Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein

Detalhes bibliográficos
Autor(a) principal: Archer, M.
Data de Publicação: 1999
Outros Autores: Carvalho, A. L., Teixeira, S., Moura, I., Moura, J. J. G., Rusnak, F., Romão, Maria João
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.1110/ps.8.7.1536
Resumo: Desulforedoxin (Dx), isolated from the sulfate reducing bacterium Desulfovibrio gigas, is a small homodimeric (2 x 36 amino acids) protein. Each subunit contains a high-spin iron atom tetrahedrally bound to four cysteinyl sulfur atoms, a metal center similar to that found in rubredoxin (Rd) type proteins. The simplicity of the active center in Dx and the possibility of replacing the iron by other metals make this protein an attractive case for the crystallographic analysis of metal-substituted derivatives. This study extends the relevance of Dx to the bioinorganic chemistry field and is important to obtain model compounds that can mimic the four sulfur coordination of metals in biology. Metal replacement experiments were carried out by reconstituting the apoprotein with In3+, Ga3+, Cd2+, Hg2+, and Ni2+ salts. The In3+ and Ga3+ derivatives are isomorphous with the iron native protein; whereas Cd2+, Hg2+, and Ni2+ substituted Dx crystallized under different experimental conditions, yielding two additional crystal morphologies; their structures were determined by the molecular replacement method. A comparison of the three-dimensional structures for all metal derivatives shows that the overall secondary and tertiary structures are maintained, while some differences in metal coordination geometry occur, namely, bond lengths and angles of the metal with the sulfur ligands. These data are discussed in terms of the entatic state theory.
id RCAP_d360eaebecc4de8b632841aea16f85db
oai_identifier_str oai:run.unl.pt:10362/63333
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type proteinCrystal structureDesulfoferrodoxinDesulforedoxinIron-sulfur proteinsMetal substitutionRubredoxin-type proteinsBiochemistryMolecular BiologyDesulforedoxin (Dx), isolated from the sulfate reducing bacterium Desulfovibrio gigas, is a small homodimeric (2 x 36 amino acids) protein. Each subunit contains a high-spin iron atom tetrahedrally bound to four cysteinyl sulfur atoms, a metal center similar to that found in rubredoxin (Rd) type proteins. The simplicity of the active center in Dx and the possibility of replacing the iron by other metals make this protein an attractive case for the crystallographic analysis of metal-substituted derivatives. This study extends the relevance of Dx to the bioinorganic chemistry field and is important to obtain model compounds that can mimic the four sulfur coordination of metals in biology. Metal replacement experiments were carried out by reconstituting the apoprotein with In3+, Ga3+, Cd2+, Hg2+, and Ni2+ salts. The In3+ and Ga3+ derivatives are isomorphous with the iron native protein; whereas Cd2+, Hg2+, and Ni2+ substituted Dx crystallized under different experimental conditions, yielding two additional crystal morphologies; their structures were determined by the molecular replacement method. A comparison of the three-dimensional structures for all metal derivatives shows that the overall secondary and tertiary structures are maintained, while some differences in metal coordination geometry occur, namely, bond lengths and angles of the metal with the sulfur ligands. These data are discussed in terms of the entatic state theory.Instituto de Tecnologia Química e Biológica António Xavier (ITQB)DQ - Departamento de QuímicaCQFB-REQUIMTE - Centro de Química Fina e Biotecnologia (Lab. Associado REQUIMTE)RUNArcher, M.Carvalho, A. L.Teixeira, S.Moura, I.Moura, J. J. G.Rusnak, F.Romão, Maria João2019-03-14T23:15:40Z1999-01-011999-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10application/pdfhttps://doi.org/10.1110/ps.8.7.1536eng0961-8368PURE: 12115487http://www.scopus.com/inward/record.url?scp=0032805156&partnerID=8YFLogxKhttps://doi.org/10.1110/ps.8.7.1536info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:30:01Zoai:run.unl.pt:10362/63333Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:33:54.512701Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
title Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
spellingShingle Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
Archer, M.
Crystal structure
Desulfoferrodoxin
Desulforedoxin
Iron-sulfur proteins
Metal substitution
Rubredoxin-type proteins
Biochemistry
Molecular Biology
title_short Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
title_full Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
title_fullStr Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
title_full_unstemmed Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
title_sort Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
author Archer, M.
author_facet Archer, M.
Carvalho, A. L.
Teixeira, S.
Moura, I.
Moura, J. J. G.
Rusnak, F.
Romão, Maria João
author_role author
author2 Carvalho, A. L.
Teixeira, S.
Moura, I.
Moura, J. J. G.
Rusnak, F.
Romão, Maria João
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Instituto de Tecnologia Química e Biológica António Xavier (ITQB)
DQ - Departamento de Química
CQFB-REQUIMTE - Centro de Química Fina e Biotecnologia (Lab. Associado REQUIMTE)
RUN
dc.contributor.author.fl_str_mv Archer, M.
Carvalho, A. L.
Teixeira, S.
Moura, I.
Moura, J. J. G.
Rusnak, F.
Romão, Maria João
dc.subject.por.fl_str_mv Crystal structure
Desulfoferrodoxin
Desulforedoxin
Iron-sulfur proteins
Metal substitution
Rubredoxin-type proteins
Biochemistry
Molecular Biology
topic Crystal structure
Desulfoferrodoxin
Desulforedoxin
Iron-sulfur proteins
Metal substitution
Rubredoxin-type proteins
Biochemistry
Molecular Biology
description Desulforedoxin (Dx), isolated from the sulfate reducing bacterium Desulfovibrio gigas, is a small homodimeric (2 x 36 amino acids) protein. Each subunit contains a high-spin iron atom tetrahedrally bound to four cysteinyl sulfur atoms, a metal center similar to that found in rubredoxin (Rd) type proteins. The simplicity of the active center in Dx and the possibility of replacing the iron by other metals make this protein an attractive case for the crystallographic analysis of metal-substituted derivatives. This study extends the relevance of Dx to the bioinorganic chemistry field and is important to obtain model compounds that can mimic the four sulfur coordination of metals in biology. Metal replacement experiments were carried out by reconstituting the apoprotein with In3+, Ga3+, Cd2+, Hg2+, and Ni2+ salts. The In3+ and Ga3+ derivatives are isomorphous with the iron native protein; whereas Cd2+, Hg2+, and Ni2+ substituted Dx crystallized under different experimental conditions, yielding two additional crystal morphologies; their structures were determined by the molecular replacement method. A comparison of the three-dimensional structures for all metal derivatives shows that the overall secondary and tertiary structures are maintained, while some differences in metal coordination geometry occur, namely, bond lengths and angles of the metal with the sulfur ligands. These data are discussed in terms of the entatic state theory.
publishDate 1999
dc.date.none.fl_str_mv 1999-01-01
1999-01-01T00:00:00Z
2019-03-14T23:15:40Z
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 https://doi.org/10.1110/ps.8.7.1536
url https://doi.org/10.1110/ps.8.7.1536
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0961-8368
PURE: 12115487
http://www.scopus.com/inward/record.url?scp=0032805156&partnerID=8YFLogxK
https://doi.org/10.1110/ps.8.7.1536
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 10
application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799137960850882560