Index | Gene Name Primary | Protein Name | Uniprot ID | Gene Name Synonym | Ligand Name | Structure | PDB Code | ligand desolvation | Ligand Structure | Compound Affinity nM |
1 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fqq | Crystal structure of human KDM4A in complex with compound 19d | 6h4w | 74.98 | | no data |
2 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fqh | Crystal structure of human KDM4A in complex with compound 18a | 6h4o | 80.22 | | no data |
3 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fqe | Crystal structure of human KDM4A in complex with compound 16m | 6h4s | 76.97 | | no data |
4 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fqb | Crystal structure of human KDM4A in complex with compound 17f | 6h4r | 82.74 | | no data |
5 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fow | Crystal structure of human KDM4A in complex with compound 19a | 6h4t | 74.51 | | no data |
6 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fo8 | Crystal structure of human KDM4A in complex with compound 17e | 6h4y | 82.1 | | no data |
7 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | fo2 | Crystal structure of human KDM4A in complex with compound 34a | 6h4q | 83.77 | | no data |
8 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | kc6 | Crystal structure of JMJD2A complexed with bipyridyl inhibitor | 3pdq | 76.39 | | 180. |
9 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | mmk | Crystal structure of human JMJD2A in complex with compound KDOAM20A | 5fpv | 86.96 | | no data |
10 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | vao | Crystal structure of human JMJD2A in complex with compound 43 | 5a7n | 83.17 | | no data |
11 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 7wh | Crystal structure of human JMJD2A in complex with compound 42 | 5a7o | 85.13 | | no data |
12 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 6z1 | Crystal structure of human JMJD2A in complex with compound 36 | 5a7p | 76.13 | | no data |
13 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | kch | Crystal structure of human JMJD2A in complex with compound 30 | 5a7q | 84.15 | | no data |
14 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | s2x | Crystal structure of human JMJD2A in complex with compound 44 | 5a7s | 82.72 | | no data |
15 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 35m | Crystal structure of human JMJD2A in complex with compound 35 | 5a7w | 78.5 | | no data |
16 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 9cj | Crystal structure of human JMJD2A in complex with compound 40 | 5a80 | 75.22 | | no data |
17 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 5yq | inhibitors of JumonjiC domain-containing histone demethylases | 5anq | 87.49 | | 3980. |
18 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 5u8 | Crystal structure of human KDM4A in complex with compound 52d | 5f3c | 77.86 | | 900. |
19 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 5uo | Crystal structure of human KDM4A in complex with compound 54a | 5f3e | 79.25 | | 138. |
20 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 5ul | Crystal structure of human KDM4A in complex with compound 53a | 5f3g | 69.52 | | 126. |
21 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 5uj | Crystal structure of human KDM4A in complex with compound 54j | 5f3i | 80.75 | | 80. |
22 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 5v1 | Crystal Structure of human JMJD2A complexed with KDOOA011340 | 5f5i | 94.04 | | 950. |
23 | KDM4A | Lysine-specific demethylase 4A | O75164 | JHDM3A JMJD2 JMJD2A KIAA0677 | 9dj | Crystal Structure of KDM4 with the Small Molecule Inhibitor QC6352 | 5vgi | 75.46 | | 104. |
24 | KDM4C | Lysine-specific demethylase 4C | Q9H3R0 | GASC1 JHDM3C JMJD2C KIAA0780 | mmk | Crystal structure of human JMJD2C catalytic domain in complex with epitherapuetic compound 2-(((2-((2-(dimethylamino)ethyl) (ethyl)amino) -2-oxoethyl)amino)methyl)isonicotinic acid | 5fjh | 86.01 | | no data |
25 | KDM4D | Lysine-specific demethylase 4D | Q6B0I6 | JHDM3D JMJD2D | cqt | Crystal Structure of KDM4D with tetrazole ligand GF049 | 6f5s | 86.97 | | no data |
26 | KDM4D | Lysine-specific demethylase 4D | Q6B0I6 | JHDM3D JMJD2D | 5v0 | Crystal Structure of human JMJD2D complexed with KDOAM16 | 5f5a | 94.01 | | no data |
27 | KDM4D | Lysine-specific demethylase 4D | Q6B0I6 | JHDM3D JMJD2D | 5v3 | Crystal Structure of human JMJD2D complexed with KDOPP7 | 5f5c | 90.39 | | no data |
