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  2. Histidine - Wikipedia

    en.wikipedia.org/wiki/Histidine

    Histidine ball and stick model spinning. Histidine (symbol His or H) [2] is an essential amino acid that is used in the biosynthesis of proteins.It contains an α-amino group (which is in the protonated –NH 3 + form under biological conditions), a carboxylic acid group (which is in the deprotonated –COO − form under biological conditions), and an imidazole side chain (which is partially ...

  3. Histidine (data page) - Wikipedia

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

    Hydrogen bond: donor ... (L-histidine) ^a CID 71083 from PubChem (D-histidine) ^a CID 6274 from PubChem (L-histidine) This page was last edited on 12 April ...

  4. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    The terms "polar" and "nonpolar" are usually applied to covalent bonds, that is, bonds where the polarity is not complete. To determine the polarity of a covalent bond using numerical means, the difference between the electronegativity of the atoms is used.

  5. Active site - Wikipedia

    en.wikipedia.org/wiki/Active_site

    Hydrogen bond: A hydrogen bond is a specific type of dipole-dipole interaction between a partially positive hydrogen atom and a partially negative electron donor that contain a pair of electrons such as oxygen, fluorine and nitrogen. The strength of hydrogen bond depends on the chemical nature and geometric arrangement of each group.

  6. Catalytic triad - Wikipedia

    en.wikipedia.org/wiki/Catalytic_triad

    Compared to oxygen, sulfur's extra d orbital makes it larger (by 0.4 Å) [29] and softer, allows it to form longer bonds (d C-X and d X-H by 1.3-fold), and gives it a lower pK a (by 5 units). [30] Serine is therefore more dependent than cysteine on optimal orientation of the acid-base triad members to reduce its p K a [ 30 ] in order to achieve ...

  7. Hydrophobicity scales - Wikipedia

    en.wikipedia.org/wiki/Hydrophobicity_scales

    Hydrogen bonds between molecules of liquid water. The hydrophobic effect represents the tendency of water to exclude non-polar molecules. The effect originates from the disruption of highly dynamic hydrogen bonds between molecules of liquid water. Polar chemical groups, such as OH group in methanol do not cause the

  8. Aromatic amino acid - Wikipedia

    en.wikipedia.org/wiki/Aromatic_amino_acid

    Aromatic amino acids often serve as the precursors to important biochemicals. Histidine is the precursor to histamine.; Tryptophan is the precursor to 5-hydroxytryptophan and then serotonin, tryptamine, auxin, kynurenines, and melatonin.

  9. Salt bridge (protein and supramolecular) - Wikipedia

    en.wikipedia.org/wiki/Salt_bridge_(protein_and...

    Hydrogen bonds contribute to the stability of ion pairs with e.g. protonated ammonium ions, and with anions is formed by deprotonation as in the case of carboxylate, phosphate etc; then the association constants depend on the pH. Entropic driving forces for ion pairing (in absence of significant H-bonding contributions) are also found in ...