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Reviews on structure and function of aromatic amino acid hydroxylases

  1. Annenkov, G.A. (1982) Genetical heterogeneity of phenylketonuria. Vopr. Med. Khim. (Moscow) 28, 62-70.
  2. Arango, V., Underwood, M.D. and Mann, J.J. (1997) Biologic alterations in the brainstem of suicides. Psychiatr. Clin. North Am. 20, 581-593.
  3. Bailey, S.W., Boerth, S.R., Dillard, S.B. and Ayling JE. (1993) The mechanism of cofactor regeneration during phenylalanine hydroxylation. Adv. Exp. Med. Biol. 338, 47-54.
  4. Barranger, J.A. (1976) The implications of multiple forms of phenylalanine hydroxylase in phenylketonuria and related diseases of phenylalanine metabolism. Biochem. Med. 15, 55-86.
  5. Bender, D.A. (1983) Biochemistry of tryptophan in health and disease. Mol. Aspects Med. 6, 101-197.
  6. Boadle­Biber, M.C. (1993) Regulation of serotonin synthesis. Prog. Biophys. Mol. Biol. 60, 1-15.
  7. Burgmayer, S.J.N. (1998) Electron transfer in transition metal-pteridine systems. Structure and Bonding 92, 67-119.
  8. Carlsson, A. (1974) Measurements of monoamine synthesis and turnover with special reference to 5­hydroxytryptamine. Adv. Biochem. Psychopharmacol. 10, 75-81.
  9. Cotton, R.G.H. (1990) Heterogeneity of phenylketonuria at the clinical, protein and DNA levels. J. Inherit. Metab. Dis. 13, 739-750.
  10. DiLella, A.G. and Woo, S.L.C. (1987) Molecular basis of phenylketonuria and its clinical applications. Mol. Biol. Med. 4, 183-192.
  11. Eisensmith, R.C. and Woo, S.L.C. (1991) Phenylketonuria and the phenylalanine hydroxylase gene. Mol. Biol. Med. 8, 3-18.
  12. Eisensmith, R.C. and Woo, S.L.C. (1992) Molecular basis of phenylketonuria and related hyperphenylalaninemias: Mutations and polymorphisms in the human phenylalanine hydroxylase gene. Hum. Mutat. 1, 13-23.
  13. Eisensmith, R.C. and Woo, S.L.C. (1995) Molecular genetics of phenylketonuria: from molecular anthropology to gene therapy. Adv. Genet. 32, 199-271.
  14. Erlandsen, H., Fusetti, F., Martínez, A., Hough, E., Flatmark, T. and Stevens, R.C. (1997) Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria. Nature Struct. Biol. 4, 995-1000.
  15. Fuller, R.W. and Steinberg, M. (1976) Regulation of enzymes that synthesize neurotransmitter monoamines. Adv. Enzyme Regul. 14, 347-390.
  16. Goldstein, D.S. (1998) Novel catecholaminergic systems. Overview. Adv. Pharmacol. 42, 819-824.
  17. Harayama, S., Kok, M. and Neidle, E.L. (1992) Functional and evolutionary relationships among diverse oxygenases. Annu. Rev. Microbiol. 46, 565-601.
  18. Hufton, S.E., Jennings, I.G. and Cotton, R.G.H. (1995) Structure and function of the aromatic amino acid hydroxylases. Biochem. J. 311, 353-366.
  19. Ichiyama, A., Hasegawa, H., Tohyama, C., Dohmoto, C. and Kataoka, T. (1976) Some properties of bovine pineal tryptophan hydroxylase. Adv. Exp. Med. Biol. 74, 103-117.
  20. Icard­Liepkalns, C., Berrard, S., Faucon Biguet, N., Lebourdelles, B., Ravassard, P., Robert, J.J. and Mallet, J. (1993) Tyrosine hydroxylase regulation in neurotransmission and neuroplasticity. J. Physiol. (Paris) 87, 153-157.
  21. Jaruzelska, J. and Slomski, R. (1990) Molekularne podloze fenyloketonurii. [Molecular basis of phenylketonuria] Postepy Biochem. 36, 24-31.
