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Structural basis for activation of Dot1L methyltransferase on the nucleosome by histone H2BK120 ubiquitylation

Cathy J. Anderson, Matthew R. Baird, Allen Hsu, Emily H. Barbour, Yuka Koyama, Mario J. Borgnia, Robert K. McGinty
doi: https://doi.org/10.1101/503128
Cathy J. Anderson
1Department of Biochemistry and Biophysics, School of Medicine, The University of North Carolina, Chapel Hill, NC 27599, USA
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Matthew R. Baird
2Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, The University of North Carolina, Chapel Hill, NC 27599, USA
4Present address: Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA
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Allen Hsu
3Genome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, NC 27709
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Emily H. Barbour
2Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, The University of North Carolina, Chapel Hill, NC 27599, USA
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Yuka Koyama
2Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, The University of North Carolina, Chapel Hill, NC 27599, USA
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Mario J. Borgnia
3Genome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, NC 27709
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Robert K. McGinty
2Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, The University of North Carolina, Chapel Hill, NC 27599, USA
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  • For correspondence: rmcginty@email.unc.edu
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Posted December 20, 2018.
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Structural basis for activation of Dot1L methyltransferase on the nucleosome by histone H2BK120 ubiquitylation
Cathy J. Anderson, Matthew R. Baird, Allen Hsu, Emily H. Barbour, Yuka Koyama, Mario J. Borgnia, Robert K. McGinty
bioRxiv 503128; doi: https://doi.org/10.1101/503128
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Structural basis for activation of Dot1L methyltransferase on the nucleosome by histone H2BK120 ubiquitylation
Cathy J. Anderson, Matthew R. Baird, Allen Hsu, Emily H. Barbour, Yuka Koyama, Mario J. Borgnia, Robert K. McGinty
bioRxiv 503128; doi: https://doi.org/10.1101/503128

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