The Crystal Structure of BRAF in Complex with an Organoruthenium Inhibitor Reveals a Mechanism for Inhibition of an Active Form of BRAF Kinase
Substitution mutations in the BRAF serine/threonine kinase are found in a variety of human cancers. Such mutations occur in approximately 70% of human malignant melanomas, and a single hyperactivating V600E mutation is found in the activation segment of the kinase domain and accounts for more than 9...
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Main Authors: | , , , , , , |
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格式: | Artigo |
语言: | 英语 |
出版: |
2009
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在线阅读: | https://doi.org/10.1021/bi802067u |
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