| pubmed-article:3018530 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0036025 | lld:lifeskim |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0040711 | lld:lifeskim |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0035696 | lld:lifeskim |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0162807 | lld:lifeskim |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0205216 | lld:lifeskim |
| pubmed-article:3018530 | lifeskim:mentions | umls-concept:C0683607 | lld:lifeskim |
| pubmed-article:3018530 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:3018530 | pubmed:dateCreated | 1986-10-8 | lld:pubmed |
| pubmed-article:3018530 | pubmed:abstractText | The CYC1-239-O mutation in the yeast Saccharomyces cerevisiae produces a -His-Leu- replacement of the normal -Ala-Gly- sequence at amino acid positions 5 and 6, which lie within a dispensable region of iso-1-cytochrome c; this mutation can accommodate the formation of a hairpin structure at the corresponding site in the mRNA. The amount of the altered protein was diminished to 20% of the wild-type level, whereas the amount of the mRNA remained normal. However, in contrast to the normal CYC1+ mRNA that is associated mainly with four to seven ribosomes, the bulk of the CYC1-239-O mRNA is associated with one to four ribosomes. These results suggest that the stable secondary structure within the translated region of the CYC1 mRNA diminishes translation by inhibiting elongation. | lld:pubmed |
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| pubmed-article:3018530 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3018530 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3018530 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3018530 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3018530 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:3018530 | pubmed:issn | 0270-7306 | lld:pubmed |
| pubmed-article:3018530 | pubmed:author | pubmed-author:EusticeD CDC | lld:pubmed |
| pubmed-article:3018530 | pubmed:author | pubmed-author:ShermanFF | lld:pubmed |
| pubmed-article:3018530 | pubmed:author | pubmed-author:PietrasD FDF | lld:pubmed |
| pubmed-article:3018530 | pubmed:author | pubmed-author:BaimS BSB | lld:pubmed |
| pubmed-article:3018530 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3018530 | pubmed:volume | 5 | lld:pubmed |
| pubmed-article:3018530 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3018530 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3018530 | pubmed:pagination | 1839-46 | lld:pubmed |
| pubmed-article:3018530 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:3018530 | pubmed:meshHeading | pubmed-meshheading:3018530-... | lld:pubmed |
| pubmed-article:3018530 | pubmed:year | 1985 | lld:pubmed |
| pubmed-article:3018530 | pubmed:articleTitle | A mutation allowing an mRNA secondary structure diminishes translation of Saccharomyces cerevisiae iso-1-cytochrome c. | lld:pubmed |
| pubmed-article:3018530 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3018530 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:3018530 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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