Search Count: 23
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Crystal Structure Of Cdk2 Bound By Compound 4
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.16 Å Release Date: 2025-09-10 Classification: TRANSFERASE Ligands: A1INI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1INI
 |
Crystal Structure Of Cdk2-Cyclin E1 Bound By Compound 30
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.16 Å Release Date: 2025-09-10 Classification: TRANSFERASE Ligands: A1IOI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1IOI
 |
Crystal Structure Of Cdk2-Cyclin E1 Bound By Compound 11 (Azd8421)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.45 Å Release Date: 2025-09-10 Classification: TRANSFERASE Ligands: A1IOP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1IOP
 |
Discovery Of Irak4 Inhibitor 41
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2024-01-31 Classification: TRANSFERASE Ligands: R73 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-01-31
Ligands: R73
 |
Discovery Of Irak4 Inhibitor 40
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.17 Å Release Date: 2024-01-31 Classification: TRANSFERASE Ligands: R6I, ACT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-01-31
Ligands: R6I, ACT
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Discovery Of Irak4 Inhibitors Bay1834845 And Bay1830839
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.12 Å Release Date: 2024-01-31 Classification: TRANSFERASE Ligands: R6R |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-01-31
Ligands: R6R
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Discovery Of Irak4 Inhibitor 16
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2023-11-29 Classification: TRANSFERASE Ligands: O0H, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-11-29
Ligands: O0H, GOL
 |
Discovery Of Irak4 Inhibitor 23
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.46 Å Release Date: 2023-09-06 Classification: TRANSFERASE Ligands: O6X |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-09-06
Ligands: O6X
 |
Discovery Of Irak4 Inhibitor 38
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.17 Å Release Date: 2023-09-06 Classification: TRANSFERASE Ligands: O06 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-09-06
Ligands: O06
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Clathrin Heavy Chain N-Terminal Domain Complexed With Peptide From Protein Mu-Ns Of Reovirus Type 1
Organism: Homo sapiens, Mammalian orthoreovirus 1 lang
Method: X-RAY DIFFRACTION Resolution:1.97 Å Release Date: 2022-03-02 Classification: TRANSPORT PROTEIN Ligands: PG4 |
Organism: Homo sapiens, Mammalian orthoreovirus 1 lang
Method: X-RAY DIFFRACTION
Release Date: 2022-03-02
Ligands: PG4
 |
Clathrin Heavy Chain N-Terminal Domain Bound To Non Structured Protein 3 From Eastern Equine Encephalitis Virus
Organism: Homo sapiens, Eastern equine encephalitis virus
Method: X-RAY DIFFRACTION Resolution:1.97 Å Release Date: 2022-03-02 Classification: TRANSPORT PROTEIN Ligands: SO4, PO4 |
Organism: Homo sapiens, Eastern equine encephalitis virus
Method: X-RAY DIFFRACTION
Release Date: 2022-03-02
Ligands: SO4, PO4
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Crystal Structure Of C-Terminal Domain Of Pabpc1 In Complex With Nucleoprotein From Human Coronavirus 229E
Organism: Homo sapiens, Human coronavirus 229e
Method: X-RAY DIFFRACTION Resolution:1.93 Å Release Date: 2022-03-02 Classification: TRANSCRIPTION Ligands: SO4, GOL |
Organism: Homo sapiens, Human coronavirus 229e
Method: X-RAY DIFFRACTION
Release Date: 2022-03-02
Ligands: SO4, GOL
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Crystal Structure Of Human Pde1B Catalytic Domain In Complex With Inhibitor 16J (6-(4-Methoxybenzyl)-9-((Tetrahydro-2H-Pyran-4-Yl)Methyl)-8,9,10,11-Tetrahydropyrido[4',3':4,5]Thieno[3,2-E][1,2,4]Triazolo[1,5-C]Pyrimidin-5(6H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.82 Å Release Date: 2017-04-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 8HM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: ZN, MG, 8HM
 |
Crystal Structure Of Human Pde1B Catalytic Domain In Complex With Inhibitor 3 (6-(4-Chlorobenzyl)-8,9,10,11-Tetrahydrobenzo[4,5]Thieno[3,2-E][1,2,4]Triazolo[1,5-C]Pyrimidin-5(6H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2017-04-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 8HP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: ZN, MG, 8HP
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Crystal Structure Of Human Pde10A In Complex With Inhibitor 16D
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.87 Å Release Date: 2017-04-26 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 8Q7, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: 8Q7, ZN, MG
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Crystal Structure Of Human Phosphodiesterase 2A In Complex With [1,2,4]Triazolo[1,5-A]Pyrimidin-7-Yl}-N-(Naphthalene-2-Yl)Piperidine-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2017-02-22 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 7OM, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: 7OM, ZN, MG
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Crystal Structure Of Human Phosphodiesterase 2A With 3-{5-Methyl-[1,2,4]Triazolo[1,5-A]Pyrimidin-7-Yl-1-[(Naphthalene-2-Yl)Carbonyl]Piperidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2017-02-22 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 7OG, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: 7OG, ZN, MG
 |
Crystal Structure Of Human Pde2A In Complex With (5S)-1-[(3-Bromo-4-Fluorophenyl)Carbonyl]-3,3-Difluoro-5-{5-Methyl-[1,2,4]Triazolo[1,5-A]Pyrimidin-7-Yl}Piperidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.36 Å Release Date: 2017-02-22 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 7OJ, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: 7OJ, ZN, MG
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Crystal Structure Of Human Phosphodiesterase 2A In Complex With 3,3-Difluoro-1-[(4-Fluorophenyl)Carbonyl]-5-{5-Methyl-[1,2,4]Triazolo[1,5-A]Pyrimidin-7-Yl}Piperidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2017-02-22 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 7OP, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: 7OP, ZN, MG
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Crystal Structure Of Human Phosphodiesterase 2A In Complex With 1-[(3,4-Difluorophenyl)Carbonyl]-3,3-Difluoro-5-{5-Methyl-[1,2,4]Triazolo[1,5-A]Pyrimidin-7-Yl}Piperidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.59 Å Release Date: 2017-02-22 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 7P4, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: 7P4, ZN, MG