CodonTable Team9/25/2026

Learn the 20 amino acid one-letter and three-letter codes with a quick reference, D/E/N/Q comparisons, simple memory cues, and five practice questions.

Amino Acid Code Mnemonics

Start with the 11 codes that match the first letter of the amino acid name. Then focus on the nine exceptions. The memory cues below are learning aids; they are not all historical reasons for assigning the letters.

The 20 codes at a glance

Amino acid Three-letter One-letter Memory cue
Alanine Ala A First letter
Cysteine Cys C First letter
Aspartate (aspartic acid) Asp D Pair D with E: the shorter acidic side chain
Glutamate (glutamic acid) Glu E Glutamate; one extra CH₂ compared with D
Phenylalanine Phe F “Ph” sounds like F
Glycine Gly G First letter
Histidine His H First letter
Isoleucine Ile I First letter; Ile, not “Iso”
Lysine Lys K K sits just before L; L is leucine
Leucine Leu L First letter
Methionine Met M First letter
Asparagine Asn N Asparagine; Asn
Proline Pro P First letter
Glutamine Gln Q “Q-tamine” as a personal memory cue
Arginine Arg R arginine
Serine Ser S First letter
Threonine Thr T First letter; distinguish Thr from Trp and Tyr
Valine Val V First letter
Tryptophan Trp W A bulky W for its double-ring side chain
Tyrosine Tyr Y tyrosine; T is already threonine

Code groups: six unique initials C H I M S V, five shared-initial assignments A G L P T, and nine exceptions D E F K N Q R W Y.

Six names have unique initials: C, H, I, M, S and V. Five others use a shared initial: A, G, L, P and T. That leaves nine codes to practise separately.

Distinguish D, E, N and Q

Learn these as two related pairs instead of four unrelated letters:

  • D / Asp and E / Glu have acidic side chains. E has one more CH₂ group than D.
  • N / Asn and Q / Gln are the corresponding amides. Q has one more CH₂ group than N.
  • In the three-letter codes, Asp/Glu identify the acids and Asn/Gln identify the amides. Notice the final n in both amide abbreviations.

Side-chain comparison near neutral pH: D is CH₂–COO⁻, E is CH₂–CH₂–COO⁻, N is CH₂–CONH₂ and Q is CH₂–CH₂–CONH₂. E and Q each have an extra CH₂.

The diagram shows only side chains, attached to the same amino acid backbone. Near neutral pH, the D/E side chains are usually negatively charged; N/Q side chains are uncharged. The CH₂ comparison is a useful cue, not a claim about why the letters were chosen.

Remember K, F, R, W and Y

K versus L: leucine uses L; remember lysine as the neighbouring letter K. Keep the three-letter forms alongside them: Lys = K and Leu = L.

F and R: “Ph” in phenylalanine sounds like F; the R in arginine is another useful sound association.

W versus Y: Trp = tryptophan = W; Tyr = tyrosine = Y. Associate the bulky W with tryptophan’s fused double-ring side chain, and find Y inside tyrosine. Do not treat “WHY-rosine” as its pronunciation.

Test yourself

Cover the table, answer these questions, then check below:

  1. What are the one-letter codes for Asp, Asn, Glu and Gln, in that order?
  2. Convert Lys–Leu–Trp–Tyr to one-letter codes.
  3. Expand F–R–M to three-letter codes.
  4. Which has the longer side chain: aspartate or glutamate?
  5. Which three-letter code means isoleucine: Ile or Leu?

Answers: 1. D–N–E–Q. 2. K–L–W–Y. 3. Phe–Arg–Met. 4. Glutamate, by one CH₂. 5. Ile; Leu is leucine.

Practise both directions with the Amino Acid Converter. For sequence notation and background, read the one-letter code guide.

The IUPAC–IUB nomenclature recommendations, section 3AA-21.2 document the code assignments. They describe the unambiguous initials, the shared-initial assignments, F/R sound associations and the bulky W association. K and Y were selected from remaining letters for their alphabetical proximity to the names’ initials. The additional cues in this article are optional study aids.

Looking for PURE As Gold or CUT the Py? Those describe nucleotide bases, not amino acids. See purines versus pyrimidines for that separate topic.