Literature DB >> 12568710

Modulation of DNA-binding domains for sequence-specific DNA recognition.

Ronen Marmorstein1, Mary X Fitzgerald.   

Abstract

Sequence-specific DNA-binding proteins use diverse mechanisms to recognize their cognate DNA sites. In addition to direct sequence-specific DNA contacts made by DNA recognition domains, extrinsic factors such as ligand binding, homo- and hetero-dimeric protein associations, and association via other transcription factors can also modulate the DNA-recognition properties of DNA-binding domains. In each case, these extrinsic factors act as molecular switches to facilitate cognate DNA recognition. In this article we review the available structural examples of how such extrinsic factors can modulate the way in which a DNA-binding domain can recognize DNA. Together, these examples reveal a variety of ways in which such extrinsic factors can significantly extend the repertoire of DNA sites recognized by a given DNA-binding domain.

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Year:  2003        PMID: 12568710     DOI: 10.1016/s0378-1119(02)01207-6

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  7 in total

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Authors:  Michael F Berger; Martha L Bulyk
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5.  Structural basis for dimerization in DNA recognition by Gal4.

Authors:  Manqing Hong; Mary X Fitzgerald; Sandy Harper; Cheng Luo; David W Speicher; Ronen Marmorstein
Journal:  Structure       Date:  2008-07       Impact factor: 5.006

6.  A dimer-specific function of the transcription factor NFATp.

Authors:  James V Falvo; Charles H Lin; Alla V Tsytsykova; Peter K Hwang; Dimitris Thanos; Anne E Goldfeld; Tom Maniatis
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7.  ENPD - A Database of Eukaryotic Nucleic Acid Binding Proteins: Linking Gene Regulations to Proteins.

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  7 in total

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