Van Troys M, Vandekerckhove J, Ampe C
Flanders Interuniversity Institute for Biotechnology, Department of Biochemistry, Faculty of Medicine, University of Gent, Belgium.
Biochim Biophys Acta. 1999 Jan 11;1448(3):323-48. doi: 10.1016/s0167-4889(98)00152-9.
The number of actin binding proteins for which (part of) the three-dimensional structure is known, is steadily increasing. This has led to a picture in which defined structural modules with actin binding capacity are shared between different actin binding proteins. A classification of these based on their common three-dimensional modules appears a logical future step and in this review we provide an initial list starting from the currently known structures. The discussed cases illustrate that a comparison of the similarities and variations within the common structural actin binding unit of different members of a particular class may ultimately provide shortcuts for defining their actin target site and for understanding their effect on actin dynamics. Within this concept, the multitude of possible interactions by an extensive, and still increasing, list of actin binding proteins becomes manageable because they can be presented as variations upon a limited number of structural themes. We discuss the possible evolutionary routes that may have produced the present array of actin binding modules.
已知(部分)三维结构的肌动蛋白结合蛋白的数量正在稳步增加。这使得人们看到一幅画面:不同的肌动蛋白结合蛋白之间共享具有肌动蛋白结合能力的特定结构模块。基于它们共同的三维模块对这些蛋白进行分类似乎是未来合理的一步,在本综述中,我们从目前已知的结构出发提供了一个初始列表。所讨论的案例表明,比较特定类别不同成员的共同结构肌动蛋白结合单元内的异同,最终可能为确定它们的肌动蛋白靶位点以及理解它们对肌动蛋白动力学的影响提供捷径。在这个概念中,大量肌动蛋白结合蛋白(其数量广泛且仍在增加)之间可能的相互作用变得易于管理,因为它们可以被呈现为有限数量结构主题的变体。我们讨论了可能产生当前一系列肌动蛋白结合模块的进化途径。