Search Count: 60
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X-Ray Co-Crystal Structure Of Ncgc00685960 / Ncats-Sm9335 In Nnmt
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.41 Å Release Date: 2025-03-05 Classification: TRANSFERASE Ligands: A1AF6 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-03-05
Ligands: A1AF6
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Structure Of The Catalytic Domain Of Ppm1D/Wip1 Serine/Threonine Phosphatase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2024-06-12 Classification: HYDROLASE Ligands: MG, PEG, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-06-12
Ligands: MG, PEG, GOL
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Human Lactate Dehydrogenase A In Complex With Inhibitor Chk-336
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.34 Å Release Date: 2024-01-24 Classification: OXIDOREDUCTASE Ligands: NAI, YBO, EDO, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-01-24
Ligands: NAI, YBO, EDO, PEG
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Crystal Structure Of Adp-Bound Galactokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2021-09-29 Classification: SUGAR BINDING PROTEIN Ligands: GLA, ADP, PO4, MG, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: GLA, ADP, PO4, MG, NA
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Crystal Structure Of Adp-Bound Galactokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2021-09-29 Classification: SUGAR BINDING PROTEIN Ligands: ADP, GLA, PO4, MG, NA, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: ADP, GLA, PO4, MG, NA, GOL
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Crystal Structure Of Inhibitor-Bound Galactokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2021-09-29 Classification: Transferase/Inhibitor Ligands: GLA, 4QI, PO4, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: GLA, 4QI, PO4, NA
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Crystal Structure Of Inhibitor-Bound Galactokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2021-09-29 Classification: Transferase/Inhibitor Ligands: GLA, V3V, NA, PO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: GLA, V3V, NA, PO4
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Crystal Structure Of Human Lactate Dehydrogenase A With Inhibitor Compound 15
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2021-07-14 Classification: OXIDOREDUCTASE Ligands: NAI, SO4, EDO, GOL, PEG, YOJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-07-14
Ligands: NAI, SO4, EDO, GOL, PEG, YOJ
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Crystal Structure Analysis Of Pip4K2A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.71 Å Release Date: 2020-12-09 Classification: TRANSFERASE Ligands: UHJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-12-09
Ligands: UHJ
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Crystal Structure Of Ldha In Complex With Compound Ncgc00384414-01 At 2.05 A Resolution
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2020-09-23 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE inhibitor Ligands: PO4, P8M, NAI, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-09-23
Ligands: PO4, P8M, NAI, GOL
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Crystal Structure Of Ldha In Complex With Compound Ncgc00420737-09 At 2.00 A Resolution
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2020-09-23 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE inhibitor Ligands: NAI, P8V, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-09-23
Ligands: NAI, P8V, EDO
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Linked Kdm5A Jmj Domain Bound To The Potential Hydrolysis Product Of Inhibitor N45 I.E. 3-((6-(4-(2-Cyano-3-Methylbut-2-Enoyl)-1,4-Diazepan-1-Yl)-2-(Pyridin-2-Yl)Pyrimidin-4-Yl)Amino)Propanoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2019-06-12 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: H6M, MN, EDO, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: H6M, MN, EDO, GOL
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Linked Kdm5A Jmj Domain Bound To The Inhibitor N50 I.E. 2-(4-((2-(Dimethylamino)Ethyl)(Ethyl)Carbamoyl)-5-(4-Methoxyphenyl)-1H-Pyrazol-1-Yl)Isonicotinic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.76 Å Release Date: 2019-06-12 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: H5Y, MN, DMS, GOL, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: H5Y, MN, DMS, GOL, SO4
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Linked Kdm5A Jmj Domain Bound To The Inhibitor N53 I.E. 2-(5-([1,1'-Biphenyl]-3-Yl)-4-(1-(2-(Piperidin-1-Yl)Ethoxy)Ethyl)-1H-Pyrazol-1-Yl)Isonicotinic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2019-06-12 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: H67, MN, GOL, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: H67, MN, GOL, DMS
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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
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2019-06-12 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: H6A, MN, GOL, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: H6A, MN, GOL, DMS
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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
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2019-06-12 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: H61, MN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: H61, MN
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Crystal Structure Of Human Brd4(1) In Complex With Cn210 (Compound 19)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.11 Å Release Date: 2019-04-03 Classification: PROTEIN BINDING Ligands: JBS, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-04-03
Ligands: JBS, GOL
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Wdr5 In Complex With A Win Site Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2019-03-13 Classification: TRANSFERASE/TRANSFERASE inhibitor Ligands: HH7, DMS, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-03-13
Ligands: HH7, DMS, SO4
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Wdr5 In Complex With A Win Site Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.56 Å Release Date: 2019-03-13 Classification: TRANSFERASE/TRANSFERASE inhibitor Ligands: HHM, SO4, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-03-13
Ligands: HHM, SO4, DMS
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Discovery Of Potent 2-Aryl-6,7-Dihydro-5Hpyrrolo[ 1,2-A]Imidazoles As Wdr5 Win-Site Inhibitors Using Fragment-Based Methods And Structure-Based Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.22 Å Release Date: 2019-03-13 Classification: gene regulation/inhibitor Ligands: HLM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-03-13
Ligands: HLM