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相似文献

1
Structural models for non-helical DNA.非螺旋DNA的结构模型
EMBO J. 1986 Jul;5(7):1719-25. doi: 10.1002/j.1460-2075.1986.tb04416.x.
2
Conformational studies of nucleic acids: IV. The conformational energetics of oligonucleotides: d(ApApApA) and ApApApA.核酸的构象研究:IV. 寡核苷酸d(ApApApA)和ApApApA的构象能量学
J Biomol Struct Dyn. 1986 Aug;4(1):69-98. doi: 10.1080/07391102.1986.10507647.
3
DNA stretching and compression: large-scale simulations of double helical structures.DNA拉伸与压缩:双螺旋结构的大规模模拟
J Mol Biol. 1999 Jun 25;289(5):1301-26. doi: 10.1006/jmbi.1999.2798.
4
The occurence of the syn-C3' endo conformation and the distorted backbone conformations for C4'-C5' and P-O5' in oligo and polynucleotides.寡核苷酸和多核苷酸中C3' 内型构象的出现以及C4'-C5' 和P-O5' 的扭曲主链构象。
J Biomol Struct Dyn. 2001 Jun;18(6):824-31. doi: 10.1080/07391102.2001.10506710.
5
Hexagonal crystal structure of the A-DNA octamer d(GTGTACAC) and its comparison with the tetragonal structure: correlated variations in helical parameters.A-DNA八聚体d(GTGTACAC)的六方晶体结构及其与四方结构的比较:螺旋参数的相关变化
Biochemistry. 1991 Apr 9;30(14):3567-76. doi: 10.1021/bi00228a030.
6
The crystal structure of d(CCCCGGGG): a new A-form variant with an extended backbone conformation.d(CCCCGGGG)的晶体结构:一种具有延伸主链构象的新型A 型变体。
J Biomol Struct Dyn. 1987 Oct;5(2):199-217. doi: 10.1080/07391102.1987.10506390.
7
Determination of nucleic acid backbone conformation by 1H NMR.通过核磁共振氢谱确定核酸主链构象
Biochemistry. 1992 Apr 14;31(14):3564-74. doi: 10.1021/bi00129a003.
8
Nucleic acid model building: the multiple backbone solutions associated with a given base morphology.核酸模型构建:与特定碱基形态相关的多种主链解决方案。
J Biomol Struct Dyn. 1987 Jun;4(6):895-938. doi: 10.1080/07391102.1987.10507690.
9
Polypurine/polypyrimidine hairpins form a triple helix structure at low pH.聚嘌呤/聚嘧啶发夹在低pH值下形成三螺旋结构。
Nucleic Acids Res. 1990 Nov 25;18(22):6523-9. doi: 10.1093/nar/18.22.6523.
10
DNA bending and sequence-dependent backbone conformation NMR and computer experiments.DNA弯曲与序列依赖性主链构象:核磁共振与计算机实验
Eur J Biochem. 1999 Oct 1;265(1):35-53. doi: 10.1046/j.1432-1327.1999.00639.x.

引用本文的文献

1
Backbone-base inclination as a fundamental determinant of nucleic acid self- and cross-pairing.主链碱基倾斜作为核酸自身配对和交叉配对的基本决定因素。
Nucleic Acids Res. 2007;35(19):6611-24. doi: 10.1093/nar/gkm612. Epub 2007 Sep 28.
2
A new DNA nanostructure, the G-wire, imaged by scanning probe microscopy.一种新的DNA纳米结构——G线,通过扫描探针显微镜成像。
Nucleic Acids Res. 1995 Feb 25;23(4):696-700. doi: 10.1093/nar/23.4.696.
3
Stable DNA unwinding, not "breathing," accounts for single-strand-specific nuclease hypersensitivity of specific A+T-rich sequences.稳定的DNA解旋而非“呼吸”作用,是特定富含A+T序列单链特异性核酸酶超敏反应的原因。
Proc Natl Acad Sci U S A. 1988 Dec;85(24):9464-8. doi: 10.1073/pnas.85.24.9464.
4
Dam methyltransferase sites located within the loop region of the oligopurine-oligopyrimidine sequences capable of forming H-DNA are undermethylated in vivo.位于能够形成H-DNA的寡嘌呤-寡嘧啶序列环区的Dam甲基转移酶位点在体内发生低甲基化。
Nucleic Acids Res. 1990 Feb 11;18(3):605-11. doi: 10.1093/nar/18.3.605.

