Characterization of Covalent Pyrazolopyrimidine-MKK7 Complexes and a Report on a Unique DFG-in/Leu-in Conformation of Mitogen-Activated Protein Kinase Kinase 7 (MKK7)

被引:12
|
作者
Wolle, Patrik [1 ,2 ]
Engel, Julian [1 ,3 ]
Smith, Steven [1 ,4 ]
Goebel, Lisa [1 ,2 ]
Hennes, Elisabeth [1 ,5 ]
Lategahn, Jonas [1 ,2 ,6 ]
Rauh, Daniel [1 ,2 ]
机构
[1] TU Dortmund Univ, Fac Chem & Chem Biol, Otto Hahn Str 4a, D-44227 Dortmund, Germany
[2] ZIW, DDHD, D-44227 Dortmund, Germany
[3] Lead Discovery Ctr GmbH, Otto Hahn Str 15, D-44227 Dortmund, Germany
[4] Agap2 Frankfurt, Bockenheimer Landstr 72, D-60323 Frankfurt, Germany
[5] Max Planck Inst Mol Physiol, Otto Hahn Str 11, D-44227 Dortmund, Germany
[6] PearlRiver Bio GmbH, Otto Hahn Str 15, D-44227 Dortmund, Germany
关键词
DRUG-RESISTANCE; INHIBITORS; EGFR; DISCOVERY; INSIGHTS;
D O I
10.1021/acs.jmedchem.9b00472
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pyrazolopyrimidines are well-established as covalent inhibitors of protein kinases such as the epidermal growth factor receptor or Bruton's tyrosine kinase, and we recently described their potential in targeting mitogen-activated protein kinase kinase 7 (MKK7). Herein, we report the structure activity relationship of pyrazolopyrimidine-based MKK7 inhibitors and solved several complex crystal structures to gain insights into their binding mode. In addition, we present two structures of apo-MKK7, exhibiting a DFG-out and an unprecedented DFG-in/Leu-in conformation.
引用
收藏
页码:5541 / 5546
页数:6
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