Walkinshaw M D, Saenger W, Maelicke A
Proc Natl Acad Sci U S A. 1980 May;77(5):2400-4. doi: 10.1073/pnas.77.5.2400.
The three-dimensional structure of alpha-cobra-toxin, the "long" neurotoxin from the venom of Naja naja siamensis, has been determined at 2.8-A resolution. Crystals grown as hexagonal needles have space group P6522 with unit cell parameters a = b = 74.59 A, c = 42.89 A; one molecule per asymmetric unit. Phases were determined with a single isomorphous derivative with HgI2 by using the anomalous scattering of the single-site HgI2 molecule to resolve the phase ambiguity. The polypeptide chain folds into three major loops and one tail emerging from a globular head. The protruding long central loop (residues 21-40) is flanked on either side by two shorter loops (residues 4-13 and 44-55); the tail piece (residues 63-71) hangs behind this loop. The molecular conformation is determined by four disulfides in the head and one at the tip of the long loop, by a triple-stranded beta-pleated sheet involving this loop, and by hydrophobic interactions stabilizing the other two loops. The structure of alpha-cobratoxin is compared to that described for the "short" erabutoxin b which shows similar arrangement of structurally and functionally invariant groups.
已在2.8埃分辨率下测定了眼镜王蛇毒中“长”神经毒素α-眼镜蛇毒素的三维结构。以六方针状生长的晶体属于空间群P6522,晶胞参数为a = b = 74.59埃,c = 42.89埃;每个不对称单元中有一个分子。通过利用单位点HgI2分子的反常散射来解决相位模糊问题,用HgI2的单个同晶型衍生物确定了相位。多肽链折叠成三个主要环和一条从球状头部伸出的尾巴。突出的长中央环(残基21 - 40)两侧是两个较短的环(残基4 - 13和44 - 55);尾段(残基63 - 71)悬在这个环的后面。分子构象由头部的四个二硫键和长环末端的一个二硫键、涉及该环的三股β-折叠片以及稳定其他两个环的疏水相互作用决定。将α-眼镜蛇毒素的结构与已描述的“短”海蛇毒素b的结构进行了比较,后者显示出结构和功能不变基团的类似排列。