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Superfamilies SDR and MDR: from early ancestry to present forms. Emergence of three lines, a Zn-metalloenzyme, and distinct variabilities.

  • Read more about Superfamilies SDR and MDR: from early ancestry to present forms. Emergence of three lines, a Zn-metalloenzyme, and distinct variabilities.

Architecture of Eph receptor clusters.

  • Read more about Architecture of Eph receptor clusters.

Crystal structure of human RNA helicase A (DHX9): structural basis for unselective nucleotide base binding in a DEAD-box variant protein.

  • Read more about Crystal structure of human RNA helicase A (DHX9): structural basis for unselective nucleotide base binding in a DEAD-box variant protein.

High-throughput production of human proteins for crystallization: the SGC experience.

  • Read more about High-throughput production of human proteins for crystallization: the SGC experience.

Structural basis for Par-4 recognition by the SPRY domain- and SOCS box-containing proteins SPSB1, SPSB2, and SPSB4.

  • Read more about Structural basis for Par-4 recognition by the SPRY domain- and SOCS box-containing proteins SPSB1, SPSB2, and SPSB4.

Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor.

  • Read more about Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor.

A chemiluminescence-based method for identification of histone lysine methyltransferase inhibitors.

  • Read more about A chemiluminescence-based method for identification of histone lysine methyltransferase inhibitors.

Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired.

  • Read more about Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired.

Arp1, an actin-related protein, in Plasmodium berghei.

  • Read more about Arp1, an actin-related protein, in Plasmodium berghei.

Protein lysine methyltransferase G9a inhibitors: design, synthesis, and structure activity relationships of 2,4-diamino-7-aminoalkoxy-quinazolines.

  • Read more about Protein lysine methyltransferase G9a inhibitors: design, synthesis, and structure activity relationships of 2,4-diamino-7-aminoalkoxy-quinazolines.

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