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Search Count: 74

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9Y9K image
Hiv-1 Nef Sf2 Core Domain Bound To The Human Hck Sh3 Domain

10DT image
Crystal Structure Of Human Wild-Type Fgr Sh3-Sh2-Linker Domains.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.80 Å Release Date: 2026-07-15
Classification: TRANSFERASE
Ligands: GOL

10FS image
Crystal Structure Of Human Fgr Sh3-Sh2-High Affinity Linker Mutant 1 (Hal1) Domains.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.30 Å Release Date: 2026-07-15
Classification: TRANSFERASE
Ligands: GOL, PEG

10FV image
Crystal Structure Of Human Fgr Sh3-Sh2-High Affinity Linker Mutant 2 (Hal2) Domains.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.80 Å Release Date: 2026-07-15
Classification: TRANSFERASE
Ligands: SO4, GOL, FLC

10GA image
Crystal Structure Of Human Fgr Sh3-Sh2-High Affinity Linker Mutant 3 (Hal3) Domains.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.60 Å Release Date: 2026-07-15
Classification: TRANSFERASE
Ligands: GOL

9Y58 image
Nef Sf2 Dimerization Mutant Bound To Hck Sh3

9NCT image
Crystal Structure Of Wdr5 In Complex With Triazole-Based Inhibitors

9NCV image
Crystal Structure Of Wdr5 In Complex With Triazole-Based Inhibitors

9NCW image
Crystal Structure Of Wdr5 In Complex With Triazole-Based Inhibitors

9BYJ image
Crystal Structure Of Hck In Complex With The Src-Family Kinase Inhibitor A-419259
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.80 Å Release Date: 2024-10-09
Classification: TRANSFERASE
Ligands: VSE, EDO, DMS, SCN

8F2P image
Nef Sf2 Dimerization Mutant Bound To Hck Sh3

7UY0 image
Crystal Structure Of Human Fgr Tyrosine Kinase In Complex With A-419259
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.55 Å Release Date: 2022-12-28
Classification: TRANSFERASE
Ligands: GOL, VSE, CL, PO4

7UY3 image
Crystal Structure Of Human Fgr Tyrosine Kinase In Complex With Tl02-59
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.99 Å Release Date: 2022-12-28
Classification: TRANSFERASE
Ligands: OJL, EDO, GOL, PO4

7UAS image
Discovery Of Potent Orally Bioavailable Wd Repeat Domain 5 (Wdr5) Inhibitors Using A Pharmacophore-Based Optimization

7U9Y image
Wdr5 Bound To 2-(3,5-Dimethoxybenzyl)-7-((2-Methyl-1H-Imidazol-1-Yl)Methyl)-5-(1-Methyl-3-(Trifluoromethyl)-1H-Pyrazol-4-Yl)-3,4-Dihydroisoquinolin-1(2H)-One

7LMD image
Sars-Cov-2 3Clpro In Complex With 2-(Benzotriazol-1-Yl)-N-[4-(1H-Pyrazol-4-Yl)Phenyl]-N-(3-Thienylmethyl)Acetamide

7LME image
Sars-Cov-2 3Clpro In Complex With N-[4-[[2-(Benzotriazol-1-Yl)Acetyl]-(3-Thienylmethyl)Amino]Phenyl]Cyclopropanecarboxamide

7LMF image
Sars-Cov-2 3Clpro In Complex With 2-(Benzotriazol-1-Yl)-N-[4-(1H-Imidazol-4-Yl)Phenyl]-N-(3-Thienylmethyl)Acetamide

7LMG image
Sars-Cov-1 3Clpro In Complex With N-(4-(1H-Imidazol-4-Yl)Phenyl)-2-(1H-Benzo[D][1,2,3]Triazol-1-Yl)-N-(Thiophen-3-Ylmethyl)Acetamide

7LMH image
Sars-Cov-1 3Clpro In Complex With 2-(1H-Benzo[D][1,2,3]Triazol-1-Yl)-N-(4-(Pyridin-3-Yl)Phenyl)-N-(Thiophen-3-Ylmethyl)Acetamide
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