| Literature DB >> 31083997 |
Patrik Wolle1,2, Julian Engel1, Steven Smith1, Lisa Goebel1,2, Elisabeth Hennes1, Jonas Lategahn1,2, Daniel Rauh1,2.
Abstract
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.Entities:
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Year: 2019 PMID: 31083997 DOI: 10.1021/acs.jmedchem.9b00472
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446