5V61

Phospho-ERK2 bound to bivalent inhibitor SBP2

Summary for 5V61

• Entry DOI: 10.2210/pdb5v61/pdb
• Related: 5V60 5V62
• Descriptor: Mitogen-activated protein kinase 1, Ribosomal protein S6 kinase alpha-1,Protein Tat, GLYCEROL, ... (6 entities in total)
• Functional Keywords: kinase, mapk, phosphorylation, cancer, transferase-transferase inhibitor complex, transferase-inhibitor complex, transferase/inhibitor
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 2
• Total formula weight: 45698.41

Authors

Lechtenberg, B.C.,Riedl, S.J. (deposition date: 2017-03-15, release date: 2017-07-26, Last modification date: 2024-11-06)

Primary citation

Lechtenberg, B.C.,Mace, P.D.,Sessions, E.H.,Williamson, R.,Stalder, R.,Wallez, Y.,Roth, G.P.,Riedl, S.J.,Pasquale, E.B.
Structure-Guided Strategy for the Development of Potent Bivalent ERK Inhibitors.
ACS Med Chem Lett, 8:726-731, 2017

PubMed Abstract: ERK is the effector kinase of the RAS-RAF-MEK-ERK signaling cascade, which promotes cell transformation and malignancy in many cancers and is thus a major drug target in oncology. Kinase inhibitors targeting RAF or MEK are already used for the treatment of certain cancers, such as melanoma. Although the initial response to these drugs can be dramatic, development of drug resistance is a major challenge, even with combination therapies targeting both RAF and MEK. Importantly, most resistance mechanisms still rely on activation of the downstream effector kinase ERK, making it a promising target for drug development efforts. Here, we report the design and structural/functional characterization of a set of bivalent ERK inhibitors that combine a small molecule inhibitor that binds to the ATP-binding pocket with a peptide that selectively binds to an ERK protein interaction surface, the D-site recruitment site (DRS). Our studies show that the lead bivalent inhibitor, SBP3, has markedly improved potency compared to the small molecule inhibitor alone. Unexpectedly, we found that SBP3 also binds to several ERK-related kinases that contain a DRS, highlighting the importance of experimentally verifying the predicted specificity of bivalent inhibitors. However, SBP3 does not target any other kinases belonging to the same CMGC branch of the kinome. Additionally, our modular click chemistry inhibitor design facilitates the generation of different combinations of small molecule inhibitors with ERK-targeting peptides.

PubMed: 28740606
DOI: 10.1021/acsmedchemlett.7b00127

Experimental method

X-RAY DIFFRACTION (2.2 Å)