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Neutron crystallographic study on rubredoxin from Pyrococcus furiosus by BIX-3 a single-crystal diffractometer for biomacromolecules

机译:用生物大分子单晶衍射仪BIX-3对激烈热球菌中的红还膜氧化还蛋白进行中子晶体学研究

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摘要

The structure of a partially deuterated rubredoxin from the hyperthermophilic archaeon Pyrococcus furiosus, an organism that grows optimally at 100°C, was determined by using the neutron single-crystal diffractometer dedicated for biological macromolecules (BIX-3) at the JRR-3M reactor of the Japan Atomic Energy Research Institute. Data were collected at room temperature up to a resolution of 1.5 Å, and the completeness factor of the data set was 81.9%. The model contains 306 H and 50 D atoms. A total of 37 hydration water molecules were identified, with 15 having all three atoms fully located and the remaining D2O molecules partially defined. The model has been refined to final agreement factors of R = 18.6% and Rfree = 21.7%. Several orientations of the O–D bonds of side chains, whose assignments from x-ray data were previously ambiguous, were clearly visible in the neutron structure. Although most backbone N–H bonds had undergone some degree of H/D exchange throughout the rubredoxin molecule, 5 H atom positions still had distinctly negative (H) peaks. The neutron Fourier maps clearly showed the details of an extensive set of H bonds involving the ND3+ terminus that may contribute to the unusual thermostability of this molecule.
机译:通过在JRR-3M反应堆中使用专用于生物大分子的中子单晶衍射仪(BIX-3),确定了在100°C最佳生长的高温嗜热古细菌激烈热球菌(Pyrococcus furiosus)产生的部分氘化的氧化还原蛋白的结构。日本原子能研究所。在室温下以高达1.5Å的分辨率收集数据,数据集的完整性因子为81.9%。该模型包含306个H和50个D原子。总共鉴定出37个水合水分子,其中15个分子完全位于所有三个原子中,其余D2O分子被部分限定。该模型已精炼为最终协议因子R = 18.6%和Rfree = 21.7%。在中子结构中,可以清楚地看到侧链的O-D键的几种取向,这些取向以前在X射线数据中的分配是模棱两可的。尽管大多数骨架N–H键在整个Rubredoxin分子中都经历了一定程度的H / D交换,但5个H原子位置仍具有明显的负(H)峰。中子傅立叶图清楚地显示了涉及ND3 + 末端的大量H键的详细信息,这可能有助于该分子异常的热稳定性。

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