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. 2011 Aug 22;5:85–94. doi: 10.2174/1875397301005010085

Fig. (2).

Fig. (2)

Architecture of the catalytic domain. The canonical SET domain (green) includes all residues critical to catalysis. The I-SET (cyan) and Post-SET (blue) domains are observed in all structures, and form the docking platform for the substrate peptide (magenta). The substrate lysine inserts into a narrow channel (top right) and is shielded from solvent. The cofactor (white sticks – top left) and peptide substrate bind at distinct druggable pockets, thereby providing multiple opportunities for chemical inhibition. Diverse combinations of N-SET (gray), Pre-SET (orange), MYND (yellow), and CTD (red) domains can dress the core SET domain, and offer distinct interfaces to specific interaction partners. The truncated version of the Post-SET domain observed in PRDM structures (bottom left) is probably linked to the absence of activity of these constructs. (PDB codes are indicated in square brackets).