Index | Gene Name Primary | Protein Name | Uniprot ID | Gene Name Synonym | Ligand Name | Structure | PDB Code | ligand desolvation | Ligand Structure | Compound Affinity nM |
1 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | sx0 | Crystal structure of Dot1l in complex with a brominated SAH analog | 3sx0 | 98.92 | | no data |
2 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | aw3 | Crystal Structure of human DOT1L in complex with inhibitor SGC0947 | 4er7 | 81.68 | | no data |
3 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | aw1 | Crystal Structure of human DOT1L in complex with inhibitor FED1 | 4er0 | 83.59 | | no data |
4 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | aw0 | Crystal structure of human DOT1L in complex with inhibitor FED2 | 4eqz | 92.41 | | no data |
5 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 5ek | Crystal structure of Dot1L in complex with inhibitor CPD3 [N-(1-(2-chlorophenyl)-1H-indol-6-yl)-2-(2-(5-(2-chlorophenyl)-1H-tetrazol-1-yl)acetyl)hydrazinecarboxamide] | 5dry | 89.5 | | 20. |
6 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 0qk | Crystal Structure of DOT1L in complex with EPZ004777 | 4eki | 90.35 | | 0.1 |
7 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 0qk | Crystal Structure of Human DOT1L in complex with inhibitor EPZ004777 | 4er3 | 87.03 | | no data |
8 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 0qj | Crystal Structure of DOT1L in Complex with EPZ003696 | 4ekg | 90.46 | | 1.7 |
9 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | ep4 | Crystal structure of DOT1L in complex with EPZ000004 | 4ek9 | 92.47 | | 38000. |
10 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | adn | Crystal structure of Dot1L in complex with adenosine and inhibitor CPD1 [N6-(2,6-dichlorophenyl)-N6-(pent-2-yn-1-yl)quinoline-4,6-diamine] | 5mvs | 77.43 | | no data |
11 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 5id | Crystal structure of Dot1l in complex with 5-iodotubercidin | 3uwp | 84.66 | | no data |
12 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 5eg | Crystal structure of Dot1L in complex with inhibitor CPD2 [2-(2-(5-((2-chlorophenoxy)methyl)-1H-tetrazol-1-yl)acetyl)-N-(4-chlorophenyl)hydrazinecarboxamide] | 5drt | 85.64 | | 4400. |
13 | DOT1L | Histone-lysine N-methyltransferase, H3 lysine-79 specific | Q8TEK3 | KIAA1814 KMT4 | 5f6 | Crystal structure of Dot1L in complex with inhibitor CPD3 [(2,6-dichlorophenyl)(quinolin-6-yl)methanone] | 5dtq | 91.9 | | 139000. |