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Nonpolar, Aliphatic R groups
Glycine, Gly, G
Alanine, Ala, A
Proline, Pro, P
Valine, Val, V
Leucine, Leu, L
Isoleucine, Ile, I
Methionine, Met, M
Aromatic R groups
phenylalanine, Phe, F
Tyrosine, Tyr, Y
Tryptophan, Trp, W
Polar, Uncharged R groups
Serine, Ser, S
Threonine, Thr, T
Cysteine, Cys, C
Asparagine, Asn, N
Glutamine, Gln, Q
Positively Charged R groups
Lysine, Lys, K
Histidine, His, H
Arginine, Arg, R
Negatively Charged R groups
Aspartate, Asp, D
Glutamate, Glu, E
Hydrogen Bonds
when 2 closely spaced EN atoms share a proton
EN atom: partial negative
proton: partial positive
N,O,F
Hydrophobic interactions
stabilize bimolecular structure
has the hydrophilic heads and the hydrophobic tails
2 reasons why non-polar groups avoid interaction with water
can’t H bond to water, so when in water, they reduce the number of H bonds water can make (UNFAVORABLE CHANGE IN ENTHALPY)
water molecules on their surface become highly ordered (UNFAVORABLE CHANGE IN ENTROPY)
4 Types of non-covalent interactions
H bonds
b/w neutral groups
peptide bonds
Ionic Interactions
attraction
repulsion
Hydrophobic Interactions
Van der Waals: 2 atoms close in proximity
Structure of an Amino Acid
Amino Group
Carboxyl Group
H
R group
Residue
single building block (monomer) in a polymer
Glycine
Gly, G
nonpolar, aliphatic

Alanine
Ala, A
Nonpolar, aliphatic

Proline
Pro, P
Nonpolar, aliphatic

Valine
Val, V
nonpolar, aliphatic

Leucine
Leu, L
nonpolar, aliphatic

Isoleucine
Ile, I
nonpolar, aliphatic

Methionine
Met, M
nonpolar, aliphatic

Phenylalanine
Phe, F
Aromatic

Tyrosine
Tyr, Y
Aromatic

Tryptophan
Trp, W
Aromatic

Serine
Ser, S
Polar, uncharged

Threonine
Thr, T
Polar, uncharged

Cysteine
Cys, C
Polar, uncharged
can form disulfide bonds
covalent bonds between 2 cysteine residues
Polar, uncharged

Asparagine
Asn, N
Polar, uncharged

Glutamine
Gln, G
Polar, uncharged

Aspartate
Asp, D
Neg charge

Glutamate
Glu, E
Neg charge

Lysine
Lys, K
Pos charge

Histidine
His, H
Pos charge

Arginine
Arg, R
Pos Charge