  22. Kaufman, S. (1971) The phenylalanine hydroxylating system from mammalian liver. Adv. Enzymol. Relat. Areas Mol. Biol. 35, 245-319.
  23. Kaufman, S. (1983) Phenylketonuria and its variants. Adv. Hum. Genet. 13, 217-297.
  24. Kaufman, S. (1986) Regulation of the activity of hepatic phenylalanine hydroxylase. Adv. Enzyme Regul. 25, 37-64.
  25. Kaufman, S. (1987) Enzymology of the phenylalanine­hydroxylating system. Enzyme 38, 286-295.
  26. Kaufman, S. (1992a) Novel aspects of metabolism and function of tetrahydrobiopterin. J. Nutr. Sci. Vitaminol. (Tokyo) Spec No., 492-496.
  27. Kaufman, S. (1992b) Biopterin­responsive hyperphenylalaninemia. J. Nutr. Sci. Vitaminol. (Tokyo) Spec No., 601-606.
  28. Kaufman, S. (1993) The phenylalanine hydroxylating system. Adv. Enzymol. Relat. Areas Mol. Biol. 67, 77-264.
  29. Kaufman, S. (1995) Tyrosine hydroxylase. Adv. Enzymol. Relat. Areas Mol. Biol. 70, 103-220.
  30. Konecki, D.S. and Lichter­Konecki, U. (1991) The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations. Hum. Genet. 87, 377-388.
  31. Kumer, S.C. and Vrana, K.E. (1996) Intricate regulation of tyrosine hydroxylase activity and gene expression. J. Neurochem. 67, 443-462.
  32. Leonard, B.E. (1997) The role of noradrenaline in depression: a review. J. Psychopharmacol. 11, S39-S47.
  33. Levy, H.L. (1987) Maternal phenylketonuria. Review with emphasis on pathogenesis. Enzyme 38, 312-320.
  34. Levy, H.L. (1989) Molecular genetics of phenylketonuria and its implications. Am. J. Hum. Genet. 45, 667-670.
  35. Lovenberg, W. and Victor, S.J. (1974a) Tryptophan hydroxylase of the central nervous system: Effect of intraventricular 5,6­ and 5,7­dihydroxytryptamine. Adv. Biochem. Psychopharmacol. 10, 93-101.
  36. Lovenberg, W. and Victor, S.J. (1974b) Regulation of tryptophan and tyrosine hydroxylase. Life Sci. 14, 2337-2353.
  37. Lutsenko, N.G. and Suvorov, N.N. (1982) Regulation of serotonin biosynthesis in the central nervous system. Usp. Sovrem. Biol. (Moscow) 94, 243-252.
  38. McGeer, P.L. and McGeer, E.G. (1973) Neurotransmitter synthetic enzymes. Prog. Neurobiol. 2, 69-117.
  39. Mallet, J. (1996) The TiPS/TINS lecture. Catecholamines: from gene regulation to neuropsychiatric disorders. Trends Pharmacol. Sci. 17, 129-135.
  40. Mallet, J., Meloni, R. and Laurent, C. (1994) Catecholamine metabolism and psychiatric or behavioral disorders. Curr. Opin. Genet. Dev. 4, 419-426.
  41. Mandell, A.J. (1978) Redundant mechanisms regulating brain tyrosine and tryptophan hydroxylases. Annu. Rev. Pharmacol. Toxicol. 18, 461-493.
  42. Mandell, A.J. and Knapp, S. (1982) Regulation of tryptophan hydroxylase: variational kinetics suggest a neuropharmacology of phase. Adv. Biochem. Psychopharmacol. 34, 1-15.
  43. Mandell, A.J., Knapp, S. and Hsu, L.L. (1974) Some factors in the regulation of central serotonergic synapses. Life Sci. 14, 1-17.
  44. Nagatsu, T. (1991) Application of high­performance liquid chromatography to the study of biogenic amine­related enzymes. J. Chromatogr. 566, 287-307.
