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ReadOut: structure-based calculation of direct and indirect readout energies and specificities for protein-DNA recognition.

Authors :
Ahmad S
Kono H
Araúzo-Bravo MJ
Sarai A
Source :
Nucleic acids research [Nucleic Acids Res] 2006 Jul 01; Vol. 34 (Web Server issue), pp. W124-7.
Publication Year :
2006

Abstract

Protein-DNA interactions play a central role in regulatory processes at the genetic level. DNA-binding proteins recognize their targets by direct base-amino acid interactions and indirect conformational energy contribution from DNA deformations and elasticity. Knowledge-based approach based on the statistical analysis of protein-DNA complex structures has been successfully used to calculate interaction energies and specificities of direct and indirect readouts in protein-DNA recognition. Here, we have implemented the method as a webserver, which calculates direct and indirect readout energies and Z-scores, as a measure of specificity, using atomic coordinates of protein-DNA complexes. This server is freely available at http://gibk26.bse.kyutech.ac.jp/jouhou/readout/. The only input to this webserver is the Protein Data Bank (PDB) style coordinate data of atoms or the PDB code itself. The server returns total energy Z-scores, which estimate the degree of sequence specificity of the protein-DNA complex. This webserver is expected to be useful for estimating interaction energy and DNA conformation energy, and relative contributions to the specificity from direct and indirect readout. It may also be useful for checking the quality of protein-DNA complex structures, and for engineering proteins and target DNAs.

Details

Language :
English
ISSN :
1362-4962
Volume :
34
Issue :
Web Server issue
Database :
MEDLINE
Journal :
Nucleic acids research
Publication Type :
Academic Journal
Accession number :
16844974
Full Text :
https://doi.org/10.1093/nar/gkl104