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  2. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    It does not participate in protein biosynthesis although it is found in proteins in small amounts - particularly aged proteins and food proteins that have been processed. The biological functions of D -amino acids remain unclear, although D -phenylalanine has pharmacological activity at niacin receptor 2 .

  3. Tryptophan hydroxylase - Wikipedia

    en.wikipedia.org/wiki/Tryptophan_hydroxylase

    Analogously to phenylalanine hydroxylase and tyrosine hydroxylase, this enzyme uses (6R)-L-erythro-5,6,7,8-tetrahydrobiopterin (BH 4) and dioxygen as cofactors. [ 2 ] In humans, the stimulation of serotonin production by administration of tryptophan has an antidepressant effect [ 3 ] [ 4 ] and inhibition of tryptophan hydroxylase (e.g. by p ...

  4. Biopterin-dependent aromatic amino acid hydroxylase - Wikipedia

    en.wikipedia.org/wiki/Biopterin-dependent...

    These enzymes primarily hydroxylate the amino acids L-phenylalanine, L-tyrosine, and L-tryptophan, respectively. The AAAH enzymes are functionally and structurally related proteins which act as rate-limiting catalysts for important metabolic pathways. [1]

  5. Phenylalanine hydroxylase - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine_hydroxylase

    Phenylalanine hydroxylase (PAH) (EC 1.14.16.1) is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine.PAH is one of three members of the biopterin-dependent aromatic amino acid hydroxylases, a class of monooxygenase that uses tetrahydrobiopterin (BH 4, a pteridine cofactor) and a non-heme iron for catalysis.

  6. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    If phenylalanine is in excess in the blood, it will saturate the transporter. Excessive levels of phenylalanine tend to decrease the levels of other LNAAs in the brain. As these amino acids are necessary for protein and neurotransmitter synthesis, Phe buildup hinders the development of the brain, causing intellectual disability. [26]

  7. Phenylethanolamine N-methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Phenylethanolamine_N...

    The active site binding region for the cofactor SAM contains a rich number of pi bonds from phenylalanine and tyrosine residues in the active site help to keep it in its binding pocket through pi stacking. Among all known PNMT variants in nature there are 7 crucial aromatic residues conserved in the active site.

  8. Phenylalanine (data page) - Wikipedia

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

    Structure. Crystal data: Spectral data. UV-Vis: IR: NMR: MS ... (D-phenylalanine) ^a CID 6140 from PubChem (L-phenylalanine) This page was last edited on 12 January ...

  9. Phenylalanine—tRNA ligase - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine—tRNA_ligase

    Phenylalanine-tRNA synthetase (PheRS) is known to be among the most complex enzymes of the aaRS (Aminoacyl-tRNA synthetase) family. Bacterial and mitochondrial PheRSs share a ferredoxin -fold anticodon binding (FDX-ACB) domain , which represents a canonical double split alpha+beta motif having no insertions.