| pubmed-article:1409590 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1409590 | lifeskim:mentions | umls-concept:C0014834 | lld:lifeskim |
| pubmed-article:1409590 | lifeskim:mentions | umls-concept:C0242640 | lld:lifeskim |
| pubmed-article:1409590 | lifeskim:mentions | umls-concept:C1708726 | lld:lifeskim |
| pubmed-article:1409590 | pubmed:issue | 19 | lld:pubmed |
| pubmed-article:1409590 | pubmed:dateCreated | 1992-11-10 | lld:pubmed |
| pubmed-article:1409590 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1409590 | pubmed:abstractText | An Escherichia coli chromosomal DNA fragment cloned on a multicopy plasmid conferred resistance to carbonylcyanide m-chlorophenylhydrazone, nalidixic acid, and a number of other toxic compounds. The sequence of the cloned emr locus located at minute 57.5 of the chromosome revealed two open reading frames, emrA and emrB. emrB encodes a highly hydrophobic 56.2-kDa peptide, with 14 potential alpha-helices to span the inner membrane. The peptide is homologous to QacA, a multidrug-resistant pump from Staphylococcus aureus, and belongs to a gene family that includes tetracycline-resistant pumps of Gram-positive bacteria and the galactose/H+ symporter of E. coli. emrA encodes a putative 42.7-kDa peptide containing a single hydrophobic domain and a large C-terminal hydrophilic domain. An active pho-fusion to the C domain suggested that EmrA is a membrane protein. Disruption of emrB significantly increased sensitivity of cells to uncouplers. The cellular content of uncoupler increased in the order: overexpressed emrB cells greater than wild type greater than emrB-. | lld:pubmed |
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| pubmed-article:1409590 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:1409590 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1409590 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1409590 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:1409590 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:1409590 | pubmed:author | pubmed-author:LewisKK | lld:pubmed |
| pubmed-article:1409590 | pubmed:author | pubmed-author:LomovskayaOO | lld:pubmed |
| pubmed-article:1409590 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1409590 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:1409590 | pubmed:volume | 89 | lld:pubmed |
| pubmed-article:1409590 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1409590 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1409590 | pubmed:pagination | 8938-42 | lld:pubmed |
| pubmed-article:1409590 | pubmed:dateRevised | 2010-9-7 | lld:pubmed |
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| pubmed-article:1409590 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1409590 | pubmed:articleTitle | Emr, an Escherichia coli locus for multidrug resistance. | lld:pubmed |
| pubmed-article:1409590 | pubmed:affiliation | Department of Biology, Massachusetts Institute of Technology, Cambridge 02139. | lld:pubmed |
| pubmed-article:1409590 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1409590 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:1409590 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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