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Journal Abstract Search

259 related items for PubMed ID: 11471246

  • 21.
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  • 22. 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
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  • 26. Evolution of bacterial RNA polymerase: implications for large-scale bacterial phylogeny, domain accretion, and horizontal gene transfer.
    Iyer LM, Koonin EV, Aravind L.
    Gene; 2004 Jun 23; 335():73-88. PubMed ID: 15194191
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  • 28. Prediction of a common beta-propeller catalytic domain for fructosyltransferases of different origin and substrate specificity.
    Pons T, Hernández L, Batista FR, Chinea G.
    Protein Sci; 2000 Nov 23; 9(11):2285-91. PubMed ID: 11305239
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  • 29. Nickel trafficking: insights into the fold and function of UreE, a urease metallochaperone.
    Musiani F, Zambelli B, Stola M, Ciurli S.
    J Inorg Biochem; 2004 May 23; 98(5):803-13. PubMed ID: 15134926
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  • 30. The Zn2 position in metallo-beta-lactamases is critical for activity: a study on chimeric metal sites on a conserved protein scaffold.
    González JM, Medrano Martín FJ, Costello AL, Tierney DL, Vila AJ.
    J Mol Biol; 2007 Nov 09; 373(5):1141-56. PubMed ID: 17915249
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  • 31. Structural aspects for evolution of beta-lactamases from penicillin-binding proteins.
    Meroueh SO, Minasov G, Lee W, Shoichet BK, Mobashery S.
    J Am Chem Soc; 2003 Aug 13; 125(32):9612-8. PubMed ID: 12904027
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  • 34. Connectivity between catalytic landscapes of the metallo-β-lactamase superfamily.
    Baier F, Tokuriki N.
    J Mol Biol; 2014 Jun 26; 426(13):2442-56. PubMed ID: 24769192
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  • 35. Molecular architecture of the Mn2+-dependent lactonase UlaG reveals an RNase-like metallo-beta-lactamase fold and a novel quaternary structure.
    Garces F, Fernández FJ, Montellà C, Penya-Soler E, Prohens R, Aguilar J, Baldomà L, Coll M, Badia J, Vega MC.
    J Mol Biol; 2010 May 21; 398(5):715-29. PubMed ID: 20359483
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  • 36. Structure-based phylogeny of the metallo-beta-lactamases.
    Garau G, Di Guilmi AM, Hall BG.
    Antimicrob Agents Chemother; 2005 Jul 21; 49(7):2778-84. PubMed ID: 15980349
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  • 38. Prediction of coenzyme specificity in dehydrogenases/reductases. A hidden Markov model-based method and its application on complete genomes.
    Kallberg Y, Persson B.
    FEBS J; 2006 Mar 21; 273(6):1177-84. PubMed ID: 16519683
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  • 39. Positively cooperative binding of zinc ions to Bacillus cereus 569/H/9 beta-lactamase II suggests that the binuclear enzyme is the only relevant form for catalysis.
    Jacquin O, Balbeur D, Damblon C, Marchot P, De Pauw E, Roberts GC, Frère JM, Matagne A.
    J Mol Biol; 2009 Oct 09; 392(5):1278-91. PubMed ID: 19665032
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  • 40. Crystal structure of TTHA0252 from Thermus thermophilus HB8, a RNA degradation protein of the metallo-beta-lactamase superfamily.
    Ishikawa H, Nakagawa N, Kuramitsu S, Masui R.
    J Biochem; 2006 Oct 09; 140(4):535-42. PubMed ID: 16945939
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