SEARCHING FOR PROTEIN INTERACTING WITH YEAST MPH1

寻找与酵母 MPH1 相互作用的蛋白质

• 批准号: 7602149
• 负责人: Kyungjae Myung
• 金额: $ 1.04万
• 依托单位: UNIVERSITY OF WASHINGTON
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-01 至 2008-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7602149
• 关键词: Computer Retrieval of Information on Scientific Projects Database; DNA; DNA Damage; Fanconi' s Anemia; Funding; Genetic; Grant; Homologous Gene; Institution; Libraries; Pathway interactions; Proteins; Research; Research Personnel; Resources; Source; United States National Institutes of Health; Yeasts; helicase; homologous recombination; protein metabolism; yeast two hybrid system

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Mph1, a yeast Fanconi Anemia M (FANCM) homolog is 3'-5' DNA helicase. It has been suggested to function in DNA damage avoidance through genetic interaction with homologous recombination pathway. However, its interaction with other known DNA metabolism proteins is not clearly understood. To understand whether Mph1 interacts with any DNA metabolism proteins, I propose to screen yeast two hybrid library in the absence or presence of DNA damaging agent, MMS.

该副本是利用众多研究子项目之一 由NIH/NCRR资助的中心赠款提供的资源。子弹和 调查员（PI）可能已经从其他NIH来源获得了主要资金， 因此可以在其他清晰的条目中代表。列出的机构是 对于中心，这不一定是调查员的机构。 MPH1，酵母菌芳烃M（FANCM）同源物为3'-5'DNA解旋酶。有人建议通过与同源重组途径的遗传相互作用来避免DNA损伤。但是，它与其他已知的DNA代谢蛋白的相互作用尚不清楚。为了了解MPH1是否与任何DNA代谢蛋白相互作用，我建议在不存在或存在DNA损伤剂MMS的情况下筛选酵母两个杂种库MMS。