Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin

Background: The TlyA protein has a controversial function as a virulence factor in Mycobacterium tuberculosis (M. tuberculosis). At present, its dual activity as hemolysin and RNA methyltransferase in M. tuberculosis has been indirectly proposed based on in vitro results. There is no evidence howeve...

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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:10336/21885
Acceso en línea:
https://doi.org/10.1186/1472-6807-11-16
https://repository.urosario.edu.co/handle/10336/21885
Palabra clave:
Tuberculosis
Enfermedades
AdoMet
Mycobacterium Species
Subcellular Localization Prediction
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License
Abierto (Texto Completo)
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repository_id_str
dc.title.spa.fl_str_mv Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
title Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
spellingShingle Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
Tuberculosis
Enfermedades
AdoMet
Mycobacterium Species
Subcellular Localization Prediction
title_short Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
title_full Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
title_fullStr Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
title_full_unstemmed Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
title_sort Molecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysin
dc.subject.spa.fl_str_mv Tuberculosis
topic Tuberculosis
Enfermedades
AdoMet
Mycobacterium Species
Subcellular Localization Prediction
dc.subject.ddc.spa.fl_str_mv Enfermedades
dc.subject.keyword.spa.fl_str_mv AdoMet
Mycobacterium Species
Subcellular Localization Prediction
description Background: The TlyA protein has a controversial function as a virulence factor in Mycobacterium tuberculosis (M. tuberculosis). At present, its dual activity as hemolysin and RNA methyltransferase in M. tuberculosis has been indirectly proposed based on in vitro results. There is no evidence however for TlyA relevance in the survival of tubercle bacilli inside host cells or whether both activities are functionally linked. A thorough analysis of structure prediction for this mycobacterial protein in this study shows the need for reevaluating TlyA's function in virulence. Results: Bioinformatics analysis of TlyA identified a ribosomal protein binding domain (S4 domain), located between residues 5 and 68 as well as an FtsJ-like methyltranferase domain encompassing residues 62 and 247, all of which have been previously described in translation machinery-associated proteins. Subcellular localization prediction showed that TlyA lacks a signal peptide and its hydrophobicity profile showed no evidence of transmembrane helices. These findings suggested that it may not be attached to the membrane, which is consistent with a cytoplasmic localization. Three-dimensional modeling of TlyA showed a consensus structure, having a common core formed by a six-stranded β-sheet between two α-helix layers, which is consistent with an RNA methyltransferase structure. Phylogenetic analyses showed high conservation of the tlyA gene among Mycobacterium species. Additionally, the nucleotide substitution rates suggested purifying selection during tlyA gene evolution and the absence of a common ancestor between TlyA proteins and bacterial pore-forming proteins. Conclusion: Altogether, our manual in silico curation suggested that TlyA is involved in ribosomal biogenesis and that there is a functional annotation error regarding this protein family in several microbial and plant genomes, including the M. tuberculosis genome. © 2011 Arenas et al; licensee BioMed Central Ltd.
