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Crystallographic Studies of Polyphosphate Kinase

Crystallographic Studies of Polyphosphate Kinase
聚磷酸激酶的晶体学研究
批准号:
7166085
负责人:
Wenqing Xu
金额:
$28.75万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-07-01 至 2008-06-30

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中文摘要
翻译
聚磷酸盐(poly(P))是由数百个正磷酸盐(Pi)残基通过以下连接而成的线性聚合物: 高能磷酸酐键。许多证据表明,聚(P)在以下方面起着关键作用: 对压力和营养缺乏的调节反应。多磷酸激酶(PPK)是一种酶, 负责从ATP可逆合成poly(P)。最近已经表明,PPK是必不可少的 生物膜的发展,群体感应,运动和许多病原体的毒力因子的释放 微生物,包括铜绿假单胞菌。PPK基因的敲除导致细胞活力的丧失, 病原微生物因此,PPK特异性抑制剂可能成为一个新的抗生素家族, 对于克服囊性纤维化和其他免疫缺陷患者的抗生素耐药性非常有用, 可以在打击生物恐怖主义方面发挥作用。 PPK是一种膜相关酶,与其他酶没有明显的序列同源性。 proteins. PPK系列没有三维结构信息。我们最近 纯化并结晶全长E. coli PPK,以及X-结构测定的初始阶段 射线晶体学。该提案的主要目标是确定晶体 PPK及其与各种底物和反应中间体模拟物的复合物的结构。我们的结构 研究将有助于确定PPK催化机制,并为药物设计提供见解。 城市,州)
英文摘要
Polyphosphate (poly(P)) is a linear polymer of hundreds of orthophosphate (Pi) residues linked by high-energy phosphoanhydride bonds. Many lines of evidence indicate that poly(P) plays a critical role in regulatory responses to stresses and nutritional deficiencies. Polyphosphate kinase (PPK) is an enzyme responsible for the reversible synthesis of poly(P) from ATP. It has been shown recently that PPK is essential for biofilm development, quorum sensing, motility and release of virulence factors of many pathogenic microorganisms, including P. aeruginosa. Knockout of the PPK gene leads to the loss of viability of the pathogenic microorganism. Thus PPK specific inhibitors could become a novel family of antibiotics, which can be very useful to overcome antibiotic resistance in cystic fibrosis and other immunodeficient patients, and could play a role in combating bioterrorism. PPK is a membrane-associated enzyme that does not have apparent sequence homology with other proteins. No three-dimensional structural information is available for the PPK family. We have recently purified and crystallized the full-length E. coli PPK, and the initial phases for structure determination by X- ray crystallography have been obtained. The main goal of this proposal is the determination of crystal structures of PPK and its complexes with various substrates and reaction intermediate mimics. Our structural studies will aid in determining the PPK catalytic mechanism and provide insights into drug design. city, state)
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An inducible protein knockout strategy based on an orthogonal, ligand-activated E3 ubiquitin ligase
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    9112804
  • 项目类别:
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    $23.15万
  • 财政年份:
    2016
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  • 财政年份:
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Structural Basis of Norrin-induced Wnt/beta-catenin signaling
  • 批准号:
    9006448
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  • 财政年份:
    2016
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  • 批准号:
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  • 项目类别:
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  • 财政年份:
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海外基金