课题基金 / 基金详情

Structure, Function and Evolution of DNA Repair Enzymes

Structure, Function and Evolution of DNA Repair Enzymes
DNA修复酶的结构、功能和进化
批准号:
7119940
负责人:
SUSAN S. WALLACE
金额:
$141.48万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-03 至 2009-08-31

项目摘要

项目成果

SUSAN S. WALLACE的其他基金

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overall goal of the Program Project Structure, Function and Evolution of DNA Repair Enzymes is to understand the fundamental mechanisms underpinning the Nth Superfamily and the Fpg Family of DNA glycosylases and the RecA recombinases, enzymes that process ionizing radiation-induced DNA damages, damages known to initiate the carcinogenic process. The central hypothesis underpinning this Program Project is that the families of the DNA repair enzymes in question each have a structural framework that supports a variety of significant changes in specificity or regulatory properties with only a small number of sequence alterations. To test this hypothesis a novel phylogenetic/structural analysis will be used to develop algorithms not only to identify natural protein variants that are orthologous, but have different activities, but also to determine which amino acids in a particular protein should be varied to potentially alter substrate specificity or other protein functions. Since the DNA glycosylases that initiate Base Excision Repair and the RecA recombinases involved in Double Strand Break Repair are highly conserved across all three kingdoms, they are particularly suited to this approach. The proposed Program Project consists of three Projects and three Cores. Core A, the Bioinformatics Core, will use a number of methodologies to select the proteins to be examined in the projects to test our hypothesis. Project 1 is designed to delineate and alter the substrate specificities of the oxidative DNA glycosylases targeted by Core A. Project 2 will focus on particular DNA glycosylases and determine their crystal structures. Project 3 will use similar computational, biochemical and structural approaches to understand variations in the biochemical properties of the RecA recombinases. The projects directly depend on Core A to provide the analysis of the natural protein sequences and to provide support for experimental design and will test the hypotheses derived so that there is continued iteration among the projects. All three projects will be supported by the Expression, Characterization, and Crystallization Core (Core B) and the Administrative Core (Core C).
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会议论文
9th International Workshop on "Radiation Damage to DNA"
Structure and Function of DNA Repair Enzymes
Administration
Structure, Function and Evolution of DNA Repair Enzymes