首页> 美国卫生研究院文献>Acta Crystallographica Section F: Structural Biology and Crystallization Communications >A 2.2 Å resolution structure of the USP7 catalytic domain in a new space group elaborates upon structural rearrangements resulting from ubiquitin binding
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A 2.2 Å resolution structure of the USP7 catalytic domain in a new space group elaborates upon structural rearrangements resulting from ubiquitin binding

机译:新空间基团中USP7催化结构域的2.2Å分辨率结构详细说明了泛素结合导致的结构重排

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摘要

A sparse-matrix screen for new crystallization conditions for the USP7 catalytic domain (USP7CD) led to the identification of a condition in which crystals grow reproducibly in 24–48 h. Variation of the halide metal, growth temperature and seed-stock concentration resulted in a shift in space group from P21 with two molecules in the asymmetric unit to C2 with one molecule in the asymmetric unit. Representative structures from each space group were determined to 2.2 Å resolution and these structures support previous findings that the catalytic triad and switching loop are likely to be in unproductive conformations in the absence of ubiquitin (Ub). Importantly, the new structures reveal previously unobserved electron density for blocking loop 1 (BL1) residues 410–419. The new structures indicate a distinct rearrangement of the USP7 BL1 compared with its position in the presence of bound Ub.
机译:针对USP7催化域(USP7CD)的新结晶条件的稀疏矩阵筛选导致鉴定出一种条件,其中晶体可在24–48 growh内可再现地生长。卤化物金属,生长温度和种子原料浓度的变化导致空间群从不对称单元中有两个分子的P21变为不对称单元中有一个分子的C2。确定每个空间群的代表性结构的分辨率为2.2Å,这些结构支持以前的发现,即在没有泛素(Ub)的情况下催化三联体和转换环可能处于非生产构象。重要的是,新结构揭示了封闭环1(BL1)残基410-419的先前未观察到的电子密度。新结构表明USP7 BL1与在结合的Ub存在下的位置相比有明显的重排。

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