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Search Count: 14

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7TUQ image
Crystal Structure Of Brd4 Bromodomain 1 In Complex With Monoacetylated Sars-Cov-2 E

7TV0 image
Crystal Structure Of Brd4 Bromodomain 1 In Complex With Dual-Acetylated Sars-Cov-2 E

4QPZ image
Crystal Structure Of The Formolase Fls_V2 In Space Group P 21

4QQ8 image
Crystal Structure Of The Formolase Fls In Space Group P 43 21 2

4X7H image
Co-Crystal Structure Of Perk Bound To N-{5-[(6,7-Dimethoxyquinolin-4-Yl)Oxy]Pyridin-2-Yl}-1-Methyl-3-Oxo-2-Phenyl-5-(Pyridin-4-Yl)-2,3-Dihydro-1H-Pyrazole-4-Carboxamide Inhibitor

4X7J image
Co-Crystal Structure Of Perk With 2-Amino-N-[4-Methoxy-3-(Trifluoromethyl)Phenyl]-4-Methyl-3-[2-(Methylamino)Quinazolin-6-Yl]Benzamide Inhibitor

4X7K image
Co-Crystal Structure Of Perk Bound To 4-{2-Amino-3-[5-Fluoro-2-(Methylamino)Quinazolin-6-Yl]-4-Methylbenzoyl}-1-Methyl-2,5-Diphenyl-1,2-Dihydro-3H-Pyrazol-3-One Inhibitor

4X7L image
Co-Crystal Structure Of Perk Bound To 4-{2-Amino-4-Methyl-3-[2-(Methylamino)-1,3-Benzothiazol-6-Yl]Benzoyl}-1-Methyl-2,5-Diphenyl-1,2-Dihydro-3H-Pyrazol-3-One Inhibitor

4X7N image
Co-Crystal Structure Of Perk Bound To 4-[2-Amino-4-Methyl-3-(2-Methylquinolin-6-Yl)Benzoyl]-1-Methyl-2,5-Diphenyl-1,2-Dihydro-3H-Pyrazol-3-One Inhibitor

4X7O image
Co-Crystal Structure Of Perk Bound To 1-[5-(4-Amino-2,7-Dimethyl-7H-Pyrrolo[2,3-D]Pyrimidin-5-Yl)-2,3-Dihydro-1H-Indol-1-Yl]-2-[3-Fluoro-5-(Trifluoromethyl)Phenyl]Ethanone Inhibitor

4EGC image
Crystal Structure Of Mbp-Fused Human Six1 Bound To Human Eya2 Eya Domain

4FLH image
Crystal Structure Of Human Pi3K-Gamma In Complex With Amg511

4DK5 image
Crystal Structure Of Human Pi3K-Gamma In Complex With A Pyridyl-Triazine Inhibitor

3IDP image
B-Raf V600E Kinase Domain In Complex With An Aminoisoquinoline Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.70 Å Release Date: 2009-10-06
Classification: TRANSFERASE
Ligands: L1E
Protein Functional Filters:
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