28 | KDM4D | Lysine-specific demethylase 4D | Q6B0I6 | JHDM3D JMJD2D | yc8 | Crystal structure of human KDM4D in complex with 3-(4- phenylbutanamido)pyridine-4-carboxylic acid | 5fp4 | 86.39 | | no data |
29 | KDM4D | Lysine-specific demethylase 4D | Q6B0I6 | JHDM3D JMJD2D | yc8 | Crystal structure of human KDM4D in complex with 3-4-methylthiophen-2- yl methylaminopyridine-4-carboxylic acid | 5fp7 | 86.39 | | no data |
30 | KDM4D | Lysine-specific demethylase 4D | Q6B0I6 | JHDM3D JMJD2D | ha6 | Crystal structure of human KDM4D in complex with 2-1H-pyrazol-4-yloxy- 3H,4H-pyrido-3,4-d-pyrimidin-4-one | 5fpb | 94.89 | | no data |
31 | KDM5A | Lysine-specific demethylase 5A | P29375 | JARID1A RBBP2 RBP2 | h6a | LINKED KDM5A JMJ DOMAIN BOUND TO THE INHIBITOR N67 i.e. 2-(5-phenyl-4-(phenyl(2-(piperidin-1-yl)ethoxy)methyl)-1H-pyrazol-1-yl)isonicotinic acid | 6dqe | 77.94 | | no data |
32 | KDM5A | Lysine-specific demethylase 5A | P29375 | JARID1A RBBP2 RBP2 | h61 | LINKED KDM5A JMJ DOMAIN BOUND TO THE INHIBITOR N68 i.e. 2-(1-(2-(piperidin-1-yl)ethyl)-1H-benzo[d]imidazol-2-yl)thieno[3,2-b]pyridine-7-carboxylic acid | 6dqf | 66.33 | | no data |
33 | KDM5A | Lysine-specific demethylase 5A | P29375 | JARID1A RBBP2 RBP2 | lqt | Linked KDM5A Jmj Domain Bound to the Inhibitor 2-(((2-((2-(dimethylamino)ethyl)(ethyl)amino)-2-oxoethyl)amino)methyl)isonicotinamid | 5iwf | 82.05 | | no data |
34 | KDM5A | Lysine-specific demethylase 5A | P29375 | JARID1A RBBP2 RBP2 | mmk | Linked KDM5A Jmj Domain Bound to the Inhibitor C49 (2-{[(2-{[(E)-2-(dimethylamino)ethenyl](ethyl)amino}-2-oxoethyl)amino]methyl}pyridine-4-carboxylic acid) | 5isl | 78.78 | | 52. |
35 | KDM5A | Lysine-specific demethylase 5A | P29375 | JARID1A RBBP2 RBP2 | 90v | LINKED KDM5A JMJ DOMAIN BOUND TO THE INHIBITOR (R)-N-(1-(3-isopropyl-1H-pyrazole-5-carbonyl)pyrrolidin-3-yl)cyclopropanecarboxamide (Compound N54) | 6bh2 | 95.36 | | no data |
36 | KDM5A | Lysine-specific demethylase 5A | P29375 | JARID1A RBBP2 RBP2 | dqj | LINKED KDM5A JMJ DOMAIN BOUND TO THE INHIBITOR (S)-N-(1-(3-isopropyl-1H-pyrazole-5-carbonyl)pyrrolidin-3-yl)cyclopropanecarboxamide (Compound N55) | 6bh3 | 95.85 | | no data |
37 | KDM5B | Lysine-specific demethylase 5B | Q9UGL1 | JARID1B PLU1 RBBP2H1 | fqk | Crystal structure of human KDM5B in complex with compound 34f | 6h51 | 84.37 | | no data |
38 | KDM5B | Lysine-specific demethylase 5B | Q9UGL1 | JARID1B PLU1 RBBP2H1 | b7z | Crystal structure of KDM5B in complex with S49365a. | 6ein | 72.13 | | no data |
39 | KDM5B | Lysine-specific demethylase 5B | Q9UGL1 | JARID1B PLU1 RBBP2H1 | 90v | Crystal structure of KDM5B in complex with S49195a. | 6ek6 | 91.76 | | no data |
40 | KDM5B | Lysine-specific demethylase 5B | Q9UGL1 | JARID1B PLU1 RBBP2H1 | wqs | Crystal structure of the catalytic domain of human JARID1B in complex with 3D fragment (5-fluoro-2-oxo-2,3-dihydro-1H-indol-3-yl)acetic acid (N09996a) | 5fyt | 91.6 | | no data |
41 | KDM5C | Lysine-specific demethylase 5C | P41229 | DXS1272E JARID1C SMCX XE169 | mmk | Crystal structure of human JARID1C in complex with KDM5-C49 | 5fwj | 83.7 | | 13. |
42 | KDM6A | Lysine-specific demethylase 6A | O15550 | UTX | k0i | Crystal structure of UTX complexed with GSK-J1 | 6g8f | 86.28 | | no data |
43 | KDM6B | Lysine-specific demethylase 6B | O15054 | JMJD3 KIAA0346 | yc8 | Cell penetrant inhibitors of the JMJD2 (KDM4) and JARID1 (KDM5) families of histone lysine demethylases | 5fp3 | 97.89 | | no data |
44 | KDM6B | Lysine-specific demethylase 6B | O15054 | JMJD3 KIAA0346 | k0i | CRYSTAL STRUCTURE OF JMJD3 WITH GSK-J1 | 4ask | 81.19 | | 60. |
45 | KDM7A | Lysine-specific demethylase 7A | Q6ZMT4 | JHDM1D KDM7 KIAA1718 | e67 | E67-2 selectively inhibits KIAA1718, a human histone H3 lysine 9 Jumonji demethylase | 3u78 | 67.99 | | 2500. |
46 | UTY | Histone demethylase UTY | O14607 | KDM6C | k0i | Crystal structure of JmjC domain of human histone demethylase UTY with bound GSK J1 | 3zpo | 83.89 | | no data |
47 | UTY | Histone demethylase UTY | O14607 | KDM6C | s2i | Crystal structure of JmjC domain of human histone demethylase UTY with S21056a | 5a1l | 81.89 | | no data |
48 | UTY | Histone demethylase UTY | O14607 | KDM6C | mmk | Crystal structure of JmjC domain of human histone demethylase UTY in complex with epitherapuetic compound 2-(((2-((2-(dimethylamino)ethyl) (ethyl)amino)-2-oxoethyl)amino)methyl)isonicotinic acid. | 4uf0 | 71.89 | | no data |