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Journal Abstract Search


181 related items for PubMed ID: 2043633

  • 1. Reaction of indole and analogues with amino acid complexes of Escherichia coli tryptophan indole-lyase: detection of a new reaction intermediate by rapid-scanning stopped-flow spectrophotometry.
    Phillips RS.
    Biochemistry; 1991 Jun 18; 30(24):5927-34. PubMed ID: 2043633
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  • 2. Effects of alpha-deuteration and of aza and thia analogs of L-tryptophan on formation of intermediates in the reaction of Escherichia coli tryptophan indole-lyase.
    Sloan MJ, Phillips RS.
    Biochemistry; 1996 Dec 17; 35(50):16165-73. PubMed ID: 8973188
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  • 3. Mechanism of binding of substrate analogues to tryptophan indole-lyase: studies using rapid-scanning and single-wavelength stopped-flow spectrophotometry.
    Phillips RS, Bender SL, Brzovic P, Dunn MF.
    Biochemistry; 1990 Sep 18; 29(37):8608-14. PubMed ID: 2271544
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  • 4. Effects of tyrosine ring fluorination on rates and equilibria of formation of intermediates in the reactions of carbon-carbon lyases.
    Phillips RS, Von Tersch RL, Secundo F.
    Eur J Biochem; 1997 Mar 01; 244(2):658-63. PubMed ID: 9119037
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  • 7. Crystals of tryptophan indole-lyase and tyrosine phenol-lyase form stable quinonoid complexes.
    Phillips RS, Demidkina TV, Zakomirdina LN, Bruno S, Ronda L, Mozzarelli A.
    J Biol Chem; 2002 Jun 14; 277(24):21592-7. PubMed ID: 11934889
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  • 11. Stereoelectronic control of bond formation in Escherichia coli tryptophan synthase: substrate specificity and enzymatic synthesis of the novel amino acid dihydroisotryptophan.
    Roy M, Keblawi S, Dunn MF.
    Biochemistry; 1988 Sep 06; 27(18):6698-704. PubMed ID: 3058204
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  • 12. Cleavage of Escherichia coli tryptophan indole-lyase by trypsin at Lys406 affects the transmission of conformational changes associated with monovalent cation activation.
    Phillips RS, Doshi KJ.
    Eur J Biochem; 1998 Jul 15; 255(2):508-15. PubMed ID: 9716394
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  • 13. Evidence of preorganization in quinonoid intermediate formation from L-Trp in H463F mutant Escherichia coli tryptophan indole-lyase from effects of pressure and pH.
    Phillips RS, Kalu U, Hay S.
    Biochemistry; 2012 Aug 21; 51(33):6527-33. PubMed ID: 22852771
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  • 14. Role of aspartate-133 and histidine-458 in the mechanism of tryptophan indole-lyase from Proteus vulgaris.
    Demidkina TV, Zakomirdina LN, Kulikova VV, Dementieva IS, Faleev NG, Ronda L, Mozzarelli A, Gollnick PD, Phillips RS.
    Biochemistry; 2003 Sep 30; 42(38):11161-9. PubMed ID: 14503866
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  • 15. Indole protects tryptophan indole-lyase, but not tryptophan synthase, from inactivation by trifluoroalanine.
    Phillips RS, Dua RK.
    Arch Biochem Biophys; 1992 Aug 01; 296(2):489-96. PubMed ID: 1632641
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  • 16. The crystal structure of Proteus vulgaris tryptophan indole-lyase complexed with oxindolyl-L-alanine: implications for the reaction mechanism.
    Phillips RS, Buisman AA, Choi S, Hussaini A, Wood ZA.
    Acta Crystallogr D Struct Biol; 2018 Aug 01; 74(Pt 8):748-759. PubMed ID: 30082510
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  • 17. Application of rapid-scanning, stopped-flow spectroscopy to the characterization of intermediates formed in the reactions of L- and D-tryptophan and beta-mercaptoethanol with Escherichia coli tryptophan synthase.
    Drewe WF, Koerber SC, Dunn MF.
    Biochimie; 1989 Apr 01; 71(4):509-19. PubMed ID: 2503056
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  • 18. [Interaction of tryptophanase with substrate analogs].
    Zakomyrdina LN, Sakharova IS, Torchinskiĭ IuM.
    Mol Biol (Mosk); 1988 Apr 01; 22(1):187-94. PubMed ID: 3287134
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  • 19. The reaction of indole with the aminoacrylate intermediate of Salmonella typhimurium tryptophan synthase: observation of a primary kinetic isotope effect with 3-[(2)H]indole.
    Cash MT, Miles EW, Phillips RS.
    Arch Biochem Biophys; 2004 Dec 15; 432(2):233-43. PubMed ID: 15542062
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  • 20. Binding of phenol and analogues to alanine complexes of tyrosine phenol-lyase from Citrobacter freundii: implications for the mechanisms of alpha,beta-elimination and alanine racemization.
    Chen H, Phillips RS.
    Biochemistry; 1993 Nov 02; 32(43):11591-9. PubMed ID: 8218227
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