Schreuder H A, Prick P A, Wierenga R K, Vriend G, Wilson K S, Hol W G, Drenth J
Laboratory of Chemical Physics, University of Groningen, The Netherlands.
J Mol Biol. 1989 Aug 20;208(4):679-96. doi: 10.1016/0022-2836(89)90158-7.
Using synchrotron radiation, the X-ray diffraction intensities of crystals of p-hydroxy-benzoate hydroxylase, complexed with the substrate p-hydroxybenzoate, were measured to a resolution of 1.9 A. Restrained least-squares refinement alternated with rebuilding in electron density maps yielded an atom model of the enzyme-substrate complex with a crystallographic R-factor of 15.6% for 31,148 reflections between 6.0 and 1.9 A. A total of 330 solvent molecules was located. In the final model, only three residues have deviating phi-psi angle combinations. One of them, the active site residue Arg44, has a well-defined electron density and may be strained to adopt this conformation for efficient catalysis. The mode of binding of FAD is distinctly different for the different components of the coenzyme. The adenine ring is engaged in three water-mediated hydrogen bonds with the protein, while making only one direct hydrogen bond with the enzyme. The pyrophosphate moiety makes five water-mediated versus three direct hydrogen bonds. The ribityl and ribose moieties make only direct hydrogen bonds, in all cases, except one, with side-chain atoms. The isoalloxazine ring also makes only direct hydrogen bonds, but virtually only with main-chain atoms. The conformation of FAD in p-hydroxybenzoate hydroxylase is strikingly similar to that in glutathione reductase, while the riboflavin-binding parts of these two enzymes have no structural similarity at all. The refined 1.9 A structure of the p-hydroxybenzoate hydroxylase-substrate complex was the basis of further refinement of the 2.3 A structure of the enzyme-product complex. The result was a final R-factor of 16.7% for 14,339 reflections between 6.0 and 2.3 A and an improved geometry. Comparison between the complexes indicated only small differences in the active site region, where the product molecule is rotated by 14 degrees compared with the substrate in the enzyme-substrate complex. During the refinements of the enzyme-substrate and enzyme-product complexes, the flavin ring was allowed to bend or twist by imposing planarity restraints on the benzene and pyrimidine ring, but not on the flavin ring as a whole. The observed angle between the benzene ring and the pyrimidine ring was 10 degrees for the enzyme-substrate complex and 19 degrees for the enzyme-product complex. Because of the high temperature factors of the flavin ring in the enzyme-product complex, the latter value should be treated with caution. Six out of eight peptide residues near the flavin ring are oriented with their nitrogen atom pointing towards the ring.(ABSTRACT TRUNCATED AT 400 WORDS)
利用同步辐射,测量了与底物对羟基苯甲酸复合的对羟基苯甲酸羟化酶晶体的X射线衍射强度,分辨率达到1.9埃。在电子密度图中进行约束最小二乘精修与重建交替操作,得到了酶-底物复合物的原子模型,对于6.0至1.9埃之间的31,148个反射,晶体学R因子为15.6%。共定位了330个溶剂分子。在最终模型中,只有三个残基具有偏离的φ-ψ角组合。其中一个,活性位点残基Arg44,具有明确的电子密度,可能因有效催化而被迫采用这种构象。对于辅酶的不同组分,FAD的结合模式明显不同。腺嘌呤环与蛋白质通过三个水介导的氢键结合,同时仅与酶形成一个直接氢键。焦磷酸部分形成五个水介导的氢键与三个直接氢键。除一种情况外,核糖醇和核糖部分仅与侧链原子形成直接氢键。异咯嗪环也仅形成直接氢键,但实际上几乎仅与主链原子形成氢键。对羟基苯甲酸羟化酶中FAD的构象与谷胱甘肽还原酶中的构象惊人地相似,而这两种酶的核黄素结合部分在结构上毫无相似之处。对羟基苯甲酸羟化酶-底物复合物经精修的1.9埃结构是对酶-产物复合物2.3埃结构进一步精修的基础。结果是对于6.0至2.3埃之间的14,339个反射,最终R因子为16.7%,且几何结构得到改善。复合物之间的比较表明,活性位点区域只有微小差异,其中产物分子相对于酶-底物复合物中的底物旋转了14度。在酶-底物和酶-产物复合物的精修过程中,通过对苯环和嘧啶环施加平面性约束,使黄素环能够弯曲或扭曲,但不是对整个黄素环施加约束。对于酶-底物复合物,苯环与嘧啶环之间观察到的角度为10度,对于酶-产物复合物为19度。由于酶-产物复合物中黄素环的温度因子较高,后一个值应谨慎对待。黄素环附近的八个肽残基中有六个的氮原子朝向环排列。(摘要截断于400字)