publishDate 2011
dc.date.created.none.fl_str_mv 2011
dc.date.issued.none.fl_str_mv 2011
dc.date.accessioned.none.fl_str_mv 2020-05-07T04:31:39Z
dc.date.available.none.fl_str_mv 2020-05-07T04:31:39Z
dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1186/1472-6807-11-16
dc.identifier.issn.none.fl_str_mv 1472-6807
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/21885
url https://doi.org/10.1186/1472-6807-11-16
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dc.language.iso.spa.fl_str_mv eng
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dc.relation.citationTitle.none.fl_str_mv BMC Structural Biology
dc.relation.citationVolume.none.fl_str_mv Vol. 11
dc.relation.ispartof.spa.fl_str_mv BMC Structural Biology, ISSN: 1472-6807 Vol. 11, (2011)
dc.relation.uri.spa.fl_str_mv https://bmcstructbiol.biomedcentral.com/articles/10.1186/1472-6807-11-16
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institution Universidad del Rosario
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spelling ee05c44e-ed29-4b05-a582-d0b1f5ea2fe66004fda4c81-5558-46e6-a038-005cc454bf3a600c79accae-eea1-4a41-94ae-947d6e0e7d8c6009de1cfc2-5d95-4925-a819-b9b2b20ff2d260010ecd4f9-843f-4ef2-bec0-7d39d3381a13600796530656002b63a153-9280-4b36-8b5f-5fc163a6b1036002020-05-07T04:31:39Z2020-05-07T04:31:39Z20112011Background: The TlyA protein has a controversial function as a virulence factor in Mycobacterium tuberculosis (M. tuberculosis). At present, its dual activity as hemolysin and RNA methyltransferase in M. tuberculosis has been indirectly proposed based on in vitro results. There is no evidence however for TlyA relevance in the survival of tubercle bacilli inside host cells or whether both activities are functionally linked. A thorough analysis of structure prediction for this mycobacterial protein in this study shows the need for reevaluating TlyA's function in virulence. Results: Bioinformatics analysis of TlyA identified a ribosomal protein binding domain (S4 domain), located between residues 5 and 68 as well as an FtsJ-like methyltranferase domain encompassing residues 62 and 247, all of which have been previously described in translation machinery-associated proteins. Subcellular localization prediction showed that TlyA lacks a signal peptide and its hydrophobicity profile showed no evidence of transmembrane helices. These findings suggested that it may not be attached to the membrane, which is consistent with a cytoplasmic localization. Three-dimensional modeling of TlyA showed a consensus structure, having a common core formed by a six-stranded β-sheet between two α-helix layers, which is consistent with an RNA methyltransferase structure. Phylogenetic analyses showed high conservation of the tlyA gene among Mycobacterium species. Additionally, the nucleotide substitution rates suggested purifying selection during tlyA gene evolution and the absence of a common ancestor between TlyA proteins and bacterial pore-forming proteins. Conclusion: Altogether, our manual in silico curation suggested that TlyA is involved in ribosomal biogenesis and that there is a functional annotation error regarding this protein family in several microbial and plant genomes, including the M. tuberculosis genome. © 2011 Arenas et al; licensee BioMed Central Ltd.application/pdfhttps://doi.org/10.1186/1472-6807-11-161472-6807https://repository.urosario.edu.co/handle/10336/21885engBMC Structural BiologyVol. 11BMC Structural Biology, ISSN: 1472-6807 Vol. 11, (2011)https://bmcstructbiol.biomedcentral.com/articles/10.1186/1472-6807-11-16Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURTuberculosisEnfermedades616600AdoMetMycobacterium SpeciesSubcellular Localization PredictionMolecular modeling and in silico characterization of Mycobacterium tuberculosis TlyA : Possible misannotation of this tubercle bacilli-hemolysinarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Arenas, Nelson ESalazar, Luz MSoto, Carlos YVizcaíno, CarolinaPatarroyo, Manuel E.Patarroyo, Manuel A.Gómez, ArleyArenas, Nelson ESalazar, Luz MSoto, Carlos YVizcaíno, CarolinaPatarroyo, Manuel EPatarroyo, Manuel AGámez, ArleyORIGINALMolecular_modeling_and_in_silico_characterization_of_Mycobacterium_tuberculosis.pdfapplication/pdf5480210https://repository.urosario.edu.co/bitstreams/2a267f72-4533-494e-9425-f470eccbf90e/download03311e00f4db19e4dc699048cbbca9b9MD51TEXTMolecular_modeling_and_in_silico_characterization_of_Mycobacterium_tuberculosis.pdf.txtMolecular_modeling_and_in_silico_characterization_of_Mycobacterium_tuberculosis.pdf.txtExtracted texttext/plain46926https://repository.urosario.edu.co/bitstreams/b5542a99-f816-451e-9dc1-412d6800f557/download227b917411f60acd483f0e5d1b548892MD52THUMBNAILMolecular_modeling_and_in_silico_characterization_of_Mycobacterium_tuberculosis.pdf.jpgMolecular_modeling_and_in_silico_characterization_of_Mycobacterium_tuberculosis.pdf.jpgGenerated Thumbnailimage/jpeg4580https://repository.urosario.edu.co/bitstreams/074d833c-d5a0-449a-8f8a-65c0dfd81b19/download6453fd21bc40a449dd4aefecfcbd1bfcMD5310336/21885oai:repository.urosario.edu.co:10336/218852020-05-13 14:48:18.169https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co