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Analysis of Gal4-directed transcription activation using Tra1 mutants selectively defective for interaction with Gal4

NIAID Data Ecosystem2026-03-09 收录

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Gal4-Tra1相互作用

数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE31391 数据链接链接失效反馈

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资源简介：

This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

应用场景：

创建时间：

2016-07-01

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DNA相互作用

ToxR bacterial transcriptional regulator bound to 25 bp toxT promoter DNA Descriptor: Cholera toxin transcriptional activator, DNA (25-MER) Authors: Canals, A, Pieretti, S, Muriel, M, El Yaman, N, Fab

Protein Data Bank Japan2024-06-19 更新50

Nucleoporin 153 links nuclear pore complex to chromatin architecture by mediating CTCF and cohesin binding [RNA-Seq]

染色质三维构象调控

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Establishment of cell lineage specification, maintenance of cellular states and cellular responses to developmental cues rely on gene regulation and spatial genome organization during early developmen

NIAID Data Ecosystem50

Dual regulation of open-complex formation and promoter clearance by Arc explains a novel repressor to activator switch.

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基因表达

In studies of variants of the P(ant) promoter of bacteriophage P22, the Arc protein was found not only to slow the rate at which RNA polymerase forms open complexes but also to accelerate the rate at

PubMed Central1996-08-20 更新30

Table S1 from Disruption of TFIIH activities generates a stress gene expression response and reveals possible new targets against cancer

癌症靶向治疗

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Disruption of the enzymatic activities of the transcription factor TFIIH by the small molecules Triptolide (TPL) or THZ1 could be used against cancer. Here, we used the MCF10A-ErSrc oncogenesis model

Figshare2020-06-01 更新50

The Nature of the TRAP:Anti-TRAP complex

蛋白质结构解析

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The Nature of the TRAP:Anti-TRAP complex Descriptor: TRYPTOPHAN, Transcription attenuation protein mtrB, Tryptophan RNA-binding attenuator protein-inhibitory protein, ... Authors: Watanabe, M, Heddle,

Protein Data Bank Japan2023-11-01 更新40

Analysis of Gal4-directed transcription activation using Tra1 mutants selectively defective for interaction with Gal4

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