Amino Acid Code Converter¶
Convert between one-letter and three-letter amino acid codes. Includes a complete reference table with chemical properties for all 20 standard amino acids.
Converter¶
Conversion Result
Amino Acid Reference Table¶
| One-Letter | Three-Letter | Name | Side Chain Class | MW (Da) | pKa (R group) | Hydropathy |
|---|---|---|---|---|---|---|
| A | Ala | Alanine | Nonpolar, Aliphatic | 71.08 | — | +1.800 |
| C | Cys | Cysteine | Polar, Sulfur | 103.14 | 8.37 | +2.500 |
| D | Asp | Aspartic Acid | Acidic | 115.09 | 3.90 | -3.500 |
| E | Glu | Glutamic Acid | Acidic | 129.12 | 4.07 | -3.500 |
| F | Phe | Phenylalanine | Aromatic | 147.18 | — | +2.800 |
| G | Gly | Glycine | Nonpolar, Aliphatic | 57.05 | — | -0.400 |
| H | His | Histidine | Basic, Aromatic | 137.14 | 6.00 | -3.200 |
| I | Ile | Isoleucine | Nonpolar, Aliphatic | 113.16 | — | +4.500 |
| K | Lys | Lysine | Basic | 128.17 | 10.50 | -3.900 |
| L | Leu | Leucine | Nonpolar, Aliphatic | 113.16 | — | +3.800 |
| M | Met | Methionine | Nonpolar, Sulfur | 131.19 | — | +1.900 |
| N | Asn | Asparagine | Polar, Amide | 114.10 | — | -3.500 |
| P | Pro | Proline | Cyclic (Imino) | 97.12 | — | -1.600 |
| Q | Gln | Glutamine | Polar, Amide | 128.13 | — | -3.500 |
| R | Arg | Arginine | Basic | 156.19 | 12.48 | -4.500 |
| S | Ser | Serine | Polar, Hydroxyl | 87.08 | — | -0.800 |
| T | Thr | Threonine | Polar, Hydroxyl | 101.10 | — | -0.700 |
| V | Val | Valine | Nonpolar, Aliphatic | 99.13 | — | +4.200 |
| W | Trp | Tryptophan | Aromatic | 186.21 | — | -0.900 |
| Y | Tyr | Tyrosine | Aromatic | 163.18 | 10.10 | -1.300 |
Amino Acid Classification Guide¶
| Category | Amino Acids | Properties |
|---|---|---|
| Nonpolar Aliphatic | Gly, Ala, Val, Leu, Ile, Pro | Hydrophobic, buried in protein cores |
| Aromatic | Phe, Tyr, Trp | Absorb UV at 280nm (important for spectroscopy) |
| Polar Uncharged | Ser, Thr, Cys, Asn, Gln | Hydrophilic, surface-exposed |
| Acidic (Negative) | Asp, Glu | Negatively charged at pH 7; pKa ~4 |
| Basic (Positive) | Lys, Arg, His | Positively charged at pH 7 (except His, pKa 6) |
| Special | Cys (disulfide), Pro (rigid), Gly (flexible) | Unique structural roles |
Amino Acid Properties at a Glance¶
- Hydrophobicity: Most hydrophobic = Ile, Val, Leu; Most hydrophilic = Arg, Asp, Lys
- Molecular weight: Smallest = Gly (57 Da); Largest = Trp (186 Da)
- Charge at pH 7: Positive = Arg, Lys; Negative = Asp, Glu; Neutral = all others
Common Usage Patterns¶
- In peptide sequences: single-letter codes are standard for sequences over 5 AA
- In publications: three-letter codes for individual residues in text
- In databases: single-letter codes for sequence storage
- In patents: both formats used interchangeably
Frequently Asked Questions¶
The three-letter system was developed first and is more descriptive, making it useful in written text. The one-letter system was introduced later to support computer sequence analysis and compact representation of long sequences. Both standards are maintained by IUPAC.
A few mnemonic aids: A = Alanine (first letter), C = Cysteine (first letter), G = Glycine (first letter), H = Histidine (first letter), P = Proline (first letter), S = Serine (first letter), V = Valine (first letter). For others: F = Phenylalanine (ph → F), R = aRginine (letter R in name), Y = tYrosine, K = lysine (sounds like K), D = asparDic acid, E = glutamEic acid, M = M (contains M), T = T (contains T), W = tW (tryptophan, double ring), I = I (contains I), L = L (contains L), N = N (contains N), Q = Q (sounds like "cue" → glutamine).
Non-standard amino acids (e.g., selenocysteine Sec/U, pyrrolysine Pyl/O, hydroxyproline Hyp) do not have universally accepted one-letter codes. In sequences, they are often represented by special letters (U for selenocysteine, O for pyrrolysine) or written out in full. The converter above handles only the 20 standard amino acids.
Isoleucine (I) and Leucine (L) are structural isomers — they share the same molecular formula (C₆H₁₃NO₂) and therefore the same molecular weight (113.16 Da). However, they differ in the arrangement of their side chains: Leu has an unbranched isobutyl side chain, while Ile has a branched sec-butyl side chain. This structural difference gives them distinct biochemical properties and roles in proteins.
The letter U stands for selenocysteine (Sec), the 21st proteinogenic amino acid. It is a cysteine analog where sulfur is replaced by selenium. Selenocysteine is encoded by a special UGA codon (normally a stop codon) in the presence of a selenocysteine insertion sequence (SECIS) element. It is found in several selenoproteins important for antioxidant defense.
Related Tools¶
- Molecular Weight Calculator — Calculate peptide mass from sequence
- Peptide Properties Calculator — Compute pI, charge, GRAVY
- Peptide Comparison Tool — Compare peptides side-by-side