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Journal Abstract Search


469 related items for PubMed ID: 9761692

  • 1. Crystal structure of carbonic anhydrase from Neisseria gonorrhoeae and its complex with the inhibitor acetazolamide.
    Huang S, Xue Y, Sauer-Eriksson E, Chirica L, Lindskog S, Jonsson BH.
    J Mol Biol; 1998; 283(1):301-10. PubMed ID: 9761692
    [Abstract] [Full Text] [Related]

  • 2. Crystal structure of human carbonic anhydrase XIII and its complex with the inhibitor acetazolamide.
    Di Fiore A, Monti SM, Hilvo M, Parkkila S, Romano V, Scaloni A, Pedone C, Scozzafava A, Supuran CT, De Simone G.
    Proteins; 2009 Jan; 74(1):164-75. PubMed ID: 18618712
    [Abstract] [Full Text] [Related]

  • 3. Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II "selective" inhibitor celecoxib.
    Di Fiore A, Pedone C, D'Ambrosio K, Scozzafava A, De Simone G, Supuran CT.
    Bioorg Med Chem Lett; 2006 Jan 15; 16(2):437-42. PubMed ID: 16290146
    [Abstract] [Full Text] [Related]

  • 4. Drug-protein interactions. Refined structures of three sulfonamide drug complexes of human carbonic anhydrase I enzyme.
    Chakravarty S, Kannan KK.
    J Mol Biol; 1994 Oct 21; 243(2):298-309. PubMed ID: 7932756
    [Abstract] [Full Text] [Related]

  • 5. Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with a topically acting antiglaucoma sulfonamide.
    Abbate F, Casini A, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2004 May 03; 14(9):2357-61. PubMed ID: 15081040
    [Abstract] [Full Text] [Related]

  • 6. Crystallographic studies of inhibitor binding sites in human carbonic anhydrase II: a pentacoordinated binding of the SCN- ion to the zinc at high pH.
    Eriksson AE, Kylsten PM, Jones TA, Liljas A.
    Proteins; 1988 May 03; 4(4):283-93. PubMed ID: 3151020
    [Abstract] [Full Text] [Related]

  • 7. Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of 5-amino-1,3,4-thiadiazole-2-sulfonamide and 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide to human isoform II.
    Menchise V, De Simone G, Di Fiore A, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2006 Dec 15; 16(24):6204-8. PubMed ID: 17000110
    [Abstract] [Full Text] [Related]

  • 8. Carbonic anhydrase activators: X-ray crystal structure of the adduct of human isozyme II with L-histidine as a platform for the design of stronger activators.
    Temperini C, Scozzafava A, Puccetti L, Supuran CT.
    Bioorg Med Chem Lett; 2005 Dec 01; 15(23):5136-41. PubMed ID: 16214338
    [Abstract] [Full Text] [Related]

  • 9. Refined structure of bovine carbonic anhydrase III at 2.0 A resolution.
    Eriksson AE, Liljas A.
    Proteins; 1993 May 01; 16(1):29-42. PubMed ID: 8497481
    [Abstract] [Full Text] [Related]

  • 10. Crystal structure of the complex between human carbonic anhydrase II and the aromatic inhibitor 1,2,4-triazole.
    Mangani S, Liljas A.
    J Mol Biol; 1993 Jul 05; 232(1):9-14. PubMed ID: 8331673
    [Abstract] [Full Text] [Related]

  • 11. Carbonic anhydrase inhibitors. Zonisamide is an effective inhibitor of the cytosolic isozyme II and mitochondrial isozyme V: solution and X-ray crystallographic studies.
    De Simone G, Di Fiore A, Menchise V, Pedone C, Antel J, Casini A, Scozzafava A, Wurl M, Supuran CT.
    Bioorg Med Chem Lett; 2005 May 02; 15(9):2315-20. PubMed ID: 15837316
    [Abstract] [Full Text] [Related]

  • 12. Carbonic anhydrase activators. Activation of isozymes I, II, IV, VA, VII, and XIV with l- and d-histidine and crystallographic analysis of their adducts with isoform II: engineering proton-transfer processes within the active site of an enzyme.
    Temperini C, Scozzafava A, Vullo D, Supuran CT.
    Chemistry; 2006 Sep 18; 12(27):7057-66. PubMed ID: 16807956
    [Abstract] [Full Text] [Related]

  • 13. Reversal of the hydrogen bond to zinc ligand histidine-119 dramatically diminishes catalysis and enhances metal equilibration kinetics in carbonic anhydrase II.
    Huang CC, Lesburg CA, Kiefer LL, Fierke CA, Christianson DW.
    Biochemistry; 1996 Mar 19; 35(11):3439-46. PubMed ID: 8639494
    [Abstract] [Full Text] [Related]

  • 14. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition.
    Weber A, Casini A, Heine A, Kuhn D, Supuran CT, Scozzafava A, Klebe G.
    J Med Chem; 2004 Jan 29; 47(3):550-7. PubMed ID: 14736236
    [Abstract] [Full Text] [Related]

  • 15. Homology modeling and receptor-based 3D-QSAR study of carbonic anhydrase IX.
    Tuccinardi T, Ortore G, Rossello A, Supuran CT, Martinelli A.
    J Chem Inf Model; 2007 Jan 29; 47(6):2253-62. PubMed ID: 17949069
    [Abstract] [Full Text] [Related]

  • 16. Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms.
    Biswas S, Aggarwal M, Güzel Ö, Scozzafava A, McKenna R, Supuran CT.
    Bioorg Med Chem; 2011 Jun 15; 19(12):3732-8. PubMed ID: 21620713
    [Abstract] [Full Text] [Related]

  • 17. Crystal structure of the soluble domain of the major anaerobically induced outer membrane protein (AniA) from pathogenic Neisseria: a new class of copper-containing nitrite reductases.
    Boulanger MJ, Murphy ME.
    J Mol Biol; 2002 Feb 01; 315(5):1111-27. PubMed ID: 11827480
    [Abstract] [Full Text] [Related]

  • 18. Carbonic anhydrase inhibitors: the X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors.
    Temperini C, Winum JY, Montero JL, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2007 May 15; 17(10):2795-801. PubMed ID: 17346964
    [Abstract] [Full Text] [Related]

  • 19. Positions of His-64 and a bound water in human carbonic anhydrase II upon binding three structurally related inhibitors.
    Smith GM, Alexander RS, Christianson DW, McKeever BM, Ponticello GS, Springer JP, Randall WC, Baldwin JJ, Habecker CN.
    Protein Sci; 1994 Jan 15; 3(1):118-25. PubMed ID: 8142888
    [Abstract] [Full Text] [Related]

  • 20. Carbonic anhydrase inhibitors: inhibition of human, bacterial, and archaeal isozymes with benzene-1,3-disulfonamides--solution and crystallographic studies.
    Alterio V, De Simone G, Monti SM, Scozzafava A, Supuran CT.
    Bioorg Med Chem Lett; 2007 Aug 01; 17(15):4201-7. PubMed ID: 17540563
    [Abstract] [Full Text] [Related]


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