Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax
Plasmodium vivax malaria caused is a public health problem that produces very high morbidity worldwide. During invasion of red blood cells the parasite requires the intervention of high molecular weight complex rhoptry proteins that are also essential for cytoadherence. PfClag9, a member of the Rhop...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2011
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/24131
- Acceso en línea:
- https://doi.org/10.1016/j.gene.2011.03.007
https://repository.urosario.edu.co/handle/10336/24131
- Palabra clave:
- Protein pfclag9
Protein pvclag7
Protozoal protein
Unclassified drug
Animal experiment
Animal model
Article
Bioinformatics
Cell cycle
Clinical article
Controlled study
Enzyme linked immunosorbent assay
Erythrocyte
Gene identification
Gene location
Human
Molecular biology
Nonhuman
Plasmodium vivax
Plasmodium vivax malaria
Priority journal
Western blotting
Chromosome mapping
Erythrocytes
Humans
Multigene family
Plasmodium vivax
Protozoan proteins
Plasmodium falciparum
Plasmodium vivax
Cytoadherence
Malaria
Multigene family
Plasmodium falciparum
Plasmodium vivax
Rhoptry
- Rights
- License
- Abierto (Texto Completo)
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c9f8488e-233e-49ce-836d-08c9130edc0c-1cfa5e7e8-4baf-4228-a98f-fe5ee81a2510-1fdb00374-1c80-49a4-8df0-97ba3454c983-1a2e26084-98d9-47b7-99c4-27d7e3dab0cf-19fc64f6d-a903-48f1-ac2e-4e55fd2ed9af-12020-05-26T00:08:58Z2020-05-26T00:08:58Z2011Plasmodium vivax malaria caused is a public health problem that produces very high morbidity worldwide. During invasion of red blood cells the parasite requires the intervention of high molecular weight complex rhoptry proteins that are also essential for cytoadherence. PfClag9, a member of the RhopH multigene family, has been identified as being critical during Plasmodium falciparum infection. This study describes identifying and characterizing the pfclag9 ortholog in P. vivax (hereinafter named pvclag7). The pvclag7 gene is transcribed at the end of the intraerythrocytic cycle and is recognized by sera from humans who have been infected by P. vivax. PvClag7 subcellular localization has been also determined and, similar to what occurs with PfClag9, it co-localize with other proteins from the Rhoptry high molecular weight complex. © 2011 Elsevier B.V.application/pdfhttps://doi.org/10.1016/j.gene.2011.03.0073781119https://repository.urosario.edu.co/handle/10336/24131eng23No. 117GeneVol. 481Gene, ISSN:3781119, Vol.481, No.1 (2011); pp. 17-23https://www.scopus.com/inward/record.uri?eid=2-s2.0-79957655332&doi=10.1016%2fj.gene.2011.03.007&partnerID=40&md5=b718697e49b95a11722a906b8645f6f9Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURProtein pfclag9Protein pvclag7Protozoal proteinUnclassified drugAnimal experimentAnimal modelArticleBioinformaticsCell cycleClinical articleControlled studyEnzyme linked immunosorbent assayErythrocyteGene identificationGene locationHumanMolecular biologyNonhumanPlasmodium vivaxPlasmodium vivax malariaPriority journalWestern blottingChromosome mappingErythrocytesHumansMultigene familyPlasmodium vivaxProtozoan proteinsPlasmodium falciparumPlasmodium vivaxCytoadherenceMalariaMultigene familyPlasmodium falciparumPlasmodium vivaxRhoptryIdentifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivaxarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Moreno-Perez D.A.Mongui A.Soler L.N.Sanchez-Ladino M.Patarroyo M.A.ORIGINALIdentifying_and_characterizing_a_member.pdfapplication/pdf564985https://repository.urosario.edu.co/bitstreams/b67037a4-1589-4c64-b652-6c54d5b6f566/download3ccd536964af2d7794aacb6f18738d17MD51TEXTIdentifying_and_characterizing_a_member.pdf.txtIdentifying_and_characterizing_a_member.pdf.txtExtracted texttext/plain43117https://repository.urosario.edu.co/bitstreams/6637b4b3-9472-4cf5-a7f9-702d97091461/download97234ac60f67d33b4c2ca3626073eaedMD52THUMBNAILIdentifying_and_characterizing_a_member.pdf.jpgIdentifying_and_characterizing_a_member.pdf.jpgGenerated Thumbnailimage/jpeg4330https://repository.urosario.edu.co/bitstreams/6acff875-3261-4e8f-9212-3233a97e7a46/downloada95e7d3342256e78a03e461ddc042f55MD5310336/24131oai:repository.urosario.edu.co:10336/241312022-05-02 07:37:21.528554https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
