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首页> 外文期刊>Acta crystallographica, Section F. Structural biology and crystallization communications >Crystallization, characterization and preliminary X-ray crystallographic analysis of GK2848, a putative carbonic anhydrase of Geobacillus kaustophilus
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Crystallization, characterization and preliminary X-ray crystallographic analysis of GK2848, a putative carbonic anhydrase of Geobacillus kaustophilus

机译:GK2848的结晶,表征和初步X射线晶体学分析,一种推测的嗜碱芽孢杆菌碳酸酐酶

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摘要

GK2848, a hypothetical protein from the thermophilic organism Geobacillus kaustophilus, was cloned and overexpressed in Escherichia coli. The protein was purified to homogeneity using Ni-NTA affinity-column and gel-filtration chromatography. The purified protein was crystallized using the sitting-drop vapour-diffusion method. The crystals diffracted to a resolution of 2.70 angstrom and belonged to the orthorhombic space group P2(1)2(1)2. GK2848 bears sequence homology to carbonic anhydrases of various bacterial species, indicating that it belongs to the carbonic anhydrase family of proteins. A subsequent carbonic anhydrase activity assay of GK2848 using the Wilbur-Anderson method confirmed its function as a carbonic anhydrase. A preliminary structure solution was obtained by molecular replacement using MOLREP. Mutation and biochemical characterization of the protein are in progress. The structure and functional analysis of GK2848 might provide valuable information on a novel class of carbonic anhydrases, as none of its homologous structures have been characterized.
机译:GK2848是嗜热生物嗜碱芽孢杆菌的一种假设蛋白,已在大肠杆菌中克隆并过表达。使用Ni-NTA亲和柱和凝胶过滤色谱将蛋白质纯化至均质。使用坐滴蒸气扩散法使纯化的蛋白质结晶。晶体衍射到2.70埃的分辨率,并属于正交晶体空间群P2(1)2(1)2。 GK2848与各种细菌的碳酸酐酶具有序列同源性,表明它属于蛋白质的碳酸酐酶家族。随后使用Wilbur-Anderson方法进行的GK2848碳酸酐酶活性测定证实了其作为碳酸酐酶的功能。通过使用MOLREP的分子置换获得初步结构的溶液。蛋白质的突变和生物化学表征正在进行中。 GK2848的结构和功能分析可能会提供有关一类新型碳酸酐酶的有价值的信息,因为尚未鉴定出其同源结构。

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