Search Count: 50
 |
Influenza A Virus Polymerase Pa Subunit Endonuclease Domain Bound To Inhibitor Compound 19A
Organism: Influenza a virus
Method: X-RAY DIFFRACTION Resolution:1.48 Å Release Date: 2025-01-29 Classification: HYDROLASE/INHIBITOR Ligands: MN, A1A8U, MLI |
Organism: Influenza a virus
Method: X-RAY DIFFRACTION
Release Date: 2025-01-29
Ligands: MN, A1A8U, MLI
 |
Crystal Structure Of Mbp-Trem2 Ig Domain Fusion With Fragment, 2-((4-Bromophenyl)Amino)Ethan-1-Ol
Organism: Methanosarcina mazei, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.47 Å Release Date: 2021-02-17 Classification: SIGNALING PROTEIN Ligands: V5S, DMS |
Organism: Methanosarcina mazei, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-02-17
Ligands: V5S, DMS
 |
Structure Of Fusion Glycoprotein From Human Respiratory Syncytial Virus
Organism: Human respiratory syncytial virus a2, Human immunodeficiency virus 1, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.40 Å Release Date: 2019-10-30 Classification: VIRAL PROTEIN/Immune system Ligands: NAG |
Organism: Human respiratory syncytial virus a2, Human immunodeficiency virus 1, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-10-30
Ligands: NAG
 |
Pde2 Complexed With 2-[6-Fluoro-8-Methylsulfonyl-9-[(1R)-1-[4-(Trifluoromethyl)Phenyl]Ethyl]-1,2,3,4-Tetrahydrocarbazol-1-Yl]Acetic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.11 Å Release Date: 2018-11-14 Classification: Hydrolase/Hydrolase inhibitor Ligands: DY1, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-11-14
Ligands: DY1, ZN, MG
 |
Hiv Reverse Transcriptase Complexed With (E)-3-(Pyrimidin-2-Yl)-N-(5-(5,6,7,8-Tetrahydronaphthalen-2-Yl)-1H-Pyrazol-3-Yl)Acrylamide
Organism: Human immunodeficiency virus type 1
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2018-05-30 Classification: TRANSFERASE/INHIBITOR Ligands: 9TV |
Organism: Human immunodeficiency virus type 1
Method: X-RAY DIFFRACTION
Release Date: 2018-05-30
Ligands: 9TV
 |
Crystal Structure Of Hiv Protease Complexed With (S)-N-(3-Fluoro-2-(2-(1-(Phenylsulfonyl)Piperazin-2-Yl)Ethyl)Phenyl)-3,3-Bis(4-Fluorophenyl)Propanamide
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.63 Å Release Date: 2018-01-03 Classification: VIRAL PROTEIN/INHIBITOR Ligands: CL, CKD |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CL, CKD
 |
Crystal Structure Of Hiv Protease Complexed With N-(3-Fluoro-2-(2-((2S,6R)-6-Methyl-1-(Phenylsulfonyl)Piperazin-2-Yl)Ethyl)Phenyl)-3,3-Bis(4-Fluorophenyl)Propanamide
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.48 Å Release Date: 2018-01-03 Classification: VIRAL PROTEIN/INHIBITOR Ligands: CL, CKM |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CL, CKM
 |
Crystal Structure Of Hiv Protease Complexed With N-(3-Fluoro-2-(2-((2S,6R)-6-Methyl-1-(Phenylsulfonyl)Piperazin-2-Yl)Ethyl)Phenyl)-3,3-Bis(4-Fluorophenyl)Propanamide
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2018-01-03 Classification: VIRAL PROTEIN/INHIBITOR Ligands: CL, CKS |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CL, CKS
 |
Crystal Structure Of Hiv Protease Complexed With N-(3-Fluoro-2-(2-((2S,5S)-5-Methyl-1-(Phenylsulfonyl)Piperazin-2-Yl)Ethyl)Phenyl)-3,3-Bis(4-Fluorophenyl)Propanamide
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.46 Å Release Date: 2018-01-03 Classification: VIRAL PROTEIN/INHIBITOR Ligands: CL, CKV |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CL, CKV
 |
Crystal Structure Of Hiv Protease Complexed With N-(3-Fluoro-2-(2-((2S,6S)-6-Methyl-1-(Phenylsulfonyl)Piperazin-2-Yl)Ethyl)Phenyl)-3,3-Bis(4-Fluorophenyl)Propanamide
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2018-01-03 Classification: VIRAL PROTEIN/INHIBITOR Ligands: CL, CKY |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CL, CKY
 |
Crystal Structure Of Hiv Protease Complexed With N-(2-(2-((6R,9S)-2,2-Dioxido-2-Thia-1,7-Diazabicyclo[4.3.1]Decan-9-Yl)Ethyl)-3-Fluorophenyl)-3,3-Bis(4-Fluorophenyl)Propanamide
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.62 Å Release Date: 2018-01-03 Classification: VIRAL PROTEIN/INHIBITOR Ligands: CN4, CL |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CN4, CL
 |
Crystal Structure Of Pde2 In Complex With Compound 16
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2017-11-22 Classification: HYDROLASE Ligands: ZN, MG, CZV, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-11-22
Ligands: ZN, MG, CZV, EDO
 |
Crystal Structure Of Pde2 In Complex With Complex 9
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.76 Å Release Date: 2017-11-22 Classification: HYDROLASE Ligands: ZN, MG, CZY, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-11-22
Ligands: ZN, MG, CZY, EDO
 |
Pde2 In Complex With Compound 1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.97 Å Release Date: 2017-11-22 Classification: HYDROLASE Ligands: ZN, MG, D07 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-11-22
Ligands: ZN, MG, D07
 |
Mark2 Complex With 7-[(1S)-1-(4-Fluorophenyl)Ethyl]-5,5-Dimethyl-2-(3-Pyridylamino)Pyrrolo[2,3-D]Pyrimidin-6-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.20 Å Release Date: 2017-05-31 Classification: Transferase/Transferase Inhibitor Ligands: 6Z2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 6Z2
 |
Mark2 Complex With 7-[(1S)-1-(4-Fluorophenyl)Ethyl]-5,5-Dimethyl-2-(3-Pyridylamino)Pyrrolo[2,3-D]Pyrimidin-6-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.21 Å Release Date: 2017-05-31 Classification: Transferase/Transferase Inhibitor Ligands: 6Z5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-31
Ligands: 6Z5
 |
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