Search Count: 32
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Crystal Structure Of Human Arginase-1 At Ph 7.0 In Complex With Abh
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2019-12-11 Classification: HYDROLASE Ligands: MN, ABH, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-12-11
Ligands: MN, ABH, NA
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Crystal Structure Of Human Arginase-1 At Ph 9.0 In Complex With Abh
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.66 Å Release Date: 2019-12-11 Classification: HYDROLASE Ligands: MN, ABH, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-12-11
Ligands: MN, ABH, NA
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Crystal Structure Of Human Arginase-1 At Ph 9.0 In Complex With Cb-1158/Incb001158
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.61 Å Release Date: 2019-12-11 Classification: HYDROLASE Ligands: MN, XC3, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-12-11
Ligands: MN, XC3, NA
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Ttk Kinase Domain In Complex With Mpi-0479605
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.52 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: 8PT, 7PE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 8PT, 7PE
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Ttk Kinase Domain In Complex With Mps-Bay2B
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: 8Q5, NA, PG0 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 8Q5, NA, PG0
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Ttk Kinase Domain In Complex With Ntrc 0066-0
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.29 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: N66, PGF, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: N66, PGF, NA
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Ttk Kinase Domain In Complex With Tc-Mps1-12
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: 8QE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 8QE
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Ttk Kinase Domain In Complex With Bay 1161909
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: 8QW |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 8QW
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Ttk Kinase Domain In Complex With A Peg-Linked Pyrimido-Indolizine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: 8QZ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 8QZ
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Ttk Kinase Domain In Complex With Bay 1217389
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2017-05-31 Classification: TRANSFERASE Ligands: 8RH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 8RH
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6-Phenyl-1H-Imidazo[4,5-C]Pyridine-4-Carbonitrile As Cathepsin S Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2011-04-06 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: EF3, DMS, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-04-06
Ligands: EF3, DMS, SO4
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Cathepsin K Covalently Bound To A Cyano-Pyrimidine Inhibitor With Improved Selectivity Over Herg
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2011-03-30 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: O47 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-03-30
Ligands: O47
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Cathepsin S In Complex With A Covalent Inhibitor With An Aldehyde Warhead
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.49 Å Release Date: 2010-12-22 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: O64, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-22
Ligands: O64, DMS
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Cathepsin K In Complex With A Covalent Inhibitor With A Ketoamide Warhead
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.02 Å Release Date: 2010-12-22 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: O96, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-22
Ligands: O96, SO4
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Cathepsin K Covalently Bound To A 2-Cyano Pyrimidine Inhibitor With A Benzyl P3 Group.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2010-10-06 Classification: HYDROLASE Ligands: SO4, O75 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-06
Ligands: SO4, O75
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4-(3-Trifluoromethylphenyl)-Pyrimidine-2-Carbonitrile As Cathepsin S Inhibitors: N3, Not N1 Is Critically Important
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2010-07-14 Classification: HYDROLASE Ligands: PEG, DMS, 935, 93N, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-07-14
Ligands: PEG, DMS, 935, 93N, SO4, GOL
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X-Ray Structure Of Gw3965 Synthetic Agonist Bound To The Lxr-Alpha
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2010-06-02 Classification: TRANSCRIPTION Ligands: 965, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-06-02
Ligands: 965, SO4
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X-Ray Structure Of Benzisoxazole Synthetic Agonist Bound To The Lxr-Alpha
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.26 Å Release Date: 2010-06-02 Classification: TRANSCRIPTION Ligands: SO4, O90 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-06-02
Ligands: SO4, O90
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X-Ray Structure Of Benzisoxazole Urea Synthetic Agonist Bound To The Lxr-Alpha
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2010-06-02 Classification: TRANSCRIPTION Ligands: O40, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-06-02
Ligands: O40, SO4
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Ru486 Bound To The Progesterone Receptor In A Destabilized Agonistic Conformation
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2009-04-28 Classification: RECEPTOR Ligands: 486, SO4, NDR, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-04-28
Ligands: 486, SO4, NDR, EDO