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  2. Threonine - Wikipedia

    en.wikipedia.org/wiki/Threonine

    Threonine (symbol Thr or T) [2] is an amino acid that is used in the biosynthesis of proteins.It contains an α-amino group (which is in the protonated −NH + 3 form when dissolved in water), a carboxyl group (which is in the deprotonated −COO − form when dissolved in water), and a side chain containing a hydroxyl group, making it a polar, uncharged amino acid.

  3. Threonic acid - Wikipedia

    en.wikipedia.org/wiki/Threonic_acid

    Threonic acid is a sugar acid derived from threose. The l - isomer is a metabolite of ascorbic acid (vitamin C). [ 1 ] One study suggested that because l -threonate inhibits DKK1 expression in vitro , it may have potential in treatment of androgenic alopecia .

  4. Catalytic triad - Wikipedia

    en.wikipedia.org/wiki/Catalytic_triad

    Threonine proteases use the amino acid threonine as their catalytic nucleophile. Unlike cysteine and serine, threonine is a secondary hydroxyl (i.e. has a methyl group). This methyl group greatly restricts the possible orientations of triad and substrate as the methyl clashes with either the enzyme backbone or histidine base. [2]

  5. Allothreonine - Wikipedia

    en.wikipedia.org/wiki/Allothreonine

    Allothreonine is an amino acid with the formula CH 3 CH(OH)CH(NH 2)CO 2 H. It is the diastereomer of the amino acid threonine. Like most other amino acids, allothreonine is a water-soluble colorless solid. Although not one of the proteinogenic amino acids, it has often been the subject for the synthesis of novel proteins using an expanded ...

  6. Threonine protease - Wikipedia

    en.wikipedia.org/wiki/Threonine_protease

    Threonine proteases use the secondary alcohol of their N-terminal threonine as a nucleophile to perform catalysis. [1] [2] The threonine must be N-terminal since the terminal amine of the same residue acts as a general base by polarising an ordered water which deprotonates the alcohol to increase its reactivity as a nucleophile.

  7. Deamidation - Wikipedia

    en.wikipedia.org/wiki/Deamidation

    Asn-Gly (NG),is the most flexible and since it is acidic, it is most prone to deamidation with a half-life around 24 h under physiological conditions (pH 7.4, 37 °C). [3] As a free amino acid, or as the N-terminal residue of a peptide or protein, glutamine deamidates readily to form pyroglutamic acid (5-oxoproline). The reaction proceeds via ...

  8. Threonine—tRNA ligase - Wikipedia

    en.wikipedia.org/wiki/Threonine—tRNA_ligase

    Threonyl-tRNA synthetase (TARS) from Escherichia coli is encoded by the thrS gene.It is a homodimeric enzyme that aminoacylates tRNA(Thr) with the amino acid threonine. [1] In addition, TARS has the ability to bind to its own messenger RNA (mRNA) immediately upstream of the AUG start codon, to inhibit its translation by competing with ribosome binding, and thus to negatively regulate the ...

  9. Aromatic amino acid - Wikipedia

    en.wikipedia.org/wiki/Aromatic_amino_acid

    In plants, the shikimate pathway first leads to the formation of chorismate, which is the precursor of phenylalanine, tyrosine, and tryptophan.These aromatic amino acids are the precursors of many secondary metabolites, all essential to a plant's biological functions, such as the hormones salicylate and auxin.