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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Backbone and side chain NMR assignments for the N-terminal domain of the cell division regulator MinC from Bacillus subtilis

Texto completo
Autor(es):
Castellen, Patricia [1, 2] ; Sforca, Mauricio L. [2] ; Gueiros-Filho, Frederico J. [1] ; de Mattos Zeri, Ana Carolina [2]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-01498 Sao Paulo - Brazil
[2] CNPEM, LNBio, Campinas, SP - Brazil
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: BIOMOLECULAR NMR ASSIGNMENTS; v. 9, n. 1, p. 1-5, APR 2015.
Citações Web of Science: 0
Resumo

Bacterial cell division proteins must assemble at the middle of the cell to ensure the viability of both daughter cells. The first step in the assembly of the cell division apparatus is the polymerization of the tubulin-like protein FtsZ into a ring-shaped scaffold, the Z-ring. The Min system contributes to the spatial precision of division by inhibiting FtsZ polymerization at the cell poles. The component of this system that interacts with FtsZ is MinC, a 25 kDa protein that has two domains. The N-terminal domain of MinC is the main responsible for FtsZ inhibition, being sufficient to block Z-ring assembly when overexpressed in vivo, and to inhibit FtsZ polymerization in vitro. Despite intensive studies, little is known about the MinC binding site for FtsZ. We have assigned the backbone and side chain resonances of the MinC N-terminal domain of Bacillus subtilis through NMR spectroscopy. These assignments provide the basis to characterize the interaction between the N-terminal domain of MinC and FtsZ by NMR methods. (AU)

Processo FAPESP: 10/51866-0 - SMolBNet 2.0: combinando genética e RMN para dissecar interações proteína-proteína fundamentais para o funcionamento do complexo de divisão bacteriana
Beneficiário:Frederico José Gueiros Filho
Modalidade de apoio: Auxílio à Pesquisa - Regular