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Titlebook: Evolving Methods for Macromolecular Crystallography; The Structural Path Randy J. Read,Joel L. Sussman Conference proceedings 2007 Springe

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书目名称Evolving Methods for Macromolecular Crystallography
副标题The Structural Path
编辑Randy J. Read,Joel L. Sussman
视频videohttp://file.papertrans.cn/319/318111/318111.mp4
概述Arises from the renowned Erice Schools on Macromolecular Crystallography.Chapters by leading experts in modern methods of macromolecular crystallography.Spans the range from detailed practical advice
丛书名称NATO Science Series II: Mathematics, Physics and Chemistry
图书封面Titlebook: Evolving Methods for Macromolecular Crystallography; The Structural Path  Randy J. Read,Joel L. Sussman Conference proceedings 2007 Springe
描述This volume comprises papers presented at the 2005 edition of the “Crystallography of Molecular Biology” courses that have been held since 1976 at the Ettore Majorana Centre for Scientific Culture in Erice, Italy. This series of courses is renowned for bringing leaders in the field of macromo- cular crystallography together with highly motivated students, in a beautiful and intimate location that encourages people to interact. The warm and informal atmosphere at these Erice conferences, especially these on cryst- lography, has helped to foster long-term scientific interactions and new int- national friendships that have often lasted for the lifetime of the scientists. The course was financed by NATO as an Advanced Study Institute and by the European Commission as a EuroSummerSchool. The papers span the breadth of material presented in the course, which emphasized the practical aspects of modern macromolecular crystallography and its applications. One must start with crystals: Bergfors showed how to improve initial crystals through seeding, while Byrne discussed the difficult problem of crystallizing membrane proteins. The collection of optimal diffraction data requires both careful
出版日期Conference proceedings 2007
关键词3D; Crystallography; X-ray; bioinformatics; biology; genome; imaging; proteins
版次1
doihttps://doi.org/10.1007/978-1-4020-6316-9
isbn_softcover978-1-4020-6315-2
isbn_ebook978-1-4020-6316-9Series ISSN 1568-2609
issn_series 1568-2609
copyrightSpringer Science+Business Media B.V. 2007
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Macromolecular cryo-crystallography,ly collected with the sample held at around 100 K, significantly reducing the secondary radiation damage, and usually resulting in higher resolution and better quality data. However, at synchrotron X-ray sources, even at cryo-temperatures there has now been frequent observation of both degradation o
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Processing diffraction data with mosflm,crystal; second, obtaining refined values for these parameters; and third, integrating the diffraction images. The basic principles underlying autoindexing, parameter refinement, and spot integration by summation integration and profile fitting are described.
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Stochastic molecular replacement,mensionality. Due to their divide-and-conquer approach, these methods necessarily ignore (at least during their early stages) the very knowledge that a target crystal structure may comprise, for example, more than one copy of a search model, or, several models of different types. Here, we describe a
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Structural genomics of mycobacterium tuberculosis: a search for function and new drug targets,o the discovery of function from structure, and the characterization of new drug targets. The TB Structural Genomics Consortium (TBSGC), an international collaboration of more than 50 laboratories, was formed to address the worldwide problem of TB, through its focus on ., the causative agent. The go
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