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Targeting human SET1/MLL family of proteins.
Vedadi, Masoud; Blazer, Levi; Eram, Mohammad S; Barsyte-Lovejoy, Dalia; Arrowsmith, Cheryl H; Hajian, Taraneh.
Afiliación
  • Vedadi M; Structural Genomics Consortium, University of Toronto, Toronto, ON, M5G 1L7.
  • Blazer L; Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON, M5S 1A8.
  • Eram MS; Structural Genomics Consortium, University of Toronto, Toronto, ON, M5G 1L7.
  • Barsyte-Lovejoy D; Structural Genomics Consortium, University of Toronto, Toronto, ON, M5G 1L7.
  • Arrowsmith CH; Structural Genomics Consortium, University of Toronto, Toronto, ON, M5G 1L7.
  • Hajian T; Structural Genomics Consortium, University of Toronto, Toronto, ON, M5G 1L7.
Protein Sci ; 26(4): 662-676, 2017 04.
Article en En | MEDLINE | ID: mdl-28160335
The SET1 family of proteins, and in particular MLL1, are essential regulators of transcription and key mediators of normal development and disease. Here, we summarize the detailed characterization of the methyltransferase activity of SET1 complexes and the role of the key subunits, WDR5, RbBP5, ASH2L, and DPY30. We present new data on full kinetic characterization of human MLL1, MLL3, SET1A, and SET1B trimeric, tetrameric, and pentameric complexes to elaborate on substrate specificities and compare our findings with what has been reported before. We also review exciting recent work identifying potent inhibitors of oncogenic MLL1 function through disruption of protein-protein interactions within the MLL1 complex.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: N-Metiltransferasa de Histona-Lisina / Inhibidores Enzimáticos / Proteína de la Leucemia Mieloide-Linfoide / Complejos Multienzimáticos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Protein Sci Asunto de la revista: BIOQUIMICA Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: N-Metiltransferasa de Histona-Lisina / Inhibidores Enzimáticos / Proteína de la Leucemia Mieloide-Linfoide / Complejos Multienzimáticos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Protein Sci Asunto de la revista: BIOQUIMICA Año: 2017 Tipo del documento: Article