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Titlebook: Data Mining in Structural Biology; Signal Transduction I. Schlichting,U. Egner Conference proceedings 2001 Springer-Verlag Berlin Heidelbe

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發(fā)表于 2025-3-21 19:08:50 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Data Mining in Structural Biology
副標(biāo)題Signal Transduction
編輯I. Schlichting,U. Egner
視頻videohttp://file.papertrans.cn/263/262967/262967.mp4
叢書名稱Ernst Schering Foundation Symposium Proceedings
圖書封面Titlebook: Data Mining in Structural Biology; Signal Transduction  I. Schlichting,U. Egner Conference proceedings 2001 Springer-Verlag Berlin Heidelbe
描述Structural biology is becoming a routine technique for structure de- termination in pharmaceutical industries. The advances in molecular biology, crystal handling and data collection techniques, tunable syn- chrotron radiation sources, and high-performance computing have all contributed to developments such as the production and expression of tailored protein domains, the use of the MAD (Multiple Anomalous Dispersion) method, and the collection of X-ray data from tiny crystals at cryogenic temperature. The number of protein structures deposited in the Protein Databank has increased tremendously over the last 3-4 years. Since 1997, more than 1,500 structures have been deposited each year, and during the first 7 months of this year, 1,500 protein structures were already deposited. The numerous initiatives in the field of "structural genomics" distributed all over the world have led to the development of techniques for high-throughput structure determina- tion, thereby contributing to the increase in the determination of three- dimensional protein structures. This structural information is being ex- plored in various ways in the drug discovery process. It is not only used in structure
出版日期Conference proceedings 2001
關(guān)鍵詞DNA; Transcription Factors; biology; cell; cell cycle; data mining; drug design; protein; protein structure;
版次1
doihttps://doi.org/10.1007/978-3-662-04645-6
isbn_softcover978-3-662-04647-0
isbn_ebook978-3-662-04645-6Series ISSN 0947-6075
issn_series 0947-6075
copyrightSpringer-Verlag Berlin Heidelberg 2001
The information of publication is updating

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Common Eye Diseases and their Management thyroid hormone receptor. A growing subgroup of NRs, for which no ligand has yet been characterized, is called the orphan receptors (Gronemeyer and Laudet 1995). Steroid hormone receptors regulate complex gene networks involved in growth, cellular differentiation, homeostasis, and morphogenesis and organ genesis.
板凳
發(fā)表于 2025-3-22 02:20:30 | 只看該作者
N. R. Galloway BA, MB, ChB, DO, FRCS, MDdevoid of kinase activity but which interact with cytoplasmic tyrosine kinases. Another important family of cytokines is the transforming growth factor-β (TGF-β) family; these factors have important roles in pattern formation during embryonal development and often inhibit cell growth via binding to protein serine/threonine kinase receptors.
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N. R. Galloway BA, MB, ChB, DO, FRCS, MDes and pharmaceutical and biotechnology companies. Recent crystallographic data on complexes of PTKs with selective and non-selective inhibitors (see below) has opened the door, in principle, to the improvement of rational drug design.
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發(fā)表于 2025-3-22 14:45:19 | 只看該作者
Common Eye Diseases and their Managementny new technologies, in particular high-throughput methods in screening and chemistry, has greatly changed the way in which drug discovery research is carried out. In parallel, structure-based methods have been further developed, resulting in successful de novo design and new applications such as virtual screening and library design.
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Structural Basis for Substrate Recognition and Control in Protein Kinases,ains no genuine eukaryotic protein kinase among its 4,288 genes, although it does contain several histidine kinases as part of the prokaryotic dual response mechanism to environmental factors. The genome of ., a bacterium that exhibits a more complex life style than ., contains 11 protein kinase genes.
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發(fā)表于 2025-3-23 04:14:48 | 只看該作者
The Selectivity of Small Molecules Towards Protein Tyrosine Kinases,es and pharmaceutical and biotechnology companies. Recent crystallographic data on complexes of PTKs with selective and non-selective inhibitors (see below) has opened the door, in principle, to the improvement of rational drug design.
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