Search Count: 18
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Crystal Structure Of Human Lysophosphatidic Acid Receptor 1 In Complex With Ono9780307
Organism: Homo sapiens, Escherichia coli
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2015-06-03 Classification: TRANSPORT PROTEIN/inhibitor Ligands: ON7, 1WV |
Organism: Homo sapiens, Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2015-06-03
Ligands: ON7, 1WV
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Crystal Structure Of Human Lysophosphatidic Acid Receptor 1 In Complex With Ono-9910539
Organism: Homo sapiens, Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2015-06-03 Classification: TRANSPORT PROTEIN/inhibitor Ligands: ON9, 1WV |
Organism: Homo sapiens, Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2015-06-03
Ligands: ON9, 1WV
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Crystal Structure Of Human Lysophosphatidic Acid Receptor 1 In Complex With Ono-3080573
Organism: Homo sapiens, Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2015-06-03 Classification: TRANSPORT PROTEIN/inhibitor Ligands: ON3, 1WV |
Organism: Homo sapiens, Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2015-06-03
Ligands: ON3, 1WV
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14-3-3Gamma Complexed With The N-Terminal Sequence Of Tyrosine Hydroxylase (Residues 1-43)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.08 Å Release Date: 2013-10-02 Classification: HYDROLASE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-02
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Structure Of The Human Kappa Opioid Receptor In Complex With Jdtic
Organism: Homo sapiens, Enterobacteria phage t4
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2012-03-21 Classification: Hormone receptor/antagonist Ligands: JDC, CIT, OLC, PEG |
Organism: Homo sapiens, Enterobacteria phage t4
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: JDC, CIT, OLC, PEG
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Crystal Structure Of A Covalently Bound Alpha-Ketoheterocycle Inhibitor (Phenhexyl/Oxadiazole/Pyridine) To A Humanized Variant Of Fatty Acid Amide Hydrolase
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2011-11-16 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: JG2, CL, PEG |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-11-16
Ligands: JG2, CL, PEG
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Crystal Structure Of A Noncovalently Bound Alpha-Ketoheterocycle Inhibitor (Phenhexyl/Oxadiazole/Pyridine) To A Humanized Variant Of Fatty Acid Amide Hydrolase
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.78 Å Release Date: 2011-11-09 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: JG1, CL, F, PEG, 1DO |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-11-09
Ligands: JG1, CL, F, PEG, 1DO
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Alpha-Ketoheterocycle Inhibitors Of Fatty Acid Amide Hydrolase Containing Additional Conformational Contraints In The Acyl Side Chain
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2011-07-06 Classification: Hydrolase/Hydrolase Inhibitor Ligands: OJ8, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-07-06
Ligands: OJ8, CL
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Crystal Structure Of The Alpha-Neurexin-1 Ectodomain, Lns 2-6
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:3.02 Å Release Date: 2011-06-08 Classification: CELL ADHESION Ligands: BGC |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2011-06-08
Ligands: BGC
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3D-Crystal Structure Of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With The Drug-Like Urea Inhibitor Pf-3845 At 2.42A Resolution
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.42 Å Release Date: 2010-06-09 Classification: HYDROLASE Ligands: PIX, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2010-06-09
Ligands: PIX, CL
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3D-Crystal Structure Of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With Carbamate Inhibitor Urb597
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2010-06-09 Classification: HYDROLASE Ligands: OHO, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2010-06-09
Ligands: OHO, CL
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Crystal Structure Analysis Of A Phenhexyl/Oxazole/Carboxypyridine Alpha-Ketoheterocycle Inhibitor Bound To A Humanized Variant Of Fatty Acid Amide Hydrolase'
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2009-12-01 Classification: HYDROLASE Ligands: F2C, CL, NA |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2009-12-01
Ligands: F2C, CL, NA
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Crystal Structure Analysis Of A Biphenyl/Oxazole/Carboxypyridine Alpha-Ketoheterocycle Inhibitor Bound To A Humanized Variant Of Fatty Acid Amide Hydrolase
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2009-12-01 Classification: HYDROLASE Ligands: F27, CL, 1DO |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2009-12-01
Ligands: F27, CL, 1DO
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Crystal Structure Analysis Of A Oleyl/Oxadiazole/Pyridine Inhibitor Bound To A Humanized Variant Of Fatty Acid Amide Hydrolase
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2009-12-01 Classification: HYDROLASE Ligands: K84, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2009-12-01
Ligands: K84, CL
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3D-Crystal Structure Of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With 7-Phenyl-1-(4-(Pyridin-2-Yl)Oxazol-2-Yl)Heptan- 1-One, An Alpha-Ketooxazole
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2009-09-15 Classification: HYDROLASE Ligands: S99, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2009-09-15
Ligands: S99, CL
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3D-Crystal Structure Of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With 7-Phenyl-1-(5-(Pyridin-2-Yl)Oxazol-2-Yl)Heptan- 1-One, An Alpha-Ketooxazole
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.55 Å Release Date: 2009-09-15 Classification: HYDROLASE Ligands: OL1, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2009-09-15
Ligands: OL1, CL
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3D-Crystal Structure Of Humanized-Rat Fatty Acid Amide Hydrolase (Faah) Conjugated With The Drug-Like Urea Inhibitor Pf-3845
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2009-05-05 Classification: HYDROLASE Ligands: PIX, CL, NA |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2009-05-05
Ligands: PIX, CL, NA
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Crystal Structure Of Fatty Acid Amide Hydrolase Conjugated With The Drug-Like Inhibitor Pf-750
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2008-09-09 Classification: HYDROLASE Ligands: UNX, PF7, CL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2008-09-09
Ligands: UNX, PF7, CL