Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/103748
Type: Artigo de evento
Title: Molecular Dynamics Simulations Of A Set Of Isoniazid Derivatives Bound To Inha, The Enoyl-acp Reductase From M. Tuberculosis
Author: Pasqualoto K.F.M.
Ferreira M.M.C.
Santos-Filho O.A.
Hopfinger A.J.
Abstract: Ligand-receptor molecular dynamics simulations (MDS) were carried out for a set of hydrazides bound to the enoyl-acp reductase from M. tuberculosis, InhA (PDB entry code 1zid). The hypothesized active conformations resulting from a previous receptorindependent (RI) 4D-QSAR analysis and related optimum model/alignment were used in this study. The molecular dynamics simulations (MDS) protocol employed 500000 steps for each ligand-receptor complex, the step size was 0.001 ps (1 fs), and the simulation temperature was 310 K, the same temperature used in the biological assay. An output trajectory file was saved every 20 simulation steps, resulting in 25,000 conformations. The hydration shell model was used to calculate the solvation energy of the lowest-energy conformation obtained from each MDS. Structural parameters as well as binding energy contributions were considered in this analysis. The thermodynamic descriptors ELE1,4, ELtors, ELel, EL el, and ELel+Hb appear to be more relevant to the biological activity. These findings can be meaningful for developing QSAR studies and for designing new antiruberculosis agents. © 2006 Wiley Periodicals, Inc.
Editor: 
Rights: fechado
Identifier DOI: 10.1002/qua.21055
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-33749183078&partnerID=40&md5=3e4cac0c61432b5c18b4522734129d10
Date Issue: 2006
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
2-s2.0-33749183078.pdf246.53 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.