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Mechanism of BRAF Activation through Biochemical Characterization of the Recombinant Full‐Length Protein
ChemBioChem ( IF 2.6 ) Pub Date : 2018-08-17 , DOI: 10.1002/cbic.201800359 Nicholas Cope 1 , Christine Candelora 1 , Kenneth Wong 1 , Sujeet Kumar 1 , Haihan Nan 1 , Michael Grasso 2 , Borna Novak 1 , Yana Li 3 , Ronen Marmorstein 2 , Zhihong Wang 1
ChemBioChem ( IF 2.6 ) Pub Date : 2018-08-17 , DOI: 10.1002/cbic.201800359 Nicholas Cope 1 , Christine Candelora 1 , Kenneth Wong 1 , Sujeet Kumar 1 , Haihan Nan 1 , Michael Grasso 2 , Borna Novak 1 , Yana Li 3 , Ronen Marmorstein 2 , Zhihong Wang 1
Affiliation
Home of the BRAF: A strategy to obtain full‐length BRAF that is significantly more active than its truncated counterpart is reported. To gain a better understanding of BRAF regulation, a detailed kinetic analysis of purified full‐length BRAF is conducted to investigate the impact of BRAF inhibitors, MEK binding, RAS binding, and heterodimerization with CRAF on kinase activity in vitro.
中文翻译:
通过重组全长蛋白质的生化表征进行BRAF活化的机制
BRAF的所在地:据报道,获得了一种全长BRAF的策略,该策略比截短的BRAF更活跃。为了更好地了解BRAF调控,对纯化的全长BRAF进行了详细的动力学分析,以研究BRAF抑制剂,MEK结合,RAS结合以及CRAF异二聚化对体外激酶活性的影响。
更新日期:2018-08-17
中文翻译:
通过重组全长蛋白质的生化表征进行BRAF活化的机制
BRAF的所在地:据报道,获得了一种全长BRAF的策略,该策略比截短的BRAF更活跃。为了更好地了解BRAF调控,对纯化的全长BRAF进行了详细的动力学分析,以研究BRAF抑制剂,MEK结合,RAS结合以及CRAF异二聚化对体外激酶活性的影响。