Search Count: 20
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Pde1B Complexed With Compound 3S
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2018-05-30 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, MG, 0NY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-05-30
Ligands: ZN, MG, 0NY
 |
Pde2 Catalytic Domain Complexed With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2017-06-28 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 19F, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-06-28
Ligands: 19F, ZN, MG
 |
Pde2 Catalytic Domain Complexed With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2017-06-28 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 7XS, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-06-28
Ligands: 7XS, ZN, MG
 |
Pde2 Catalytic Domain Complexed With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2017-06-28 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 7XV, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-06-28
Ligands: 7XV, ZN, MG
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Pde2 Catalytic Domain Complexed With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.06 Å Release Date: 2017-06-28 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, MG, 7Y1, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-06-28
Ligands: ZN, MG, 7Y1, CL
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Pde2 Catalytic Domain Complexed With Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.38 Å Release Date: 2017-06-28 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 7Y4, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-06-28
Ligands: 7Y4, ZN, MG
 |
Crystal Structure Of Human Pde1B Bound To Inhibitor 7A (6,7,8-Trimethoxy-N-(Pentan-3-Yl)Quinazolin-4-Amine)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2014-07-16 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 0NK, MG, ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-07-16
Ligands: 0NK, MG, ZN
 |
Crystal Structure Of Human Pde1B Bound To Inhibitor 19A (7,8-Dimethoxy-N-[(2S)-1-(3-Methyl-1H-Pyrazol-5-Yl)Propan-2-Yl]Quinazolin-4-Amine)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2014-07-16 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 0NY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-07-16
Ligands: ZN, MG, 0NY
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Ck1D In Complex With 1-{4-[3-(4-Fluorophenyl)-1-Methyl-1H-Pyrazol-4-Yl]Pyridin-2-Yl}-N-Methylmethanamine Ligand
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2013-09-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1QN, SO4, 1QO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: 1QN, SO4, 1QO
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Ck1D In Complex With 9-[3-(4-Fluorophenyl)-1-Methyl-1H-Pyrazol-4-Yl]-2,3,4,5-Tetrahydropyrido[2,3-F][1,4]Oxazepine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2013-09-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1QM, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: 1QM, SO4
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Ck1D In Complex With {4-[3-(4-Fluorophenyl)-1H-Pyrazol-4-Yl]Pyridin-2-Yl}Methanol Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2013-09-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1QJ, SO4, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: 1QJ, SO4, EDO
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Ck1D In Complex With (3S)-3-{4-[3-(4-Fluorophenyl)-1-Methyl-1H-Pyrazol-4-Yl]Pyridin-2-Yl}Morpholine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2013-09-18 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1QG, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: 1QG, SO4
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Discovery Of A Novel, Potent And Selective Inhibitor Of 3-Phosphoinositide Dependent Kinase (Pdk1)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.92 Å Release Date: 2011-11-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, SO4, ABQ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-11-16
Ligands: GOL, SO4, ABQ
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Discovery Of A Novel, Potent And Selective Inhibitor Of 3-Phosphoinositide Dependent Kinase (Pdk1)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.55 Å Release Date: 2011-11-16 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3RW, GOL, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-11-16
Ligands: 3RW, GOL, SO4
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Structure Of Pde10-Inhibitor Complex
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2011-06-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: SO4, ZN, MG, PFK |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-06-15
Ligands: SO4, ZN, MG, PFK
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Structure Of Pde10-Inhibitor Complex
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2011-06-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: SO4, ZN, MG, PFR |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-06-15
Ligands: SO4, ZN, MG, PFR
 |
Structure Of Pde10-Inhibitor Complex
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2011-06-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, SO4, DMS, PFW |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-06-15
Ligands: ZN, MG, SO4, DMS, PFW
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Crystal Structure Of The Catalytic Domain Of Rat Phosphodiesterase 10A
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2007-03-06 Classification: HYDROLASE Ligands: SO4, ZN, MG, PFH |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2007-03-06
Ligands: SO4, ZN, MG, PFH
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Crystal Structure Of The Catalytic Domain Of Rat Phosphodiesterase 10A
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2007-03-06 Classification: HYDROLASE Ligands: SO4, ZN, MG, PFJ |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2007-03-06
Ligands: SO4, ZN, MG, PFJ
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Crystal Structure Of The Catalytic Domain Of Rat Phosphodiesterase 10A
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2007-01-09 Classification: HYDROLASE Ligands: ZN, MG, 227 |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2007-01-09
Ligands: ZN, MG, 227