dc.date.accessioned2023-09-06T20:45:11Z
dc.date.accessioned2024-04-24T13:22:09Z
dc.date.available2023-09-06T20:45:11Z
dc.date.available2024-04-24T13:22:09Z
dc.date.created2023-09-06T20:45:11Z
dc.date.issued2023
dc.identifierhttps://hdl.handle.net/20.500.12866/14104
dc.identifierhttps://doi.org/10.1016/j.tube.2023.102375
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9231338
dc.description.abstractTo better understand the interaction between the host and the Mycobacterium tuberculosis pathogen, it is critical to identify its potential secreted proteins. While various experimental methods have been successful in identifying proteins under specific culture conditions, they have not provided a comprehensive characterisation of the secreted proteome. We utilized a combination of bioinformatics servers and in-house software to identify all potentially secreted proteins from six mycobacterial genomes through the three secretion systems: SEC, TAT, and T7SS. The results are presented in a database that can be crossed referenced to selected proteomics and transcriptomics studies (https://secretomyc.cbs.cnrs.fr). In addition, thanks to the recent availability of Alphafold models, we developed a tool in order to identify the structural homologues among the mycobacterial genomes.
dc.languageeng
dc.publisherElsevier
dc.relationTuberculosis
dc.relation1873-281X
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectSecretion
dc.subjectHost-pathogen
dc.subjectMycobacteria
dc.subjectAlphafold
dc.titleSecretoMyc, a web-based database on mycobacteria secreted proteins and structure-based homology identification using bio-informatics tools
dc.typeinfo:eu-repo/semantics/article


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