Ploux O - Search Results

1

S-adenosyl-N-decyl-aminoethyl, a potent bisubstrate inhibitor of mycobacterium tuberculosis mycolic acid methyltransferases.

Vaubourgeix J, Bardou F, Boissier F, Julien S, Constant P, Ploux O, Daffé M, Quémard A, Mourey L. Vaubourgeix J, et al. Among authors: ploux o. J Biol Chem. 2009 Jul 17;284(29):19321-30. doi: 10.1074/jbc.M809599200. Epub 2009 May 13. J Biol Chem. 2009. PMID: 19439410 Free PMC article.

2

Synthesis and evaluation of analogues of S-adenosyl-L-methionine, as inhibitors of the E. coli cyclopropane fatty acid synthase.

Guérard C, Bréard M, Courtois F, Drujon T, Ploux O. Guérard C, et al. Among authors: ploux o. Bioorg Med Chem Lett. 2004 Apr 5;14(7):1661-4. doi: 10.1016/j.bmcl.2004.01.051. Bioorg Med Chem Lett. 2004. PMID: 15026045

3

Analysis of tachykinin binding site interactions using constrained analogues of tachykinins.

Lavielle S, Chassaing G, Ploux O, Loeuillet D, Besseyre J, Julien S, Marquet A, Convert O, Beaujouan JC, Torrens Y, et al. Lavielle S, et al. Among authors: ploux o. Biochem Pharmacol. 1988 Jan 1;37(1):41-9. doi: 10.1016/0006-2952(88)90753-8. Biochem Pharmacol. 1988. PMID: 2827684 Review. No abstract available.

4

Inhibition of 7,8-diaminopelargonic acid aminotransferase from Mycobacterium tuberculosis by chiral and achiral anologs of its substrate: biological implications.

Mann S, Colliandre L, Labesse G, Ploux O. Mann S, et al. Among authors: ploux o. Biochimie. 2009 Jul;91(7):826-34. doi: 10.1016/j.biochi.2009.03.019. Epub 2009 Apr 2. Biochimie. 2009. PMID: 19345718

5

Interaction of tachykinins with their receptors studied with cyclic analogues of substance P and neurokinin B.

Ploux O, Lavielle S, Chassaing G, Julien S, Marquet A, d'Orléans-Juste P, Dion S, Regoli D, Beaujouan JC, Bergström L, et al. Ploux O, et al. Proc Natl Acad Sci U S A. 1987 Nov;84(22):8095-9. doi: 10.1073/pnas.84.22.8095. Proc Natl Acad Sci U S A. 1987. PMID: 2446317 Free PMC article.

6

7,8-Diaminoperlargonic acid aminotransferase from Mycobacterium tuberculosis, a potential therapeutic target. Characterization and inhibition studies.

Mann S, Ploux O. Mann S, et al. Among authors: ploux o. FEBS J. 2006 Oct;273(20):4778-89. doi: 10.1111/j.1742-4658.2006.05479.x. Epub 2006 Sep 19. FEBS J. 2006. PMID: 16984394 Free article.

7

Identification of new inhibitors of E. coli cyclopropane fatty acid synthase using a colorimetric assay.

Guianvarc'h D, Drujon T, Leang TE, Courtois F, Ploux O. Guianvarc'h D, et al. Among authors: ploux o. Biochim Biophys Acta. 2006 Aug;1764(8):1381-8. doi: 10.1016/j.bbapap.2006.06.002. Epub 2006 Jun 18. Biochim Biophys Acta. 2006. PMID: 16872920

8

Structure of the prolyl-acyl carrier protein oxidase involved in the biosynthesis of the cyanotoxin anatoxin-a.

Moncoq K, Regad L, Mann S, Méjean A, Ploux O. Moncoq K, et al. Among authors: ploux o. Acta Crystallogr D Biol Crystallogr. 2013 Dec;69(Pt 12):2340-52. doi: 10.1107/S0907444913021859. Epub 2013 Nov 19. Acta Crystallogr D Biol Crystallogr. 2013. PMID: 24311576

9

Identification of inhibitors of the E. coli cyclopropane fatty acid synthase from the screening of a chemical library: In vitro and in vivo studies.

Guianvarc'h D, Guangqi E, Drujon T, Rey C, Wang Q, Ploux O. Guianvarc'h D, et al. Among authors: ploux o. Biochim Biophys Acta. 2008 Nov;1784(11):1652-8. doi: 10.1016/j.bbapap.2008.04.019. Epub 2008 May 5. Biochim Biophys Acta. 2008. PMID: 18501724

10

An active site mutant of Escherichia coli cyclopropane fatty acid synthase forms new non-natural fatty acids providing insights on the mechanism of the enzymatic reaction.

E G, Drujon T, Correia I, Ploux O, Guianvarc'h D. E G, et al. Among authors: ploux o. Biochimie. 2013 Dec;95(12):2336-44. doi: 10.1016/j.biochi.2013.08.007. Epub 2013 Aug 15. Biochimie. 2013. PMID: 23954860

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