The Catalytic Acid in the Dephosphorylation of the Cdk2-pTpY/CycA Protein Complex by Cdc25B Phosphatase


Autoria(s): ARANTES, Guilherme Menegon
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

The development of anticancer therapeutics that target Cdc25 phosphatases is now an active area of research. A complete understanding of the Cdc25 catalytic mechanism would certainly allow a more rational inhibitor design. However, the identity of the catalytic acid used by Cdc25 has been debated and not established unambiguously. Results of molecular dynamics simulations with a calibrated hybrid potential for the first reaction step catalyzed by Cdc25B in complex with its natural substrate, the Cdk2-pTpY/CycA protein complex, are presented here. The calculated reaction free-energy profiles are in very good agreement with experimental measurements and are used to discern between different proposals for the general acid. In addition, the simulations give useful insight on interactions that can be explored for the design of inhibitors specific to Cdc25.

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)[07/52772-6]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)[07/59345-6]

Identificador

JOURNAL OF PHYSICAL CHEMISTRY B, v.112, n.47, p.15244-15247, 2008

1520-6106

http://producao.usp.br/handle/BDPI/30871

10.1021/jp8070019

http://dx.doi.org/10.1021/jp8070019

Idioma(s)

eng

Publicador

AMER CHEMICAL SOC

Relação

Journal of Physical Chemistry B

Direitos

restrictedAccess

Copyright AMER CHEMICAL SOC

Palavras-Chave #DUAL-SPECIFICITY PHOSPHATASES #CRYSTAL-STRUCTURE #FREE-ENERGY #CELL-CYCLE #SIMULATIONS #MECHANISM #INHIBITORS #TARGETS #CANCER #Chemistry, Physical
Tipo

article

original article

publishedVersion