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124 related items for PubMed ID: 8053906

  • 1. Interactions of plant acetohydroxy acid isomeroreductase with reaction intermediate analogues: correlation of the slow, competitive, inhibition kinetics of enzyme activity and herbicidal effects.
    Dumas R, Cornillon-Bertrand C, Guigue-Talet P, Genix P, Douce R, Job D.
    Biochem J; 1994 Aug 01; 301 ( Pt 3)(Pt 3):813-20. PubMed ID: 8053906
    [Abstract] [Full Text] [Related]

  • 2. Isolation and kinetic properties of acetohydroxy acid isomeroreductase from spinach (Spinacia oleracea) chloroplasts overexpressed in Escherichia coli.
    Dumas R, Job D, Ortholand JY, Emeric G, Greiner A, Douce R.
    Biochem J; 1992 Dec 15; 288 ( Pt 3)(Pt 3):865-74. PubMed ID: 1472001
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  • 4. Oxalyl hydroxamates as reaction-intermediate analogues for ketol-acid reductoisomerase.
    Aulabaugh A, Schloss JV.
    Biochemistry; 1990 Mar 20; 29(11):2824-30. PubMed ID: 2189496
    [Abstract] [Full Text] [Related]

  • 5. Characterization of the conformational changes of acetohydroxy acid isomeroreductase induced by the binding of Mg2+ ions, NADPH, and a competitive inhibitor.
    Halgand F, Dumas R, Biou V, Andrieu JP, Thomazeau K, Gagnon J, Douce R, Forest E.
    Biochemistry; 1999 May 11; 38(19):6025-34. PubMed ID: 10320328
    [Abstract] [Full Text] [Related]

  • 6. Crystallization and preliminary crystallographic data for acetohydroxy acid isomeroreductase from Spinacia oleracea.
    Dumas R, Job D, Douce R, Pebay-Peyroula E, Cohen-Addad C.
    J Mol Biol; 1994 Sep 30; 242(4):578-81. PubMed ID: 7932712
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  • 7. Stepwise building of a 115-kDa macromolecular edifice monitored by electrospray mass spectrometry. The case of acetohydroxy acid isomeroreductase.
    Laprévote O, Serani L, Das BC, Halgand F, Forest E, Dumas R.
    Eur J Biochem; 1999 Jan 30; 259(1-2):356-9. PubMed ID: 9914514
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  • 8. Kinetic and mass spectrometric analyses of the interactions between plant acetohydroxy acid isomeroreductase and thiadiazole derivatives.
    Halgand F, Vives F, Dumas R, Biou V, Andersen J, Andrieu JP, Cantegril R, Gagnon J, Douce R, Forest E, Job D.
    Biochemistry; 1998 Apr 07; 37(14):4773-81. PubMed ID: 9537993
    [Abstract] [Full Text] [Related]

  • 9. Evidence for two catalytically different magnesium-binding sites in acetohydroxy acid isomeroreductase by site-directed mutagenesis.
    Dumas R, Butikofer MC, Job D, Douce R.
    Biochemistry; 1995 May 09; 34(18):6026-36. PubMed ID: 7742305
    [Abstract] [Full Text] [Related]

  • 10. Metabolic effects of inhibitors of two enzymes of the branched-chain amino acid pathway in Salmonella typhimurium.
    Epelbaum S, Chipman DM, Barak Z.
    J Bacteriol; 1996 Feb 09; 178(4):1187-96. PubMed ID: 8576056
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  • 12. A loop deletion in the plant acetohydroxy acid isomeroreductase homodimer generates an active monomer with reduced stability and altered magnesium affinity.
    Wessel PM, Biou V, Douce R, Dumas R.
    Biochemistry; 1998 Sep 15; 37(37):12753-60. PubMed ID: 9737852
    [Abstract] [Full Text] [Related]

  • 13. Branched-chain-amino-acid biosynthesis in plants: molecular cloning and characterization of the gene encoding acetohydroxy acid isomeroreductase (ketol-acid reductoisomerase) from Arabidopsis thaliana (thale cress).
    Dumas R, Curien G, DeRose RT, Douce R.
    Biochem J; 1993 Sep 15; 294 ( Pt 3)(Pt 3):821-8. PubMed ID: 8379936
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  • 14. The herbicidally active experimental compound Hoe 704 is a potent inhibitor of the enzyme acetolactate reductoisomerase.
    Schulz A, Spönemann P, Köcher H, Wengenmayer F.
    FEBS Lett; 1988 Oct 10; 238(2):375-8. PubMed ID: 3049163
    [Abstract] [Full Text] [Related]

  • 15. Structure of spinach acetohydroxyacid isomeroreductase complexed with its reaction product dihydroxymethylvalerate, manganese and (phospho)-ADP-ribose.
    Thomazeau K, Dumas R, Halgand F, Forest E, Douce R, Biou V.
    Acta Crystallogr D Biol Crystallogr; 2000 Apr 10; 56(Pt 4):389-97. PubMed ID: 10739911
    [Abstract] [Full Text] [Related]

  • 16. Crystal Structures of Staphylococcus aureus Ketol-Acid Reductoisomerase in Complex with Two Transition State Analogues that Have Biocidal Activity.
    Patel KM, Teran D, Zheng S, Kandale A, Garcia M, Lv Y, Schembri MA, McGeary RP, Schenk G, Guddat LW.
    Chemistry; 2017 Dec 22; 23(72):18289-18295. PubMed ID: 28975665
    [Abstract] [Full Text] [Related]

  • 17. Inhibition studies of ketol-acid reductoisomerases from pathogenic microorganisms.
    Wun SJ, Johnson LA, You L, McGeary RP, Brueck T, Schenk G, Guddat LW.
    Arch Biochem Biophys; 2020 Oct 15; 692():108516. PubMed ID: 32745463
    [Abstract] [Full Text] [Related]

  • 18. Role of acetohydroxy acid isomeroreductase in biosynthesis of pantothenic acid in Salmonella typhimurium.
    Primerano DA, Burns RO.
    J Bacteriol; 1983 Jan 15; 153(1):259-69. PubMed ID: 6401279
    [Abstract] [Full Text] [Related]

  • 19. Crystal structure of class I acetohydroxy acid isomeroreductase from Pseudomonas aeruginosa.
    Ahn HJ, Eom SJ, Yoon HJ, Lee BI, Cho H, Suh SW.
    J Mol Biol; 2003 Apr 25; 328(2):505-15. PubMed ID: 12691757
    [Abstract] [Full Text] [Related]

  • 20. Crystal structure of Mycobacterium tuberculosis ketol-acid reductoisomerase at 1.0 Å resolution - a potential target for anti-tuberculosis drug discovery.
    Lv Y, Kandale A, Wun SJ, McGeary RP, Williams SJ, Kobe B, Sieber V, Schembri MA, Schenk G, Guddat LW.
    FEBS J; 2016 Apr 25; 283(7):1184-96. PubMed ID: 26876563
    [Abstract] [Full Text] [Related]


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