MAPK variant effect atlas

Contextual variant effects across the MAPK pathway

This atlas maps how 186,676 variants in 17 proteins of the RAS–MAPK pathway, the signaling pathway most often mutated in cancer, change each protein's abundance and the activity of the pathway in human cells. We also measured variants in altered cellular contexts: with the chaperone HSP90 inhibited, which showed that the abundance of most missense variants depends on HSP90; with RAS switched on from upstream; and with LZTR1, which marks RAS for degradation, knocked out. Finally, we used the variant effects to test hundreds of protein–protein interactions seen in experimental and predicted structures. For nearly all of them, mutations in the contact surface disrupted protein abundance or pathway activity more than mutations elsewhere on the protein's surface, pinpointing the contacts the pathway relies on.

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pERK pathway activity(measured) ReceptorTyrosineKinases GRB2 SOS SHP2 RAS KSR MEK RAF

Adapted from the PDB-101 Raf/MEK/ERK pathway figure (CC BY 4.0): re-rendered with Illustrate (Goodsell, Autin & Olson, Structure 2019) from PDB 3NJP, 2M20, 3GOP, 1GRI, 1AZE, 6CRF, 1AYA, 1XD2, 5P21, 6XI7, 6Q0J, 7MFD, 2Y4I, 2ERK, with disordered regions and the KSR2 N-terminal domains from AlphaFold DB models.

All proteins

Receptor tyrosine kinaseEGFRERBB2HGFRRET
PhosphataseSHP2
AdapterGRB2
GTPaseKRASMRAS
RAF kinaseARAFBRAFCRAF
MEK kinaseMEK1MEK2
Scaffold pseudokinaseKSR1KSR2