Search Count: 17
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P110Delta/P85Alpha With Taselisib (Gdc-0032)
Organism: Homo sapiens, Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.91 Å Release Date: 2017-01-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 799 |
Organism: Homo sapiens, Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2017-01-11
Ligands: 799
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Crystal Structure Of Murine Nf-Kappab Inducing Kinase (Nik) Bound To Imidazobenzoxepin Compound 3
Organism: Mus musculus
Method: X-RAY DIFFRACTION Resolution:2.41 Å Release Date: 2017-01-11 Classification: TRANSFERASE Ligands: SO4, 76Z |
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Release Date: 2017-01-11
Ligands: SO4, 76Z
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Crystal Structure Of Murine Nf-Kappab Inducing Kinase (Nik) Bound To Benzoxepin Compound 2
Organism: Mus musculus
Method: X-RAY DIFFRACTION Resolution:2.32 Å Release Date: 2017-01-11 Classification: TRANSFERASE Ligands: 774, SO4 |
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Release Date: 2017-01-11
Ligands: 774, SO4
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Crystal Structure Of Murine Nf-Kappab Inducing Kinase (Nik) Bound To Aryl Pyrrole Fragment 17
Organism: Mus musculus
Method: X-RAY DIFFRACTION Resolution:2.63 Å Release Date: 2017-01-11 Classification: TRANSFERASE Ligands: SO4, 76Y |
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Release Date: 2017-01-11
Ligands: SO4, 76Y
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Crystal Structure Of Actin-Like Protein Alp7A
Organism: Bacillus subtilis
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2016-11-02 Classification: STRUCTURAL PROTEIN Ligands: GOL, ADP, MG |
Organism: Bacillus subtilis
Method: X-RAY DIFFRACTION
Release Date: 2016-11-02
Ligands: GOL, ADP, MG
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Phuz201 Filament
Organism: Pseudomonas phage 201phi2-1
Method: ELECTRON MICROSCOPY Resolution:7.10 Å Release Date: 2014-03-26 Classification: VIRAL PROTEIN Ligands: GDP, MG |
Organism: Pseudomonas phage 201phi2-1
Method: ELECTRON MICROSCOPY
Release Date: 2014-03-26
Ligands: GDP, MG
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Itk Kinase Domain In Complex With Benzothiazole Inhibitor Compound 12A (1S,2S)-2-{4-[(Dimethylamino)Methyl]Phenyl}-N-[6-(Pyridin-3-Yl)-1,3-Benzothiazol-2-Yl]Cyclopropanecarboxamide (12A)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.67 Å Release Date: 2013-11-13 Classification: transferase/transferase inhibitor Ligands: 29Z |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-13
Ligands: 29Z
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Itk Kinase Domain In Complex With Benzothiazole Inhibitor 12B (1S,2S)-2-{4-[(Dimethylamino)Methyl]Phenyl}-N-[6-(1H-Pyrazol-4-Yl)-1,3-Benzothiazol-2-Yl]Cyclopropanecarboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.11 Å Release Date: 2013-11-13 Classification: transferase/transferase inhibitor Ligands: 29Y |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-13
Ligands: 29Y
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Crystal Structure Of Cpd 15 Bound To Keap1 Kelch Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.59 Å Release Date: 2013-05-15 Classification: TRANSCRIPTION Ligands: PO4, 4ID |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: PO4, 4ID
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Crystal Structure Of Cpd 16 Bound To Keap1 Kelch Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.97 Å Release Date: 2013-05-15 Classification: TRANSCRIPTION Ligands: IQK |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: IQK
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Structure Of The Phage Tubulin Phuz-Gdp
Organism: Pseudomonas phage 201phi2-1
Method: X-RAY DIFFRACTION Resolution:1.67 Å Release Date: 2012-07-04 Classification: UNKNOWN FUNCTION Ligands: GDP, MG |
Organism: Pseudomonas phage 201phi2-1
Method: X-RAY DIFFRACTION
Release Date: 2012-07-04
Ligands: GDP, MG
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Structure Of The Phage Tubulin Phuz(Semet)-Gdp
Organism: Pseudomonas phage 201phi2-1
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2012-07-04 Classification: UNKNOWN FUNCTION Ligands: GDP, MG |
Organism: Pseudomonas phage 201phi2-1
Method: X-RAY DIFFRACTION
Release Date: 2012-07-04
Ligands: GDP, MG
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Fragment Based Discovery And Optimisation Of Bace-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2011-06-01 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: EV6, IOD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-06-01
Ligands: EV6, IOD
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Structure Of Bace (Beta Secretase) In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2010-07-14 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: EV3, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-07-14
Ligands: EV3, GOL
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Fragment Based Discovery And Optimisation Of Bace-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2010-07-14 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: IOD, GOL, EV4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-07-14
Ligands: IOD, GOL, EV4
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Fragment Based Discovery And Optimisation Of Bace-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2010-07-14 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: IOD, EV5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-07-14
Ligands: IOD, EV5
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Plasticity Of Pas Domain And Potential Role For Signal Transduction In The Histidine-Kinase Dcus
Organism: Escherichia coli
Method: SOLID-STATE NMR Release Date: 2008-09-30 Classification: TRANSFERASE |
Organism: Escherichia coli
Method: SOLID-STATE NMR
Release Date: 2008-09-30