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The crystal structures of histone methyltransferase SET7/9 in complexes with two previously developed AdoMet analogues revealed the structural bases for the efficient inhibition of SET7/9 by DAAM-3 and the stabilization of AAM-1, a weaker inhibitor than DAAM-3, within SET7/9 in the crystal.

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This study presents crystal structures of the catalytic domain of human DUSP26 and a catalytically inactive mutant at 1.67 and 2.20 Å resolution, respectively.
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