-
2023Synthesis and structure-activity relationship studies of original cyclic diadenosine derivatives as nanomolar inhibitors of NAD kinase from pathogenic bacteria., Eur J Med Chem 2023 Jan; 246(): 114941.
-
2022Structure-based design, synthesis and biological evaluation of a NAD+ analogue targeting Pseudomonas aeruginosa NAD kinase., FEBS J 2022 Aug; (): .
-
2021Noncanonical DNA polymerization by aminoadenine-based siphoviruses., Science 2021 04; 372(6541): 520-524.
-
2020New Chemical Probe Targeting Bacterial NAD Kinase., Molecules 2020 Oct; 25(21): .
-
2020From Substrate to Fragments to Inhibitor Active In Vivo against Staphylococcus aureus., ACS Infect Dis 2020 Mar; 6(3): 422-435.
-
2020An expedient synthesis of flexible nucleosides through enzymatic glycosylation of proximal and distal fleximer bases, Chembiochem 2020 Jan;.
-
2019Crystal structure of the Trypanosoma cruzi EIF4E5 translation factor homologue in complex with mRNA cap-4, Nucleic Acids Res. 2019 Jun;47(11):5973-5987.
-
20192′-Deoxyribonucleoside 5′-triphosphates bearing 4-phenyl and 4-pyrimidinyl imidazoles as DNA polymerase substrates, Org. Biomol. Chem. 2019 01;17(2):290-301.
-
2018Enzymatic synthesis of random sequences of RNA and RNA analogues by DNA polymerase theta mutants for the generation of aptamer libraries, Nucleic Acids Res. 2018 07;46(12):6271-6284.
-
2017An expedient synthesis of flexible nucleosides via a regiocontrolled enzymatic glycosylation of functionalized imidazoles, Org. Biomol. Chem., 2017, 15, 8193.
-
20168-Thioalkyl-adenosine derivatives inhibit Listeria monocytogenes NAD kinase through a novel binding mode., Eur J Med Chem 2016 Nov; 124(): 1041-1056.
-
2016Expedient and generic synthesis of imidazole nucleosides by enzymatic transglycosylation, Org. Biomol. Chem., 2016, 14, 3638.
-
2015Unprecedented formation of 8(R),5′-O-cycloribonucleosides through a triflation reaction of purine ribonucleosides, Tetrahedron, 71, 2525-2529..
-
2014A convenient synthesis of 4(5)-(hetero)aryl-1H-imidazoles via microwave-assisted Suzuki-Miyaura cross-coupling reaction, Tetrahedron Lett. 2014; 55(46);6347–6350.
-
20146-(Hetero)Arylpurine nucleotides as inhibitors of the oncogenic target DNPH1: synthesis, structural studies and cytotoxic activities, Eur J Med Chem 2014 Oct;85:418-37.
-
2014Synthesis of novel 9-aryl and heteroarylpurine derivatives via copper mediated coupling reaction, Tetrahedron Letters 02/2014; 55(9):1625–1627. .
-
2013N (6)-substituted AMPs inhibit mammalian deoxynucleotide N-hydrolase DNPH1, PLoS ONE 2013;8(11):e80755.
-
2013Structure of the oncoprotein Rcl bound to three nucleotide analogues, Acta Crystallogr. D Biol. Crystallogr. 2013 Feb;69(Pt 2):247-55.
-
2012Screening and in situ synthesis using crystals of a NAD kinase lead to a potent antistaphylococcal compound., Structure 2012 Jun; 20(6): 1107-17.
-
2012Drug design and identification of potent leads against mycobacterium tuberculosis thymidine monophosphate kinase, Curr Top Med Chem 2012;12(7):694-705.
-
2011In-plate protein crystallization, in situ ligand soaking and X-ray diffraction, Acta Crystallogr. D Biol. Crystallogr. 2011 Sep;67(Pt 9):747-55.
-
2010Probing the active site of the deoxynucleotide N-hydrolase Rcl encoded by the rat gene c6orf108, J. Biol. Chem. 2010 Dec;285(53):41806-14.
