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The Fk1 Domain Of Fkbp51 In Complex With (1S,5S,6R)-10-(Benzo[D]Thiazol-6-Ylsulfonyl)-5-(Methoxymethyl)-3-(Pyridin-2-Ylmethyl)-3,10-Diazabicyclo[4.3.1]Decan-2-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.09 Å Release Date: 2021-11-10 Classification: ISOMERASE Ligands: RQW |
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The Fk1 Domain Of Fkbp51 In Complex With ((1S,5S,6R)-10-((3,5-Dichlorophenyl)Sulfonyl)-2-Oxo-5-Vinyl-3,10-Diazabicyclo[4.3.1]Decan-3-Yl)Acetic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.13 Å Release Date: 2021-11-10 Classification: ISOMERASE Ligands: RRZ |
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The Fk1 Domain Of Fkbp51 In Complex With (1S,5S,6R)-10-(Benzo[D]Thiazol-6-Ylsulfonyl)-5-(Methoxymethyl)-3-(Pyridin-2-Ylethyl)-3,10-Diazabicyclo[4.3.1]Decan-2-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:0.89 Å Release Date: 2021-11-10 Classification: CHAPERONE Ligands: RSB |
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The Fk1 Domain Of Fkbp51 In Complex With (2S)-2-((1S,5R,6R)-10-((3,5-Dichlorophenyl)Sulfonyl)-2-Oxo-5-Vinyl-3,10-Diazabicyclo[4.3.1]Decan-3-Yl)Propanoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:0.94 Å Release Date: 2021-11-03 Classification: ISOMERASE Ligands: RR5 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.86 Å Release Date: 2019-12-04 Classification: TRANSFERASE/INHIBITOR Ligands: CKO |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2011-03-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: AKI |
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Crystal Structure Of Human Ppar-Gamma Ligand Binding Domain Complexed With A Potent And Selective Agonist
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2009-12-29 Classification: ligand binding protein Ligands: 2PQ |
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2.9 A Resolution Structure Of Malate Dehydrogenase From Archaeoglobus Fulgidus In Complex With Nadh
Organism: Archaeoglobus fulgidus dsm 4304
Method: X-RAY DIFFRACTION Resolution:2.91 Å Release Date: 2009-12-22 Classification: OXIDOREDUCTASE Ligands: NAI, SO4, NA |
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2.8 A Resolution Structure Of Malate Dehydrogenase From Archaeoglobus Fulgidus In Complex With Etheno-Nad
Organism: Archaeoglobus fulgidus dsm 4304
Method: X-RAY DIFFRACTION Resolution:2.79 Å Release Date: 2009-12-22 Classification: OXIDOREDUCTASE Ligands: ENA, SO4 |
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Structure-Based Drug Design Of Novel Aurora Kinase A Inhibitors: Structure Basis For Potency And Specificity
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2009-09-15 Classification: TRANSFERASE Ligands: MMH |
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Structural Basis For The Structure-Activity Relationships Of Peroxisome Proliferator-Activated Receptor Agonists
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.97 Å Release Date: 2007-08-07 Classification: LIGAND BINDING PROTEIN Ligands: DRY |
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Structural Basis For The Structure-Activity Relationships Of Peroxisome Proliferator-Activated Receptor Agonists
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.34 Å Release Date: 2007-08-07 Classification: LIGAND BINDING PROTEIN Ligands: DRD |
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Crystal Structure Of The Ligand Binding Domain Of Human Ppar-Gamma Im Complex With An Agonist
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.28 Å Release Date: 2006-08-25 Classification: TRANSCRIPTION Ligands: 3EA |
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Structure-Based Drug Design Of A Novel Family Of Ppar Partial Agonists: Virtual Screening, X-Ray Crystallography And In Vitro/In Vivo Biological Activities
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.54 Å Release Date: 2006-05-16 Classification: TRANSCRIPTION ACTIVATOR Ligands: SP0 |
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Structure-Based Drug Design Of A Novel Family Of Ppar Partial Agonists: Virtual Screening, X-Ray Crystallography And In Vitro/In Vivo Biological Activities
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2006-05-16 Classification: TRANSCRIPTION ACTIVATOR Ligands: SP3 |
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Crystal Structure Of The Ligand Binding Domain Of Human Ppar-Gamma In Complex With An Agonist
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.07 Å Release Date: 2006-02-14 Classification: TRANSCRIPTION ACTIVATOR Ligands: EHA |