Kabsch W, Mannherz H G, Suck D
EMBO J. 1985 Aug;4(8):2113-8. doi: 10.1002/j.1460-2075.1985.tb03900.x.
The shape of an actin subunit has been derived from an improved 6 A map of the complex of rabbit skeletal muscle actin and bovine pancreatic DNase I obtained by X-ray crystallographic methods. The three-dimensional structure of DNase I determined independently at 2.5 A resolution was compared with the DNase I electron density in the actin:DNase map. The two structures are very similar at 6 A resolution thus leading to an unambiguous identification of actin as well as DNase I electron density. Furthermore the correct hand of the actin structure is determined from the DNase I atomic structure. The resolution of the actin structure was extended to 4.5 A by using a single heavy-atom derivative and the knowledge of the atomic coordinates of DNase I. The dimensions of an actin subunit are 67 A X 40 A X 37 A. It consists of a small and a large domain, the small domain containing the N terminus. Actin is an alpha,beta-protein with a beta-pleated sheet in each domain. These sheets are surrounded by several alpha-helices, comprising at least 40% of the structure. The phosphate peak of the adenine nucleotide is located between the two domains. The complex of actin and DNase I as found in solution (i.e., the actin:DNase I contacts which do not depend on crystal packing) was deduced from a comparison of monoclinic with orthorhombic crystals. Residues 44-46, 51, 52, 60-62 of DNase I are close to a loop region in the small domain of actin. At a distance of approximately 15 A there is a second contact in the large domain in which Glu13 of DNase I is involved. A possible binding region for myosin is discussed.
肌动蛋白亚基的形状源自通过X射线晶体学方法获得的兔骨骼肌肌动蛋白与牛胰腺DNA酶I复合物的改进6埃图谱。将独立测定的分辨率为2.5埃的DNA酶I三维结构与肌动蛋白:DNA酶图谱中的DNA酶I电子密度进行了比较。在6埃分辨率下,这两种结构非常相似,从而能够明确识别肌动蛋白以及DNA酶I的电子密度。此外,根据DNA酶I的原子结构确定了肌动蛋白结构的正确手性。通过使用单一重原子衍生物以及DNA酶I的原子坐标知识,将肌动蛋白结构的分辨率扩展至4.5埃。肌动蛋白亚基的尺寸为67埃×40埃×37埃。它由一个小结构域和一个大结构域组成,小结构域包含N端。肌动蛋白是一种α、β蛋白,每个结构域中有一个β折叠片层。这些片层被几个α螺旋包围,α螺旋至少占结构的40%。腺嘌呤核苷酸的磷酸峰位于两个结构域之间。通过单斜晶体与正交晶体的比较,推断出溶液中存在的肌动蛋白与DNA酶I复合物(即不依赖晶体堆积的肌动蛋白:DNA酶I接触)。DNA酶I的44 - 46、51、52、60 - 62位残基靠近肌动蛋白小结构域中的一个环区。在大约15埃的距离处,大结构域中有第二个接触点,DNA酶I的Glu13参与其中。讨论了肌球蛋白的一个可能结合区域。