4HRA
Crystal Structure of DOT1L in Complex with EPZ-5676
Summary for 4HRA
Entry DOI | 10.2210/pdb4hra/pdb |
Related | 3QOW 3QOX 4EK9 4EKG 4EKI |
Descriptor | Histone-lysine N-methyltransferase, H3 lysine-79 specific, 5'-[{cis-3-[2-(5-tert-butyl-1H-benzimidazol-2-yl)ethyl]cyclobutyl}(propan-2-yl)amino]-5'-deoxyadenosine, SULFATE ION (3 entities in total) |
Functional Keywords | histone lysine methyltransferase, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Nucleus: Q8TEK3 |
Total number of polymer chains | 1 |
Total formula weight | 49321.07 |
Authors | |
Primary citation | Daigle, S.R.,Olhava, E.J.,Therkelsen, C.A.,Basavapathruni, A.,Jin, L.,Boriack-Sjodin, P.A.,Allain, C.J.,Klaus, C.R.,Raimondi, A.,Scott, M.P.,Waters, N.J.,Chesworth, R.,Moyer, M.P.,Copeland, R.A.,Richon, V.M.,Pollock, R.M. Potent inhibition of DOT1L as treatment of MLL-fusion leukemia. Blood, 122:1017-1025, 2013 Cited by PubMed: 23801631DOI: 10.1182/blood-2013-04-497644 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.15 Å) |
Structure validation
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