| pubmed-article:18445278 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18445278 | lifeskim:mentions | umls-concept:C0026926 | lld:lifeskim |
| pubmed-article:18445278 | lifeskim:mentions | umls-concept:C0162326 | lld:lifeskim |
| pubmed-article:18445278 | lifeskim:mentions | umls-concept:C2700640 | lld:lifeskim |
| pubmed-article:18445278 | lifeskim:mentions | umls-concept:C0055608 | lld:lifeskim |
| pubmed-article:18445278 | pubmed:dateCreated | 2008-5-15 | lld:pubmed |
| pubmed-article:18445278 | pubmed:abstractText | The emergence of multi- and extensively-drug resistant Mycobacterium tuberculosis strains has created an urgent need for new agents to treat tuberculosis (TB). The enzymes of shikimate pathway are attractive targets to the development of antitubercular agents because it is essential for M. tuberculosis and is absent from humans. Chorismate synthase (CS) is the seventh enzyme of this route and catalyzes the NADH- and FMN-dependent synthesis of chorismate, a precursor of aromatic amino acids, naphthoquinones, menaquinones, and mycobactins. Although the M. tuberculosis Rv2540c (aroF) sequence has been annotated to encode a chorismate synthase, there has been no report on its correct assignment and functional characterization of its protein product. | lld:pubmed |
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| pubmed-article:18445278 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:18445278 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18445278 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18445278 | pubmed:issn | 1471-2091 | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:FrazzonJevers... | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:BassoLuiz ALA | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:SantosDiógene... | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:PalmaMário... | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:ElyFernandaF | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:NunesJosé E... | lld:pubmed |
| pubmed-article:18445278 | pubmed:author | pubmed-author:SchroederEvel... | lld:pubmed |
| pubmed-article:18445278 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18445278 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:18445278 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18445278 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18445278 | pubmed:pagination | 13 | lld:pubmed |
| pubmed-article:18445278 | pubmed:dateRevised | 2010-9-22 | lld:pubmed |
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| pubmed-article:18445278 | pubmed:meshHeading | pubmed-meshheading:18445278... | lld:pubmed |
| pubmed-article:18445278 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18445278 | pubmed:articleTitle | The Mycobacterium tuberculosis Rv2540c DNA sequence encodes a bifunctional chorismate synthase. | lld:pubmed |
| pubmed-article:18445278 | pubmed:affiliation | Centro de Pesquisas em Biologia Molecular e Funcional, Pontifícia Universidade Católica do Rio Grande do Sul, RS 90619-900, Porto Alegre, Brazil. fernanda_ely@yahoo.com.br | lld:pubmed |
| pubmed-article:18445278 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18445278 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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