New catalytic mechanism for human purine nucleoside phosphorylase


Autoria(s): Canduri, F.; Fadel, V; Basso, L. A.; Palma, Mario Sergio; Santos, D. S.; de Azevedo, W. F.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

18/02/2005

Resumo

Human purine nucleoside phosphorylase has been submitted to intensive structure-based design of inhibitors, most of them using low-resolution structures of human PNP. Recently, several structures of human PNP have been reported, which allowed redefinition of the active site and understanding of the structural basis for inhibition of PNP by acyclovir and immucillin-H. Based on previously solved human PNP structures, we proposed here a new catalytic mechanism for human PNP, which is supported by crystallographic studies and explains previously determined kinetic data. (C) 2004 Elsevier B.V. All rights reserved.

Formato

646-649

Identificador

http://dx.doi.org/10.1016/j.bbrc.2004.12.052

Biochemical and Biophysical Research Communications. San Diego: Academic Press Inc. Elsevier B.V., v. 327, n. 3, p. 646-649, 2005.

0006-291X

http://hdl.handle.net/11449/19552

10.1016/j.bbrc.2004.12.052

WOS:000226674800003

Idioma(s)

eng

Publicador

Elsevier B.V.

Relação

Biochemical and Biophysical Research Communications

Direitos

closedAccess

Palavras-Chave #PNP #synchrotron radiation #Structure #drug design
Tipo

info:eu-repo/semantics/article