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Search Count: 12

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8S0R image
Cryo-Em Structure Of Cak Modified By Covalent Inhibitor Sy-1365

8S0T image
Cryo-Em Structure Of Cak In Complex With Sy-5609

7RA5 image
Cdk2 In Complex With Compound 4

4WVL image
Structure-Guided Dot1L Probe Optimization By Label-Free Ligand Displacement

4WIV image
Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A Novel Inhibitor Umb32 (N-Tert-Butyl-2-[4-(3,5-Dimethyl-1,2-Oxazol-4-Yl) Phenyl]Imidazo[1,2-A]Pyrazin-3-Amine)

4ER3 image
Crystal Structure Of Human Dot1L In Complex With Inhibitor Epz004777

4ER5 image
Crystal Structure Of Human Dot1L In Complex With 2 Molecules Of Epz004777

4ER6 image
Crystal Structure Of Human Dot1L In Complex With Inhibitor Sgc0946

4ER7 image
Crystal Structure Of Human Dot1L In Complex With Inhibitor Sgc0947

4EQZ image
Crystal Structure Of Human Dot1L In Complex With Inhibitor Fed2

4ER0 image
Crystal Structure Of Human Dot1L In Complex With Inhibitor Fed1

3UWP image
Crystal Structure Of Dot1L In Complex With 5-Iodotubercidin
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.05 Å Release Date: 2012-03-14
Classification: TRANSFERASE
Ligands: 5ID, IOD, NA, UNX
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