• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[四链DNA。具有不同碱基结合变体的聚(dT).聚(dA).聚(dA).聚(dT)规则螺旋的构象分析]

[Four-stranded DNA. Conformational analysis of regular spirals of poly(dT).poly(dA).poly(dA).poly(dT) with different base binding variations].

作者信息

Chernyĭ A A, Lysov Iu P, Il'icheva I A, Zibrov A S, Shchelkina A K, Borisova O F, Mamaeva O K, Florent'ev V L

出版信息

Mol Biol (Mosk). 1990 Sep-Oct;24(5):1399-410.

PMID:2290430
Abstract

Conformational analysis of four stranded DNA helices poly(dT).poly(dA).poly(dA).poly(dT) with parallel arrangement of the identical sugar-phosphate chains connected by twofold symmetry has been performed. All possible models of symmetrical base binding were checked. By the potential energy optimization the dihedral angles and helices parameters of stable conformations of four stranded polynucleotides were calculated. The dependences of conformational energy on the base complex structure and mutual orientation of the poly(dA).and poly(dT) chains were studied. Possible biological functions of four stranded helices are discussed.

摘要

对具有通过双重对称性连接的相同糖磷酸链平行排列的四链DNA螺旋聚(dT)·聚(dA)·聚(dA)·聚(T)进行了构象分析。检查了对称碱基结合的所有可能模型。通过势能优化计算了四链多核苷酸稳定构象的二面角和螺旋参数。研究了构象能量对碱基复合物结构以及聚(dA)和聚(dT)链相互取向的依赖性。讨论了四链螺旋可能的生物学功能。

相似文献

1
[Four-stranded DNA. Conformational analysis of regular spirals of poly(dT).poly(dA).poly(dA).poly(dT) with different base binding variations].[四链DNA。具有不同碱基结合变体的聚(dT).聚(dA).聚(dA).聚(dT)规则螺旋的构象分析]
Mol Biol (Mosk). 1990 Sep-Oct;24(5):1399-410.
2
Four-stranded DNA helices: conformational analysis of regular poly(dT).poly(dA).poly(dA).poly(dT) helices with various types of base binding.四链DNA螺旋:具有各种碱基结合类型的规则聚(dT)·聚(dA)·聚(dA)·聚(dT)螺旋的构象分析
J Biomol Struct Dyn. 1990 Dec;8(3):513-27. doi: 10.1080/07391102.1990.10507826.
3
[Parallel double DNA spiral. A conformational analysis of regular spirals of poly(dA).poly(dT) with different variations of joining bases].[平行双DNA螺旋。具有不同连接碱基变体的聚(dA)·聚(dT)规则螺旋的构象分析]
Mol Biol (Mosk). 1991 Jan-Feb;25(1):264-72.
4
[Parallel DNA double helices. II. Conformational analysis of regular helices having a second order axis of symmetry].[平行DNA双螺旋。II. 具有二阶对称轴的规则螺旋的构象分析]
Mol Biol (Mosk). 1989 Jul-Aug;23(4):1145-62.
5
[Parallel DNA helices. Conformational analysis of regular poly(dG).poly(dC) helices with different variants of base binding].[平行DNA螺旋。具有不同碱基结合变体的规则聚(dG)·聚(dC)螺旋的构象分析]
Mol Biol (Mosk). 1992 Nov-Dec;26(6):1332-7.
6
[Interaction of topotecan, DNA topoisomerase I inhibitor, with double-stranded polydeoxyribonucleotides. 4. Topotecan binds preferably to the GC base pairs of DNA].[拓扑替康(一种DNA拓扑异构酶I抑制剂)与双链多聚脱氧核糖核苷酸的相互作用。4. 拓扑替康优先结合于DNA的GC碱基对]
Mol Biol (Mosk). 2002 Sep-Oct;36(5):912-30.
7
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.
8
[Structure of the hydration envelope of the B-form of polydeoxyribonucleotides poly(dA-dC).poly(dG-dT) and poly(dA-dG).poly(dTs-dT) from the data of Monte-Carlo simulation].[基于蒙特卡洛模拟数据的聚脱氧核糖核苷酸B型poly(dA-dC).poly(dG-dT)和poly(dA-dG).poly(dT-dT)水化包膜结构]
Biofizika. 1988 May-Jun;33(3):422-9.
9
[Study of the relationship between secondary DNA strucure and base sequence by the technic of theoretical conformational analysis].[运用理论构象分析技术研究二级DNA结构与碱基序列之间的关系]
Biofizika. 1978 Mar-Apr;23(2):201-7.
10
Simultaneous binding of meso-tetrakis(N-methylpyridinium-4-yl)porphyrin and 4',6-diamidino-2-phenylindole at the minor grooves of poly(dA).poly(dT) and poly[d(A-T)(2)]: fluorescence resonance energy transfer between DNA bound drugs.中-四(N-甲基吡啶-4-基)卟啉与4',6-二脒基-2-苯基吲哚在聚(dA)·聚(dT)和聚[d(A-T)₂]小沟处的同时结合:DNA结合药物间的荧光共振能量转移
J Am Chem Soc. 2005 Mar 2;127(8):2417-24. doi: 10.1021/ja044555w.