Walter M R, Cook W J, Cole L B, Short S A, Koszalka G W, Krenitsky T A, Ealick S E
Department of Biochemistry, University of Alabama, Birmingham 35294.
J Biol Chem. 1990 Aug 15;265(23):14016-22. doi: 10.2210/pdb1tpt/pdb.
The three-dimensional structure of thymidine phosphorylase from Escherichia coli has been determined at 2.8 A resolution using multiple-isomorphous-replacement techniques. The amino acid sequence deduced from the deoA DNA sequence is also reported. Thymidine phosphorylase exists in the crystal as an S-shaped dimer in which the subunits are related by a crystallographic 2-fold axis. Each subunit is composed of a small alpha-helical domain of six helices and a large alpha/beta domain. The alpha/beta domain includes a six-stranded mixed beta-sheet and a four-stranded antiparallel beta-sheet. The active site has been identified by difference Fourier analyses of the binding of thymine and thymidine and lies in a cavity between the small and large domains. The central beta-sheet is splayed open to accommodate a putative phosphate-binding site which is probably occupied by a sulfate ion in the crystal.
利用多同晶置换技术,已在2.8埃分辨率下测定了来自大肠杆菌的胸苷磷酸化酶的三维结构。同时还报道了从deoA DNA序列推导出来的氨基酸序列。胸苷磷酸化酶在晶体中以S形二聚体形式存在,其中亚基通过一个晶体学二重轴相关联。每个亚基由一个包含六个螺旋的小α螺旋结构域和一个大的α/β结构域组成。α/β结构域包括一个六链混合β折叠和一个四链反平行β折叠。通过对胸腺嘧啶和胸苷结合的差分傅里叶分析确定了活性位点,它位于小结构域和大结构域之间的一个腔内。中央β折叠张开以容纳一个假定的磷酸结合位点,在晶体中该位点可能被一个硫酸根离子占据。