Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1107/S1744309109037567 http://hdl.handle.net/11449/22100 |
Resumo: | Nucleoside 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. |
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Repositório Institucional da UNESP |
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spelling |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania majorNucleoside 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.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Brazilian Assoc Synchrotron Light Technol, Ctr Struct Mol Biol, Campinas, SP, BrazilFFCLRP USP, Dept Chem, Ribeirao Preto, SP, BrazilIBILCE UNESP, Dept Phys, Sao Jose do Rio Preto, SP, BrazilIBILCE UNESP, Dept Phys, Sao Jose do Rio Preto, SP, BrazilFAPESP: 07/06755-2FAPESP: 07/54865CNPq: 307853/2006-3CNPq: 473997/2007-0CNPq: 471192/2007-4Wiley-Blackwell Publishing, IncBrazilian Assoc Synchrotron Light TechnolUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Costa Tonoli, Celisa CaldanaVieira, Plinio SalmazoWard, Richard JohnArni, Raghuvir Krishnaswamy [UNESP]Cavalcante de Oliveira, Arthur HenriqueMurakami, Mario Tyago2014-05-20T14:02:41Z2014-05-20T14:02:41Z2009-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1116-1119application/pdfhttp://dx.doi.org/10.1107/S1744309109037567Acta Crystallographica Section F-structural Biology and Crystallization Communications. Malden: Wiley-blackwell Publishing, Inc, v. 65, p. 1116-1119, 2009.1744-3091http://hdl.handle.net/11449/2210010.1107/S1744309109037567WOS:000271421800010WOS000271421800010.pdf91625089789458870000-0003-2460-1145Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Crystallographica Section F: Structural Biology and Crystallization Communicationsinfo:eu-repo/semantics/openAccess2023-10-06T06:01:17Zoai:repositorio.unesp.br:11449/22100Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:07:44.125440Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
title |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
spellingShingle |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major Costa Tonoli, Celisa Caldana |
title_short |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
title_full |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
title_fullStr |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
title_full_unstemmed |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
title_sort |
Production, purification, crystallization and preliminary X-ray diffraction studies of the nucleoside diphosphate kinase b from Leishmania major |
author |
Costa Tonoli, Celisa Caldana |
author_facet |
Costa Tonoli, Celisa Caldana Vieira, Plinio Salmazo Ward, Richard John Arni, Raghuvir Krishnaswamy [UNESP] Cavalcante de Oliveira, Arthur Henrique Murakami, Mario Tyago |
author_role |
author |
author2 |
Vieira, Plinio Salmazo Ward, Richard John Arni, Raghuvir Krishnaswamy [UNESP] Cavalcante de Oliveira, Arthur Henrique Murakami, Mario Tyago |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Brazilian Assoc Synchrotron Light Technol Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Costa Tonoli, Celisa Caldana Vieira, Plinio Salmazo Ward, Richard John Arni, Raghuvir Krishnaswamy [UNESP] Cavalcante de Oliveira, Arthur Henrique Murakami, Mario Tyago |
description |
Nucleoside 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. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-11-01 2014-05-20T14:02:41Z 2014-05-20T14:02:41Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1107/S1744309109037567 Acta Crystallographica Section F-structural Biology and Crystallization Communications. Malden: Wiley-blackwell Publishing, Inc, v. 65, p. 1116-1119, 2009. 1744-3091 http://hdl.handle.net/11449/22100 10.1107/S1744309109037567 WOS:000271421800010 WOS000271421800010.pdf 9162508978945887 0000-0003-2460-1145 |
url |
http://dx.doi.org/10.1107/S1744309109037567 http://hdl.handle.net/11449/22100 |
identifier_str_mv |
Acta Crystallographica Section F-structural Biology and Crystallization Communications. Malden: Wiley-blackwell Publishing, Inc, v. 65, p. 1116-1119, 2009. 1744-3091 10.1107/S1744309109037567 WOS:000271421800010 WOS000271421800010.pdf 9162508978945887 0000-0003-2460-1145 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Acta Crystallographica Section F: Structural Biology and Crystallization Communications |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1116-1119 application/pdf |
dc.publisher.none.fl_str_mv |
Wiley-Blackwell Publishing, Inc |
publisher.none.fl_str_mv |
Wiley-Blackwell Publishing, Inc |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128319175000064 |