Literature DB >> 10563583

Structural study of homeodomain protein-DNA complexes using a homology modeling approach.

C S Tung1.   

Abstract

The homeodomain is a conserved protein motif that binds to DNA and plays a central role in gene regulation. We use homeodomain as a model system to study the specific interactions between protein and DNA in a complex. Following the fundamental concept of homology modeling, we have developed an algorithm for predicting structures of both protein and DNA using the known structure of a similar complex as the template. The accuracies of the algorithm in predicting the complex structures are evaluated when two of the homeodomain protein-DNA complexes with known structures (antennapedia and MATalpha2) are selected as test systems. This algorithm allows structural studies of homeodomain binds to DNA with different sequences.

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Year:  1999        PMID: 10563583     DOI: 10.1080/07391102.1999.10508366

Source DB:  PubMed          Journal:  J Biomol Struct Dyn        ISSN: 0739-1102


  4 in total

1.  Reprogrammable recognition codes in bicoid homeodomain-DNA interaction.

Authors:  V Dave; C Zhao; F Yang; C S Tung; J Ma
Journal:  Mol Cell Biol       Date:  2000-10       Impact factor: 4.272

2.  Atomic model of the Thermus thermophilus 70S ribosome developed in silico.

Authors:  Chang-Shung Tung; Kevin Y Sanbonmatsu
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

3.  A 20 bp Duplication in Exon 2 of the Aristaless-Like Homeobox 4 Gene (ALX4) Is the Candidate Causative Mutation for Tibial Hemimelia Syndrome in Galloway Cattle.

Authors:  Bertram Brenig; Ekkehard Schütz; Michael Hardt; Petra Scheuermann; Markus Freick
Journal:  PLoS One       Date:  2015-06-15       Impact factor: 3.240

4.  Mismatched dNTP incorporation by DNA polymerase beta does not proceed via globally different conformational pathways.

Authors:  Kuo-Hsiang Tang; Marc Niebuhr; Chang-Shung Tung; Hsiu-Chien Chan; Chia-Cheng Chou; Ming-Daw Tsai
Journal:  Nucleic Acids Res       Date:  2008-04-02       Impact factor: 16.971

  4 in total

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