Search Count: 15
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Sars-Cov-2 Spike Receptor-Binding Domain (Rbd) In Complex With S2X35 Fab And S309 Fab
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:1.83 Å Release Date: 2021-07-21 Classification: VIRAL PROTEIN/IMMUNE SYSTEM Ligands: SO4, GOL, CL, POL |
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2021-07-21
Ligands: SO4, GOL, CL, POL
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Sars-Cov-2 Spike Receptor-Binding Domain (Rbd) In Complex With S2E12 Fab, S309 Fab, And S304 Fab
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:2.95 Å Release Date: 2021-07-21 Classification: VIRAL PROTEIN/IMMUNE SYSTEM Ligands: NAG, CL |
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2021-07-21
Ligands: NAG, CL
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Sars-Cov-2 Spike In Complex With The S2D106 Neutralizing Antibody Fab Fragment (Local Refinement Of The Rbd And S2D106)
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: ELECTRON MICROSCOPY Release Date: 2021-07-21 Classification: VIRAL PROTEIN/IMMUNE SYSTEM |
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: ELECTRON MICROSCOPY
Release Date: 2021-07-21
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Antibodies To The Sars-Cov-2 Receptor-Binding Domain That Maximize Breadth And Resistance To Viral Escape
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2021-05-05 Classification: VIRAL PROTEIN/IMMUNE SYSTEM Ligands: NAG |
Organism: Homo sapiens, Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2021-05-05
Ligands: NAG
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Solution Structure Of Enterocin Hf, An Antilisterial Bacteriocin Produced By Enterococcus Faecium M3K31
Organism: Enterococcus faecium
Method: SOLUTION NMR Release Date: 2015-12-02 Classification: ANTIMICROBIAL PROTEIN |
Organism: Enterococcus faecium
Method: SOLUTION NMR
Release Date: 2015-12-02
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Pyridopyrimidinone Derivatives As Potent And Selective C-Jun N-Terminal Kinase (Jnk) Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2015-05-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 4F2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-05-06
Ligands: 4F2
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Pyridopyrimidinone Derivatives As Potent And Selective C-Jun N-Terminal Kinase (Jnk) Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.06 Å Release Date: 2015-05-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 519 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-05-06
Ligands: 519
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Jnk2/3 In Complex With 3-(4-{[(2-Chlorophenyl)Carbamoyl]Amino}-1H-Pyrazol-1-Yl)-N-(2-Methylpyridin-4-Yl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.01 Å Release Date: 2015-02-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3H8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-11
Ligands: 3H8
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Jnk2/3 In Complex With N-(2-Methylpyridin-4-Yl)-3-{4-[(Phenylcarbamoyl)Amino]-1H-Pyrazol-1-Yl}Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2015-02-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3HJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-11
Ligands: 3HJ
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Jnk2/3 In Complex With 3-(4-{[(4-Fluorophenyl)Carbamoyl]Amino}-1H-Pyrazol-1-Yl)-N-(2-Methylpyridin-4-Yl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2015-02-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3HN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-11
Ligands: 3HN
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Jnk2/3 In Complex With 3-(4-{[(4-Methylphenyl)Carbamoyl]Amino}-1H-Pyrazol-1-Yl)-N-(2-Methylpyridin-4-Yl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2015-02-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3HQ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-02-11
Ligands: 3HQ
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Crystal Structure Of Trichomonas Vaginalis Triosephosphate Isomerase Ile45-Leu Mutant (Tvag_497370)
Organism: Trichomonas vaginalis
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2014-12-24 Classification: ISOMERASE |
Organism: Trichomonas vaginalis
Method: X-RAY DIFFRACTION
Release Date: 2014-12-24
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Crystal Structure Of Trichomonas Vaginalis Triosephosphate Isomerase Ile45-Tyr Mutant (Tvag_497370)
Organism: Trichomonas vaginalis
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2014-12-24 Classification: ISOMERASE |
Organism: Trichomonas vaginalis
Method: X-RAY DIFFRACTION
Release Date: 2014-12-24
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Design And Synthesis Of Highly Potent And Isoform Selective Jnk3 Inhibitors: Sar Studies On Aminopyrazole Derivatives
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2014-11-26 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 3NL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-26
Ligands: 3NL
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Synthesis Of Benzoquinone-Ansamycin-Inspired Macrocyclic Lactams From Shikimic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2013-04-10 Classification: chaperone/Inhibitor Ligands: VJ6, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-04-10
Ligands: VJ6, MG