Search Count: 45
 |
Crystal Structure Of Limk1 Mutant D460N Bound To Small Molecule Inhibitor Climk1I
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2026-07-29 Classification: SIGNALING PROTEIN Ligands: A1C13 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-07-29
Ligands: A1C13
 |
Crystal Structure Of Apo Limk1 Mutant D460N
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.26 Å Release Date: 2026-07-22 Classification: SIGNALING PROTEIN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-07-22
 |
Core Catalytic Domain Of Hiv Integrase In Complex With Virtual Screening Hit
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.32 Å Release Date: 2020-05-13 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: R2D |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2020-05-13
Ligands: R2D
 |
Factor Xia In Complex With Compound 7
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2020-05-06 Classification: BLOOD CLOTTING Ligands: CIT, R2Y |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-05-06
Ligands: CIT, R2Y
 |
Factor Xia In Complex With Compound 11
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2020-05-06 Classification: BLOOD CLOTTING Ligands: FLC, R3A |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-05-06
Ligands: FLC, R3A
 |
Crystal Structure Of Sam-Bound Prdm9 In Complex With Mrk-740 Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.58 Å Release Date: 2019-02-13 Classification: GENE REGULATION/INHIBITOR Ligands: ZN, SAM, KS7, UNX |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-02-13
Ligands: ZN, SAM, KS7, UNX
 |
Trka With (6~{R})-3-Methylsulfanyl-6-Phenyl-1-(1~{H}-Pyrazol-3-Yl)-6,7-Dihydro-5~{H}-Thieno[3,4-C]Pyridin-4-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.33 Å Release Date: 2017-08-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 69C, CL, ACT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-08-09
Ligands: 69C, CL, ACT
 |
Crystal Structure Of The Prototype Foamy Virus Intasome With A 2- Pyridinone Aminal Inhibitor (Compound 18)
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION Resolution:2.85 Å Release Date: 2017-03-29 Classification: TRANSFERASE/DNA/INHIBITOR Ligands: ZN, GOL, MG, SO4, 8G4 |
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION
Release Date: 2017-03-29
Ligands: ZN, GOL, MG, SO4, 8G4
 |
Crystal Structure Of The Prototype Foamy Virus Intasome With A 2- Pyridinone Aminal Inhibitor (Compound 31)
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION Resolution:2.61 Å Release Date: 2017-03-29 Classification: TRANSFERASE/DNA/INHIBITOR Ligands: ZN, GOL, MG, SO4, 8G1 |
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION
Release Date: 2017-03-29
Ligands: ZN, GOL, MG, SO4, 8G1
 |
Discovery Of Mli-2, An Orally Available And Selective Lrrk2 Inhibitor That Reduces Brain Kinase Activity
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2017-03-15 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 81Y, SO4 |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2017-03-15
Ligands: 81Y, SO4
 |
Trka Jm-Kinase With 1-(9{H}-Fluoren-9-Yl)-3-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.87 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UE
 |
Trka Jm-Kinase With {N}-(2-Pyridylmethyl)-2-[2-(2-Thienyl)Indol-1-Yl]Acetamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UF |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UF
 |
Trka Jm-Kinase With 2-Fluoro-{N}-[2-(4-Fluorophenyl)-6-Methyl-3-Pyridyl]-4-(Trifluoromethyl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.24 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UG
 |
Trka Jm-Kinase With 1-(5-Methyl-3-Phenyl-1,2-Oxazol-4-Yl)-3-[[2-(Trifluoromethyl)Phenyl]Methyl]Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.01 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UH
 |
Trka Jm-Kinase With 1-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)-3-(1-Naphthyl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.12 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UJ
 |
Trka Jm-Kinase With 1-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)-3-[[2-(Trifluoromethyl)Phenyl]Methyl]Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.14 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UK |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UK
 |
Trka Jm-Kinase With 1-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)-3-(2-Pyridyl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.67 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UM
 |
Crystal Structure Of The Prototype Foamy Virus Intasome With A 2-Pyridinone Aminal Inhibitor
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2015-10-07 Classification: Transferase/DNA/Inhibitor Ligands: ZN, GOL, X2P, MG, SO4 |
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION
Release Date: 2015-10-07
Ligands: ZN, GOL, X2P, MG, SO4
 |
Crystal Structure Of The Prototype Foamy Virus Intasome With A 2-Pyridinone Aminal Inhibitor
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION Resolution:2.67 Å Release Date: 2015-10-07 Classification: transferase/DNA/inhibitor Ligands: ZN, GOL, MG, SO4, 4RT |
Organism: Human spumaretrovirus
Method: X-RAY DIFFRACTION
Release Date: 2015-10-07
Ligands: ZN, GOL, MG, SO4, 4RT
 |
Synthesis And Evaluation Of Heterocyclic Catechol Mimics As Inhibitors Of Catechol-O-Methyltransferase (Comt): Structure With Cmpd18 (1-(Biphenyl-3-Yl)-3-Hydroxypyridin-4(1H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2015-04-15 Classification: transferase/transferase inhibitor Ligands: 43G, MG, SAM, MES |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-04-15
Ligands: 43G, MG, SAM, MES