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High-Resolution Structure of ClpC1-Rufomycin and Ligand Binding Studies Provide a Framework to Design and Optimize Anti-Tuberculosis Leads

机译：CLPC1-Rufomycin和配体结合研究的高分辨率结构提供了一种设计和优化抗结核铅的框架

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Nina M. Wolf; Hyun Lee; Mary P. Choules; Guido F. Pauli; Rasika Phansalkar; Jeffrey R. Anderson; Wei Gao; Jinhong Ren; Bernard D. Santarsiero; Hanki Lee; Jinhua Cheng; Ying-Yu Jin; Ngoc Anh Ho; Nguyen Minh Duc; Joo-Won Suh; Celerino Abad-Zapatero; Sanghyun Cho;
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1. High-Resolution Structure of Clpc1-Ntd-Rufomycin Complex Provides Three-Dimensional Framework For Optimization Of Cyclopeptide Anti-Tb Drug Leads [J] . Wolf Nina, Lee Hyun, Choules Mary, Protein Science: A Publication of the Protein Society . 2018,第S1期

机译：CLPC1-NTD-Rufomycin复合物的高分辨率结构提供了三维框架，用于优化环肽抗TB药物引线
2. Two crystal structures of the cytoplasmic molybdate-binding protein ModG suggest a novel cooperative binding mechanism and provide insights into ligand-binding specificity. [J] . Delarbre L, Stevenson CE, White DJ, Journal of Molecular Biology . 2001,第5期

机译：细胞质钼酸盐结合蛋白ModG的两个晶体结构表明了一种新型的协同结合机制，并为配体结合特异性提供了见识。
3. The vital role of ditopicN-Nbridging ligands with different lengths in the formation of new binuclear dioxomolybdenum(vi) complexes: synthesis, crystal structures, supramolecular framework and protein binding studies [J] . Biswal Debanjana, Roy Malini, Pramanik Nikhil Ranjan, New Journal of Chemistry . 2020,第38期

机译：DITOPICN-NBRIDGEN配体在新的双核二氧化碳钼（VI）复合物的形成中具有不同长度的重要作用：合成，晶体结构，超分子框架和蛋白质结合研究
4. Coupled plasmon aveguide resonance studies of agonist/antagonist binding to the human delta-opioid receptor provide new structural insights into the three-state model for receptor-ligand interactions [C] . Z.Salamon, I.Alves, S.Cowell, the International Peptide Symposium . 2001

机译：偶联的等离子体Aveguide对人δ-阿片受体的激动剂/拮抗剂结合的共振研究为受体 - 配体相互作用的三种模型提供了新的结构性见解
5. Optimization of lead spectinamide compounds as novel anti-tuberculosis agents with a pharmacometric approach. [D] . Trivedi, Ashit Rasendu. 2015

机译：使用药理学方法优化了作为新的抗结核药物的血氨酰胺铅化合物的优化。
6. High-Resolution Structure of ClpC1-Rufomycin and Ligand Binding Studies Provide a Framework to Design and Optimize Anti-Tuberculosis Leads [O] . Nina M. Wolf, Hyun Lee, Mary P. Choules, -1

机译：ClpC1-Rufomycin的高分辨率结构和配体结合研究为设计和优化抗结核引线提供了框架
7. Structures of Pseudomonas aeruginosa β-ketoacyl-(acyl-carrier-protein) synthase II (FabF) and a C164Q mutant provide templates for antibacterial drug discovery and identify a buried potassium ion and a ligand-binding site that is an artefact of the crystal form [O] . Baum, Bernhard, Lecker, Laura S. M., Zoltner, Martin, 2015

机译：铜绿假单胞菌β-酮酰基-（酰基载体蛋白）合酶II（FabF）和C164Q突变体的结构为发现抗菌药物提供了模板，并确定了掩埋的钾离子和配体结合位点是晶体形式的人工制品

High-Resolution Structure of ClpC1-Rufomycin and Ligand Binding Studies Provide a Framework to Design and Optimize Anti-Tuberculosis Leads

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