| pubmed-article:8022784 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C0032556 | lld:lifeskim |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C0444598 | lld:lifeskim |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C0041361 | lld:lifeskim |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C1312062 | lld:lifeskim |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C1705297 | lld:lifeskim |
| pubmed-article:8022784 | lifeskim:mentions | umls-concept:C1514562 | lld:lifeskim |
| pubmed-article:8022784 | pubmed:issue | 14 | lld:pubmed |
| pubmed-article:8022784 | pubmed:dateCreated | 1994-8-1 | lld:pubmed |
| pubmed-article:8022784 | pubmed:abstractText | Polyomavirus middle tumor antigen (MT) transforms a large number of cell types by binding to and modulating the activities of cellular proteins. Previous genetic analysis defined in MT an independent motif, NPTY (Asn-Pro-Thr-Tyr), required for transformation. This report demonstrates that NPTY is required for interaction between MT and SHC protein, a Src homology 2 (SH2)-containing protooncogene product implicated in activating Ras via association with GRB2 protein. SHC is phosphorylated on tyrosine and associates with GRB2 in MT-transformed cells. These effects require an intact NPTY motif in MT. SHC immunoprecipitates from MT-transformed cells possess kinase activity that phosphorylates not only SHC and MT but also the 85-kDa subunit of phosphatidylinositol 3-kinase. This result suggests that a complex exists that contains, at a minimum, MT, Src family tyrosine kinases, phosphatidylinositol 3-kinase, and SHC. | lld:pubmed |
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| pubmed-article:8022784 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8022784 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8022784 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8022784 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:8022784 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8022784 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:8022784 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:TUTT | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:RobertsT MTM | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:OgrisEE | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:BurkeBB | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:SchaffhausenB... | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:DrukerB JBJ | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:AugerK RKR | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:PallasD CDC | lld:pubmed |
| pubmed-article:8022784 | pubmed:author | pubmed-author:CampbellK SKS | lld:pubmed |
| pubmed-article:8022784 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8022784 | pubmed:day | 5 | lld:pubmed |
| pubmed-article:8022784 | pubmed:volume | 91 | lld:pubmed |
| pubmed-article:8022784 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8022784 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8022784 | pubmed:pagination | 6344-8 | lld:pubmed |
| pubmed-article:8022784 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
| pubmed-article:8022784 | pubmed:meshHeading | pubmed-meshheading:8022784-... | lld:pubmed |
