Search Count: 26
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Crystal Structure Of The Fis1 Cytosolic Domain Bound To A Peptide Inhibitor
Organism: Homo sapiens, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2024-09-04 Classification: PEPTIDE BINDING PROTEIN/INHIBITOR |
Organism: Homo sapiens, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2024-09-04
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Dyrk1A Kinase Domain In Complex With A 6-Azaindole Derivative, Gnf2133.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.70 Å Release Date: 2020-03-04 Classification: TRANSFERASE Ligands: Q8J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-03-04
Ligands: Q8J
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Recognition Of Mhc-Like Molecule
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.30 Å Release Date: 2019-12-18 Classification: IMMUNE SYSTEM Ligands: 2LJ, NAG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-12-18
Ligands: 2LJ, NAG
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Structure Of Jmjd6 Bound To Mono-Methyl Arginine.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2019-09-18 Classification: TRANSCRIPTION Ligands: AKG, FE, NMM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-09-18
Ligands: AKG, FE, NMM
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S. Cerevisiae Spliceosomal E Complex (Ubc4)
Organism: Saccharomyces cerevisiae (strain atcc 204508 / s288c), Saccharomyces cerevisiae s288c
Method: ELECTRON MICROSCOPY Release Date: 2019-09-18 Classification: RNA BINDING PROTEIN Ligands: ZN |
Organism: Saccharomyces cerevisiae (strain atcc 204508 / s288c), Saccharomyces cerevisiae s288c
Method: ELECTRON MICROSCOPY
Release Date: 2019-09-18
Ligands: ZN
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Saccharomyces Cerevisiae Spliceosomal E Complex (Act1)
Organism: Saccharomyces cerevisiae (strain atcc 204508 / s288c), Saccharomyces cerevisiae s288c, Saccharomyces cerevisiae
Method: ELECTRON MICROSCOPY Release Date: 2019-09-18 Classification: RNA BINDING PROTEIN Ligands: ZN |
Organism: Saccharomyces cerevisiae (strain atcc 204508 / s288c), Saccharomyces cerevisiae s288c, Saccharomyces cerevisiae
Method: ELECTRON MICROSCOPY
Release Date: 2019-09-18
Ligands: ZN
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S. Cerevisiae U1 Snrnp
Organism: Saccharomyces cerevisiae (strain atcc 204508 / s288c), Saccharomyces cerevisiae s288c
Method: ELECTRON MICROSCOPY Resolution:3.60 Å Release Date: 2019-07-24 Classification: RNA BINDING PROTEIN/RNA |
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Crystal Structure Of Qscr Bound To Agonist S3
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2018-02-28 Classification: transcription/agonist Ligands: EVY |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2018-02-28
Ligands: EVY
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Crystal Structure Of Qscr Bound To C12-Homoserine Lactone
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2018-02-28 Classification: TRANSCRIPTION Ligands: EWM |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2018-02-28
Ligands: EWM
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S. Cerevisiae Spliceosomal Post-Catalytic P Complex
Organism: Saccharomyces cerevisiae, Saccharomyces cerevisiae (strain atcc 204508 / s288c)
Method: ELECTRON MICROSCOPY Release Date: 2018-02-21 Classification: RNA BINDING PROTEIN Ligands: MG, IHP, GTP, ZN |
Organism: Saccharomyces cerevisiae, Saccharomyces cerevisiae (strain atcc 204508 / s288c)
Method: ELECTRON MICROSCOPY
Release Date: 2018-02-21
Ligands: MG, IHP, GTP, ZN
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Capsid Protein In The Staphylococcus Aureus Phage 80Alpha Mature Capsid
Organism: Staphylococcus virus 80alpha
Method: ELECTRON MICROSCOPY Resolution:5.20 Å Release Date: 2018-01-17 Classification: VIRUS |
Organism: Staphylococcus virus 80alpha
Method: ELECTRON MICROSCOPY
Release Date: 2018-01-17
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Capsid Protein In The Staphylococcus Aureus Phage 80Alpha-Derived Sapi1 Mature Capsid
Organism: Staphylococcus virus 80alpha
Method: ELECTRON MICROSCOPY Resolution:8.40 Å Release Date: 2018-01-17 Classification: VIRUS |
Organism: Staphylococcus virus 80alpha
Method: ELECTRON MICROSCOPY
Release Date: 2018-01-17
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Identification Of Potent And Selective Ripk2 Inhibitors For The Treatment Of Inflammatory Diseases
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.85 Å Release Date: 2017-10-25 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 9WS, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-10-25
Ligands: 9WS, SO4
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Identification Of Potent And Selective Ripk2 Inhibitors For The Treatment Of Inflammatory Diseases.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.89 Å Release Date: 2017-10-25 Classification: Transferase/Transferase Inhibitor Ligands: 9XA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-10-25
Ligands: 9XA
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Bruton'S Tyrosine Kinase In Complex With A T-Butyl Cyanoacrylamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2015-05-13 Classification: TRANSFERASE Ligands: 4C9, NA, EDO, SO4, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-05-13
Ligands: 4C9, NA, EDO, SO4, CL
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Crystal Structure Of The Ligand Binding Domains Of The Bovicola Ovis Ecdysone Receptor Ecr/Usp Heterodimer (Methylene Lactam Crystal)
Organism: Pediculus humanus subsp. corporis
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2014-07-30 Classification: TRANSCRIPTION |
Organism: Pediculus humanus subsp. corporis
Method: X-RAY DIFFRACTION
Release Date: 2014-07-30
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Crystal Structure Of The Ligand Binding Domains Of The Bovicola Ovis Ecdysone Receptor Ecr/Usp Heterodimer (Pona Crystal)
Organism: Pediculus humanus subsp. corporis
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2014-07-30 Classification: TRANSCRIPTION Ligands: P1A, NEQ |
Organism: Pediculus humanus subsp. corporis
Method: X-RAY DIFFRACTION
Release Date: 2014-07-30
Ligands: P1A, NEQ
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Crystal Structure Of Btk Kinase Domain Complexed With 4-Tert-Butyl-N-(3-{8-[4-(4-Methyl-Piperazine-1-Carbonyl)-Phenylamino]-Imidazo[1,2-A]Pyrazin-6-Yl}-Phenyl)-Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 481, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 481, DMS
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Crystal Structure Of Btk Kinase Domain Complexed With 4-Methanesulfonyl-N-(3-{8-[4-(Morpholine-4-Carbonyl)-Phenylamino]-Imidazo[1,2-A]Pyrazin-6-Yl}-Phenyl)-Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2V1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 2V1
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Crystal Structure Of Btk Kinase Domain Complexed With 1-[5-[3-(7-Tert-Butyl-4-Oxo-Quinazolin-3-Yl)-2-Methyl-Phenyl]-1-Methyl-2-Oxo-3-Pyridyl]-3-Methyl-Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2V2, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 2V2, DMS