Literature DB >> 21301083

Structure of the putative dihydroorotate dehydrogenase from Streptococcus mutans.

Ying Liu1, Zeng Qiang Gao, Chao Pei Liu, Jian Hua Xu, Lan Fen Li, Chao Neng Ji, Xiao Dong Su, Yu Hui Dong.   

Abstract

Streptococcus mutans is one of the pathogenic species involved in dental caries, especially in the initiation and development stages. Here, the crystal structure of SMU.595, a putative dihydroorotate dehydrogenase (DHOD) from S. mutans, is reported at 2.4 Å resolution. DHOD is a flavin mononucleotide-containing enzyme which catalyzes the oxidation of L-dihydroorotate to orotate, which is the fourth step and the only redox reaction in the de novo biosynthesis of pyrimidine nucleotides. The reductive lysine-methylation procedure was applied in order to improve the diffraction qualities of the crystals. Analysis of the S. mutans DHOD crystal structure shows that this enzyme is a class 1A DHOD and also suggests potential sites that could be exploited for the design of highly specific inhibitors using the structure-based chemotherapeutic design technique.

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Year:  2011        PMID: 21301083      PMCID: PMC3034605          DOI: 10.1107/S1744309110048414

Source DB:  PubMed          Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun        ISSN: 1744-3091


  16 in total

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Authors:  S Liu; E A Neidhardt; T H Grossman; T Ocain; J Clardy
Journal:  Structure       Date:  2000-01-15       Impact factor: 5.006

7.  Sequence analysis and identification of the pyrKDbF operon from Lactococcus lactis including a novel gene, pyrK, involved in pyrimidine biosynthesis.

Authors:  P S Andersen; J Martinussen; K Hammer
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Authors:  Tracy L Arakaki; Frederick S Buckner; J Robert Gillespie; Nicholas A Malmquist; Margaret A Phillips; Oleksandr Kalyuzhniy; Joseph R Luft; George T Detitta; Christophe L M J Verlinde; Wesley C Van Voorhis; Wim G J Hol; Ethan A Merritt
Journal:  Mol Microbiol       Date:  2008-02-26       Impact factor: 3.501

9.  Inhibitor binding in a class 2 dihydroorotate dehydrogenase causes variations in the membrane-associated N-terminal domain.

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  1 in total

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  1 in total

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