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DBMODELING - A database applied to the study of protein targets from genome projects

dc.contributor.authorda Silveira, NJF
dc.contributor.authorBonalumi, C. E.
dc.contributor.authorUchao, H. B.
dc.contributor.authorPereira, J. H.
dc.contributor.authorCanduri, F.
dc.contributor.authorde Azevedo, W. F.
dc.contributor.institutionPontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de Mato Grosso do Sul (UFMS)
dc.date.accessioned2014-05-20T15:25:49Z
dc.date.available2014-05-20T15:25:49Z
dc.date.issued2006-01-01
dc.description.abstractGenome sequencing efforts are providing us with complete genetic blueprints for hundreds of organisms. We are now faced with assigning, understanding, and modifying the functions of proteins encoded by these genomes. DBMODELING is a relational database of annotated comparative protein structure models and their metabolic pathway characterization, when identified. This procedure was applied to complete genomes such as Mycobacteritum tuberculosis and Xylella fastidiosa. The main interest in the study of metabolic pathways is that some of these pathways are not present in humans, which makes them selective targets for drug design, decreasing the impact of drugs in humans. In the database, there are currently 1116 proteins from two genomes. It can be accessed by any researcher at http://www.biocristalografia.df.ibilce.unesp.br/tools/. This project confirms that homology modeling is a useful tool in structural bioinformatics and that it can be very valuable in annotating genome sequence information, contributing to structural and functional genomics, and analyzing protein-ligand docking.en
dc.description.affiliationPUCRS, Fac Biociencias, BR-90619900 Porto Alegre, RS, Brazil
dc.description.affiliationUNESP, Programa Posgrad Biofis Mol, Dept Fis, Sao Jose do Rio Preto, SP, Brazil
dc.description.affiliationUFMS, CCBS, Dept Morfofisiol, BR-79070900 Campo Grande, MS, Brazil
dc.description.affiliationUnespUNESP, Programa Posgrad Biofis Mol, Dept Fis, Sao Jose do Rio Preto, SP, Brazil
dc.format.extent366-374
dc.identifierhttp://dx.doi.org/10.1385/CBB:44:3:366
dc.identifier.citationCell Biochemistry and Biophysics. Totowa: Humana Press Inc., v. 44, n. 3, p. 366-374, 2006.
dc.identifier.doi10.1385/CBB:44:3:366
dc.identifier.issn1085-9195
dc.identifier.urihttp://hdl.handle.net/11449/36162
dc.identifier.wosWOS:000237403800006
dc.language.isoeng
dc.publisherHumana Press Inc
dc.relation.ispartofCell Biochemistry and Biophysics
dc.relation.ispartofjcr1.455
dc.relation.ispartofsjr0,581
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectbioinformaticspt
dc.subjectDatabasept
dc.subjecthomology modelingpt
dc.subjectprotein structure, drug design, metabolic pathwaypt
dc.titleDBMODELING - A database applied to the study of protein targets from genome projectsen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights
dcterms.rightsHolderHumana Press Inc
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentFísica - IBILCEpt

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