Crystal structure of Trypanosoma cruzi dihydroorotate dehydrogenase from Y strain


Autoria(s): PINHEIRO, Matheus P.; IULEK, Jorge; NONATO, M. Cristina
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Trypanosoma cruzi is the etiological agent of Chagas` disease, a pathogenesis that affects millions of people in Latin America. Here, we report the crystal structure of dihydroorotate dehydrogenase (DHODH) from T cruzi strain Y solved at 2.2 angstrom resolution. DHODH is a flavin mononucleotide containing enzyme, which catalyses the oxidation Of L-dihydroorotate to orotate, the fourth step and only redox reaction in the de novo biosynthesis of pyrimidine nucleotides. Genetic studies have shown that DHODH is essential for T cruzi survival, validating the idea that this enzyme can be considered an attractive target for the development of antichagasic drugs. In our work, a detailed analysis of T cruzi DHODH crystal structure has allowed us to suggest potential sites to be further exploited for the design of highly specific inhibitors through the technology of structure-based drug design. (c) 2008 Elsevier Inc. All rights reserved.

Identificador

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.369, n.3, p.812-817, 2008

0006-291X

http://producao.usp.br/handle/BDPI/19942

10.1016/j.bbrc.2008.02.074

http://dx.doi.org/10.1016/j.bbrc.2008.02.074

Idioma(s)

eng

Publicador

ACADEMIC PRESS INC ELSEVIER SCIENCE

Relação

Biochemical and Biophysical Research Communications

Direitos

restrictedAccess

Copyright ACADEMIC PRESS INC ELSEVIER SCIENCE

Palavras-Chave #Trypanosoma cruzi #Y strain #dihydroorotate dehydrogenase #cloning #expression #purification #crystallization #X-ray crystallography #LACTOCOCCUS-LACTIS #CHAGAS-DISEASE #CRYSTALLIZATION #GENES #PURIFICATION #EXPRESSION #SOFTWARE #Biochemistry & Molecular Biology #Biophysics
Tipo

article

original article

publishedVersion