Literature DB >> 21601671

DNA-binding specificity prediction with FoldX.

Alejandro D Nadra1, Luis Serrano, Andreu Alibés.   

Abstract

With the advent of Synthetic Biology, a field between basic science and applied engineering, new computational tools are needed to help scientists reach their goal, their design, optimizing resources. In this chapter, we present a simple and powerful method to either know the DNA specificity of a wild-type protein or design new specificities by using the protein design algorithm FoldX. The only basic requirement is having a good resolution structure of the complex. Protein-DNA interaction design may aid the development of new parts designed to be orthogonal, decoupled, and precise in its target. Further, it could help to fine-tune the systems in terms of specificity, discrimination, and binding constants. In the age of newly developed devices and invented systems, computer-aided engineering promises to be an invaluable tool.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21601671     DOI: 10.1016/B978-0-12-385120-8.00001-2

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  6 in total

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3.  Cytosine methylation at CpCpG sites triggers accumulation of non-CpG methylation in gene bodies.

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4.  Structural basis of DNA target recognition by the B3 domain of Arabidopsis epigenome reader VAL1.

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5.  FoldX 5.0: working with RNA, small molecules and a new graphical interface.

Authors:  Javier Delgado; Leandro G Radusky; Damiano Cianferoni; Luis Serrano
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6.  Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations.

Authors:  Carlos D Bruque; Marisol Delea; Cecilia S Fernández; Juan V Orza; Melisa Taboas; Noemí Buzzalino; Lucía D Espeche; Andrea Solari; Verónica Luccerini; Liliana Alba; Alejandro D Nadra; Liliana Dain
Journal:  Sci Rep       Date:  2016-12-14       Impact factor: 4.379

  6 in total

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