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Journal Abstract Search

208 related items for PubMed ID: 15146479

  • 41. Crystal structure of the Trypanosoma cruzi trypanothione reductase.mepacrine complex.
    Jacoby EM, Schlichting I, Lantwin CB, Kabsch W, Krauth-Siegel RL.
    Proteins; 1996 Jan; 24(1):73-80. PubMed ID: 8628734
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  • 42. Docking and molecular dynamics study on the inhibitory activity of coumarins on aldose reductase.
    Wang Z, Ling B, Zhang R, Liu Y.
    J Phys Chem B; 2008 Aug 14; 112(32):10033-40. PubMed ID: 18637681
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  • 43. High resolution crystal structures of human cytosolic thiolase (CT): a comparison of the active sites of human CT, bacterial thiolase, and bacterial KAS I.
    Kursula P, Sikkilä H, Fukao T, Kondo N, Wierenga RK.
    J Mol Biol; 2005 Mar 18; 347(1):189-201. PubMed ID: 15733928
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  • 45. Crystal structures of Escherichia coli gamma-glutamyltranspeptidase in complex with azaserine and acivicin: novel mechanistic implication for inhibition by glutamine antagonists.
    Wada K, Hiratake J, Irie M, Okada T, Yamada C, Kumagai H, Suzuki H, Fukuyama K.
    J Mol Biol; 2008 Jul 04; 380(2):361-72. PubMed ID: 18555071
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  • 46. Calf spleen purine-nucleoside phosphorylase: crystal structure of the binary complex with a potent multisubstrate analogue inhibitor.
    Luić M, Koellner G, Yokomatsu T, Shibuya S, Bzowska A.
    Acta Crystallogr D Biol Crystallogr; 2004 Aug 04; 60(Pt 8):1417-24. PubMed ID: 15272165
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  • 49. Studies on the inhibitor-binding site of porcine aldehyde reductase: crystal structure of the holoenzyme-inhibitor ternary complex.
    el-Kabbani O, Carper DA, McGowan MH, Devedjiev Y, Rees-Milton KJ, Flynn TG.
    Proteins; 1997 Oct 04; 29(2):186-92. PubMed ID: 9329083
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  • 51. Radiation damage reveals promising interaction position.
    Koch C, Heine A, Klebe G.
    J Synchrotron Radiat; 2011 Sep 04; 18(Pt 5):782-9. PubMed ID: 21862860
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  • 53. Crystal structure of calf spleen purine nucleoside phosphorylase with two full trimers in the asymmetric unit: important implications for the mechanism of catalysis.
    Bzowska A, Koellner G, Wielgus-Kutrowska B, Stroh A, Raszewski G, Holý A, Steiner T, Frank J.
    J Mol Biol; 2004 Sep 17; 342(3):1015-32. PubMed ID: 15342253
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  • 54. Tyrosine-48 is the proton donor and histidine-110 directs substrate stereochemical selectivity in the reduction reaction of human aldose reductase: enzyme kinetics and crystal structure of the Y48H mutant enzyme.
    Bohren KM, Grimshaw CE, Lai CJ, Harrison DH, Ringe D, Petsko GA, Gabbay KH.
    Biochemistry; 1994 Mar 01; 33(8):2021-32. PubMed ID: 8117659
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  • 56. Structure-based optimization of aldose reductase inhibitors originating from virtual screening.
    Eisenmann M, Steuber H, Zentgraf M, Altenkämper M, Ortmann R, Perruchon J, Klebe G, Schlitzer M.
    ChemMedChem; 2009 May 01; 4(5):809-19. PubMed ID: 19301313
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  • 59. Xylose isomerase in substrate and inhibitor michaelis states: atomic resolution studies of a metal-mediated hydride shift.
    Fenn TD, Ringe D, Petsko GA.
    Biochemistry; 2004 Jun 01; 43(21):6464-74. PubMed ID: 15157080
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