A small region in HMG I(Y) is critical for cooperation with NF-kappaB on DNA. (Q38322949)

2 September 2017

title

A small region in HMG I(Y) is critical for cooperation with NF-kappaB on DNA. (English)

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2 September 2017

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Zhang XM

1

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2 September 2017

Verdine GL

series ordinal

2

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2 September 2017

language of work or name

English

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publication date

1 July 1999

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Journal of Biological Chemistry

2 September 2017

published in

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2 September 2017

volume

274

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2 September 2017

issue

29

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2 September 2017

page(s)

20235-20243

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Structural features of the HMG chromosomal proteins and their genes

2 September 2017

cites work

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The solution structure of an HMG-I(Y)-DNA complex defines a new architectural minor groove binding motif

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21 January 2018

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Functional interaction between the POU domain protein Tst-1/Oct-6 and the high-mobility-group protein HMG-I/Y

21 January 2018

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The high mobility group protein HMG I(Y) is required for NF-kappa B-dependent virus induction of the human IFN-beta gene

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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The activation domain of GAL4 protein mediates cooperative promoter binding with general transcription factors in vivo

21 January 2018

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Recruitment of CBP/p300 by the IFN beta enhanceosome is required for synergistic activation of transcription

21 January 2018

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21 January 2018

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NF-kappaB mediated transcriptional activation is enhanced by the architectural factor HMGI-C.

21 January 2018

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A novel AT-rich DNA binding protein that combines an HMG I-like DNA binding domain with a putative transcription domain

21 January 2018

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Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias

21 January 2018

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Reversal of intrinsic DNA bends in the IFN beta gene enhancer by transcription factors and the architectural protein HMG I(Y)

21 January 2018

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High mobility group protein I(Y) is required for function and for c-Rel binding to CD28 response elements within the GM-CSF and IL-2 promoters

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.274.29.20235

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2 September 2017

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