List of standard protein amino acids

Source: Internet
Author: User

Standard amino Acids (English:amino acids) or protein amino acids (proteinogenic amino acids), It is a total of 20 amino acids used in biological cells to synthesize proteins. This list mainly describes its name, marking method, structure and nature. Also included are the secondary encoding of amino acids, selenium cysteine and pyrrole lysine, respectively, with the usual termination codon UGA and UAG encoding, appearing in a few proteins. See 21st and 22nd amino acids .

Directory[Hide]
    • 1 names and symbols
    • 2 Structure
    • 3 main chemical properties
    • 4 Branched Nature
    • 5 gene expression and biochemistry
    • 6 References

Name and Symbol

The following table shows each Chinese name with English name, three letter symbol and one letter symbol. (* for secondary coding of amino acids)

Chinese name English name Short Write Abbreviations
Propionic acid Alanine A Ala
Phenylalanine (L-alanine) Phenylalanine F Phe
Cysteine Cysteine C Cys
Selenium cysteine * Selenocysteine U Sec
Aspartic acid Aspartic acid/aspartate D Asp
Aspartic amide Asparagine N Asn
Glutamate Glutamic acid/glutamate E Glu
Ammonium glutamine Glutamine Q Gln
Glycine Glycine G Gly
Histidine Histidine H His
Leucine Leucine L Leu
ISO-leucine Isoleucine I Ile
Lysine Lysine K Lys
Pyrrole lysine * Pyrrolysine O Pyl
Methionine Methionine M Met
L-Proline Proline P Pro
L-Arginine Arginine R Arg
Serine Serine S Ser
Threonine Threonine T Thr
L-Valine Valine V Val
Tryptophan Tryptophan W Trp
Tyrosine Tyrosine Y Tyr


In addition, there are some three-letter or single-letter symbols that can be used to denote undefined abbreviations:

    • ASX, B can represent aspartic acid (ASP, D) or aspartic amide (ASN, N).
    • GLX, z may represent glutamic acid (Glu, E) or glutamine (Gln, Q).
    • Xle, J may represent Leucine (Leu, L) or isoleucine (Ile, I).
    • Xaa (also with UNK), X may represent any amino acid or unknown amino acid.
structure

The following is the structure and representation of the 20 amino acids that the standard genetic code uses to directly synthesize proteins.

  • L-alanine
    (ala/a)

  • L-arginine
    (ARG/R)

  • L-aspartic amide
    (asn/n)

  • L-aspartic acid
    (ASP/D)

  • L-cysteine
    (CYS/C)

  • L-Glutamic acid
    (glu/e)

  • L-Glutamine
    (gln/q)

  • Glycine
    (gly/g)

  • L-histidine
    (his/h)

  • L-isoleucine
    (ile/i)

  • L-leucine
    (LEU/L)

  • L-lysine
    (lys/k)

  • L-methionine
    (met/m)

  • L-phenylalanine
    (phe/f)

  • L-proline
    (pro/p)

  • L-serine
    (SER/S)

  • L-threonine
    (thr/t)

  • L-Tryptophan
    (trp/w)

  • L-tyrosine
    (tyr/y)

  • L-valine
    (val/v)

  • L-Selenium cysteine
    (sec/u)

  • L-Pyrrole lysine
    (pyl/o)

Main chemical properties

The following molecular weight is the average of the abundance of isotopes in nature based on each element. In addition, due to the formation of peptide bonds, a water molecule is reduced, so the molecular weight of the single amino acid in the protein, less than the table value 18.01524 Da.

Amino Acids Molecular Weight (Da) PI pK1 (Α-cooh) pK2 (Α-+NH3)
Propionic acid 89.09404 6.01 2.35 9.87
Cysteine 121.15404 5.05 1.92 10.70
Selenium-cysteine 169.06
Aspartic acid 133.10384 2.85 1.99 9.90
Glutamate 147.13074 3.15 2.10 9.47
Phenylalanine (L-alanine) 165.19184 5.49 2.20 9.31
Glycine 75.06714 6.06 2.35 9.78
Histidine 155.15634 7.60 1.80 9.33
ISO-leucine 131.17464 6.05 2.32 9.76
Lysine 146.18934 9.60 2.16 9.06
Pyrrole lysine 255.31
Leucine 131.17464 6.01 2.33 9.74
Methionine 149.20784 5.74 2.13 9.28
Aspartic amide 132.11904 5.41 2.14 8.72
L-Proline 115.13194 6.30 1.95 10.64
Ammonium glutamine 146.14594 5.65 2.17 9.13
L-Arginine 174.20274 10.76 1.82 8.99
Serine 105.09344 5.68 2.19 9.21
Threonine 119.12034 5.60 2.09 9.10
L-Valine 117.14784 6.00 2.39 9.74
Tryptophan 204.22844 5.89 2.46 9.41
Tyrosine 181.19124 5.64 2.20 9.21
Branched chain Properties

