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首页> 外文期刊>Journal of Applied Crystallography >X-RAY SCATTERING STUDIES OF METALLOPROTEINS IN SOLUTION - A QUANTITATIVE APPROACH FOR STUDYING MOLECULAR CONFORMATIONS
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X-RAY SCATTERING STUDIES OF METALLOPROTEINS IN SOLUTION - A QUANTITATIVE APPROACH FOR STUDYING MOLECULAR CONFORMATIONS

机译:溶液中金属蛋白的X射线散射研究-研究分子构象的定量方法

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摘要

The model-independent approach based on the multipole expansion method using spherical harmonics [Stuhrmann (1970a). Acta Cryst. A26, 297-306] has been applied to obtain structural information on a variety of metalloproteins studied by synchrotron X-ray solution scattering. The method is applied to examples (nitrite reductase, transferrin and nitrogenase), not only with the view of comparing protein conformations in solution with those in the crystalline state, but also defining conformational changes and protein-protein interactions which are of functional importance. The shape restoration is found to be straightforward at low resolution (L less than or equal to 3). For correct treatment using higher harmonics, overall molecular symmetry, if present, must be included in the multipole expansion. [References: 41]
机译:基于模型的方法基于使用球谐函数的多极展开法[Stuhrmann(1970a)。 Acta Cryst。 [A26,297-306]已用于获得通过同步加速器X射线溶液散射研究的各种金属蛋白的结构信息。该方法不仅可以将溶液中的蛋白质构象与结晶态的蛋白质构象进行比较,而且可以定义具有重要功能的构象变化和蛋白质-蛋白质相互作用,从而应用于实例(亚硝酸还原酶,转铁蛋白和固氮酶)。发现形状恢复在低分辨率(L小于或等于3)时很简单。为了使用高次谐波进行正确处理,必须在多极扩展中包括整体分子对称性(如果存在)。 [参考:41]

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