-
2008Crystal structure of poxvirus thymidylate kinase: an unexpected dimerization has implications for antiviral therapy, Proc. Natl. Acad. Sci. U.S.A. 2008 Nov;105(44):16900-5.
-
2008In vivo reshaping the catalytic site of nucleoside 2′-deoxyribosyltransferase for dideoxy- and didehydronucleosides via a single amino acid substitution, J. Biol. Chem. 2008 Jul;283(29):20053-9.
-
2008Substituted benzyl-pyrimidines targeting thymidine monophosphate kinase of Mycobacterium tuberculosis: synthesis and in vitro anti-mycobacterial activity, Bioorg. Med. Chem. 2008 Jun;16(11):6075-85.
-
2008Expanding substrate specificity of nucleoside 2′-deoxyribosyltransferase, Nucleic Acids Symp Ser (Oxf) 2008;(52):495-6.
-
2007NAD kinases use substrate-assisted catalysis for specific recognition of NAD, J. Biol. Chem. 2007 Nov;282(47):33925-34.
-
2007Enantioselectivity of human AMP, dTMP and UMP-CMP kinases, Nucleic Acids Res. 2007;35(14):4895-904.
-
2007Nucleotide binding to human UMP-CMP kinase using fluorescent derivatives — a screening based on affinity for the UMP-CMP binding site, FEBS J. 2007 Jul;274(14):3704-14.
-
2007A new family of inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase, Nucleosides Nucleotides Nucleic Acids 2007;26(8-9):1057-61.
-
2007Looking for new pyrimidine acyclic nucleotide analogues designed for phosphorylation by human UMP-CMP kinase, Nucleosides Nucleotides Nucleic Acids 2007;26(10-12):1369-73.
-
2007Crystal structure and photochemical behavior in solution of the 3′-N-sulfamate analogue of thymidylyl(3′-5′)thymidine, J. Org. Chem. 2007 Jan;72(1):43-50.
-
2006Recognition of nucleotide analogs containing the 7,8-dihydro-8-oxo structure by the human MTH1 protein, J. Biochem. 2006 Dec;140(6):843-9.
-
2005Substrate specificity of vaccinia virus thymidylate kinase, FEBS J. 2005 Dec;272(24):6254-65.
-
2005LEA3D: a computer-aided ligand design for structure-based drug design, J. Med. Chem. 2005 Apr;48(7):2457-68.
-
2005Mechanism of the antiviral action of 1-beta-D-arabinofuranosylcytosine on Borna disease virus, J. Virol. 2005 Apr;79(7):4514-8.
-
2005Synthesis and incorporation into DNA fragments of the artificial nucleobase, 2-amino-8-oxopurine, Bioorg. Med. Chem. Lett. 2005 Feb;15(4):1069-73.
-
2004APOBEC3G is a single-stranded DNA cytidine deaminase and functions independently of HIV reverse transcriptase, Nucleic Acids Res. 2004;32(8):2421-9.
-
20042′-fluoro-2′-deoxycytidine inhibits Borna disease virus replication and spread, Antimicrob. Agents Chemother. 2004 Apr;48(4):1422-5.
-
2004Probing the substrate recognition mechanism of the human MTH1 protein by nucleotide analogs, J. Mol. Biol. 2004 Feb;336(4):843-50.
-
2003Replication of hexitol oligonucleotides as a prelude to the propagation of a third type of nucleic acid in vivo, C. R. Biol. 2003 Dec;326(12):1175-84.
-
2003Thymidine and thymidine-5′-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase, Bioorg. Med. Chem. Lett. 2003 Sep;13(18):3045-8.
-
20033′-C-branched-chain-substituted nucleosides and nucleotides as potent inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase, J. Med. Chem. 2003 Aug;46(18):3811-21.
-
2003Comparative study of purine and pyrimidine nucleoside analogues acting on the thymidylate kinases of Mycobacterium tuberculosis and of humans, Chembiochem 2003 Aug;4(8):742-7.
