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166 related items for PubMed ID: 18547057

  • 1. Insights into the mechanism of oxidative deamination catalyzed by DOPA decarboxylase.
    Bertoldi M, Cellini B, Montioli R, Borri Voltattorni C.
    Biochemistry; 2008 Jul 08; 47(27):7187-95. PubMed ID: 18547057
    [Abstract] [Full Text] [Related]

  • 2. A quinonoid is an intermediate of oxidative deamination reaction catalyzed by Dopa decarboxylase.
    Bertoldi M, Cellini B, Maras B, Voltattorni CB.
    FEBS Lett; 2005 Sep 26; 579(23):5175-80. PubMed ID: 16150447
    [Abstract] [Full Text] [Related]

  • 3. Reaction of dopa decarboxylase with L-aromatic amino acids under aerobic and anaerobic conditions.
    Bertoldi M, Borri Voltattorni C.
    Biochem J; 2000 Dec 01; 352 Pt 2(Pt 2):533-8. PubMed ID: 11085948
    [Abstract] [Full Text] [Related]

  • 4. Multiple roles of the active site lysine of Dopa decarboxylase.
    Bertoldi M, Voltattorni CB.
    Arch Biochem Biophys; 2009 Aug 15; 488(2):130-9. PubMed ID: 19580779
    [Abstract] [Full Text] [Related]

  • 5. Reaction of dopa decarboxylase with alpha-methyldopa leads to an oxidative deamination producing 3,4-dihydroxyphenylacetone, an active site directed affinity label.
    Bertoldi M, Dominici P, Moore PS, Maras B, Voltattorni CB.
    Biochemistry; 1998 May 05; 37(18):6552-61. PubMed ID: 9572873
    [Abstract] [Full Text] [Related]

  • 6. Dopa decarboxylase exhibits low pH half-transaminase and high pH oxidative deaminase activities toward serotonin (5-hydroxytryptamine).
    Bertoldi M, Voltattorni CB.
    Protein Sci; 2001 Jun 05; 10(6):1178-86. PubMed ID: 11369856
    [Abstract] [Full Text] [Related]

  • 7. Mutation of tyrosine 332 to phenylalanine converts dopa decarboxylase into a decarboxylation-dependent oxidative deaminase.
    Bertoldi M, Gonsalvi M, Contestabile R, Voltattorni CB.
    J Biol Chem; 2002 Sep 27; 277(39):36357-62. PubMed ID: 12118007
    [Abstract] [Full Text] [Related]

  • 8. Mammalian Dopa decarboxylase: structure, catalytic activity and inhibition.
    Bertoldi M.
    Arch Biochem Biophys; 2014 Mar 15; 546():1-7. PubMed ID: 24407024
    [Abstract] [Full Text] [Related]

  • 9. Mutation of residues in the coenzyme binding pocket of Dopa decarboxylase. Effects on catalytic properties.
    Bertoldi M, Castellani S, Bori Voltattorni C.
    Eur J Biochem; 2001 May 15; 268(10):2975-81. PubMed ID: 11358515
    [Abstract] [Full Text] [Related]

  • 10. Reaction and substrate specificity of recombinant pig kidney Dopa decarboxylase under aerobic and anaerobic conditions.
    Bertoldi M, Borri Voltattorni C.
    Biochim Biophys Acta; 2003 Apr 11; 1647(1-2):42-7. PubMed ID: 12686106
    [Abstract] [Full Text] [Related]

  • 11. Kinetic and structural studies on the catalytic role of the aspartic acid residue conserved in copper amine oxidase.
    Chiu YC, Okajima T, Murakawa T, Uchida M, Taki M, Hirota S, Kim M, Yamaguchi H, Kawano Y, Kamiya N, Kuroda S, Hayashi H, Yamamoto Y, Tanizawa K.
    Biochemistry; 2006 Apr 04; 45(13):4105-20. PubMed ID: 16566584
    [Abstract] [Full Text] [Related]

  • 12. Reaction specificity of native and nicked 3,4-dihydroxyphenylalanine decarboxylase.
    Bertoldi M, Frigeri P, Paci M, Voltattorni CB.
    J Biol Chem; 1999 Feb 26; 274(9):5514-21. PubMed ID: 10026165
    [Abstract] [Full Text] [Related]

  • 13. Behavior of fluorinated analogs of L-(3,4-dihydroxyphenyl)alanine and L-threo-(3,4-dihydroxyphenyl)serine as substrates for Dopa decarboxylase.
    Borri Voltattorni C, Bertoldi M, Bianconi S, Deng WP, Wong K, Kim I, Herbert B, Kirk KL.
    Biochem Biophys Res Commun; 2002 Jul 05; 295(1):107-11. PubMed ID: 12083775
    [Abstract] [Full Text] [Related]

  • 14. Theoretical studies on the pyridoxal-5'-phosphate dependent enzyme dopa decarboxylase: effect of thr 246 residue on the co-factor-enzyme binding and reaction mechanism.
    Chakrabarty K, Gupta SN, Das GK, Roy S.
    Indian J Biochem Biophys; 2012 Jun 05; 49(3):155-64. PubMed ID: 22803330
    [Abstract] [Full Text] [Related]

  • 15. Ornithine and glutamate decarboxylases catalyse an oxidative deamination of their alpha-methyl substrates.
    Bertoldi M, Carbone V, Borri Voltattorni C.
    Biochem J; 1999 Sep 15; 342 Pt 3(Pt 3):509-12. PubMed ID: 10477260
    [Abstract] [Full Text] [Related]

  • 16. Biochemical identification of residues that discriminate between 3,4-dihydroxyphenylalanine decarboxylase and 3,4-dihydroxyphenylacetaldehyde synthase-mediated reactions.
    Liang J, Han Q, Ding H, Li J.
    Insect Biochem Mol Biol; 2017 Dec 15; 91():34-43. PubMed ID: 29037755
    [Abstract] [Full Text] [Related]

  • 17. Oxygen reactivity with pyridoxal 5'-phosphate enzymes: biochemical implications and functional relevance.
    Bisello G, Longo C, Rossignoli G, Phillips RS, Bertoldi M.
    Amino Acids; 2020 Aug 15; 52(8):1089-1105. PubMed ID: 32844248
    [Abstract] [Full Text] [Related]

  • 18. Ruthenium-catalyzed oxidative cyanation of tertiary amines with molecular oxygen or hydrogen peroxide and sodium cyanide: sp3 C-H bond activation and carbon-carbon bond formation.
    Murahashi S, Nakae T, Terai H, Komiya N.
    J Am Chem Soc; 2008 Aug 20; 130(33):11005-12. PubMed ID: 18646852
    [Abstract] [Full Text] [Related]

  • 19. The oxidative deamination of L-aminoethylcysteine sulfoxide and sulfone by snake venom L-amino acid oxidase.
    Solinas SP, Montefoschi G, Antonucci A, Cavallini D.
    Physiol Chem Phys Med NMR; 1993 Aug 20; 25(4):281-5. PubMed ID: 8153153
    [Abstract] [Full Text] [Related]

  • 20. Acid-base chemistry of the reaction of aromatic L-amino acid decarboxylase and dopa analyzed by transient and steady-state kinetics: preferential binding of the substrate with its amino group unprotonated.
    Hayashi H, Tsukiyama F, Ishii S, Mizuguchi H, Kagamiyama H.
    Biochemistry; 1999 Nov 23; 38(47):15615-22. PubMed ID: 10569946
    [Abstract] [Full Text] [Related]

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