Search Count: 15
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Crystal Structure Of Human Nuak1-Mark3 Kinase Domain Chimera Bound With Azepane (R)-#50 Small Molecule Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2024-11-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: X5I, EDO, CL, BEZ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-11-06
Ligands: X5I, EDO, CL, BEZ
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Crystal Structure Of Human Nuak1-Mark3 Kinase Domain Chimera Bound With Small Molecule Inhibitor #10
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2024-10-23 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: EDO, NI, X4W |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-10-23
Ligands: EDO, NI, X4W
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Crystal Structure Of Human Nuak1-Mark3 Kinase Domain Chimera Bound With Small Molecule Inhibitor #65
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2024-10-23 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: X3Q, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-10-23
Ligands: X3Q, EDO
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Crystal Structure Of Human Nuak1-Mark3 (7 Mutations) Kinase Domain Chimera Bound With Small Molecule Inhibitor #31
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2024-10-23 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: X5N, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-10-23
Ligands: X5N, EDO
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Crystal Structure Of Human Nuak1-Mark3 (6 Mutations) Kinase Domain Chimera Bound With Small Molecule Inhibitor #31
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2024-10-23 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: X4H, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-10-23
Ligands: X4H, EDO
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Crystal Structure Of C-Terminal Domain Of Msk1 In Complex With In Covalently Bound Literature Rsk2 Inhibitor Pyrrolopyrimidine Cyanoacrylamide Compound 25 (Co-Crystal)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2022-08-31 Classification: TRANSFERASE Ligands: SUU, OXM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-08-31
Ligands: SUU, OXM
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Crystal Structure Of C-Terminal Domain Of Msk1 In Complex With Covalently Bound With Literature Rsk2 Inhibitor Indazole Cyanoacrylamide Compound 26 (Soak)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2022-07-20 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1LE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-07-20
Ligands: 1LE
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Crystal Structure Of C-Terminal Domain Of Msk1 In Complex With Covalently Bound Pyrrolopyrimidine Compound 20 (Co-Crystal)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2022-07-06 Classification: TRANSFERASE Ligands: O1K |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-07-06
Ligands: O1K
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Crystal Structure Of C-Terminal Domain Of Msk1 In Complex With Covalently Bound Pyrrolopyrimidine Compound 23 (Co-Crystal)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2022-07-06 Classification: TRANSFERASE Ligands: O1R, IOD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-07-06
Ligands: O1R, IOD
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Crystal Structure Of C-Terminal Domain Of Msk1 In Complex With Covalently Bound Pyrrolopyrimidine Compound 27 (Co-Crystal)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2022-07-06 Classification: TRANSFERASE Ligands: O10 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-07-06
Ligands: O10
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Discovery Of A Potent Cyclophilin Inhibitor (Compound 3) Based On Structural Simplification Of Sanglifehrin A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2017-01-25 Classification: isomerase/isomerase inhibitor Ligands: 7HG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-01-25
Ligands: 7HG
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Discovery Of A Potent Cyclophilin Inhibitor (Compound 5) Based On Structural Simplification Of Sanglifehrin A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2017-01-25 Classification: isomerase/isomerase inhibitor Ligands: 78E |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-01-25
Ligands: 78E
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Discovery Of A Potent Cyclophilin Inhibitor (Compound 6) Based On Structural Simplification Of Sanglifehrin A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2017-01-25 Classification: isomerase/isomerase inhibitor Ligands: 78R |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-01-25
Ligands: 78R
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Discovery Of A Potent Cyclophilin Inhibitor (Compound 7) Based On Structural Simplification Of Sanglifehrin A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.48 Å Release Date: 2017-01-25 Classification: isomerase/isomerase inhibitor Ligands: 78X |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-01-25
Ligands: 78X
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Discovery Of A Potent Cyclophilin Inhibitor (Compound 8) Based On Structural Simplification Of Sanglifehrin A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2017-01-25 Classification: isomerase/isomerase inhibitor Ligands: 838, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-01-25
Ligands: 838, SO4