  45. Nagatsu, T. (1995) Tyrosine hydroxylase: human isoforms, structure and regulation in physiology and pathology. Essays Biochem. 30, 15-35.
  46. Nagatsu, T. and Stjarne, L. (1998) Catecholamine synthesis and release. Overview. Adv. Pharmacol. 42, 1-14.
  47. Rey, F. and Rey, J. (1992) Catalogue des mutations du gene de la phenylalanine hydroxylase. [Catalog of mutations of the phenylalanine hydroxylase gene] Arch. Fr. Pediatr. 49, 63-65.
  48. Rey, F. Munnich, A., Lyonnet, S. and Rey, J. (1987) Classification et heterogeneite des hyperphenylalaninemies liees a un deficit en phenylalanine hydroxylase. [Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency] Arch. Fr. Pediatr. 44 Suppl. 1, 639-642.
  49. Roy, A., Rylander, G. and Sarchiapone, M. (1997a) Genetic studies of suicidal behavior. Psychiatr. Clin. North Am. 20, 595-611.
  50. Roy, A., Rylander, G. and Sarchiapone, M. (1997b) Genetics of suicides. Family studies and molecular genetics. Ann. N. Y. Acad. Sci. 836, 135-157.
  51. Scriver, C.R. and Clow, C.L. (1980a) Phenylketonuria: epitome of human biochemical genetics (part I). N. Engl. J. Med. 303, 1336-1342.
  52. Scriver, C.R. and Clow, C.L. (1980b) Phenylketonuria: epitome of human biochemical genetics (part II). N. Engl. J. Med. 303, 1394-1400.
  53. Scriver, C.R. and Clow, C.L. (1980c) Phenylketonuria and other phenylalanine hydroxylation mutants in man. Annu. Rev. Genet. 14, 179-202.
  54. Scriver, C.R., Kaufman, S. and Woo, S.L.C. (1988) Mendelian hyperphenylalaninemia. Annu. Rev. Genet. 22, 301-321.
  55. Scriver, C.R., Eisensmith, R.C., Woo, S.L.C. and Kaufman, S. (1994) The hyperphenylalaninemias of man and mouse. Annu. Rev. Genet. 28, 141-165.
  56. Scriver, C.R., Byck, S., Prevost, L. and Hoang, L. (1996) The phenylalanine hydroxylase locus: a marker for the history of phenylketonuria and human genetic diversity. PAH Mutation Analysis Consortium. Ciba Found. Symp. 197, 73-90.
  57. Singhal, R.L., Rastogi, R.B. and Hrdina, P.D. (1975) Brain biogenic amines and altered thyroid function. Life Sci. 17, 1617-1626.
  58. Tank, A.W., Piech, K.M., Osterhout, C.A., Sun, B. and Sterling, C. (1998) Regulation of tyrosine hydroxylase gene expression by transsynaptic mechanisms and cell-cell contact. Adv. Pharmacol. 42, 25-29.
  59. Vis, H.L., Elmer, C., Goyens, P. and Roumat, G. (1988) La phenylcetonurie: etat actuel de la question. [Phenylketonuria: current status of the problem] Bull. Mem. Acad. R. Med. Belg. 143, 231-247.
  60. Waters, P.J., Parniak, M.A., Nowacki, P. and Scriver, C.R. (1998) In vitro expression analysis of mutations in phenylalanine hydroxylase: Linking genotype to phenotype and structure to function. Hum. Mutat. 11, 4-17.
  61. Witkop, B. (1991) Retro­, intro­ and perspectives of trypto­fun. Adv. Exp. Med. Biol. 294, 3-13.
  62. Woo, S.L.C. (1989) Molecular basis and population genetics of phenylketonuria. Biochemistry 28, 1-7.
  63. Zigmond, R.E., Schwarzschild, M.A. and Rittenhouse, A.R. (1989) Acute regulation of tyrosine hydroxylase by nerve activity and by neurotransmitters via phosphorylation. Annu. Rev. Neurosci. 12, 415-461.
Bibliography on structural studies of aromatic amino acid hydroxylases