Crystallographic structure of PNP from Mycobacterium tuberculosis at 1.9 angstrom resolution


Autoria(s): Nolasco, D. O.; Canduri, F.; Pereira, J. H.; Cortinoz, JR; Palma, Mario Sergio; Oliveira, J. S.; Basso, L. A.; de Azevedo, W. F.; Santos, D. S.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

12/11/2004

Resumo

Even being a bacterial purine nucleoside phosphorylase (PNP), which normally shows hexameric folding, the Mycobacterium tuberculosis PNP (MtPNP) resembles the mammalian trimeric structure. The crystal structure of the MtPNP apoenzyme was solved at 1.9 Angstrom resolution. The present work describes the first structure of MtPNP in complex with phosphate. In order to develop new insights into the rational drug design, conformational changes were profoundly analyzed and discussed. Comparisons over the binding sites were specially studied to improve the discussion about the selectivity of potential new drugs. (C) 2004 Elsevier B.V. All rights reserved.

Formato

789-794

Identificador

http://dx.doi.org/10.1016/j.bbrc.2004.09.137

Biochemical and Biophysical Research Communications. San Diego: Academic Press Inc. Elsevier B.V., v. 324, n. 2, p. 789-794, 2004.

0006-291X

http://hdl.handle.net/11449/19413

10.1016/j.bbrc.2004.09.137

WOS:000224794000046

Idioma(s)

eng

Publicador

Elsevier B.V.

Relação

Biochemical and Biophysical Research Communications

Direitos

closedAccess

Palavras-Chave #tuberculosis #PNP #Crystallography #apoenzyme #selectivity
Tipo

info:eu-repo/semantics/article