Search Count: 26
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Human Serum Albumin Bound To Cerastecin Compound 5E
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.91 Å Release Date: 2024-09-04 Classification: ANTIBIOTIC Ligands: MYR, A1AZR |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-09-04
Ligands: MYR, A1AZR
 |
A. Baumannii Msba Bound To Cerastecin Compound 5
Organism: Acinetobacter baumannii
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2024-09-04 Classification: ANTIBIOTIC Ligands: ANP, MVC, MG, A1AZS |
Organism: Acinetobacter baumannii
Method: X-RAY DIFFRACTION
Release Date: 2024-09-04
Ligands: ANP, MVC, MG, A1AZS
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Hsv1 Polymerase Ternary Complex With Dsdna And Compound 44
Organism: Human alphaherpesvirus 1, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:3.83 Å Release Date: 2024-08-28 Classification: TRANSFERASE Ligands: A1AC6 |
Organism: Human alphaherpesvirus 1, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2024-08-28
Ligands: A1AC6
 |
Msba Bound To Cerastecin C
Organism: Acinetobacter baumannii
Method: ELECTRON MICROSCOPY Release Date: 2024-04-24 Classification: ANTIMICROBIAL PROTEIN Ligands: ANP, ZQF |
Organism: Acinetobacter baumannii
Method: ELECTRON MICROSCOPY
Release Date: 2024-04-24
Ligands: ANP, ZQF
 |
Sortilin-Progranulin Interaction With Compound 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2020-08-12 Classification: UNKNOWN FUNCTION Ligands: UMJ, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-08-12
Ligands: UMJ, GOL
 |
Sortilin-Progranulin Interaction With Compound 17
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2020-08-12 Classification: UNKNOWN FUNCTION Ligands: UP4, UNL, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-08-12
Ligands: UP4, UNL, GOL
 |
Sortilin-Progranulin Interaction With Compound 24
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2020-08-12 Classification: UNKNOWN FUNCTION Ligands: UOY, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-08-12
Ligands: UOY, GOL
 |
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
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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
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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
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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
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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
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Identification Of Lxrbeta Selective Agonists For The Treatment Of Alzheimer'S Disease
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2016-04-06 Classification: SIGNALING PROTEIN Ligands: 668, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-06
Ligands: 668, PEG
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Identification Of Lxrbeta Selective Agonists For The Treatment Of Alzheimer'S Disease
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2016-04-06 Classification: SIGNALING PROTEIN Ligands: 668, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-04-06
Ligands: 668, SO4
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C-Met In Complex With Osi Ligand
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2014-04-30 Classification: TRANSFERASE Ligands: 1RU, GBL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-04-30
Ligands: 1RU, GBL
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Crystal Structure Of 1-(4-{4-[7-Amino-2-(1,2,3-Benzothiadiazol-7-Yl)Furo[2,3-C]Pyridin-4-Yl]-1H-Pyrazol-1-Yl}Piperidin-1-Yl)Ethan-1-One Bound To Tak1-Tab1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.54 Å Release Date: 2013-07-03 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1UL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-07-03
Ligands: 1UL
 |
Crystal Structure Of (1R,4R)-4-{4-[7-Amino-2-(1,2,3-Benzothiadiazol-7-Yl)-3-Chlorofuro[2,3-C]Pyridin-4-Yl]-1H-Pyrazol-1-Yl}Cyclohexan-1-Ol Bound To Tak1-Tab1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.55 Å Release Date: 2013-07-03 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1UO, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-07-03
Ligands: 1UO, EDO
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Crystal Structure Of 2-(1-Benzothiophen-7-Yl)-4-[1-(Piperidin-4-Yl)-1H-Pyrazol-4-Yl]Furo[2,3-C]Pyridin-7-Amine Bound To Tak1-Tab1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.68 Å Release Date: 2013-06-19 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1UH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-06-19
Ligands: 1UH