Non-proteinogenic amino acids

Non-proteinogenic amino acids

In proteinogenic amino acids), over 140 natural amino acids are known and thousands of more combinations are possible.[1] Several non-proteinogenic amino acids are noteworthy because they are:

Definition by negation

Technically, any organic compound with an amine (-NH2) and a carboxylic acid (-COOH) functional group is an amino acid. The proteinogenic amino acids are small subset of this group that possess central carbon atom (α- or 2-) bearing an amino group, a carboxyl group, a side chain and an α-hydrogen levo conformation, with the exception of glycine, which is achiral, and proline, whose amine group is a secondary amine and is consequently frequently referred to as an imino acid for traditional reasons, albeit not an imino.

The genetic code encodes 20 standard amino acids. However, there are three extra proteinogenic amino acids: selenocysteine, pyrrolysine and N-formylmethionine. The former two do not have a dedicated codon, but are added in place of a stop codon when a specific sequence is present, UGA codon and SECIS element for selenocysteine, UAG PYLIS downstream sequence for pyrrolysine.[2][3] Formylmethionine is an amino acid encoded by the start codon AUG in bacteria, mitochondria and chloroplasts, but is often removed posttranslationaly.[4]

There are various groups of amino acids:[5]

  • 20 standard amino acids
  • 23 proteinogenic amino acids
  • over 80 amino acids created abiotically in high concentrations
  • about 900 are produced by natural pathways
  • over 118 engineered amino acids have been placed into protein

These groups overlap, but are not identical. All 23 proteinogenic amino acids are biosynthesised by organisms, but not all of them are abiotic (found in prebiotic experiments and meteorites), such as histidine. Many amino acids, such as ornithine, are metabolic intermediates produced biotically, but not coded. Others are only metabolic intermediates, such as citrulline. Others are solely found in abiotic mixes, such as α-methylnorvaline. Over 30 unnatural amino acids have been translationally inserted into protein in engineered systems, yet are not biosynthetic.[5]


In addition to the [6] (Consequently, the IUPAC names of many non-proteinogenic α-amino acids start with 2-amino and end in -ic acid.)

Natural, but non L-α-amino acids

Most natural amino acids are α-amino acids in the L conformation, but some exceptions exist.

Non alpha

Comparison of the structures of alanine and beta alanine.

Some non-α amino acids exist in organisms, such as β-alanine, GABA, and δ-Aminolevulinic acid.

The reason why α amino acids are using in protein has been attributed to their frequency in meteorites and prebiotic experiments.[8] 14. An initial speculation on the deleterious properties of β amino acids in terms of secondary structure,[8] turned out to be incorrect.[9] Additionally, several man-made inhibitors exist that are not α amino acids, such as isoserine.

D amino acids

Most bacterial cells walls are formed by peptidoglycan, a polymer composed of amino sugar crosslinked with short oligopeptides bridged between each other. The oligopeptide is non-ribosomally synthesised and contains several peculiarities, including D-amino acids, generally D-alanine and D-glutamate. A further peculiarity is that the former is racemised by a PLP-binding enzymes (encoded by alr or the homologue dadX), whereas the latter is racemised by a cofactor independent enzyme (murI). Some variants are present, in Thermotoga spp. D-lysine is present and in certain vancomycin-resistant strains D-serine is present (vanT gene).[10][11]

In animals, some D-amino acids are neurotransmitters.

Without a hydrogen on the α-carbon

All proteinogenic amino acids have at least one hydrogen on the α-carbon: this is due to the different specificity a the rybosomal transferase activity would require for a α-hydrogen versus a α-methyl and the biosynthetic problems faced with the quaternary carbon, which would block PLP-dependent catalysis (both SN2 and E2/attack).[8]

Nevertheless, some exceptions are present. In some fungi α-Amino isobutyric acid is produced as a monomer to synthesise some antibiotics.[12] This compound is similar to alanine, but possess a methyl group instead of a hydrogen, given that it possess two methyl group on the α-carbon, the latter is therefore not a stereocentre. Another compound similar to alanine without an α-hydrogen is dehydroalanine, which possess a methene sidechain.

Twin amino acid stereocentres

A subset of L α amino acids possess two ends that could be considered α amino acids (obviously only one end is the α). In protein djenkolic acid, a plant toxin from jengkol beans, is composed of two cysteines joined via two thioethers separated by a methylene group. Diaminopimelic acid is both used as a bridge in petidoglycan and is used a precursor to lysine (via its decarboxylation).


In cells, especially autotrophs, several non-proteinogenic amino acids are found as metabolic intermediates. However, despite the catalytic flexibility of PLP-binding enzymes, many amino acids are synthesised as keto-acids (e.g. 4-methyl-2-oxopentanoate to leucine) and aminated in the last step, thus keeping the number of non-proteinogenic amino acid intermediates fairly low.

Ornithine and citrulline occur in the urea cycle, part of amino acid catabolism (see below).[13]

In addition to primary metabolism, several non-proteinogenic amino acids are precursors or the final production in secondary metabolism to make compounds such as toxins.

