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Titlebook: Biophysics and Structure to Counter Threats and Challenges; Joseph D. Puglisi,Manolia V. Margaris Conference proceedings 2013 Springer Sci

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發(fā)表于 2025-3-21 19:37:42 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Biophysics and Structure to Counter Threats and Challenges
影響因子2023Joseph D. Puglisi,Manolia V. Margaris
視頻videohttp://file.papertrans.cn/189/188361/188361.mp4
發(fā)行地址Molecular dynamics and other computational approaches.Translational mechanisms and antibiotics.Structure-based drug design in biotechnology
學科分類NATO Science for Peace and Security Series B: Physics and Biophysics
圖書封面Titlebook: Biophysics and Structure to Counter Threats and Challenges;  Joseph D. Puglisi,Manolia V. Margaris Conference proceedings 2013 Springer Sci
影響因子.This ASI brought together a diverse group of experts who span virology, biology, biophysics, chemistry, physics and engineering. ?Prominent lecturers representing world renowned scientists from nine (9) different countries, and students from around the world representing eighteen (18) countries, participated in the ASI organized by Professors Joseph Puglisi (Stanford University, USA) and Alexander Arseniev (Moscow, RU). ?.The central hypothesis underlying this ASI was that interdisciplinary research, merging principles of physics, chemistry and biology, can drive new discovery in detecting and fighting chemical and bioterrorism agents, lead to cleaner environments and improved energy sources, and help propel development in NATO partner countries.? At the end of the ASI students had an appreciation of how to apply each technique to their own particular research problem and to demonstrate that multifaceted approaches and new technologies are needed to solve the biological challenges of our time.? The course succeeded in training a new generation of biologists and chemists who will probe the molecular basis for life and disease. .
Pindex Conference proceedings 2013
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System-Specific Scoring Functions: Application to Guanine-Containing Ligands and Thrombin, details of protein functioning and in drug design. Nevertheless, modern docking algorithms are still far from perfection. Development of scoring functions aimed at prediction of spatial structure and free energy of binding for molecular complexes remains a challenging task. With increasing amount o
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Structures of Novel HIV-Inactivating Lectins,PFA, using NMR spectroscopy and X-ray crystallography. We solved crystal structures of these proteins, free and complexed with α3,α6-mannopentaose, the minimal mannosyl oligosaccharide substructure of the gp120-attached mannoses that is recognized by these lectins. Our data provide the first atomic
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An Introduction to Macromolecular Crystallography Through Parable and Analogy, any electromagnetic radiation such as light. But, to make the example more concrete, let’s assume it is an invisible, cream colored, 1984 Alpha Romeo Spider (curiously, exactly like the author’s). If we have never seen such a glorious object before, how can we learn of its structure? How can we vis
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Approaches to Protein-Ligand Structure Determination by NMR Spectroscopy: Applications in Drug Bindvide structural information relatively easily. For example, chemical shift mapping has been a tool employed for many years to identify ligand binding sites and to determine the stoichiometry and affinity of ligand binding. However, the determination of a high resolution solution structure of a targe
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How Do Nascent Proteins Emerge from the Ribosome?,ctacular architecture and inherent mobility, allowing their smooth performance in decoding the genetic information as well as the formation of peptide bonds, elongation of the newly born proteins and their protection (for review see [45] ChemBioChem 10:63–72, 2009).
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