Structure-guided development of affinity probes for tyrosine kinases using chemical genetics-Reference-Cited by-同舟云学术

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Structure-guided development of affinity probes for tyrosine kinases using chemical genetics

Published:2007-03-04 Issue:4 Volume:3 Page:229-238
ISSN:1552-4450
Container-title:Nature Chemical Biology
language:en
Short-container-title:Nat Chem Biol

Author:

Blair Jimmy A,Rauh Daniel,Kung Charles,Yun Cai-Hong,Fan Qi-Wen,Rode Haridas,Zhang Chao,Eck Michael J,Weiss William A,Shokat Kevan M

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/nchembio866.pdf

Reference50 articles.

1. Cohen, P. Protein kinases–the major drug targets of the twenty-first century? Nat. Rev. Drug Discov. 1, 309–315 (2002).

2. Knight, Z.A. & Shokat, K.M. Features of selective kinase inhibitors. Chem. Biol. 12, 621–637 (2005).

3. Kung, C., Kenski, D.M., Krukenberg, K., Madhani, H.D. & Shokat, K.M. Selective kinase inhibition by exploiting differential pathway sensitivity. Chem. Biol. 13, 399–407 (2006).

4. Ventura, J.J. et al. Chemical genetic analysis of the time course of signal transduction by JNK. Mol. Cell 21, 701–710 (2006).

5. Evans, M.J. & Cravatt, B.F. Mechanism-based profiling of enzyme families. Chem. Rev. 106, 3279–3301 (2006).

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