Search Count: 11
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Structure Of Human Trpa1 In Complex With Antagonist Compound 21
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-03-31 Classification: MEMBRANE PROTEIN/Antagonist Ligands: VKM |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-03-31
Ligands: VKM
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Structure Of Human Trpa1 In Complex With Inhibitor Gdc-0334
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-02-17 Classification: MEMBRANE PROTEIN/Inhibitor Ligands: LXY |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-02-17
Ligands: LXY
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Structure Of Human Trpa1 In Complex With Agonist Gne551
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2020-11-18 Classification: MEMBRANE PROTEIN/Agonist Ligands: ULJ |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2020-11-18
Ligands: ULJ
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Structure Of Cathb With Covalently Linked Compound 28
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2017-12-27 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: C1G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-12-27
Ligands: C1G
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Pi3K-Gamma K802T In Complex With Cpd 8 10-((1-(Tert-Butyl)Piperidin-4-Yl)Sulfinyl)-2-(1-Isopropyl-1H-1,2,4-Triazol-5-Yl)-5,6-Dihydrobenzo[F]Imidazo[1,2-D][1,4]Oxazepine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.02 Å Release Date: 2017-11-15 Classification: TRANSFERASE/TRANSFERASE INHBITOR Ligands: BWY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-11-15
Ligands: BWY
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Human Nav1.7-Vsd4-Navab In Complex With Gx-936.
Organism: Arcobacter butzleri, homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.53 Å Release Date: 2015-12-23 Classification: METAL TRANSPORT Ligands: PX4, 5P2 |
Organism: Arcobacter butzleri, homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-12-23
Ligands: PX4, 5P2
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Potent And Selective Inhibitors Of Pi3K-Delta: Obtaining Isoform Selectivity From The Affinity Pocket And Tryptophan Shelf
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.67 Å Release Date: 2013-04-17 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0SC |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-17
Ligands: 0SC
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Potent And Selective Inhibitors Of Pi3K-Delta: Obtaining Isoform Selectivity From The Affinity Pocket And Tryptophan Shelf
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2013-04-17 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0SD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-17
Ligands: 0SD
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Potent And Selective Inhibitors Of Pi3K-Delta: Obtaining Isoform Selectivity From The Affinity Pocket And Tryptophan Shelf
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.94 Å Release Date: 2013-04-17 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0SE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-17
Ligands: 0SE
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Potent And Highly Selective Benzimidazole Inhibitors Of Pi3K-Delta
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.44 Å Release Date: 2012-08-22 Classification: transferase/transferase inhibitor Ligands: 0WR |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-08-22
Ligands: 0WR
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Crystal Structure Of Aurora-A In Complex With A Pentacyclic Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2009-02-17 Classification: TRANSFERASE Ligands: 83H |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-02-17
Ligands: 83H