Structural studies by X-ray diffraction on metal substituted desulforedoxin, a rubredoxin-type protein
Autor(a) principal: | |
---|---|
Data de Publicação: | 1999 |
Outros Autores: | , , , , , |
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 |