The pka values in the following list may differ from those of amino acids within the protein.

the of the aliphatic group
Amino Acids branched Water Repellent PKa Polarity charge Aromatic Family
Or
van der Waals radius
Propionic acid -ch3 X - - - - 67
Cysteine -ch2sh X 8.18 - Acid - 86
Selenium-cysteine -ch2seh X 5.73 - - -
Aspartic acid -ch2cooh - 3.90 X Acid - 91
Glutamate -ch2ch2cooh - 4.07 X Acid - 109
Phenylalanine (L-alanine) -ch2c6h5 X - - - Aromatic nature 135
Glycine -H - - - - - 48
Histidine -ch2-c3h3n2 - 6.04 X Weakly alkaline Aromatic nature 118
ISO-leucine -ch (CH3) Ch2ch3 X - - - Fat Sex 124
Lysine -(CH2) 4NH2 - 10.54 X Alkaline - 135
Pyrrole lysine -c12h21n3o3
Leucine -CH2CH (CH3) 2 X - - - Fat Sex 124
Methionine -ch2ch2sch3 X - - - - 124
Aspartic amide -ch2conh2 - - X - - 96
L-Proline -ch2ch2ch2- X - - - - 90
Ammonium glutamine -ch2ch2conh2 - - X - - 114
L-Arginine -(CH2) 3nh-c (NH) NH2 - 12.48 X Alkaline - 148
Serine -ch2oh - - X - - 73
Threonine -ch (OH) CH3 - - X Weakly acidic - 93
L-Valine -ch (CH3) 2 X - - - Fat Sex 105
Tryptophan -ch2-c8h6n X - - - Aromatic nature 163
Tyrosine -ch2-c6h4oh X 10.46 X - Aromatic nature 141
gene expression and biochemistry
of
Amino Acids Short Write Abbreviations codon in the protein
Frequency of occurrence (%)
human necessity
Off-amino acid K Lys AAA, AAG 5.9 X
Aspartic amide N Asn AAU, AAC 4.3 -
Threonine T Thr ACU, ACC, ACA, ACG 5.9 X
Methyl-L-methionine M Met The 2.3 X
ISO-leucine I Ile AUU, AUC, AUA 5.3 X
Ammonium glutamine Q Gln CAA, CAG 4.2 -
Histidine H His CAU, CAC 2.3 -
L-Proline P Pro CCU, CCC, CCA, CCG 5.2 -
L-Arginine R Arg CGU, CGC, CGA, CGG, AGA, AGG 5.1 -
Glutamate E Glu GAA, GAG 6.3 -
Aspartic acid D Asp GAU, GAC 5.3 -
Propionic acid A Ala GCU, GCC, GCA, GCG 7.8 -
Glycine G Gly Ggu, GGC, GGA, GGG 7.2 -
L-Valine V Val GUU, GUC, GUA, GUG 6.6 X
Terminating encoding - Term UAA, UAG, UGA - -
Pyrrole lysine O Pyl UAG
Tyrosine Y Tyr Uau, UAC 3.2 -
Serine S Ser UCU, UCC, UCA, UCG, AGU, AGC 6.8 -
Selenium-cysteine U Sec UGA -
Tryptophan W Trp Ugg 1.4 X
Cysteine C Cys Ugu, UGC 1.9 -
Leucine L Leu UUA, Uug, Cuu, CUC, CUA, CUG 9.1 X
Phenylalanine (L-alanine) F Phe UUU, Uuc 3.9 X
Reference Documents
      • Nelson, David L.; Cox, Michael M. Lehninger Principles of Biochemistry 3rd ed. Worth Publishers. ISBN 1-57259-153-6.
      • Kyte, J.; Doolittle, R. F. A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 1982, 157 (1): 105–132. PMID 7108955.

List of standard protein amino acids

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