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Discovery of a 2,4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a.

  • Read more about Discovery of a 2,4-diamino-7-aminoalkoxyquinazoline as a potent and selective inhibitor of histone lysine methyltransferase G9a.

A homogeneous method for investigation of methylation-dependent protein-protein interactions in epigenetics.

  • Read more about A homogeneous method for investigation of methylation-dependent protein-protein interactions in epigenetics.

Structure and functional characterization of the atypical human kinase haspin.

  • Read more about Structure and functional characterization of the atypical human kinase haspin.

Mouse Piwi interactome identifies binding mechanism of Tdrkh Tudor domain to arginine methylated Miwi.

  • Read more about Mouse Piwi interactome identifies binding mechanism of Tdrkh Tudor domain to arginine methylated Miwi.

SH2 domains: modulators of nonreceptor tyrosine kinase activity.

  • Read more about SH2 domains: modulators of nonreceptor tyrosine kinase activity.

Screening for inhibitors of low-affinity epigenetic peptide-protein interactions: an AlphaScreen-based assay for antagonists of methyl-lysine binding proteins.

  • Read more about Screening for inhibitors of low-affinity epigenetic peptide-protein interactions: an AlphaScreen-based assay for antagonists of methyl-lysine binding proteins.

Evaluation of substituted N,N'-diarylsulfonamides as activators of the tumor cell specific M2 isoform of pyruvate kinase.

  • Read more about Evaluation of substituted N,N'-diarylsulfonamides as activators of the tumor cell specific M2 isoform of pyruvate kinase.

PARP-3 is a mono-ADP-ribosylase that activates PARP-1 in the absence of DNA.

  • Read more about PARP-3 is a mono-ADP-ribosylase that activates PARP-1 in the absence of DNA.

Crystal structure of the PHF8 Jumonji domain, an Nepsilon-methyl lysine demethylase.

  • Read more about Crystal structure of the PHF8 Jumonji domain, an Nepsilon-methyl lysine demethylase.

Crystal structures of the ATPase domains of four human Hsp70 isoforms: HSPA1L/Hsp70-hom, HSPA2/Hsp70-2, HSPA6/Hsp70B', and HSPA5/BiP/GRP78.

  • Read more about Crystal structures of the ATPase domains of four human Hsp70 isoforms: HSPA1L/Hsp70-hom, HSPA2/Hsp70-2, HSPA6/Hsp70B', and HSPA5/BiP/GRP78.

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