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UDP-glucose dehydrogenase: structure and function of a potential drug target.

  • Read more about UDP-glucose dehydrogenase: structure and function of a potential drug target.

Selective inhibition of BET bromodomains.

  • Read more about Selective inhibition of BET bromodomains.

Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation.

  • Read more about Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation.

The Clp chaperones and proteases of the human malaria parasite Plasmodium falciparum.

  • Read more about The Clp chaperones and proteases of the human malaria parasite Plasmodium falciparum.

Structural basis for recognition of arginine methylated Piwi proteins by the extended Tudor domain.

  • Read more about Structural basis for recognition of arginine methylated Piwi proteins by the extended Tudor domain.

Comparative structural analysis of human DEAD-box RNA helicases.

  • Read more about Comparative structural analysis of human DEAD-box RNA helicases.

Binding of different histone marks differentially regulates the activity and specificity of polycomb repressive complex 2 (PRC2).

  • Read more about Binding of different histone marks differentially regulates the activity and specificity of polycomb repressive complex 2 (PRC2).

The crystal structure of human GLRX5: iron-sulfur cluster co-ordination, tetrameric assembly and monomer activity.

  • Read more about The crystal structure of human GLRX5: iron-sulfur cluster co-ordination, tetrameric assembly and monomer activity.

Structural basis for c-KIT inhibition by the suppressor of cytokine signaling 6 (SOCS6) ubiquitin ligase.

  • Read more about Structural basis for c-KIT inhibition by the suppressor of cytokine signaling 6 (SOCS6) ubiquitin ligase.

A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date.

  • Read more about A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date.

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