Position 12: LTK (dark kinome) cellular models, phosphoproteomics and interface dependency

Position 11: Cellular target engagement and pathway modulation in EGFR/BRAF models

Position 10: Deep-learning for polypharmacology, allosterism and resistance-aware interface design

Position 9: Structure-based & ML pipelines for interface-selective hit discovery

Position 8: Design and synthesis of MCR-based dimerization inhibitors.

Position 7: PPI-biased small-molecule discovery for kinase regulatory interfaces

Position 6: (Bi)cyclic peptide discovery against dimerization and substrate interfaces

Position 5: SMALP-stabilised kinase reconstitution to bridge structural and cellular states

Position 1: TR-FRET dimerization reporters for EGFR, BRAF and LTK under ATP-locked conditions

Position 2: Cleavable-linker bisubstrate FRET assays with covalent ATP anchors

Position 3: Single-molecule FRET maps of kinase oligomerization and ligand-biased conformations

Position 4: Cryo-EM blueprints of kinase dimerization and substrate-site architecture