Please use this identifier to cite or link to this item: http://repositorio.ufla.br/jspui/handle/1/41028
metadata.artigo.dc.title: Molecular modeling studies of Yersinia pestis dihydrofolate reductase
metadata.artigo.dc.creator: Oliveira, Aline A.
Rennó, Magdalena N.
Matos, César A. S. de
Bertuzzi, Morena D.
Ramalho, Teodorico C.
Fraga, Carlos A.M.
França, Tanos C. C.
metadata.artigo.dc.subject: Plague
Yersinia pestis
Yp DHFR
Homology modeling
Docking
Molecular dynamics
Selective inhibition
Dihydrofolate reductase (DHFR)
metadata.artigo.dc.publisher: Taylor & Francis
metadata.artigo.dc.date.issued: 2011
metadata.artigo.dc.identifier.citation: OLIVEIRA, A. A. et al. Molecular modeling studies of Yersinia pestis dihydrofolate reductase. Journal of Biomolecular Structure and Dynamics, [S.l.], v. 29, n. 2, 2011. DOI: 10.1080/07391102.2011.10507390.
metadata.artigo.dc.description.abstract: Considering the risk represented by plague today as a potential biological warfare agent, we propose cytosolic Yersinia pestis dihydrofolate reductase (Yp DHFR) as a new target to the design of selective plague chemotherapy. This enzyme has a low homology with the human enzyme and its crystallographic structure has been recently deposited in the Protein Data Bank (PDB). Comparisons of the docking energies and molecular dynamic behaviors of five known DHFR inhibitors inside a 3D model of Yp DHFR (adapted from the crystallographic structure) and human DHFR (Hss DHFR), revealed new potential interactions and suggested insights into the design of more potent Hss DHFR inhibitors as well as selective inhibitors for Yp DHFR.
metadata.artigo.dc.identifier.uri: https://www.tandfonline.com/doi/abs/10.1080/07391102.2011.10507390
http://repositorio.ufla.br/jspui/handle/1/41028
metadata.artigo.dc.language: en_US
Appears in Collections:DQI - Artigos publicados em periódicos

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