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Sub-Particle Structure Of The Iterative Acetyltransferase From Actinomycetes In Complex With Accoa And Monoacetylated Lasso Peptides
Organism: Actinosynnema mirum dsm 43827
Method: ELECTRON MICROSCOPY Resolution:3.43 Å Release Date: 2026-02-25 Classification: TRANSFERASE Ligands: ACO |
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Iterative Acetyltransferase On Lasso Peptides From Actinomycetes In Complex With Coa
Organism: Actinosynnema mirum (strain atcc 29888 / dsm 43827 / jcm 3225 / nbrc 14064 / ncimb 13271 / nrrl b-12336 / imru 3971 / 101)
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: TRANSFERASE Ligands: COA |
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Iterative Acetyltransferase On Lasso Peptides From Actinomycetes In Complex With Accoa
Organism: Actinosynnema mirum (strain atcc 29888 / dsm 43827 / jcm 3225 / nbrc 14064 / ncimb 13271 / nrrl b-12336 / imru 3971 / 101)
Method: ELECTRON MICROSCOPY Release Date: 2025-08-13 Classification: TRANSFERASE Ligands: ACO |
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Crystal Structure Of Trk-A In Complex With The Pan-Trk Kinase Inhibitor, Compound 10B.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.68 Å Release Date: 2018-07-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: FKY |
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Crystal Structure Of Trk-A In Complex With The Pan-Trk Kinase Inhibitor, Compound 13B.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.53 Å Release Date: 2018-07-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 22L, GO7 |
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Crystal Structure Of Trk-A In Complex With The Pan-Trk Kinase Inhibitor, Compound 19.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.11 Å Release Date: 2018-07-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 22L, GOD |
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Crystal Structure Of Trk-A In Complex With The Pan-Trk Kinase Inhibitor, Compound 3.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.91 Å Release Date: 2018-07-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GXA |
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Crystal Structure Of Tyrosine-Protein Kinase Receptor In Complex With 2,4-Dichloro-N-(3-Methyl-1-Phenyl-1H-Pyrazol-5-Yl)Benzamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.93 Å Release Date: 2018-05-02 Classification: TRANSFERASE/Inhibitor Ligands: FQJ |
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Crystal Structure Of Tyrosine-Protein Kinase Receptor In Complex With 5-(4-Fluorophenyl)Thieno[2,3-D]Pyrimidin-4(3H)-One Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.87 Å Release Date: 2018-05-02 Classification: TRANSFERASE/Inhibitor Ligands: FQD, GOL, FQM |
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Crystal Structure Of Tyrosine-Protein Kinase Receptor In Complex With 5-(4-Fluorophenyl)Thieno[2,3-D]Pyrimidin-4(3H)-One And 5-{[2,4-Dichloro-5-(Pyridin-2-Yl)Benzene-1-Carbonyl]Amino}-N-(2-Hydroxy-2-Methylpropyl)-1-Phenyl-1H-Pyrazole-3-Carboxamide Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2018-05-02 Classification: TRANSFERASE/Inhibitor Ligands: FQD, FQG |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.46 Å Release Date: 2018-05-02 Classification: TRANSFERASE |
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Structure Of Human Anaplastic Lymphoma Kinase In Complex With 2-[(1R)-1-{[2-Amino-5-(1,3-Dimethyl-1H-Pyrazol-4-Yl)Pyridin-3-Yl]Oxy}Ethyl]-4-Fluoro-N,N-Dimethylbenzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2016-08-17 Classification: Transferase/Transferase Inhibitor Ligands: 6YL |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With Pf- 06463922 ((10R)-7-Amino-12-Fluoro-2,10,16-Trimethyl-15-Oxo-10,15,16, 17-Tetrahydro-2H-8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11) Benzoxadiazacyclotetradecine-3-Carbonitrile).
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: 5P8 |
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Structure Of L1196M Mutant Human Anaplastic Lymphoma Kinase In Complex With Pf-06463922 ((10R)-7-Amino-12-Fluoro-2,10,16-Trimethyl- 15-Oxo-10,15,16,17-Tetrahydro-2H-8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11) Benzoxadiazacyclotetradecine-3-Carbonitrile).
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.66 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: 5P8 |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With The Inhibitor 2-((1R)-1-((3-Amino-6-(2-Methoxypyridin-3-Yl)Pyrazin-2-Yl) Oxy)Ethyl)-4-Fluoro-N-Methylbenzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: YPW |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With The Inhibitor 3-((1R)-1-(5-Fluoro-2-(2H-1,2,3-Triazol-2-Yl)Phenyl)Ethoxy)- 5-(3-(Methylsulfonyl)Phenyl)Pyridin-2-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.73 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: GWH |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With The Inhibitor (10R)-7-Amino-12-Fluoro-1,3,10,16-Tetramethyl-16,17-Dihydro- 1H-8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11)Benzoxadiazacyclotetradecin-15(10H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: IV7 |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With The Inhibitor 3-((1R)-1-(5-Fluoro-2-Methoxyphenyl)Ethoxy)-5-(1-Methyl-1H- 1,2,3-Triazol-5-Yl)Pyridin-2-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: 3U9 |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With The Inhibitor (5R)-8-Amino-3-Fluoro-5,19-Dimethyl-20-Oxo-5,18,19,20- Tetrahydro-7,11-(Azeno)Pyrido(2',1':2,3)Imidazo(4,5-H)(2,5,11) Benzoxadiazacyclotetradecine-14-Carbonitrile
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: KVC |
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Structure Of The Human Anaplastic Lymphoma Kinase In Complex With The Inhibitor 7-Amino-3-Cyclopropyl-12-Fluoro-1,10,16-Trimethyl-16,17- Dihydro-1H-8,4-(Metheno)Pyrazolo(4,3-H)(2,5,11) Benzoxadiazacyclotetradecin-15(10H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.03 Å Release Date: 2014-05-28 Classification: TRANSFERASE Ligands: J99 |