| pubmed-article:16574659 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16574659 | lifeskim:mentions | umls-concept:C0003232 | lld:lifeskim |
| pubmed-article:16574659 | lifeskim:mentions | umls-concept:C0028630 | lld:lifeskim |
| pubmed-article:16574659 | lifeskim:mentions | umls-concept:C0004022 | lld:lifeskim |
| pubmed-article:16574659 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:16574659 | lifeskim:mentions | umls-concept:C1521840 | lld:lifeskim |
| pubmed-article:16574659 | lifeskim:mentions | umls-concept:C0066511 | lld:lifeskim |
| pubmed-article:16574659 | pubmed:issue | 26 | lld:pubmed |
| pubmed-article:16574659 | pubmed:dateCreated | 2006-6-26 | lld:pubmed |
| pubmed-article:16574659 | pubmed:abstractText | Microcin C is a ribosome-synthesized heptapeptide that contains a modified adenosine monophosphate covalently attached to the C-terminal aspartate. Microcin C is a potent inhibitor of bacterial cell growth. Based on the in vivo kinetics of inhibition of macromolecular synthesis, Microcin C targets translation, through a mechanism that remained undefined. Here, we show that Microcin C is a subject of specific degradation inside the sensitive cell. The product of degradation, a modified aspartyl-adenylate containing an N-acylphosphoramidate linkage, strongly inhibits translation by blocking the function of aspartyl-tRNA synthetase. | lld:pubmed |
| pubmed-article:16574659 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16574659 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16574659 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16574659 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16574659 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:16574659 | pubmed:issn | 0021-9258 | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:SeverinovKons... | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:IbbaMichaelM | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:PavlovaOlgaO | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:Praetorius-Ib... | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:Krasheninniko... | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:KommerAigarA | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:MetlitskayaAn... | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:KazakovTeymur... | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:KolbVyachesla... | lld:pubmed |
| pubmed-article:16574659 | pubmed:author | pubmed-author:KhmelInessaI | lld:pubmed |
| pubmed-article:16574659 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16574659 | pubmed:day | 30 | lld:pubmed |
| pubmed-article:16574659 | pubmed:volume | 281 | lld:pubmed |
| pubmed-article:16574659 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16574659 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16574659 | pubmed:pagination | 18033-42 | lld:pubmed |
| pubmed-article:16574659 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:meshHeading | pubmed-meshheading:16574659... | lld:pubmed |
| pubmed-article:16574659 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16574659 | pubmed:articleTitle | Aspartyl-tRNA synthetase is the target of peptide nucleotide antibiotic Microcin C. | lld:pubmed |
| pubmed-article:16574659 | pubmed:affiliation | Institute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia. | lld:pubmed |
| pubmed-article:16574659 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16574659 | pubmed:publicationType | In Vitro | lld:pubmed |
| pubmed-article:16574659 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:16574659 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| entrez-gene:946385 | entrezgene:pubmed | pubmed-article:16574659 | lld:entrezgene |
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