RECHERCHER
Résultats de la recherche ""
Development and crystallography-aided SAR studies of multifunctional BuChE inhibitors and 5-HT6R antagonists with β-amyloid anti-aggregation properties
Publié le 14/09/2021
... Wichur, T., Godyń,J., Góral,I., Latacz,G., Bucki,A., Siwek,A., Głuch-Lutwin,M., Mordyl,B., Śniecikowska,J., Walczak,M., Knez,D., Jukic,M., Sałat,K., Gobec,S., Kołaczkowski,M., Malawska,B., Brazzolotto,X., Więckowska, A. "Development and crystallography ...
Structure-aided optimization of non-nucleoside M. tuberculosis thymidylate kinase inhibitors
Publié le 14/09/2021
... Song, L., Merceron, R., Hulpia, F., Lucía, A., Gracia, B., Jian, Y., Risseeuw, M.D.P., Verstraelen, T., Cos, P., Aínsa, J.A., Boshoff, H.I.M., Munier-Lehmann, H., Savvides, S.N., Van Calenbergh, S. "Structure-aided optimization of non-nucleoside M. ...
Nonhydrolysable Analogues of (p)ppGpp and (p)ppApp Alarmone Nucleotides as Novel Molecular Tools
Publié le 14/09/2021
... Mojr, V., Roghanian, M., Tamman, H., Pham, D.D.D., Petrová, M., Pohl, R., Takada, H., Van Nerom, K., Ainelo, H., Caballero-Montes, J., Jimmy, S., Garcia-Pino, A., Hauryliuk, V., Rejman, D. "Nonhydrolysable Analogues of (p)ppGpp and (p)ppApp Alarmone ...
Exploring the dNTP -binding site of HIV-1 reverse transcriptase for inhibitor design
Publié le 14/09/2021
... Gu, W., Martinez, S., Singh, A.K., Nguyen, H., Rozenski, J., Schols, D., Herdewijn, P., Das, K., De Jonghe, S. "Exploring the dNTP -binding site of HIV-1 reverse transcriptase for inhibitor design" European Journal of Medicinal Chemistry., 225: art.n° ...
Crystal structures capture multiple stoichiometric states of an aqueous self-assembling oligourea foldamer
Publié le 14/09/2021
... Collie, G.W., Lombardo, C.M., Yoo, S.Y., Pułka-Ziach, C., Gabelica, V., MacKereth, C.D., Rosu, F., Guichard, G. "Crystal structures capture multiple stoichiometric states of an aqueous self-assembling oligourea foldamer" Chemical Communications., 57(75): ...
Phosphopantetheinyl transferase binding and inhibition by amidino-urea and hydroxypyrimidinethione compounds
Publié le 14/09/2021
... Carivenc, C., Maveyraud, L., Blanger, C., Ballereau, S., Roy-Camille, C., Nguyen, M.C., Génisson, Y., Guilhot, C., Chalut, C., Pedelacq, J.D., Mourey, L. "Phosphopantetheinyl transferase binding and inhibition by amidino-urea and hydroxypyrimidinethione ...
The Oxoglutarate Binding Site and Regulatory Mechanism Are Conserved in Ammonium Transporter Inhibitors GlnKs from Methanococcales
Publié le 13/08/2021
... Muller, M.C., Wagner, T. "The Oxoglutarate Binding Site and Regulatory Mechanism Are Conserved in Ammonium Transporter Inhibitors GlnKs from Methanococcales" International Journal of Molecular Sciences., 22(16): art.n° 8631. (2021). ...
Biochemical and structural studies of target lectin SapL1 from the emerging opportunistic microfungus Scedosporium apiospermum
Publié le 12/08/2021
... Martínez-Alarcón, D., Balloy, V., Bouchara, J.P., Pieters, R.J., Varrot, A. "Biochemical and structural studies of target lectin SapL1 from the emerging opportunistic microfungus Scedosporium apiospermum" Scientific Reports., 11: art.n° 16109. (2021). ...
Characterization of a triad of genes in cyanophage S-2L sufficient to replace adenine by 2-aminoadenine in bacterial DNA
Publié le 07/08/2021
... Czernecki, D., Bonhomme, F., Kaminski, P.A., Delarue, M. "Characterization of a triad of genes in cyanophage S-2L sufficient to replace adenine by 2-aminoadenine in bacterial DNA" Nature Communications., 12: art.n° 4710. (2021). ...
Comment les microbes des grands fonds vivent-ils à partir d'éthane ? Des réponses obtenues dans un cristal jaune
Publié le 05/08/2021
... Divers hydrocarbures sont naturellement libérés dans les grands fonds marins, mais quelque chose les consomme directement dans les sédiments. Les responsables sont des micro-organismes spécifiques, capables de transformer ces hydrocarbures en ...