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nonpolar, aliphatic
Methionine Valine Alanine Glycine Leucine Isoleucine Proline
aromatic
Phenylalanine, Tyrosine, Tryptophan
polar, uncharged
Serine, Threonine, Cysteine, Asparagine, Glutamine
positively charged
Lysine, Histidine, Arginine
negatively charged
aspartate, Glutamate

Glycine, Gly, G
characteristic: no optical activity, symmetrical

Alanine, Ala, A

Proline, Pro, P
characteristics: only cyclic structure, 2nd amine

Leucine, Leu, L

Isoleucine, Ile, I

Methionine, Met, M
Characteristics of Nonpolar, aliphatic R groups
The hydrophobic effect stabilizes protein structure
• These amino acids are found clustered in the internal portions of proteins
Characteristics of Aromatic R Groups
absorb UV light at 270 – 280 nm
Characteristic of Polar, Uncharged R Groups
Polar R groups make H-bonds with water
Characteristics of Cysteine/Cystine
readily oxidized to form a disulfide bond
with another cysteine. The covalently linked amino
acids = cystine. This bond is hydrophobic
Characteristics of Positively Charged R Groups
basic amino acids (remove H+ from
solution)
Characteristics of Negatively Charged R Groups
acidic (donate H+ ions to
solution)

Valine, Val, V