Lecture 4: Amino Acids Flashcards
Good Rule of Thumb
At pH< pKa, protonated
At pH> pKa, deprotonated
Properties of Amino Acids
Optically active
Engage in noncovalent interactions that determine protein structure/function
Amino Acids are Optically Active
a-carbon is the chiral center of molecule
Only the L-configuration is found in proteins
Polar, negative charged amino acids
Aspartate
Glutamate
Polar, positive charged
Lysine, Arginine, Histidine
Polar uncharged (-OH)
Serine, threonine, tyrosine
Polar uncharged (Carboxamide- CONH2)
Asparagine, Glutamine
Polar uncharged (-SH group)
Cysteine
Nonpolar, aliphatic
Glycine, alanine
Branched: valine, leucine, isoleucine
Thioester: methionine
Ring structure; not aromatic: Proline
Nonpolar, aromatic
Phenylalanine, tryptophan
Amphipathic: tyrosine
*Aromatic ring structure permits absorption of UV light (280 nm)
Why is it important to know the classification and side chains/R-groups of amino acids?
Noncovalent interactions contribute to protein folding and reactivity