| pubmed-article:2160590 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2160590 | lifeskim:mentions | umls-concept:C0029016 | lld:lifeskim |
| pubmed-article:2160590 | lifeskim:mentions | umls-concept:C0206454 | lld:lifeskim |
| pubmed-article:2160590 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:2160590 | lifeskim:mentions | umls-concept:C1521840 | lld:lifeskim |
| pubmed-article:2160590 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:2160590 | pubmed:dateCreated | 1990-6-25 | lld:pubmed |
| pubmed-article:2160590 | pubmed:abstractText | An 85,000-molecular-weight polypeptide (85K polypeptide) has previously been identified as a common substrate for tyrosine phosphorylation upon polyomavirus middle T transformation or upon platelet-derived growth factor stimulation of 3T3 cells. In each case, pp85 has an associated phosphatidylinositol kinase activity. The tissue distribution of pp85 was determined by middle T blotting experiments; the highest levels were found in brain, lung, and spleen tissues. High-resolution examination of 85K by isoelectric focusing demonstrated that there are at least 10 different forms. These were resolved into two families, 85K and 86K; the ratio of the two families changed in different cells. Similar forms were found for pp85 associated with pp60v-src. Individual species within each family differed by phosphorylation. Analysis of pp85 and pp86 by immunoprecipitation with anti-phosphotyrosine antibody showed increasing phosphorylation in response to middle T or pp60v-src transformation. The association of middle T with pp85 and pp60c-src was examined in pulse-chase experiments. Association of middle T with pp60c-src was slow and was accompanied by progressive modification of middle T. pp85 formed a dissociable complex with middle T within 2.5 min. | lld:pubmed |
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| pubmed-article:2160590 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:2160590 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2160590 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2160590 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:2160590 | pubmed:issn | 0270-7306 | lld:pubmed |
| pubmed-article:2160590 | pubmed:author | pubmed-author:RobertsT MTM | lld:pubmed |
| pubmed-article:2160590 | pubmed:author | pubmed-author:CohenBB | lld:pubmed |
| pubmed-article:2160590 | pubmed:author | pubmed-author:SchaffhausenB... | lld:pubmed |
| pubmed-article:2160590 | pubmed:author | pubmed-author:DrukerBB | lld:pubmed |
| pubmed-article:2160590 | pubmed:author | pubmed-author:LieY HYH | lld:pubmed |
| pubmed-article:2160590 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2160590 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:2160590 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2160590 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2160590 | pubmed:pagination | 2909-15 | lld:pubmed |
| pubmed-article:2160590 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:2160590 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:2160590 | pubmed:articleTitle | Characterization of pp85, a target of oncogenes and growth factor receptors. | lld:pubmed |
| pubmed-article:2160590 | pubmed:affiliation | Department of Biochemistry, Tufts University Health Sciences Campus, Boston, Massachusetts 02111. | lld:pubmed |
| pubmed-article:2160590 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2160590 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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