Yamagata Y, Fujii S
Faculty of Pharmaceutical Sciences, Osaka University, Japan.
Nucleic Acids Symp Ser. 1995(34):7-8.
We report the model structure of enzyme-DNA complex based on X-ray structure of 3-methyladenine-DNA glycosylase II and mutagenic studies. The enzyme structure does not have any recognizable DNA binding motifs. The DNA was located in the large cleft between the two all alpha domains with the damaged adenine base moiety (3-methyladenine) of DNA duplex positioned in the entrance region of the cleft including the tryptophan and aspartic acid residues. For the target 3-methyladenine to interact with these residues, the 3-methyladenine has to flipped out from the DNA helix. A number of the positively charged amino acid residues adopt at the negatively charged phosphate moieties. It is necessary to kink the DNA helix slightly to form the good interactions between both molecules. The damaged base must be held in place by a number of interactions including the weak van der Waals and electrostatic attractions.
我们基于3-甲基腺嘌呤-DNA糖基化酶II的X射线结构和诱变研究报告了酶-DNA复合物的模型结构。酶结构没有任何可识别的DNA结合基序。DNA位于两个全α结构域之间的大裂隙中,DNA双链体中受损的腺嘌呤碱基部分(3-甲基腺嘌呤)位于裂隙的入口区域,包括色氨酸和天冬氨酸残基。为了使目标3-甲基腺嘌呤与这些残基相互作用,3-甲基腺嘌呤必须从DNA螺旋中翻转出来。许多带正电荷的氨基酸残基与带负电荷的磷酸基团结合。有必要使DNA螺旋稍微扭结以在两个分子之间形成良好的相互作用。受损碱基必须通过包括弱范德华力和静电引力在内的多种相互作用保持在原位。