Prebiotic amino acids and alternative biochemistries

In meteorites and in prebiotic experiments (e.g. Miller–Urey experiment) many more amino acids than the twenty standard amino acids are found, several of which at higher concentrations that the standard ones: it has been conjectured that if amino acid based life were to arise in parallel elsewhere in the universe, no more than 75% of the amino acids would be in common.[8] The most notable anomaly is the lack of aminobutyric acid.

Proportion of amino acids relative to glycine (%)
Molecule Electric discharge Murchinson meteorite
Glycine 100 100
Alanine 180 36
α-Amino-n-butyric acid 61 19
Norvaline 14 14
Valine 4.4
Norleucine 1.4
Leucine 2.6
Isoleucine 1.1
Alloisoleucine 1.2
t-leucine < 0.005
α-Amino-n-heptanoic acid 0.3
Proline 0.3 22
Pipecolic acid 0.01 11
α,β-diaminopropionic acid 1.5
α,γ-diaminobutyric acid 7.6
Ornithine < 0.01
lysine < 0.01
Aspartic acid 7.7 13
Glutamic acid 1.7 20
Serine 1.1
Threonine 0.2
Allothreonine 0.2
Methionine 0.1
Homocysteine 0.5
Homoserine 0.5
β-Alanine 4.3 10
β-Amino-n-butyric acid 0.1 5
β-Aminoisobutyric acid 0.5 7
γ-Aminobutyric acid 0.5 7
α-Aminoisobutyric acid 7 33
isovaline 1 11
Sarcosine 12.5 7
N-ethyl glycine 6.8 6
N-propyl glycine 0.5
N-isopropyl glycine 0.5
N-methyl alanine 3.4 3
N-ethyl alanine < 0.05
N-methyl β-alanine 1.0
N-ethyl β-alanine < 0.05
isoserine 1.2
α-hydroxy-γ-aminobutyric acid 17

Straight side chain

The genetic code has been described as a frozen accident and the reasons why there is only one standard amino acid with a straight chain (alanine) could simply be redundancy with valine, leucine and isoleucine.[8] However, straight chained amino acids are reported to form much more stable alpha helices.[14]


Serine, homoserine, O-methyl-homoserine and O-ethyl-homoserine possess an hydroxymethyl, hydroxyethyl, O-methyl-hydroxymethyl and O-methyl-hydroxyethyl side chain. Whereas cysteine, homocysteine, methionine and ethionine possess the thiol equivalents. The selenol equivalents are selenocysteine, selenohomocysteine, selenomethionine and selenoethionine. Amino acids with the next chalcogen down are also found in nature: several species such as Aspergillus fumigatus, Aspergillus terreus, and Penicillium chrysogenum in the absence of sulfur are able to produce and incorporate into protein tellurocysteine and telluromethionine.[15]

Hydroxyglycine, an amino acid with a hydroxyl side-chain, is highly unstable.

Expanded genetic code

Post-translationally incorporated into protein

Despite not being encoded by the genetic code as proteinogenic amino acids, some non-standard amino acids are nevertheless found in proteins. These are formed by post-translational modification of the side chains of standard amino acids present in the target protein. These modifications are often essential for the function or regulation of a protein; for example, in Gamma-carboxyglutamate the carboxylation of glutamate allows for better binding of calcium cations,[16] and in hydroxyproline the hydroxylation of proline is critical for maintaining connective tissues.[17] Another example is the formation of hypusine in the translation initiation factor EIF5A, through modification of a lysine residue.[18] Such modifications can also determine the localization of the protein, e.g., the addition of long hydrophobic groups can cause a protein to bind to a phospholipid membrane.[19]

There is some preliminary evidence that aminomalonic acid may be present, possibly by misincorporation, in protein.[20][21]

Toxic analogues

Several non-proteinogenic amino acids are toxic due to their ability to mimic certain properties of proteinogenic amino acids, such as thialysine. Some non-proteinogenic amino acids are neurotoxic by mimicking amino acids used as neurotransmitters (i.e. not for protein biosynthesis), e.g. Quisqualic acid, canavanine or azetidine-2-carboxylic acid.[22] Cephalosporin C has an α-aminoadipic acid (homoglutamate) backbone that is amidated with a cephalosporin moiety.[23] Penicillamine is therapeutic amino acid, whose mode of action is unknown.

Naturally-occurring cyanotoxins can also include non-proteinogenic amino acids. Microcystin and nodularin, for example, are both derived from ADDA, a β-amino acid.

Not amino acids

The osmolytes, sarcosine and glycine betaine are derived from amino acids, but have an secondary and quaternary amine respectively.


