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STRUCTURAL GENOMICS OF MYCOBACTERIUM TUBERCULOSIS: A SEARCH FOR FUNCTION AND NEW DRUG TARGETS

机译:结核分枝杆菌的结构基因组学:寻找功能和新药物目标

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摘要

Structural genomics initiatives have various goals: from the discovery of new folds to providing representative structures for all protein families, to 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 Mycobacterium tuberculosis, the causative agent. The goals are to characterize new drug targets and to gain a deeper understanding of TB biology. The project has now entered a very productive phase, with more than one third of the genes cloned, many proteins purified, and more than 100 structures determined. Some of these are for already-validated drug targets. Others have led to new functional understanding of important processes in the biology of the organism, providing validation of the structure-to-function paradigm.
机译:结构基因组学举措具有各种目标:从发现新折叠到为所有蛋白质家族提供代表性结构,从结构的功能发现,以及新药物靶标的表征。 TB结构基因组学联盟(TBSGC)是一项以上50多个实验室的国际合作,通过重点关注结核分枝杆菌,致病因子来解决TB的全球问题。目标是表征新的药物目标,并获得对TB生物学的更深入了解。该项目现在已经进入了非常高效的阶段,克隆了超过三分之一的基因,许多蛋白质纯化,并确定了超过100种结构。其中一些是用于已经验证的药物目标。其他人导致对生物体生物学中的重要过程的新功能理解,提供了对功能范式的验证。

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