PDB 5mw3
PDB Information
PDB | 5MW3 |
Method | X-RAY DIFFRACTION |
Host Organism | Escherichia coli |
Gene Source | Homo sapiens |
Primary Citation | Discovery of Potent, Selective, and Structurally Novel Dot1L Inhibitors by a Fragment Linking Approach.
ACS Med Chem Lett
|
Header | Transferase |
Released | 2017-01-18 |
Resolution | 2.090 |
CATH Insert Date | 07 May, 2017 |
PDB Images (7)
PDB Prints
PDB Chains (2)
Chain ID | Date inserted into CATH | CATH Status |
---|---|---|
A | 08 May, 2017 | Chopped |
B | 08 May, 2017 | Chopped |
CATH Domains (4)
Domain ID | Date inserted into CATH | Superfamily | CATH Status |
---|---|---|---|
5mw3A01 | 17 May, 2017 | 1.10.260.60 | Assigned |
5mw3A02 | 17 May, 2017 | 3.40.50.150 | Assigned |
5mw3B01 | 17 May, 2017 | 1.10.260.60 | Assigned |
5mw3B02 | 17 May, 2017 | 3.40.50.150 | Assigned |
UniProtKB Entries (2)
Accession | Gene ID | Taxon | Description |
---|---|---|---|
Q8TEK3 | DOT1L_HUMAN | Homo sapiens | Histone-lysine N-methyltransferase, H3 lysine-79 specific |
Q8TEK3 | DOT1L_HUMAN | Homo sapiens | Histone-lysine N-methyltransferase, H3 lysine-79 specific |