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Search Count: 22

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6CJ5 image
Crystal Structure Of Mnk2-D228G In Complex With Inhibitor

6CJE image
Crystal Structure Of Mnk2-D228G In Complex With Inhibitor

6CJH image
Co-Crystal Structure Of Mnk2 In Complex With An Inhibitor

6CJW image
Crystal Structure Of Mnk2-D228G In Complex With Inhibitor

6CJY image
Crystal Structure Of Mnk2-D228G In Complex With Inhibitor

6CK3 image
Co-Crytsal Structure Of Mnk2 In Complex With An Inhibitor

6CK6 image
Crystal Structure Of Mnk2-D228G In Complex With Inhibitor

6CKI image
Co-Crystal Structure Of Mnk2 In Complex With Inhibitor

5KJ2 image
The Novel P300/Cbp Inhibitor A-485 Uncovers A Unique Mechanism Of Action To Target Ar In Castrate Resistant Prostate Cancer

5U2M image
Crystal Structure Of Human Nampt With A-1293201

5U2N image
Crystal Structure Of Human Nampt With A-1326133

5UPE image
Crystal Structure Of Human Nampt With Isoindoline Urea Inhibitor Compound 5

5UPF image
Crystal Structure Of Human Nampt With Isoindoline Urea Inhibitor Compound 53

5U69 image
Polycomb Protein Eed In Complex With Inhibitor: (3R,4S)-1-[(2-Methoxyphenyl)Methyl]-N,N-Dimethyl-4-(1-Methylindol-3-Yl)Pyrrolidin-3-Amine

5U6D image
Polycomb Protein Eed In Complex With Inhibitor: 2-[4-(4-{(3S,4R)-4-(Dimethylamino)-1-[(2-Fluoro-6-Methylphenyl)Methyl]Pyrrolidin-3-Yl}Phenyl)-1H-Pyrazol-1-Yl]Acetamide

5U8A image
Polycomb Protein Eed In Complex With Inhibitor: (3R,4S)-1-[(2-Bromo-6-Fluorophenyl)Methyl]-N,N-Dimethyl-4-(1-Methyl-1H-Indol-3-Yl)Pyrrolidin-3-Amine

5U8F image
Polycomb Protein Eed In Complex With Inhibitor: (3R,4S)-1-[(1S)-7-Fluoro-2,3-Dihydro-1H-Inden-1-Yl]-N,N-Dimethyl-4-(1-Methyl-1H-Indol-3-Yl)Pyrrolidin-3-Amine

5CPR image
The Novel Suv4-20 Inhibitor A-196 Verifies A Role For Epigenetics In Genomic Integrity
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.22 Å Release Date: 2017-01-25
Classification: TRANSFERASE
Ligands: ZN, SAM, 539

5K0M image
Targeting The Prc2 Complex Through A Novel Protein-Protein Interaction Inhibitor Of Eed

4YND image
The Discovery Of A-893, A New Cell-Active Benzoxazinone Inhibitor Of Lysine Methyltransferase Smyd2
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