title |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
spellingShingle |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax Protein pfclag9 Protein pvclag7 Protozoal protein Unclassified drug Animal experiment Animal model Article Bioinformatics Cell cycle Clinical article Controlled study Enzyme linked immunosorbent assay Erythrocyte Gene identification Gene location Human Molecular biology Nonhuman Plasmodium vivax Plasmodium vivax malaria Priority journal Western blotting Chromosome mapping Erythrocytes Humans Multigene family Plasmodium vivax Protozoan proteins Plasmodium falciparum Plasmodium vivax Cytoadherence Malaria Multigene family Plasmodium falciparum Plasmodium vivax Rhoptry |
title_short |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
title_full |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
title_fullStr |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
title_full_unstemmed |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
title_sort |
Identifying and characterizing a member of the RhopH1/Clag family in Plasmodium vivax |
dc.subject.keyword.spa.fl_str_mv |
Protein pfclag9 Protein pvclag7 Protozoal protein Unclassified drug Animal experiment Animal model Article Bioinformatics Cell cycle Clinical article Controlled study Enzyme linked immunosorbent assay Erythrocyte Gene identification Gene location Human Molecular biology Nonhuman Plasmodium vivax Plasmodium vivax malaria Priority journal Western blotting Chromosome mapping Erythrocytes Humans Multigene family Plasmodium vivax Protozoan proteins Plasmodium falciparum Plasmodium vivax Cytoadherence Malaria Multigene family Plasmodium falciparum Plasmodium vivax Rhoptry |
topic |
Protein pfclag9 Protein pvclag7 Protozoal protein Unclassified drug Animal experiment Animal model Article Bioinformatics Cell cycle Clinical article Controlled study Enzyme linked immunosorbent assay Erythrocyte Gene identification Gene location Human Molecular biology Nonhuman Plasmodium vivax Plasmodium vivax malaria Priority journal Western blotting Chromosome mapping Erythrocytes Humans Multigene family Plasmodium vivax Protozoan proteins Plasmodium falciparum Plasmodium vivax Cytoadherence Malaria Multigene family Plasmodium falciparum Plasmodium vivax Rhoptry |
description |
Plasmodium vivax malaria caused is a public health problem that produces very high morbidity worldwide. During invasion of red blood cells the parasite requires the intervention of high molecular weight complex rhoptry proteins that are also essential for cytoadherence. PfClag9, a member of the RhopH multigene family, has been identified as being critical during Plasmodium falciparum infection. This study describes identifying and characterizing the pfclag9 ortholog in P. vivax (hereinafter named pvclag7). The pvclag7 gene is transcribed at the end of the intraerythrocytic cycle and is recognized by sera from humans who have been infected by P. vivax. PvClag7 subcellular localization has been also determined and, similar to what occurs with PfClag9, it co-localize with other proteins from the Rhoptry high molecular weight complex. © 2011 Elsevier B.V. |
publishDate |
2011 |
dc.date.created.spa.fl_str_mv |
2011 |
dc.date.accessioned.none.fl_str_mv |
2020-05-26T00:08:58Z |
dc.date.available.none.fl_str_mv |
2020-05-26T00:08:58Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.gene.2011.03.007 |
dc.identifier.issn.none.fl_str_mv |
3781119 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/24131 |
url |
https://doi.org/10.1016/j.gene.2011.03.007 https://repository.urosario.edu.co/handle/10336/24131 |
identifier_str_mv |
3781119 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
23 |
dc.relation.citationIssue.none.fl_str_mv |
No. 1 |
dc.relation.citationStartPage.none.fl_str_mv |
17 |
dc.relation.citationTitle.none.fl_str_mv |
Gene |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 481 |
dc.relation.ispartof.spa.fl_str_mv |
Gene, ISSN:3781119, Vol.481, No.1 (2011); pp. 17-23 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79957655332&doi=10.1016%2fj.gene.2011.03.007&partnerID=40&md5=b718697e49b95a11722a906b8645f6f9 |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
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