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Journal Abstract Search


350 related items for PubMed ID: 7756296

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Nuclear Resonance Vibrational Spectroscopy Definition of Peroxy Intermediates in Catechol Dioxygenases: Factors that Determine Extra- versus Intradiol Cleavage.
    Babicz JT, Rogers MS, DeWeese DE, Sutherlin KD, Banerjee R, Böttger LH, Yoda Y, Nagasawa N, Saito M, Kitao S, Kurokuzu M, Kobayashi Y, Tamasaku K, Seto M, Lipscomb JD, Solomon EI.
    J Am Chem Soc; 2023 Jul 19; 145(28):15230-15250. PubMed ID: 37414058
    [Abstract] [Full Text] [Related]

  • 23. Iron(III) complexes of tridentate 3N ligands as functional models for catechol dioxygenases: the role of ligand N-alkyl substitution and solvent on reaction rate and product selectivity.
    Visvaganesan K, Mayilmurugan R, Suresh E, Palaniandavar M.
    Inorg Chem; 2007 Nov 26; 46(24):10294-306. PubMed ID: 17958355
    [Abstract] [Full Text] [Related]

  • 24. Synthesis, structure, spectra and reactivity of iron(III) complexes of imidazole and pyrazole containing ligands as functional models for catechol dioxygenases.
    Dhanalakshmi T, Suresh E, Palaniandavar M.
    Dalton Trans; 2009 Oct 21; (39):8317-28. PubMed ID: 19789784
    [Abstract] [Full Text] [Related]

  • 25. Binding of 17O-labeled substrate and inhibitors to protocatechuate 4,5-dioxygenase-nitrosyl complex. Evidence for direct substrate binding to the active site Fe2+ of extradiol dioxygenases.
    Arciero DM, Lipscomb JD.
    J Biol Chem; 1986 Feb 15; 261(5):2170-8. PubMed ID: 3003098
    [Abstract] [Full Text] [Related]

  • 26. Extradiol oxidative cleavage of catechols by ferrous and ferric complexes of 1,4,7-triazacyclononane: insight into the mechanism of the extradiol catechol dioxygenases.
    Lin G, Reid G, Bugg TD.
    J Am Chem Soc; 2001 May 30; 123(21):5030-9. PubMed ID: 11457331
    [Abstract] [Full Text] [Related]

  • 27. Unravelling the Molecular Origin of the Regiospecificity in Extradiol Catechol Dioxygenases.
    Christian GJ, Neese F, Ye S.
    Inorg Chem; 2016 Apr 18; 55(8):3853-64. PubMed ID: 27050565
    [Abstract] [Full Text] [Related]

  • 28. Iron(III) complexes of N2O and N3O donor ligands as functional models for catechol dioxygenase enzymes: ether oxygen coordination tunes the regioselectivity and reactivity.
    Sundaravel K, Suresh E, Saminathan K, Palaniandavar M.
    Dalton Trans; 2011 Aug 28; 40(32):8092-107. PubMed ID: 21766098
    [Abstract] [Full Text] [Related]

  • 29. Novel square pyramidal iron(III) complexes of linear tetradentate bis(phenolate) ligands as structural and reactive models for intradiol-cleaving 3,4-PCD enzymes: Quinone formation vs. intradiol cleavage.
    Mayilmurugan R, Sankaralingam M, Suresh E, Palaniandavar M.
    Dalton Trans; 2010 Oct 28; 39(40):9611-25. PubMed ID: 20835480
    [Abstract] [Full Text] [Related]

  • 30. Aliphatic C-C Bond Cleavage of α-Hydroxy Ketones by Non-Heme Iron(II) Complexes: Mechanistic Insight into the Reaction Catalyzed by 2,4'-Dihydroxyacetophenone Dioxygenase.
    Rahaman R, Paria S, Paine TK.
    Inorg Chem; 2015 Nov 16; 54(22):10576-86. PubMed ID: 26536067
    [Abstract] [Full Text] [Related]

  • 31. Crystal structures of the reaction intermediate and its homologue of an extradiol-cleaving catecholic dioxygenase.
    Sato N, Uragami Y, Nishizaki T, Takahashi Y, Sazaki G, Sugimoto K, Nonaka T, Masai E, Fukuda M, Senda T.
    J Mol Biol; 2002 Aug 23; 321(4):621-36. PubMed ID: 12206778
    [Abstract] [Full Text] [Related]

  • 32. Substrate binding to NO-ferro-naphthalene 1,2-dioxygenase studied by high-resolution Q-band pulsed 2H-ENDOR spectroscopy.
    Yang TC, Wolfe MD, Neibergall MB, Mekmouche Y, Lipscomb JD, Hoffman BM.
    J Am Chem Soc; 2003 Jun 11; 125(23):7056-66. PubMed ID: 12783560
    [Abstract] [Full Text] [Related]

  • 33. The 1.8 A crystal structure of catechol 1,2-dioxygenase reveals a novel hydrophobic helical zipper as a subunit linker.
    Vetting MW, Ohlendorf DH.
    Structure; 2000 Apr 15; 8(4):429-40. PubMed ID: 10801478
    [Abstract] [Full Text] [Related]

  • 34. A novel tripodal ligand containing three different N-heterocyclic donor functions and its application in catechol dioxygenase mimicking.
    Wagner M, Limberg C, Tietz T.
    Chemistry; 2009 Apr 15; 15(22):5567-76. PubMed ID: 19360824
    [Abstract] [Full Text] [Related]

  • 35. Reactions of 3-ethylcatechol and 3-(methylthio)catechol with catechol dioxygenases.
    Pascal RA, Huang DS.
    Arch Biochem Biophys; 1986 Jul 15; 248(1):130-7. PubMed ID: 3015028
    [Abstract] [Full Text] [Related]

  • 36. Spectroscopic studies of the effect of ligand donor strength on the Fe-NO bond intradiol dioxygenases.
    Wasinger EC, Davis MI, Pau MY, Orville AM, Zaleski JM, Hedman B, Lipscomb JD, Hodgson KO, Solomon EI.
    Inorg Chem; 2003 Jan 27; 42(2):365-76. PubMed ID: 12693216
    [Abstract] [Full Text] [Related]

  • 37. Quantitative structure-activity relationship for the cleavage of C3/C4-substituted catechols by a prototypal extradiol catechol dioxygenase with broad substrate specificity.
    Ishida T, Tanaka H, Horiike K.
    J Biochem; 2004 Jun 27; 135(6):721-30. PubMed ID: 15213248
    [Abstract] [Full Text] [Related]

  • 38. Isolation and partial characterization of an extradiol non-haem iron dioxygenase which preferentially cleaves 3-methylcatechol.
    Wallis MG, Chapman SK.
    Biochem J; 1990 Mar 01; 266(2):605-9. PubMed ID: 2317207
    [Abstract] [Full Text] [Related]

  • 39. Dioxygen reactivity of biomimetic Fe(II) complexes with noninnocent catecholate, o-aminophenolate, and o-phenylenediamine ligands.
    Bittner MM, Lindeman SV, Popescu CV, Fiedler AT.
    Inorg Chem; 2014 Apr 21; 53(8):4047-61. PubMed ID: 24697567
    [Abstract] [Full Text] [Related]

  • 40. Iron(III) complexes of tripodal tetradentate 4N ligands as functional models for catechol dioxygenases: the electronic vs. steric effect on extradiol cleavage.
    Balamurugan M, Vadivelu P, Palaniandavar M.
    Dalton Trans; 2014 Oct 21; 43(39):14653-68. PubMed ID: 25143993
    [Abstract] [Full Text] [Related]


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