Mechanism of Allosteric Inhibition of the Enzyme IspD by Three Different Classes of Ligands.
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F. Diederich | A. Bacher | M. Fischer | M. Groll | M. Witschel | B. Illarionov | Anatol Schwab | M. Seet | A. Frank | A. Kunfermann
[1] M. Groll,et al. The Methylerythritol Phosphate Pathway to Isoprenoids. , 2017, Chemical reviews.
[2] S. Cherukupalli,et al. An insight on synthetic and medicinal aspects of pyrazolo[1,5-a]pyrimidine scaffold. , 2017, European journal of medicinal chemistry.
[3] F. Diederich,et al. Halogen-Bonded Supramolecular Capsules in the Solid State, in Solution, and in the Gas Phase. , 2017, Angewandte Chemie.
[4] Synthesis and evaluation of hydroxyazolopyrimidines as herbicides; the generation of amitrole in planta. , 2016, Pest management science.
[5] Thomas E. Exner,et al. Using Surface Scans for the Evaluation of Halogen Bonds toward the Side Chains of Aspartate, Asparagine, Glutamate, and Glutamine , 2016, J. Chem. Inf. Model..
[6] S. Faure,et al. The insect repellent N,N-diethyl-m-toluamide (DEET) induces angiogenesis via allosteric modulation of the M3 muscarinic receptor in endothelial cells , 2016, Scientific Reports.
[7] Pierangelo Metrangolo,et al. The Halogen Bond , 2016, Chemical reviews.
[8] François Diederich,et al. Addressing the Glycine-Rich Loop of Protein Kinases by a Multi-Facetted Interaction Network: Inhibition of PKA and a PKB Mimic. , 2016, Chemistry.
[9] F. Diederich,et al. Molecular recognition in chemical and biological systems. , 2015, Angewandte Chemie.
[10] P. Beer,et al. Halogen Bonding in Supramolecular Chemistry. , 2008, Chemical reviews.
[11] M. Schorn,et al. Biosynthesis of polybrominated aromatic organic compounds by marine bacteria , 2014, Nature chemical biology.
[12] F. Diederich,et al. Pseudilins: halogenated, allosteric inhibitors of the non-mevalonate pathway enzyme IspD. , 2014, Angewandte Chemie.
[13] J. Changeux. 50 years of allosteric interactions: the twists and turns of the models , 2013, Nature Reviews Molecular Cell Biology.
[14] Jing Zhang,et al. Jaguar: A high-performance quantum chemistry software program with strengths in life and materials sciences , 2013 .
[15] Arthur Christopoulos,et al. Emerging paradigms in GPCR allostery: implications for drug discovery , 2013, Nature Reviews Drug Discovery.
[16] M. Witschel,et al. In search of new herbicidal inhibitors of the non-mevalonate pathway. , 2013, Pest management science.
[17] F. Diederich,et al. Efficient Stacking on Protein Amide Fragments , 2013, ChemMedChem.
[18] A. Joerger,et al. Principles and applications of halogen bonding in medicinal chemistry and chemical biology. , 2013, Journal of medicinal chemistry.
[19] Philip A. Gale,et al. Supramolecular Chemistry: From Molecules to Nanomaterials , 2012 .
[20] S. Martino‐Catt,et al. Genetically Modified Herbicide‐Resistant Crops , 2012 .
[21] F. Diederich,et al. Inhibitors of the herbicidal target IspD: allosteric site binding. , 2011, Angewandte Chemie.
[22] F. Diederich,et al. Aromatic rings in chemical and biological recognition: energetics and structures. , 2011, Angewandte Chemie.
[23] François Diederich,et al. Systematic investigation of halogen bonding in protein-ligand interactions. , 2011, Angewandte Chemie.
[24] Ryan M. Lee,et al. Biochemical and structural consequences of a glycine deletion in the alpha-8 helix of protoporphyrinogen oxidase. , 2010, Biochimica et biophysica acta.
[25] W. Eisenreich,et al. Probing the reaction mechanism of IspH protein by x-ray structure analysis , 2009, Proceedings of the National Academy of Sciences.
[26] D. Manstein,et al. Total synthesis of pentabromo- and pentachloropseudilin, and synthetic analogues--allosteric inhibitors of myosin ATPase. , 2009, Angewandte Chemie.
[27] Bosco K. Ho,et al. HOLLOW: Generating Accurate Representations of Channel and Interior Surfaces in Molecular Structures , 2008, BMC Structural Biology.
[28] F. Diederich,et al. Fluorine in Pharmaceuticals: Looking Beyond Intuition , 2007, Science.
[29] Markus Fischer,et al. Nonmevalonate terpene biosynthesis enzymes as antiinfective drug targets: substrate synthesis and high-throughput screening methods. , 2006, The Journal of organic chemistry.
[30] W. Eisenreich,et al. The crystal structure of a plant 2C‐methyl‐D‐erythritol 4‐phosphate cytidylyltransferase exhibits a distinct quaternary structure compared to bacterial homologues and a possible role in feedback regulation for cytidine monophosphate , 2006, The FEBS journal.
[31] A. Bacher,et al. Biosynthesis of isoprenoids via the non-mevalonate pathway , 2004, Cellular and Molecular Life Sciences CMLS.
[32] F. Diederich,et al. Interactions with aromatic rings in chemical and biological recognition. , 2003, Angewandte Chemie.
[33] M. Rodríguez-Concepcíon,et al. Elucidation of the Methylerythritol Phosphate Pathway for Isoprenoid Biosynthesis in Bacteria and Plastids. A Metabolic Milestone Achieved through Genomics1 , 2002, Plant Physiology.
[34] A. J. Fisher,et al. Differential Accumulation of Dimethylallyl Diphosphate in Leaves and Needles of Isoprene- and Methylbutenol-Emitting and Nonemitting Species1 , 2002, Plant Physiology.
[35] D. Cane,et al. Structure of 4-diphosphocytidyl-2-C- methylerythritol synthetase involved in mevalonate- independent isoprenoid biosynthesis , 2001, Nature Structural Biology.
[36] M. Rohmer. The discovery of a mevalonate-independent pathway for isoprenoid biosynthesis in bacteria, algae and higher plants. , 1999, Natural product reports.
[37] H. Laatsch,et al. Marine Bakterien, II. Synthese cyclischer und sterisch gehinderter Pseudiline , 1990 .
[38] R. Andersen,et al. Autotoxic antibiotic production by a marine Chromobacterium , 1974 .
[39] P. Burkholder,et al. Production of a pyrrole antibiotic by a marine bacterium. , 1966, Applied microbiology.