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Guide · 2 min read

Peptide Sequence Notation: One-Letter and Three-Letter Codes

How peptide sequences are written: direction from N- to C-terminus, the 20 one- and three-letter codes, terminal groups like H- and -NH2, and the ambiguous codes that trip up calculators.

Reviewed 20 Oct 2026 2 references Companion tool: T-03 Sequence length

Sequences are written to a convention set by the IUPAC-IUB Joint Commission on Biochemical Nomenclature. Reading them correctly matters: a reversed or mistyped sequence gives a different molecule, even when its mass is identical.

Direction: N-terminus to C-terminus

Sequences are always written from the free amino end (N-terminus) on the left to the free carboxyl end (C-terminus) on the right. GHK means glycine carries the free amine and lysine carries the free acid. KHG has the same composition and mass, but it is a different peptide.

Three-letter codes

Three-letter codes are joined by hyphens, which stand for peptide bonds: Gly-His-Lys. Terminal groups are written explicitly when it matters. H- marks the free amine, -OH the free acid, Ac- an acetylated N-terminus and -NH2 a C-terminal amide. So Ac-Gly-His-Lys-NH2 is a capped tripeptide.

One-letter codes

One-letter codes are compact and are the norm in databases and long sequences: GEPPPGKPADDAGLV. They are usually written without separators, often in blocks of ten for readability.

Amino acid 3-letter 1-letter Amino acid 3-letter 1-letter
Alanine Ala A Leucine Leu L
Arginine Arg R Lysine Lys K
Asparagine Asn N Methionine Met M
Aspartic acid Asp D Phenylalanine Phe F
Cysteine Cys C Proline Pro P
Glutamic acid Glu E Serine Ser S
Glutamine Gln Q Threonine Thr T
Glycine Gly G Tryptophan Trp W
Histidine His H Tyrosine Tyr Y
Isoleucine Ile I Valine Val V

Codes that cause trouble

  • Ambiguity codes. B (Asx: Asp or Asn), Z (Glx: Glu or Gln) and X (any) appear in sequencing results, but they have no single formula. The calculators reject them rather than guess.
  • Look-alike letters. D is aspartic acid and E is glutamic acid. N and Q are their amides, and K is lysine, not potassium. Mixing these up is the most common transcription error.
  • Leucine and isoleucine have identical formulas and masses, so mass alone cannot tell them apart.
  • Stereochemistry. Some authors mark D-amino acids with a D- prefix or lower-case letters. D- and L-forms have the same mass, but they are different molecules. Record them explicitly.
  • Selenocysteine (U) and pyrrolysine (O) are genuine amino acids, but they are outside the 20 standard residues handled here.

Length, bonds and a quick size check

A linear peptide of n residues has n − 1 peptide bonds. The average residue mass across proteins is about 110 g/mol, so n × 110 is a quick sanity check against a calculated molecular weight. Short peptides rich in glycine or alanine will come in lighter, and those rich in Trp, Tyr or Arg heavier.

Worked example

Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val converts to GEPPPGKPADDAGLV: 15 residues and 14 peptide bonds. The size estimate is 15 × 110 ≈ 1650 g/mol. The exact average mass is 1419.56 g/mol, lighter because the sequence is rich in small residues (Gly, Ala, Pro).

References

  1. IUPAC-IUB JCBN: Nomenclature and symbolism for amino acids and peptides
  2. IUPAC Compendium of Chemical Terminology (Gold Book)