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  2. Histidine - Wikipedia

    en.wikipedia.org/wiki/Histidine

    [5] [6] [7] The imidazole/imidazolium ring of histidine is aromatic at all pH values. [8] Under certain conditions, all three ion-forming groups of histidine can be charged forming the histidinium cation. [9] The acid-base properties of the imidazole side chain are relevant to the catalytic mechanism of many enzymes. [10]

  3. His-tag - Wikipedia

    en.wikipedia.org/wiki/His-tag

    Imidazole is the side chain of histidine and is typically used at a concentration of 150 - 500 mM for elution. Histidine or histamine can also be used. Decrease in pH; When the pH decreases, the histidine residue is protonated and can no longer coordinate the metal tag, allowing the protein to be eluted.

  4. Histidine (data page) - Wikipedia

    en.wikipedia.org/wiki/Histidine_(data_page)

    Chemical formula: C 6 H 9 N 3 O 2 Molar mass: 155.16 g·mol −1 Systematic name: 2-amino-3-(3H-imidazol-4-yl)propanoic acid Abbreviations: H, His Synonyms: Imidazole alanine ({S/D})-α-amino-1H-imidazole-4-propanoic acid

  5. Catalytic triad - Wikipedia

    en.wikipedia.org/wiki/Catalytic_triad

    The aspartate is hydrogen bonded to the histidine, increasing the pK a of its imidazole nitrogen from 7 to around 12. Histidine is thus able to act as a powerful general base, activating the serine nucleophile.

  6. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Arginine has a charged guanidino group and lysine a charged alkyl amino group, and are fully protonated at pH 7. Histidine's imidazole group has a pK a of 6.0, and is only around 10% protonated at neutral pH. Because histidine is easily found in its basic and conjugate acid forms it often participates in catalytic proton transfers in enzyme ...

  7. Isoelectric point - Wikipedia

    en.wikipedia.org/wiki/Isoelectric_point

    The isoelectric point (pI, pH(I), IEP), is the pH at which a molecule carries no net electrical charge or is electrically neutral in the statistical mean. The standard nomenclature to represent the isoelectric point is pH(I). [ 1 ]

  8. Protein phosphorylation - Wikipedia

    en.wikipedia.org/wiki/Protein_phosphorylation

    The analysis of phosphorylated histidine using standard biochemical and mass spectrometric approaches is much more challenging than that of Ser, Thr or Tyr. [49] [7] [5] and [50] In prokaryotes, archaea, and some lower eukaryotes, histidine's nitrogen act as a nucleophile and binds to a phosphate group. [51]

  9. Transition metal imidazole complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_imidazole...

    Structure of the histidine complex [Ni(κ 3-histidinate) 2] 2-. [1] A transition metal imidazole complex is a coordination complex that has one or more imidazole ligands. Complexes of imidazole itself are of little practical importance. In contrast, imidazole derivatives, especially histidine, are pervasive ligands in biology where they bind ...