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Molecular models for shikimate pathway enzymes of Xylella fastidiosa

dc.contributor.authorArcuri, H. A.
dc.contributor.authorCanduri, F.
dc.contributor.authorPereira, J. H.
dc.contributor.authorda Silveira, NJF
dc.contributor.authorCamera, J. C.
dc.contributor.authorde Oliveira, J. S.
dc.contributor.authorBasso, L. A.
dc.contributor.authorPalma, Mario Sergio [UNESP]
dc.contributor.authorSantos, D. S.
dc.contributor.authorde Azevedo, W. F.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)
dc.contributor.institutionInstituto Butantan
dc.contributor.institutionPontifícia Universidade Católica do Rio Grande do Sul (PUCRS)
dc.date.accessioned2014-05-20T13:54:38Z
dc.date.available2014-05-20T13:54:38Z
dc.date.issued2004-07-30
dc.description.abstractThe Xylella fastidiosa is a bacterium that is the cause of citrus variegated chlorosis (CVC). The shikimate pathway is of pivotal importance for production of a plethora of aromatic compounds in plants, bacteria, and fungi. Putative structural differences in the enzymes from the shikimate pathway, between the proteins of bacterial origin and those of plants, could be used for the development of a drug for the control of CVC. However, inhibitors for shikimate pathway enzymes should have high specificity for X. fastidiosa enzymes, since they are also present in plants. In order to pave the way for structural and functional efforts towards antimicrobial agent development, here we describe the molecular modeling of seven enzymes of the shikimate pathway of X. fastidiosa. The structural models of shikimate pathway enzymes, complexed with inhibitors, strongly indicate that the previously identified inhibitors may also inhibit the X. fastidiosa enzymes. (C) 2004 Elsevier B.V. All rights reserved.en
dc.description.affiliationUNESP, IBILCE, Dept Phys, BR-15054000 Sao Jose do Rio Preto, SP, Brazil
dc.description.affiliationUFRGS, Dept Mol Biol & Biotecnol, BR-91501970 Porto Alegre, RS, Brazil
dc.description.affiliationUNESP, Inst Biosci, Dept Biol, Lab Struct Biol & Zoochem, BR-13506900 Rio Claro, SP, Brazil
dc.description.affiliationInst Butantan, Ctr Appl Toxicol, BR-05503900 São Paulo, SP, Brazil
dc.description.affiliationPUCRS, Ctr Res & Dev Mol Struct & Funtional Mol Biol, BR-90619900 Porto Alegre, RS, Brazil
dc.description.affiliationUnespUNESP, IBILCE, Dept Phys, BR-15054000 Sao Jose do Rio Preto, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Biosci, Dept Biol, Lab Struct Biol & Zoochem, BR-13506900 Rio Claro, SP, Brazil
dc.format.extent979-991
dc.identifierhttp://dx.doi.org/10.1016/j.bbrc.2004.05.220
dc.identifier.citationBiochemical and Biophysical Research Communications. San Diego: Academic Press Inc. Elsevier B.V., v. 320, n. 3, p. 979-991, 2004.
dc.identifier.doi10.1016/j.bbrc.2004.05.220
dc.identifier.issn0006-291X
dc.identifier.lattes2901888624506535
dc.identifier.urihttp://hdl.handle.net/11449/19551
dc.identifier.wosWOS:000222723200052
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofBiochemical and Biophysical Research Communications
dc.relation.ispartofjcr2.559
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectshikimate pathwaypt
dc.subjectstructural bioinformaticspt
dc.subjectdrug designpt
dc.subjectXylella fastidiosapt
dc.titleMolecular models for shikimate pathway enzymes of Xylella fastidiosaen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes2901888624506535
unesp.author.orcid0000-0003-4971-463X[9]
unesp.author.orcid0000-0002-7363-8211[8]
unesp.author.orcid0000-0003-0903-2407[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentBiologia - IBpt
unesp.departmentFísica - IBILCEpt

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