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• W1903298945 endingPage "3042" @default.
• W1903298945 startingPage "3035" @default.
• W1903298945 abstract "The protein substrates for the tyrosine protein kinases in cells transformed by avian sarcoma viruses were analyzed by gel electrophoresis in combination with immunoblotting or immunoprecipitation by antibodies against phosphotyrosine. We found that greater than 90% of phosphotyrosine-containing cellular proteins can be immunoprecipitated by these antibodies. The level of phosphotyrosine-containing cellular proteins detectable by this method markedly increased upon transformation with Rous sarcoma virus, and more than 20 distinct bands of such proteins were found in lysates of Rous sarcoma virus-transformed cells. Most of these phosphotyrosine-containing proteins had not been identified by other methods, and their presence appeared to correlate with morphological transformation in cells infected with various Rous sarcoma virus mutants and Y73, PRCII, and Fujinami sarcoma viruses. However, considerably different patterns were obtained with cells infected with nontransforming Rous sarcoma virus mutants that encode nonmyristylated src kinases, indicating that most substrates that correlate with transformation can only be recognized by p60v-src associated with the plasma membrane." @default.
• W1903298945 created "2016-06-24" @default.
• W1903298945 creator A5068776411 @default.
• W1903298945 creator A5072279288 @default.
• W1903298945 creator A5073313983 @default.
• W1903298945 date "1988-08-01" @default.
• W1903298945 modified "2023-09-27" @default.
• W1903298945 title "Phosphorylation of cellular proteins in Rous sarcoma virus-infected cells: analysis by use of anti-phosphotyrosine antibodies." @default.
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• W1903298945 doi "https://doi.org/10.1128/mcb.8.8.3035" @default.
• W1903298945 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/363529" @default.
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• W1903298945 hasPublicationYear "1988" @default.
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