Search Count: 15
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Sars-Cov-2 Main Protease With Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2025-10-22 Classification: VIRAL PROTEIN, HYDROLASE Ligands: A1B3B, BTB, EDO |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2025-10-22
Ligands: A1B3B, BTB, EDO
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Sars-Cov-2 Main Protease With Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2025-09-10 Classification: VIRAL PROTEIN Ligands: A1A3N |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1A3N
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Sars-Cov-2 Main Protease With Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2025-09-10 Classification: VIRAL PROTEIN Ligands: A1A3O |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1A3O
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Cryo-Em Structure Of K+-Bound Herg Channel
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-01-20 Classification: TRANSPORT PROTEIN Ligands: K |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-01-20
Ligands: K
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Cryo-Em Structure Of K+-Bound Herg Channel In The Presence Of Astemizole
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-01-20 Classification: TRANSPORT PROTEIN Ligands: K |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-01-20
Ligands: K
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Structure Of Rorgt In Complex With A Novel Inverse Agonist 2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.18 Å Release Date: 2018-08-01 Classification: signaling protein/agonist Ligands: CFJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-08-01
Ligands: CFJ
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Structure Of Rorgt In Complex With A Novel Isoquinoline Inverse Agonist.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.18 Å Release Date: 2018-03-21 Classification: transcription/agonist Ligands: MPD, E3S |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: MPD, E3S
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Structure Of Rorgt In Complex With A Novel Inverse Agonist Tak-828.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2018-03-21 Classification: transcription/agonist Ligands: MPD, E3V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: MPD, E3V
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Structure Of Rorgt In Complex With A Novel Inverse Agonist 1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.69 Å Release Date: 2018-01-03 Classification: SIGNALING PROTEIN Ligands: CFG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-01-03
Ligands: CFG
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Crystal Structure Of Human Brr2 In Complex With T-3905516
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2017-07-19 Classification: Hydrolase/Hydrolase Inhibitor Ligands: GOL, 8LS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-07-19
Ligands: GOL, 8LS
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Crystal Structure Of Human Brr2 In Complex With T-3935799
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.95 Å Release Date: 2017-07-19 Classification: Hydrolase/Hydrolase Inhibitor Ligands: GOL, 8LP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-07-19
Ligands: GOL, 8LP
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Crystal Structure Of Human Brr2 In Complex With T-1206548
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2017-07-19 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 8LV |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-07-19
Ligands: 8LV
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Crystal Structure Of Human K-Ras G12D Mutant In Complex With Gdp And Cyclic Inhibitory Peptide
Organism: Homo sapiens, Enterobacteria phage t7
Method: X-RAY DIFFRACTION Resolution:1.25 Å Release Date: 2017-05-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: GDP, EDO |
Organism: Homo sapiens, Enterobacteria phage t7
Method: X-RAY DIFFRACTION
Release Date: 2017-05-24
Ligands: GDP, EDO
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Crystal Structure Of Human Parp14 Bound To 2-{[(1-Methylpiperidin-4-Yl)Methyl]Amino}-5,6,7,8-Tetrahydro[1]Benzothieno[2,3-D]Pyrimidin-4(3H)-One Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2017-05-10 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 91J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-10
Ligands: 91J
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Crystal Structure Of Parp14 Bound To N-{4-[4-(Diphenylmethoxy)Piperidin-1-Yl]Butyl}[1,2,4]Triazolo[4,3-B]Pyridazin-6-Amine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2017-05-03 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 91V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-03
Ligands: 91V