本文引用的文献

1
The structure of DNA.DNA的结构。
Cold Spring Harb Symp Quant Biol. 1953;18:123-31. doi: 10.1101/sqb.1953.018.01.020.
2
Left-handed double helical DNA: variations in the backbone conformation.左手双螺旋DNA:主链构象的变化
Science. 1981 Jan 9;211(4478):171-6. doi: 10.1126/science.7444458.
3
X-ray diffraction study of a new crystal form of the nucleosome core showing higher resolution.对具有更高分辨率的核小体核心新晶体形式的X射线衍射研究。
J Mol Biol. 1981 Feb 5;145(4):757-69. doi: 10.1016/0022-2836(81)90313-2.
4
Visualization of an unwound DNA duplex.解旋DNA双链的可视化。
Nature. 1980 Oct 9;287(5782):561-3. doi: 10.1038/287561a0.
5
Structure of a B-DNA dodecamer: conformation and dynamics.一种B型DNA十二聚体的结构:构象与动力学
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2179-83. doi: 10.1073/pnas.78.4.2179.
6
Sequence-dependent conformation of an A-DNA double helix. The crystal structure of the octamer d(G-G-T-A-T-A-C-C).A-DNA双螺旋的序列依赖性构象。八聚体d(G-G-T-A-T-A-C-C)的晶体结构。
J Mol Biol. 1983 May 15;166(2):183-201. doi: 10.1016/s0022-2836(83)80005-9.
7
An analysis of the sequence dependence of the structure and energy of A- and B-DNA models using molecular mechanics.使用分子力学对A-DNA和B-DNA模型的结构与能量的序列依赖性进行分析。
Biopolymers. 1983 Mar;22(3):969-1002. doi: 10.1002/bip.360220316.
8
Antibodies to left-handed Z-DNA bind to interband regions of Drosophila polytene chromosomes.抗左旋Z-DNA的抗体与果蝇多线染色体的间带区域结合。
Nature. 1981 Dec 3;294(5840):417-22. doi: 10.1038/294417a0.
9
A + T-rich linkers define functional domains in eukaryotic DNA.富含A + T的接头定义了真核生物DNA中的功能域。
Nature. 1982 Jan 21;295(5846):260-2. doi: 10.1038/295260a0.
10
DNA structural variations in the E. coli tyrT promoter.大肠杆菌tyrT启动子中的DNA结构变异
Cell. 1984 Jun;37(2):491-502. doi: 10.1016/0092-8674(84)90379-9.

非螺旋DNA的结构模型

Structural models for non-helical DNA.

作者信息

Yagil G, Sussman J L

出版信息

EMBO J. 1986 Jul;5(7):1719-25. doi: 10.1002/j.1460-2075.1986.tb04416.x.

DOI:10.1002/j.1460-2075.1986.tb04416.x
PMID:3017709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1166999/
Abstract

Structural modelling techniques are employed to explore the energetic requirements for the transformation of classical B DNA into unwound yet double-stranded DNA structures. Structural idealization using CORELS computer program of Sussman et al. followed by energy minimization using the EREF program of Levitt, leads to two regular non-helical models. In both models, the bases are conventionally paired and stacked, yet there is no net rotation between successive base pairs. One model, N1, has a 1-bp repeating unit; the second, N2, has a 2-bp repeating unit. The dihedral angles of the backbone all have values found either in the B or the Z form of DNA, except for the P-O5'-C5'-C4' angle, which is in the unprecedented g+ or g- domains. The energy difference found between the two N form models and B form DNA are 6.6 and 3.4 kcal/mol/nucleotide for N1 and N2 respectively. These relatively low energy differences encourage the idea that non-helical forms of DNA may contribute to the alternate DNA structures found in S1 nuclease sensitive and other regulatory regions of active genes.

摘要

采用结构建模技术来探索将经典B型DNA转变为解旋但仍为双链DNA结构所需的能量。使用苏斯曼等人的CORELS计算机程序进行结构理想化,随后使用莱维特的EREF程序进行能量最小化,得到了两种规则的非螺旋模型。在这两种模型中,碱基按常规方式配对和堆积,但连续碱基对之间没有净旋转。一种模型N1有一个1碱基对的重复单元;第二种模型N2有一个2碱基对的重复单元。主链的二面角除了P - O5'-C5'-C4'角处于前所未有的g+或g-区域外,其他值均在DNA的B型或Z型中出现。N1和N2这两种N型模型与B型DNA之间的能量差分别为6.6和3.4千卡/摩尔/核苷酸。这些相对较低的能量差支持了这样一种观点,即DNA的非螺旋形式可能有助于在活跃基因的S1核酸酶敏感区域和其他调控区域中发现的交替DNA结构。