Search Count: 12
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Crystal Structure Of Syk In Complex With Compound 1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2015-10-07 Classification: TRANSFERASE/INHIBITOR Ligands: 50H |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-10-07
Ligands: 50H
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Crystal Structure Of Syk In Complex With Compound 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2015-10-07 Classification: TRANSFERASE/INHIBITOR Ligands: 50J, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-10-07
Ligands: 50J, GOL
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Crystal Structure Of Syk Kinase Domain With 1-(5-(6,7-Dimethoxyquinolin-4-Yloxy)Pyridin-2-Yl)-3-((1R,2S)-2-Phenylcyclopropyl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.23 Å Release Date: 2012-08-29 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: FPU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: FPU
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Crystal Structure Of Syk Kinase Domain With 1-Benzyl-N-(5-(6,7-Dimethoxyquinolin-4-Yloxy)Pyridin-2-Yl)-2-Oxo-1,2-Dihydropyridine-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2012-08-29 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: FPW |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: FPW
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Crystal Structure Of Syk Kinase Domain With N-(4-Methyl-3-(8-Methyl-7-Oxo-2-(Phenylamino)-7,8-Dihydropyrido[2,3-D]Pyrimidin-6-Yl)Phenyl)-3-(Trifluoromethyl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.33 Å Release Date: 2012-08-29 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: FPX |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: FPX
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Amcase In Complex With Compound 1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2011-08-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 3RM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
Ligands: 3RM
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Amcase In Complex With Compound 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2011-08-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: RM8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
Ligands: RM8
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Amcase In Complex With Compound 3
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2011-08-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 613 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
Ligands: 613
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Amcase In Complex With Compound 5
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2011-08-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: GOL, A1BEM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-08-24
Ligands: GOL, A1BEM
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Acidic Mammalian Chinase, Catalytic Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2009-03-10 Classification: HYDROLASE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-10
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The Acidic Mammalian Chitinase Catalytic Domain In Complex With Methylallosamidin
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2009-03-10 Classification: HYDROLASE Ligands: AMI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-03-10
Ligands: AMI
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Crystal Structure Of Pkc-Theta Complexed With Staurosporine At 2A Resolution
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2004-10-19 Classification: TRANSFERASE Ligands: STU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2004-10-19
Ligands: STU