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  2. Protein pKa calculations - Wikipedia

    en.wikipedia.org/wiki/Protein_pKa_calculations

    The pH-dependence of the activity displayed by enzymes and the pH-dependence of protein stability, for example, are properties that are determined by the pK a values of amino acid side chains. The p K a values of an amino acid side chain in solution is typically inferred from the p K a values of model compounds (compounds that are similar to ...

  3. Hydrophobicity scales - Wikipedia

    en.wikipedia.org/wiki/Hydrophobicity_scales

    Also, amino acid side chain affinity for water was measured using vapor phases. [14] Vapor phases represent the simplest non polar phases, because it has no interaction with the solute. [18] The hydration potential and its correlation to the appearance of amino acids on the surface of proteins was studied by Wolfenden.

  4. File:ProteinogenicAminoAcids.svg - Wikipedia

    en.wikipedia.org/wiki/File:ProteinogenicAmino...

    Trying again to fix the text alignment in some of the amino acids: 00:33, 19 April 2022: 941 × 753 (293 KB) TungstenEinsteinium: Made fonts and alignments more consistent (again) 23:51, 18 April 2022: 941 × 753 (296 KB) TungstenEinsteinium: Made fonts and alignments more consistent: 23:33, 18 April 2022: 941 × 753 (297 KB) TungstenEinsteinium

  5. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    The 21 proteinogenic α-amino acids found in eukaryotes, grouped according to their side chains' pK a values and charges carried at physiological pH (7.4) 2-, alpha-, or α-amino acids [21] have the generic formula H 2 NCHRCOOH in most cases, [b] where R is an organic substituent known as a "side chain". [22]

  6. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    Phenylalanine (symbol Phe or F) [3] is an essential α-amino acid with the formula C 9 H 11 NO 2.It can be viewed as a benzyl group substituted for the methyl group of alanine, or a phenyl group in place of a terminal hydrogen of alanine.

  7. Tryptophan - Wikipedia

    en.wikipedia.org/wiki/Tryptophan

    Like other amino acids, tryptophan is a zwitterion at physiological pH where the amino group is protonated (– NH + 3; pK a = 9.39) and the carboxylic acid is deprotonated ( –COO −; pK a = 2.38). [5] Humans and many animals cannot synthesize tryptophan: they need to obtain it through their diet, making it an essential amino acid.

  8. Isoelectric point - Wikipedia

    en.wikipedia.org/wiki/Isoelectric_point

    Some improvements in the methodology (especially in the determination of the pK values for modified amino acids) have been also proposed. [ 8 ] [ 9 ] More advanced methods take into account the effect of adjacent amino acids ±3 residues away from a charged aspartic or glutamic acid , the effects on free C terminus, as well as they apply a ...

  9. Pleckstrin homology domain - Wikipedia

    en.wikipedia.org/wiki/Pleckstrin_homology_domain

    Pleckstrin homology domain (PH domain) or (PHIP) is a protein domain of approximately 120 amino acids that occurs in a wide range of proteins involved in intracellular signaling or as constituents of the cytoskeleton.