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Добірка наукової літератури з теми "Phosphatidyl-myo-Inositol Mannosides"
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Статті в журналах з теми "Phosphatidyl-myo-Inositol Mannosides"
Scherman, Hataichanok, Devinder Kaur, Ha Pham, Henrieta Škovierová, Mary Jackson, and Patrick J. Brennan. "Identification of a Polyprenylphosphomannosyl Synthase Involved in the Synthesis of Mycobacterial Mannosides." Journal of Bacteriology 191, no. 21 (August 28, 2009): 6769–72. http://dx.doi.org/10.1128/jb.00431-09.
Повний текст джерелаSancho-Vaello, Enea, David Albesa-Jové, Ane Rodrigo-Unzueta, and Marcelo E. Guerin. "Structural basis of phosphatidyl-myo-inositol mannosides biosynthesis in mycobacteria." Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1862, no. 11 (November 2017): 1355–67. http://dx.doi.org/10.1016/j.bbalip.2016.11.002.
Повний текст джерелаGilleron, Martine, Buko Lindner, and Germain Puzo. "MS/MS Approach for Characterization of the Fatty Acid Distribution on Mycobacterial Phosphatidyl-myo-inositol Mannosides." Analytical Chemistry 78, no. 24 (December 2006): 8543–48. http://dx.doi.org/10.1021/ac061574a.
Повний текст джерелаFront, Sophie, Nathalie Court, Marie-Laure Bourigault, Stéphanie Rose, Bernhard Ryffel, François Erard, Valérie F. J. Quesniaux, and Olivier R. Martin. "Phosphatidyl myo-Inositol Mannosides Mimics Built on an Acyclic or Heterocyclic Core: Synthesis and Anti-inflammatory Properties." ChemMedChem 6, no. 11 (September 7, 2011): 2081–93. http://dx.doi.org/10.1002/cmdc.201100291.
Повний текст джерелаOmahdi, Zakaria, Yuto Horikawa, Masamichi Nagae, Kenji Toyonaga, Akihiro Imamura, Koichi Takato, Takamasa Teramoto, Hideharu Ishida, Yoshimitsu Kakuta, and Sho Yamasaki. "Structural insight into the recognition of pathogen-derived phosphoglycolipids by C-type lectin receptor DCAR." Journal of Biological Chemistry 295, no. 17 (March 5, 2020): 5807–17. http://dx.doi.org/10.1074/jbc.ra120.012491.
Повний текст джерелаSchami, Alyssa, Wei Ke, Anna Allué-Guardia, Angélica M. Olmo-Fontánez, John Chan, and Jordi B. Torrelles. "The Rv2623-Rv1747 interaction influences phosphatidyl-myo-inositol levels on the cell envelope of Mycobacterium tuberculosis." Journal of Immunology 208, no. 1_Supplement (May 1, 2022): 58.19. http://dx.doi.org/10.4049/jimmunol.208.supp.58.19.
Повний текст джерелаTorrelles, Jordi B., Abul K. Azad, and Larry S. Schlesinger. "Fine Discrimination in the Recognition of Individual Species of Phosphatidyl-myo-Inositol Mannosides fromMycobacterium tuberculosisby C-Type Lectin Pattern Recognition Receptors." Journal of Immunology 177, no. 3 (July 18, 2006): 1805–16. http://dx.doi.org/10.4049/jimmunol.177.3.1805.
Повний текст джерелаCala-De Paepe, Diane, Emilie Layre, Gaëlle Giacometti, Luis F. Garcia-Alles, Lucia Mori, Daniel Hanau, Gennaro de Libero, Henri de la Salle, Germain Puzo, and Martine Gilleron. "Deciphering the Role of CD1e Protein in Mycobacterial Phosphatidyl-myo-inositol Mannosides (PIM) Processing for Presentation by CD1b to T Lymphocytes." Journal of Biological Chemistry 287, no. 37 (July 10, 2012): 31494–502. http://dx.doi.org/10.1074/jbc.m112.386300.
Повний текст джерелаRhoades, Elizabeth R., Angela S. Archambault, Rebecca Greendyke, Fong-Fu Hsu, Cassandra Streeter та Thomas F. Byrd. "Mycobacterium abscessusGlycopeptidolipids Mask Underlying Cell Wall Phosphatidyl-myo-Inositol Mannosides Blocking Induction of Human Macrophage TNF-α by Preventing Interaction with TLR2". Journal of Immunology 183, № 3 (13 липня 2009): 1997–2007. http://dx.doi.org/10.4049/jimmunol.0802181.
Повний текст джерелаPatel, Onisha, Rajini Brammananth, Weiwen Dai, Santosh Panjikar, Ross L. Coppel, Isabelle S. Lucet, and Paul K. Crellin. "Crystal structure of the putative cell-wall lipoglycan biosynthesis protein LmcA from Mycobacterium smegmatis." Acta Crystallographica Section D Structural Biology 78, no. 4 (March 11, 2022): 494–508. http://dx.doi.org/10.1107/s2059798322001772.
Повний текст джерелаДисертації з теми "Phosphatidyl-myo-Inositol Mannosides"
Piechowiak, Julien. "Conception et synthèse de molécules ciblant la biosynthèse des PIMs." Electronic Thesis or Diss., Orléans, 2025. https://theses.univ-orleans.fr/prive/accesESR/2025ORLE1004_va.pdf.
Повний текст джерелаMycobacterium tuberculosis (M.tb) is the second most deadly infectious agent in the world. Drug treatment requires daily dosage of two to four drugs over six months. Most recently, there has been an alarming rise of multi-drug resistant tuberculosis (TB), making the discovery of new drugs crucial. Current anti-TB drugs target diverse biological processes, but no molecules are designed to target PIMs biosynthesis. PIMs (Phosphatidyl-myo-Inositol Mannosides) are essential constituents of mycobacteria cell wall and the precursors of two major lipoglycans implicated in host-pathogen interactions. The acyltransferase PatA, catalyzing the transfer of a palmitoyl moiety to the 6-position of the mannose linked to inositol in PIM1 or PIM2, is essential for mycobacteria growth. Therefore, with the aim of developing PatA inhibitors, we synthesized a panel of molecules based on a mannopyranosyl scaffold. In addition, the structures present different groups (octyl, carbonate, carbamate, phosphonate, triazole, galactoside) on the aglycone to mimic the phosphatidyl part and different groups (fluorine, sulfonamide, phosphonate) on the 6-position of mannose in order to mimic either the substrate or the acylation tetrahedral transition state. The inhibitory activity of these compounds on PatA was evaluated and the Minimum Inhibitory Concentrations (MIC) were determined on M.tb