-
2003Design of Mycobacterium tuberculosis thymidine monophosphate kinase inhibitors, Nucleosides Nucleotides Nucleic Acids 2003 May-Aug;22(5-8):801-4.
-
2003Synthesis and recognition by DNA polymerases of a reactive nucleoside for DNA diversification, Nucleosides Nucleotides Nucleic Acids 2003 May-Aug;22(5-8):1665-7.
-
2003A short path synthesis of [13C/15N] multilabeled pyrimidine nucleosides starting from glucopyranose nucleosides, J. Org. Chem. 2003 Mar;68(5):1867-71.
-
2002A parallel synthesis scheme for generating libraries of DNA polymerase substrates and inhibitors, Chembiochem 2002 Dec;3(12):1251-6.
-
2002Synthesis and evaluation of thymidine-5′-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase, Bioorg. Med. Chem. Lett. 2002 Oct;12(19):2695-8.
-
2002Synthesis and recognition by DNA polymerases of a reactive nucleoside, 1-(2-deoxy-beta-D-erythro-pentofuranosyl)-imidazole-4-hydrazide, Nucleic Acids Res. 2002 May;30(9):1869-78.
-
2002Nucleoside analogues as inhibitors of thymidylate kinases: possible therapeutic applications, Chembiochem 2002 Jan;3(1):108-10.
-
2002Substrate recognition by the human MTH1 protein, Nucleic Acids Res. Suppl. 2002;(2):85-6.
-
2001Reverse transcriptase incorporation of 1,5-anhydrohexitol nucleotides, Nucleic Acids Res. 2001 Aug;29(15):3154-63.
-
2001Thymidylate kinase of Mycobacterium tuberculosis: a chimera sharing properties common to eukaryotic and bacterial enzymes, Protein Sci. 2001 Jun;10(6):1195-205.
-
2000Enzymatic incorporation in DNA of 1,5-anhydrohexitol nucleotides, Biochemistry 2000 Oct;39(42):12757-65.
-
1999Assay of nucleoside 2-deoxyribosyltransferase activity with pyruvate kinase/lactate dehydrogenase coupling system, Anal. Biochem. 1999 Jul;271(2):192-3.
-
1996Ambiguous base pairing of the purine analogue 1-(2-deoxy-beta-D-ribofuranosyl)-imidazole-4-carboxamide during PCR, Nucleic Acids Res. 1996 Sep;24(17):3302-6.
-
1996Construction of a self-complementary nucleoside from deoxyguanosine, C. R. Acad. Sci. III, Sci. Vie 1996 Jan;319(1):1-7.
-
1994Genetic characterization of polypeptide deformylase, a distinctive enzyme of eubacterial translation, EMBO J. 1994 Feb;13(4):914-23.
-
1993Directed evolution of biosynthetic pathways. Recruitment of cysteine thioethers for constructing the cell wall of Escherichia coli, J. Biol. Chem. 1993 Dec;268(36):26827-35.
-
1990Synthesis and enzymatic polymerisation of 5-amino-1-(2′-deoxy-beta-D-ribofuranosyl)imidazole-4-carboxamide-5′- triphosphate, Nucleic Acids Res. 1990 Dec;18(23):7127-31.
-
1989Preparation and use of a universal primed Sepharose for the purification of DNA-binding proteins, Eur. J. Biochem. 1989 Feb;179(2):359-63.
-
1988IR and UV studies on stability and conformations of short DNA duplexes containing a no-base residue: coexistence of B and Z conformations, J. Biomol. Struct. Dyn. 1988 Aug;6(1):167-79.
-
1988Solid-supported ligation primer, Nucleic Acids Res. 1988 Feb;16(4):1619.
-
1986NMR, CD and IR spectroscopies of a tridecanucleotide containing a no-base residue: coexistence of B and Z conformations, Nucleic Acids Res. 1986 Jan;14(2):1107-26.