  1. ^ Ambrogelly, A.; Palioura, S.; Söll, D. (2007). "Natural expansion of the genetic code". Nature Chemical Biology 3 (1): 29–35.  
  2. ^ Böck, A.; Forchhammer, K.; Heider, J.; Baron, C. (1991). "Selenoprotein synthesis: An expansion of the genetic code". Trends in biochemical sciences 16 (12): 463–467.  
  3. ^ Théobald-Dietrich, A.; Giegé, R.; Rudinger-Thirion, J. L. (2005). "Evidence for the existence in mRNAs of a hairpin element responsible for ribosome dependent pyrrolysine insertion into proteins". Biochimie 87 (9–10): 813–817.  
  4. ^ Sherman, F.; Stewart, J. W.; Tsunasawa, S. (1985). "Methionine or not methionine at the beginning of a protein". BioEssays 3 (1): 27–31.  
  5. ^ a b Lu, Y.; Freeland, S. (2006). "On the evolution of the standard amino-acid alphabet". Genome Biology 7 (1): 102.  
  6. ^ Voet, D.; Voet, J. G. (2004). Biochemistry (3rd ed.). John Wiley & Sons.  
  7. ^ Chakauya, E.; Coxon, K. M.; Ottenhof, H. H.; Whitney, H. M.; Blundell, T. L.; Abell, C.; Smith, A. G. (2005). "Pantothenate biosynthesis in higher plants". Biochemical Society Transactions 33 (4): 743–746.  
  8. ^ a b c d e Weber, A. L.; Miller, S. L. (1981). "Reasons for the occurrence of the twenty coded protein amino acids". Journal of molecular evolution 17 (5): 273–284.  
  9. ^ Koyack, M. J.; Cheng, R. P. (2006). "Protein Design". Methods in molecular biology (Clifton, N.J.) 340: 95–109.  
  10. ^ Boniface, A.; Parquet, C.; Arthur, M.; Mengin-Lecreulx, D.; Blanot, D. (2009). "The Elucidation of the Structure of Thermotoga maritima Peptidoglycan Reveals Two Novel Types of Cross-link". Journal of Biological Chemistry 284 (33): 21856–21862.  
  11. ^ Arias, C. A.; Martín-Martinez, M.; Blundell, T. L.; Arthur, M.; Courvalin, P.; Reynolds, P. E. (1999). "Characterization and modelling of VanT: A novel, membrane-bound, serine racemase from vancomycin-resistant Enterococcus gallinarum BM4174". Molecular microbiology 31 (6): 1653–1664.  
  12. ^ Gao, X.; Chooi, Y. H.; Ames, B. D.; Wang, P.; Walsh, C. T.; Tang, Y. (2011). "Fungal Indole Alkaloid Biosynthesis: Genetic and Biochemical Investigation of the Tryptoquialanine Pathway inPenicillium aethiopicum". Journal of the American Chemical Society 133 (8): 2729–2741.  
  13. ^ Curis, E.; Nicolis, I.; Moinard, C.; Osowska, S.; Zerrouk, N.; Bénazeth, S.; Cynober, L. (2005). "Almost all about citrulline in mammals". Amino Acids 29 (3): 177–205.  
  14. ^ Padmanabhan, S.; Baldwin, R. L. (1991). "Straight-chain non-polar amino acids are good helix-formers in water". Journal of molecular biology 219 (2): 135–137.  
  15. ^ Ramadan, S. E.; Razak, A. A.; Ragab, A. M.; El-Meleigy, M. (1989). "Incorporation of tellurium into amino acids and proteins in a tellurium-tolerant fungi". Biological trace element research 20 (3): 225–232.  
  16. ^ Vermeer, C. (1990). "Gamma-carboxyglutamate-containing proteins and the vitamin K-dependent carboxylase". The Biochemical journal 266 (3): 625–636.  
  17. ^ Bhattacharjee, A.; Bansal, M. (2005). "Collagen Structure: The Madras Triple Helix and the Current Scenario". IUBMB Life (International Union of Biochemistry and Molecular Biology: Life) 57 (3): 161–172.  
  18. ^ Park, M. H. (2006). "The Post-Translational Synthesis of a Polyamine-Derived Amino Acid, Hypusine, in the Eukaryotic Translation Initiation Factor 5A (eIF5A)". Journal of Biochemistry 139 (2): 161–169.  
  19. ^ Blenis, J.; Resh, M. D. (1993). "Subcellular localization specified by protein acylation and phosphorylation". Current opinion in cell biology 5 (6): 984–989.  
  20. ^ Copley, S. D.; Frank, E.; Kirsch, W. M.; Koch, T. H. (1992). "Detection and possible origins of aminomalonic acid in protein hydrolysates". Analytical biochemistry 201 (1): 152–157.  
  21. ^ Van Buskirk, J. J.; Kirsch, W. M.; Kleyer, D. L.; Barkley, R. M.; Koch, T. H. (1984). "Aminomalonic acid: Identification in Escherichia coli and atherosclerotic plaque". Proceedings of the National Academy of Sciences of the United States of America 81 (3): 722–725.  
  22. ^ Dasuri, K.; Ebenezer, P. J.; Uranga, R. M.; Gavilán, E.; Zhang, L.; Fernandez-Kim, S. O. K.; Bruce-Keller, A. J.; Keller, J. N. (2011). "Amino acid analog toxicity in primary rat neuronal and astrocyte cultures: Implications for protein misfolding and TDP-43 regulation". Journal of Neuroscience Research 89 (9): 1471–1477.  
  23. ^ Trown, P. W.; Smith, B.; Abraham, E. P. (1963). "Biosynthesis of cephalosporin C from amino acids". The Biochemical journal 86 (2): 284–291.