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Mismodeled purines: implicit alternates and hidden Hoogsteens

机译:Mismodeled嘌呤:隐式交替和隐藏Hoogsteens

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摘要

Hoogsteen base pairs are seen in DNA crystal structures, but only rarely. This study tests whether Hoogsteens or other syn purines are either under‐modeled or over‐modeled, which are known problems for rare conformations. Candidate purines needing a syn / anti 180° flip were identified by diagnostic patterns of difference electron‐density peaks. Manual inspection narrowed 105 flip candidates to 20 convincing cases, all at ≤2.7?? resolution. Rebuilding and refinement confirmed that 14 of these were authentic purine flips. Seven examples are modeled as Watson–Crick base pairs but should be Hoogsteens (commonest at duplex termini), and three had the opposite issue. Syn / anti flips were also needed for some single‐stranded purines. Five of the 20 convincing cases arose from an unmodeled alternate duplex running in the opposite direction. These are in semi‐palindromic DNA sequences bound by a homodimeric protein and show flipped‐purine‐like difference peaks at residues where the palindrome is imperfect. This study documents types of incorrect modeling which are worth avoiding. However, the primary conclusions are that such mistakes are infrequent, the bias towards fitting anti purines is very slight, and the occurrence rate of Hoogsteen base pairs in DNA crystal structures remains unchanged from earlier estimates at ~0.3%.
机译:Hoogsteen碱基对中DNA晶体结构,但很少。是否Hoogsteens或其他syn嘌呤无论是在地理建模或者在建模,罕见的构象的已知问题。嘌呤需要syn /反180°翻转被诊断的模式不同电子密度的峰值。缩小105翻转候选人20令人信服情况下,所有在≤2.7 ? ?细化证实,这些都是14真实的嘌呤翻转。建模为沃森克里克碱基对但应该在双末端Hoogsteens(常见),和三个了相反的问题。也需要一些单量困吗嘌呤。从一个未建模替代双中运行相反的方向。homodimeric蛋白质和DNA序列结合高嘌呤类区域显示了不同的山峰残留的回文是不完美的。文件类型不正确的建模研究是需要避免。结论是这样的错误罕见的,偏向反嘌呤很轻微的,发生的吗Hoogsteen碱基对的DNA晶体结构从早些时候估计在保持不变~0.3%.

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