Redundant targeting of Isr1 by two CDKs in mitotic cells
Author:
Funder
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00294-020-01110-x.pdf
Reference32 articles.
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2. Benanti JA, Cheung SK, Brady MC, Toczyski DP (2007) A proteomic screen reveals SCFGrr1 targets that regulate the glycolytic–gluconeogenic switch. Nat Cell Biol 9:1184–1191. https://doi.org/10.1038/ncb1639
3. Bishop AC, Ubersax JA, Petsch DT, Matheos DP, Gray NS, Blethrow J, Shimizu E, Tsien JZ, Schultz PG, Rose MD, Wood JL, Morgan DO, Shokat KM (2000) A chemical switch for inhibitor-sensitive alleles of any protein kinase. Nature 407:395–401. https://doi.org/10.1038/35030148
4. Carroll AS, Bishop AC, DeRisi JL, Shokat KM, O’Shea EK (2001) Chemical inhibition of the Pho85 cyclin-dependent kinase reveals a role in the environmental stress response. Proc Natl Acad Sci USA 98:12578–12583. https://doi.org/10.1073/pnas.211195798
5. Dephoure N, Howson RW, Blethrow JD, Shokat KM, O’Shea EK (2005) Combining chemical genetics and proteomics to identify protein kinase substrates. Proc Natl Acad Sci 102:17940–17945. https://doi.org/10.1073/pnas.0509080102
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