Search Count: 13
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Cryo Em Structure Of Dcaf2
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.36 Å Release Date: 2025-10-01 Classification: LIGASE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-01
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Cryo Em Structure Of Dcaf2:Compound 1 Complex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.05 Å Release Date: 2025-10-01 Classification: LIGASE Ligands: A1AUM |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-01
Ligands: A1AUM
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Cryo Em Structure Of A Dcaf2:Degrader:Brd4 Ternary Complex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.36 Å Release Date: 2025-10-01 Classification: LIGASE Ligands: A1AUO |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-10-01
Ligands: A1AUO
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Crystal Structure Of Mnk2-D228G In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: ZN, F4G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, F4G
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Crystal Structure Of Mnk2-D228G In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.36 Å Release Date: 2018-05-09 Classification: Transferase/Transferase Inhibitor Ligands: ZN, F4A |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, F4A
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Co-Crystal Structure Of Mnk2 In Complex With An Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.60 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: ZN, ET8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, ET8
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Crystal Structure Of Mnk2-D228G In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.38 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: ZN, FYV |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, FYV
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Crystal Structure Of Mnk2-D228G In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.05 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: ZN, F4J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, F4J
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Co-Crytsal Structure Of Mnk2 In Complex With An Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: ZN, F67, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, F67, CL
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Crystal Structure Of Mnk2-D228G In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.32 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, N45 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, N45
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Co-Crystal Structure Of Mnk2 In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.95 Å Release Date: 2018-05-09 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: ZN, FZJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-09
Ligands: ZN, FZJ
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Crystal Structure Of Cyclin-Dependent Kinase 2 (Cdk2-Wt) Complex With N-[5-[[[5-(1,1-Dimethylethyl)-2-Oxazolyl] Methyl]Thio]-2-Thiazolyl]-4-Piperidinecarboxamide (Bms-387032)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2015-08-12 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 56H |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-08-12
Ligands: 56H
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Crystal Structure Of Cyclin-Dependent Kinase 2 (Cdk2-Wt) Complex With (2S)-N-(5-(((5-Tert-Butyl-1,3-Oxazol-2-Yl)Methyl)Sulfanyl)-1,3-Thiazol-2-Yl)-2-Phenylpropanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2013-10-02 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1YG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-02
Ligands: 1YG