Necrotic activity of ExhC from Mammaliicoccus sciuri is mediated by specific amino acid residues

Registro completo de metadados
MetadadosDescriçãoIdioma
Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.contributorBrazilian Center for Research in Energy and Materials (CNPEM)-
Autor(es): dc.creatorGismene, Carolina-
Autor(es): dc.creatorGonzález, Jorge Enrique Hernández-
Autor(es): dc.creatorde Freitas Calmon, Marília-
Autor(es): dc.creatorNascimento, Andrey Fabricio Ziem-
Autor(es): dc.creatorSantisteban, Angela Rocio Niño-
Autor(es): dc.creatorCalil, Felipe Antunes-
Autor(es): dc.creatorda Silva, Alana Della Torre-
Autor(es): dc.creatorRahal, Paula-
Autor(es): dc.creatorGóes, Rejane Maira-
Autor(es): dc.creatorArni, Raghuvir Krishnaswamy-
Autor(es): dc.creatorMariutti, Ricardo Barros-
Data de aceite: dc.date.accessioned2025-08-21T21:38:03Z-
Data de disponibilização: dc.date.available2025-08-21T21:38:03Z-
Data de envio: dc.date.issued2025-04-29-
Data de envio: dc.date.issued2023-12-31-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.1016/j.ijbiomac.2023.127741-
Fonte completa do material: dc.identifierhttps://hdl.handle.net/11449/305562-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/305562-
Descrição: dc.descriptionMammaliicoccus sciuri, a commensal and pathogenic bacterium of significant clinical and veterinary relevance, expresses exfoliative toxin C (ExhC), a specific glutamyl endopeptidase belonging to the chymotrypsin family as the principal virulence factor. However, unlike most members of this family, ETs are inactive against a wide range of substrates and possess exquisite specificity for desmoglein-1 (Dsg1), a cadherin-like adhesion molecule that is crucial to maintain tissue integrity, thereby preventing the separation of skin cells and the entry of pathogens. ExhC is of clinical importance since in addition to causing exfoliation in pigs and mice, it induces necrosis in multiple mammalian cell lines, a property not observed for other ETs. Previous experiments have implicated the ExhC79–128 fragment in causing necrosis. Site-directed mutagenesis of specific residues within this fragment were studied and led to the design of an ExhC variant containing four-point mutations (ExhCmut4) lacking necrotic potential but retaining nearly wild-type (wt) levels of enzymatic activity. Moreover, the determination of the ExhCwt and ExhCmut4 crystal structures identified the conformation in the necrosis-linked region. These results constitute an important step toward the understanding of the mechanisms underlying the necrotic and epidermolytic activity of ExhC.-
Descrição: dc.descriptionPró-Reitoria de Pesquisa, Universidade Federal do Rio Grande do Sul-
Descrição: dc.descriptionUniversidade Estadual Paulista-
Descrição: dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
Descrição: dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
Descrição: dc.descriptionMultiuser Center for Biomolecular Innovation São Paulo State University - UNESP, SP-
Descrição: dc.descriptionLaboratory of Genomic Studies São Paulo State University - UNESP, SP-
Descrição: dc.descriptionBrazilian Synchrotron Light Laboratory (LNLS) Brazilian Center for Research in Energy and Materials (CNPEM), SP-
Descrição: dc.descriptionDepartment of Biological Sciences São Paulo State University - UNESP, SP-
Descrição: dc.descriptionMultiuser Center for Biomolecular Innovation São Paulo State University - UNESP, SP-
Descrição: dc.descriptionLaboratory of Genomic Studies São Paulo State University - UNESP, SP-
Descrição: dc.descriptionDepartment of Biological Sciences São Paulo State University - UNESP, SP-
Descrição: dc.descriptionFAPESP: 2019/10230-0-
Descrição: dc.descriptionFAPESP: 2020/08615-8-
Descrição: dc.descriptionFAPESP: 2020/10214-1-
Descrição: dc.descriptionFAPESP: 2020/10214-1M-
Descrição: dc.descriptionFAPESP: 2020/13921-0-
Descrição: dc.descriptionFAPESP: 2022/03901-8-
Descrição: dc.descriptionFAPESP: 2022/10941-6-
Descrição: dc.descriptionFAPESP: 2022/14362-0-
Descrição: dc.descriptionCNPq: 309940/2019-2-
Idioma: dc.languageen-
Relação: dc.relationInternational Journal of Biological Macromolecules-
???dc.source???: dc.sourceScopus-
Palavras-chave: dc.subjectEnzymatic activity-
Palavras-chave: dc.subjectExfoliative toxin C-
Palavras-chave: dc.subjectMammaliicoccus sciuri-
Palavras-chave: dc.subjectMoonlighting protein-
Palavras-chave: dc.subjectNecrosis-linked region-
Palavras-chave: dc.subjectNecrotic activity-
Título: dc.titleNecrotic activity of ExhC from Mammaliicoccus sciuri is mediated by specific amino acid residues-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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