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176 related items for PubMed ID: 18782082

  • 1. Arabidopsis thaliana GLX2-1 contains a dinuclear metal binding site, but is not a glyoxalase 2.
    Limphong P, Crowder MW, Bennett B, Makaroff CA.
    Biochem J; 2009 Jan 01; 417(1):323-30. PubMed ID: 18782082
    [Abstract] [Full Text] [Related]

  • 2. Structural studies on a mitochondrial glyoxalase II.
    Marasinghe GP, Sander IM, Bennett B, Periyannan G, Yang KW, Makaroff CA, Crowder MW.
    J Biol Chem; 2005 Dec 09; 280(49):40668-75. PubMed ID: 16227621
    [Abstract] [Full Text] [Related]

  • 3. The binding of iron and zinc to glyoxalase II occurs exclusively as di-metal centers and is unique within the metallo-beta-lactamase family.
    Wenzel NF, Carenbauer AL, Pfiester MP, Schilling O, Meyer-Klaucke W, Makaroff CA, Crowder MW.
    J Biol Inorg Chem; 2004 Jun 09; 9(4):429-38. PubMed ID: 15067523
    [Abstract] [Full Text] [Related]

  • 4. Converting GLX2-1 into an active glyoxalase II.
    Limphong P, Adams NE, Rouhier MF, McKinney RM, Naylor M, Bennett B, Makaroff CA, Crowder MW.
    Biochemistry; 2010 Sep 21; 49(37):8228-36. PubMed ID: 20715794
    [Abstract] [Full Text] [Related]

  • 5. Human glyoxalase II contains an Fe(II)Zn(II) center but is active as a mononuclear Zn(II) enzyme.
    Limphong P, McKinney RM, Adams NE, Bennett B, Makaroff CA, Gunasekera T, Crowder MW.
    Biochemistry; 2009 Jun 16; 48(23):5426-34. PubMed ID: 19413286
    [Abstract] [Full Text] [Related]

  • 6. Flexible metal binding of the metallo-beta-lactamase domain: glyoxalase II incorporates iron, manganese, and zinc in vivo.
    Schilling O, Wenzel N, Naylor M, Vogel A, Crowder M, Makaroff C, Meyer-Klaucke W.
    Biochemistry; 2003 Oct 14; 42(40):11777-86. PubMed ID: 14529289
    [Abstract] [Full Text] [Related]

  • 7. Arabidopsis thaliana mitochondrial glyoxalase 2-1 exhibits beta-lactamase activity.
    Limphong P, Nimako G, Thomas PW, Fast W, Makaroff CA, Crowder MW.
    Biochemistry; 2009 Sep 15; 48(36):8491-3. PubMed ID: 19735113
    [Abstract] [Full Text] [Related]

  • 8. The metal ion requirements of Arabidopsis thaliana Glx2-2 for catalytic activity.
    Limphong P, McKinney RM, Adams NE, Makaroff CA, Bennett B, Crowder MW.
    J Biol Inorg Chem; 2010 Feb 15; 15(2):249-58. PubMed ID: 19834746
    [Abstract] [Full Text] [Related]

  • 9. Structural and functional characterization of Salmonella enterica serovar Typhimurium YcbL: an unusual Type II glyoxalase.
    Stamp AL, Owen P, El Omari K, Nichols CE, Lockyer M, Lamb HK, Charles IG, Hawkins AR, Stammers DK.
    Protein Sci; 2010 Oct 15; 19(10):1897-905. PubMed ID: 20669241
    [Abstract] [Full Text] [Related]

  • 10. Biochemical and structural characterization of Salmonella typhimurium glyoxalase II: new insights into metal ion selectivity.
    Campos-Bermudez VA, Leite NR, Krog R, Costa-Filho AJ, Soncini FC, Oliva G, Vila AJ.
    Biochemistry; 2007 Oct 02; 46(39):11069-79. PubMed ID: 17764159
    [Abstract] [Full Text] [Related]

  • 11. Glyoxalase II from A. thaliana requires Zn(II) for catalytic activity.
    Crowder MW, Maiti MK, Banovic L, Makaroff CA.
    FEBS Lett; 1997 Dec 01; 418(3):351-4. PubMed ID: 9428743
    [Abstract] [Full Text] [Related]

  • 12. Spectroscopic studies on Arabidopsis ETHE1, a glyoxalase II-like protein.
    Holdorf MM, Bennett B, Crowder MW, Makaroff CA.
    J Inorg Biochem; 2008 Sep 01; 102(9):1825-30. PubMed ID: 18656261
    [Abstract] [Full Text] [Related]

  • 13. Metal content of metallo-beta-lactamase L1 is determined by the bioavailability of metal ions.
    Hu Z, Gunasekera TS, Spadafora L, Bennett B, Crowder MW.
    Biochemistry; 2008 Jul 29; 47(30):7947-53. PubMed ID: 18597493
    [Abstract] [Full Text] [Related]

  • 14. Arabidopsis thaliana glyoxalase 2-1 is required during abiotic stress but is not essential under normal plant growth.
    Devanathan S, Erban A, Perez-Torres R, Kopka J, Makaroff CA.
    PLoS One; 2014 Jul 29; 9(4):e95971. PubMed ID: 24760003
    [Abstract] [Full Text] [Related]

  • 15. Identification of putative zinc hydrolase genes of the metallo-beta-lactamase superfamily from Campylobacter jejuni.
    Alfredson DA, Korolik V.
    FEMS Immunol Med Microbiol; 2007 Feb 29; 49(1):159-64. PubMed ID: 17266723
    [Abstract] [Full Text] [Related]

  • 16. Identification of metal binding residues for the binuclear zinc phosphodiesterase reveals identical coordination as glyoxalase II.
    Vogel A, Schilling O, Meyer-Klaucke W.
    Biochemistry; 2004 Aug 17; 43(32):10379-86. PubMed ID: 15301536
    [Abstract] [Full Text] [Related]

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  • 18. Characterization of the metal-binding sites of the beta-lactamase from Bacteroides fragilis.
    Crowder MW, Wang Z, Franklin SL, Zovinka EP, Benkovic SJ.
    Biochemistry; 1996 Sep 17; 35(37):12126-32. PubMed ID: 8810919
    [Abstract] [Full Text] [Related]

  • 19. Explaining the inhibition of glyoxalase II by 9-fluorenylmethoxycarbonyl-protected glutathione derivatives.
    Yang KW, Sobieski DN, Carenbauer AL, Crawford PA, Makaroff CA, Crowder MW.
    Arch Biochem Biophys; 2003 Jun 15; 414(2):271-8. PubMed ID: 12781779
    [Abstract] [Full Text] [Related]

  • 20. Promiscuous metallo-β-lactamases: MIM-1 and MIM-2 may play an essential role in quorum sensing networks.
    Miraula M, Schenk G, Mitić N.
    J Inorg Biochem; 2016 Sep 15; 162():366-375. PubMed ID: 26775612
    [Abstract] [Full Text] [Related]

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