| pubmed-article:10517594 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10517594 | lifeskim:mentions | umls-concept:C0006837 | lld:lifeskim |
| pubmed-article:10517594 | lifeskim:mentions | umls-concept:C0009015 | lld:lifeskim |
| pubmed-article:10517594 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:10517594 | lifeskim:mentions | umls-concept:C0242417 | lld:lifeskim |
| pubmed-article:10517594 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:10517594 | lifeskim:mentions | umls-concept:C0332453 | lld:lifeskim |
| pubmed-article:10517594 | pubmed:dateCreated | 2000-1-10 | lld:pubmed |
| pubmed-article:10517594 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10517594 | pubmed:abstractText | A multicopper oxidase gene from the human pathogenic yeast Candida albicans was isolated and characterized. An open reading frame of 1872 bp, designated CaFET3, was identified, encoding a predicted protein of 624 amino acids and a molecular mass of 70.5 kDa. The identity between the deduced amino acid sequences of CaFET3 and the Saccharomyces cerevisiae FET3 gene is 55%. CaFET3 was localized on chromosome 6. A null mutant (fet3delta/fet3delta) was constructed by sequential gene disruption. Unlike the C. albicans SC5314 wild-type strain the fet3delta mutant was unable to grow in low-iron medium. The lack of growth of a S. cerevisiae fet3delta mutant in iron-limited medium was compensated by transformation with CaFET3. The null mutant strain showed no change in pathogenicity compared with the wild-type strain in the mouse model of systemic candidiasis. | lld:pubmed |
| pubmed-article:10517594 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10517594 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10517594 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10517594 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:10517594 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10517594 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10517594 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:10517594 | pubmed:issn | 1350-0872 | lld:pubmed |
| pubmed-article:10517594 | pubmed:author | pubmed-author:KünkelWW | lld:pubmed |
| pubmed-article:10517594 | pubmed:author | pubmed-author:HärtlAA | lld:pubmed |
| pubmed-article:10517594 | pubmed:author | pubmed-author:RoemerEE | lld:pubmed |
| pubmed-article:10517594 | pubmed:author | pubmed-author:EckRR | lld:pubmed |
| pubmed-article:10517594 | pubmed:author | pubmed-author:HundtSS | lld:pubmed |
| pubmed-article:10517594 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10517594 | pubmed:volume | 145 ( Pt 9) | lld:pubmed |
| pubmed-article:10517594 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10517594 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10517594 | pubmed:pagination | 2415-22 | lld:pubmed |
| pubmed-article:10517594 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:10517594 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10517594 | pubmed:articleTitle | A multicopper oxidase gene from Candida albicans: cloning, characterization and disruption. | lld:pubmed |
| pubmed-article:10517594 | pubmed:affiliation | Hans-Knöll-Institut für Naturstoff-Forschung eV, Abteilung Mikrobielle Infektionsbiologie, Jena, Germany. reck@pmail.hki-jena.de | lld:pubmed |
| pubmed-article:10517594 | pubmed:publicationType | Journal Article | lld:pubmed |
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