Sternglanz H, Bugg C E
Biochim Biophys Acta. 1975 Jan 6;378(1):1-11. doi: 10.1016/0005-2787(75)90130-6.
Three-dimensional X-ray diffraction data were used to determine the crystal structures of 5-chlorouracil and 5-bromouracil, two mutagenic pyrimidine analogs that can substitute for thymine in DNA. Crystals of the two compounds are nearly isostructural. The space group is P21/c, with a equals 8.450(6), b equals 6.842(3), c equals 11.072(16) angstrom, beta equals 123.53(19) degrees for 5-chlorouracil, and a equals 8.598(3), b equals 6.886(1), c equals 11.417(5) angstrom, beta equals 123.93(3) degrees for 5-bromouracil. Intensity data were collected with an automated diffractometer. The structures were refined by full-matrix least-squares to R equals 0.058 for 5-chlorouracil and R equals 0.027 for 5-bromouracil. The analogs from planar, hydrogen-bonded ribbons that are nearly identical to those found in the crystal structure of thymine monohydrate. As in many other structures of 5-halogenated uracil derivatives, the bases assume a stacking pattern that permits intimate contacts between the halogen substituents and the pyrimidine rings of adjacent bases. This stacking pattern involves halogen contacts that are significantly shorter than normal van der Waals interactions. The crystallographic results provide additional evidence that halogen substituents influence the stacking patterns of uracil derivatives, while exerting little direct effect on the hydrogen-bonding properties. The observed stacking patterns are consistent with the hypothesis that altered stacking interactions may account for the mis-pairing between 5-halogenated uracil bases and guanine residues within double-helical nucleic acids.
利用三维X射线衍射数据测定了5-氯尿嘧啶和5-溴尿嘧啶的晶体结构,这两种诱变嘧啶类似物可在DNA中替代胸腺嘧啶。这两种化合物的晶体几乎是同构的。空间群为P21/c,5-氯尿嘧啶的a等于8.450(6)埃,b等于6.842(3)埃,c等于11.072(16)埃,β等于123.53(19)度;5-溴尿嘧啶的a等于8.598(3)埃,b等于6.886(1)埃,c等于11.417(5)埃,β等于123.93(3)度。强度数据用自动衍射仪收集。结构通过全矩阵最小二乘法进行精修,5-氯尿嘧啶的R等于0.058,5-溴尿嘧啶的R等于0.027。这些类似物形成平面的、氢键连接的条带,与一水合胸腺嘧啶晶体结构中的条带几乎相同。与许多其他5-卤代尿嘧啶衍生物的结构一样,碱基呈现出一种堆积模式,使得卤素取代基与相邻碱基的嘧啶环之间能够紧密接触。这种堆积模式涉及的卤素接触明显短于正常的范德华相互作用。晶体学结果提供了额外的证据,表明卤素取代基影响尿嘧啶衍生物的堆积模式,而对氢键性质几乎没有直接影响。观察到的堆积模式与以下假设一致,即堆积相互作用的改变可能解释了双螺旋核酸中5-卤代尿嘧啶碱基与鸟嘌呤残基之间的错配。