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Amino acids

Charge, hydrogen donor and acceptor atoms, and polarity of the amino acid side chains

Charge of the amino acid side chains

Charged side chains

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.

  1. Negative charged (acidic side chains): aspartic acid and glutamic acid

    At a pH superior to their pK (Table 2), the carboxylic side chains lose an H+ ion (proton) and are negative charged. They are therefore acid.

    acidic

    At a pH inferior to their pK, the aspartic acid and glutamic acid side chains are uncharged.

  2. Positive charged (basic side chains): lysine, arginine and histidine

    At a pH superior to their pK (Table 2), the amine side chains are uncharged.
    At a pH inferior to their pK, the lysine, arginine and histidine side chains accept an H+ ion (proton) and are positive charged. They are therefore basic.

    basic

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 acidpK of the side chain group
Aspartic acid3.9
Glutamic acid4.2
Lysine10.5
Arginine12.5
Histidine6.0

The arginine side chain is very basic because its positive charge is stabilized by resonance.

arg1

The two nitrogens of the histidine side chain have a relatively weak affinity for an H+ and are only partly positive at neutral pH.

his1

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.

pk table

Uncharged side chains

Fifteen AA have uncharged side chains. They are: A, N, C, Q, G, I, L, M, F, P, S, T, W, Y, V.

Hydrogen donor and acceptor atoms of the amino acid side chains

Click here for Amino acid atoms nomenclature.

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.

Polarity of the amino acid side chains

Amino acid side chains with hydrogen donor and/or acceptor atoms are polar

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:

Amino acid side chains without hydrogen donor and/or acceptor atoms are nonpolar

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.

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