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Binding of Escherichia coli RNA polymerase holoenzyme to bacteriophage T7 DNA. Measurements of the rate of open complex formation at T7 promoter A.

作者信息

Rosenberg S, Kadesch T R, Chamberlin M J

出版信息

J Mol Biol. 1982 Feb 15;155(1):31-51. doi: 10.1016/0022-2836(82)90490-9.

DOI:10.1016/0022-2836(82)90490-9
PMID:7042986
Abstract
摘要

相似文献

1
Binding of Escherichia coli RNA polymerase holoenzyme to bacteriophage T7 DNA. Measurements of the rate of open complex formation at T7 promoter A.大肠杆菌RNA聚合酶全酶与噬菌体T7 DNA的结合。T7启动子A处开放复合物形成速率的测定。
J Mol Biol. 1982 Feb 15;155(1):31-51. doi: 10.1016/0022-2836(82)90490-9.
2
Binding of Escherichia coli RNA polymerase holoenzyme to bacteriophage T7 DNA. Measurements of binding at bacteriophage T7 promoter A1 using a template competition assay.大肠杆菌RNA聚合酶全酶与噬菌体T7 DNA的结合。使用模板竞争分析法对噬菌体T7启动子A1处的结合进行测量。
J Mol Biol. 1982 Feb 15;155(1):1-29. doi: 10.1016/0022-2836(82)90489-2.
3
Binding of Escherichia coli ribonucleic acid polymerase holoenzyme to a bacteriophage T7 promoter-containing fragment: evaluation of promoter binding constants as a function of solution conditions.大肠杆菌核糖核酸聚合酶全酶与含噬菌体T7启动子片段的结合:作为溶液条件函数的启动子结合常数评估
Biochemistry. 1980 Jul 22;19(15):3504-15. doi: 10.1021/bi00556a015.
4
Binding of Escherichia coli ribonucleic acid polymerase holoenzyme to a bacteriophage T7 promoter-containing fragment: selectivity exists over a wide range of solution conditions.大肠杆菌核糖核酸聚合酶全酶与含有噬菌体T7启动子的片段的结合:在广泛的溶液条件范围内存在选择性。
Biochemistry. 1980 Jul 22;19(15):3496-504. doi: 10.1021/bi00556a014.
5
On the promoter complex formation rate of E. coli RNA polymerases with T7 phage DNA.关于大肠杆菌RNA聚合酶与T7噬菌体DNA的启动子复合物形成速率
Nucleic Acids Res. 1980 Mar 25;8(6):1391-404. doi: 10.1093/nar/8.6.1391.
6
Bacteriophage T7 E promoter: identification and measurement of kinetics of association with Escherichia coli RNA polymerase.噬菌体T7 E启动子:与大肠杆菌RNA聚合酶结合动力学的鉴定与测定
Biochemistry. 1985 Apr 23;24(9):2219-27. doi: 10.1021/bi00330a016.
7
[Transcription initiation: influence of ionic strength and actinomycin D on the kinetics of the open promoter complex formation between Escherichia coli RNA-polymerase and T7 DNA].[转录起始:离子强度和放线菌素D对大肠杆菌RNA聚合酶与T7 DNA之间开放启动子复合物形成动力学的影响]
Mol Biol (Mosk). 1979 Sep-Oct;13(5):1077-84.
8
[RNA polymerase of a rifampicin-resistant mutant of Escherichia coli has an altered selectivity to phage T7 DNA promoters].[大肠杆菌利福平抗性突变体的RNA聚合酶对噬菌体T7 DNA启动子的选择性发生改变]
Mol Biol (Mosk). 1988 Mar-Apr;22(2):384-92.
9
Studies of the binding of Escherichia coli RNA polymerase to DNA. V. T7 RNA chain initiation by enzyme-DNA complexes.大肠杆菌RNA聚合酶与DNA结合的研究。V. 酶-DNA复合物引发的T7 RNA链起始
J Mol Biol. 1972 Sep 28;70(2):221-37. doi: 10.1016/0022-2836(72)90535-9.
10
[The effect of mutation in the beta-subunit of Escherichia coli RNA polymerase on the selectivity of complex formation with T7 DNA promoters].[大肠杆菌RNA聚合酶β亚基突变对与T7 DNA启动子形成复合物的选择性的影响]
Dokl Akad Nauk SSSR. 1989;309(2):487-91.

引用本文的文献

1
Stepwise Promoter Melting by Bacterial RNA Polymerase.逐步启动子熔解由细菌 RNA 聚合酶。
Mol Cell. 2020 Apr 16;78(2):275-288.e6. doi: 10.1016/j.molcel.2020.02.017. Epub 2020 Mar 10.
2
Promoter-specific transcription inhibition in Staphylococcus aureus by a phage protein.噬菌体蛋白对金黄色葡萄球菌启动子特异性转录的抑制作用。
Cell. 2012 Nov 21;151(5):1005-16. doi: 10.1016/j.cell.2012.10.034.
3
Solute probes of conformational changes in open complex (RPo) formation by Escherichia coli RNA polymerase at the lambdaPR promoter: evidence for unmasking of the active site in the isomerization step and for large-scale coupled folding in the subsequent conversion to RPo.
大肠杆菌RNA聚合酶在λPR启动子上形成开放复合物(RPo)过程中构象变化的溶质探针:异构化步骤中活性位点暴露以及随后转化为RPo过程中大规模耦合折叠的证据。
Biochemistry. 2006 Feb 21;45(7):2161-77. doi: 10.1021/bi051835v.
4
Mutations affecting two different steps in transcription initiation at the phage lambda PRM promoter.影响噬菌体λ PRM启动子转录起始两个不同步骤的突变。
Proc Natl Acad Sci U S A. 1983 Jan;80(2):496-500. doi: 10.1073/pnas.80.2.496.
5
RNA polymerase II ternary transcription complexes generated in vitro.体外生成的RNA聚合酶II三元转录复合物。
Nucleic Acids Res. 1983 Sep 10;11(17):6041-64. doi: 10.1093/nar/11.17.6041.
6
Sequence distributions associated with DNA curvature are found upstream of strong E. coli promoters.与DNA弯曲相关的序列分布在大肠杆菌强启动子的上游被发现。
Nucleic Acids Res. 1987 Jan 26;15(2):785-96. doi: 10.1093/nar/15.2.785.
7
Association of RNA polymerase having increased Km for ATP and UTP with hyperexpression of the pyrB and pyrE genes of Salmonella typhimurium.对ATP和UTP具有增加的米氏常数的RNA聚合酶与鼠伤寒沙门氏菌pyrB和pyrE基因的过表达之间的关联。
J Bacteriol. 1986 Jun;166(3):857-65. doi: 10.1128/jb.166.3.857-865.1986.
8
Promoter recognition and promoter strength in the Escherichia coli system.大肠杆菌系统中的启动子识别与启动子强度
EMBO J. 1987 Oct;6(10):3139-44. doi: 10.1002/j.1460-2075.1987.tb02624.x.
9
Topography of intermediates in transcription initiation of E.coli.
EMBO J. 1990 Jul;9(7):2215-20. doi: 10.1002/j.1460-2075.1990.tb07391.x.