You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/22100
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCosta Tonoli, Celisa Caldana-
dc.contributor.authorVieira, Plinio Salmazo-
dc.contributor.authorWard, Richard John-
dc.contributor.authorArni, Raghuvir Krishnaswamy-
dc.contributor.authorCavalcante de Oliveira, Arthur Henrique-
dc.contributor.authorMurakami, Mario Tyago-
dc.date.accessioned2014-05-20T14:02:41Z-
dc.date.available2014-05-20T14:02:41Z-
dc.date.issued2009-11-01-
dc.identifierhttp://dx.doi.org/10.1107/S1744309109037567-
dc.identifier.citationActa Crystallographica Section F-structural Biology and Crystallization Communications. Malden: Wiley-blackwell Publishing, Inc, v. 65, p. 1116-1119, 2009.-
dc.identifier.issn1744-3091-
dc.identifier.urihttp://hdl.handle.net/11449/22100-
dc.description.abstractNucleoside diphosphate kinases (NDKs; EC 2.7.4.6) play an essential role in the synthesis of nucleotides from intermediates in the salvage pathway in all parasitic trypanosomatids and their structural studies will be instrumental in shedding light on the biochemical machinery involved in the parasite life cycle and host-parasite interactions. In this work, NDKb from Leishmania major was overexpressed in Escherichia coli, purified to homogeneity and crystallized using the sitting-drop vapour-diffusion method. The NDK crystal diffracted to 2.2 angstrom resolution and belonged to the trigonal crystal system, with unit-cell parameters a = 114.2, c = 93.9 angstrom. Translation-function calculations yielded an unambiguous solution in the enantiomorphic space group P3(2)21.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent1116-1119-
dc.language.isoeng-
dc.publisherWiley-Blackwell Publishing, Inc-
dc.sourceWeb of Science-
dc.titleProduction, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania majoren
dc.typeoutro-
dc.contributor.institutionBrazilian Assoc Synchrotron Light Technol-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationBrazilian Assoc Synchrotron Light Technol, Ctr Struct Mol Biol, Campinas, SP, Brazil-
dc.description.affiliationFFCLRP USP, Dept Chem, Ribeirao Preto, SP, Brazil-
dc.description.affiliationIBILCE UNESP, Dept Phys, Sao Jose do Rio Preto, SP, Brazil-
dc.description.affiliationUnespIBILCE UNESP, Dept Phys, Sao Jose do Rio Preto, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 07/06755-2-
dc.description.sponsorshipIdFAPESP: 07/54865-
dc.description.sponsorshipIdCNPq: 307853/2006-3-
dc.description.sponsorshipIdCNPq: 473997/2007-0-
dc.description.sponsorshipIdCNPq: 471192/2007-4-
dc.identifier.doi10.1107/S1744309109037567-
dc.identifier.wosWOS:000271421800010-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000271421800010.pdf-
dc.relation.ispartofActa Crystallographica Section F: Structural Biology and Crystallization Communications-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.