When an amino acid (AA) is incorporated into a polypeptide, the charges on the amino and carboxyl groups disappear. Among the 20 common amino acids, five have a side chain which can be charged. At pH=7, two are negative charged: aspartic acid (Asp, D) and glutamic acid (Glu, E) (acidic side chains), and three are positive charged: lysine (Lys, K), arginine (Arg, R) and histidine (His, H) (basic side chains).
The charge on the amino acid side chain depends on the pK of the AA (Table 1) and on the pH of the solution.
At a pH inferior to their pK, the aspartic acid and glutamic acid side chains are uncharged.
Table 1: pK of the amino acid side chain group. The pK of the side chain group is the pH at which exactly half of a carboxylic or amine group is charged.
Amino acid | pK of the side chain group |
---|---|
Aspartic acid | 3.9 |
Glutamic acid | 4.2 |
Lysine | 10.5 |
Arginine | 12.5 |
Histidine | 6.0 |
The arginine side chain is very basic because its positive charge is stabilized by resonance.
The two nitrogens of the histidine side chain have a relatively weak affinity for an H+ and are only partly positive at neutral pH.
Table 2: Charge of the amino acid side chains. Only the side chains are shown.
At pH=7, side chains of the 5 amino acids are charged.
Fifteen AA have uncharged side chains. They are: A, N, C, Q, G, I, L, M, F, P, S, T, W, Y, V.
Table 3: Hydrogen donor and acceptor atoms in amino acid side chains.
Amino acids | Hydrogen donor atoms a | Hydrogen acceptor atoms b |
---|---|---|
Arginine (Arg, R) | NE, NH1 (2), NH2 (2) | |
Asparagine (Asn, N) | ND2 (2) | OD1 (2) |
Aspartic acid (Asp, D) | OD1 (2), OD2 (2) | |
Glutamine (Gln, Q) | NE2 (2) | OE1 (2) |
Glutamic acid (Glu, E) | OE1 (2), OE2 (2) | |
Histidine (His, H) | ND1, NE2 | ND1, NE2 |
Lysine (Lys, K) | NZ (3) | |
Serine (Ser, S) | OG | OG (2) |
Threonine (Thr, T) | OG1 | OG1 (2) |
Tryptophan (Trp, W) | NE1 | |
Tyrosine (Tyr, Y) | OH | OH |
a Between parentheses, number of "sp hydrogens" that a donor atom can donate, if more than one.
b Between parentheses, number of hydrogen bonds that an acceptor atom can accept, if more than one.
There are 10 polar amino acids (same amino acids as in Table 3, except tryptophan usually nonpolar): D, E, H, K, R, N, Q, S, T, Y, that fall into 2 categories:
There are 10 nonpolar amino acids (including the tryptophan, despite an hydrogen donor atom): A, C, G, I, L, M, F, P, V, W.
These nonpolar amino acids:
Paired cysteines allow disulfide bonds.