therefore both carboxylic acids and amines. The physical and chemical properties unique to each result from the properties of the R group, particularly its tendency to interact with water and its charge (if any). Amino acids joined linearly by peptide bonds (see covalent bond) in a particular order make up peptides and proteins. Of over 100 natural amino acids, each with a different R group, only 20 make up the proteins of all living organisms. Humans can synthesize 10 of them (by interconversions) from each other or from other molecules of intermediary metabolism, but the other 10 (essential amino acids: arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine) must be consumed in the diet.
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amino acid summary
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Learn about the structure and properties of amino acids
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asparagine Summary
Asparagine, an amino acid closely related to aspartic acid, and an important component of proteins. First isolated in 1932 from asparagus, from which its name is derived, asparagine is widely distributed in plant proteins. It is one of several so-called nonessential amino acids in warm-blooded
arginine Summary
Arginine, an amino acid obtainable by hydrolysis of many common proteins but particularly abundant in protamines and histones, proteins associated with nucleic acids. First isolated from animal horn (1895), arginine plays an important role in mammals in the synthesis of urea, the principal form in