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Search Count: 10

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6SBA image
Crystal Structure Of Mtead With A Vgl4 Tertiary Structure Mimetic

6T8U image
Complement Factor B In Complex With 5-Bromo-3-Chloro-N-(4,5-Dihydro-1H-Imidazol-2-Yl)-7-Methyl-1H-Indol-4-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.84 Å Release Date: 2020-03-04
Classification: HYDROLASE
Ligands: MVZ, SO4

6T8V image
Complement Factor B In Complex With (S)-5,7-Dimethyl-4-((2-Phenylpiperidin-1-Yl)Methyl)-1H-Indole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.29 Å Release Date: 2020-03-04
Classification: HYDROLASE
Ligands: SO4, MVK, ZN

6T8W image
Complement Factor B In Complex With (-)-4-(1-((5,7-Dimethyl-1H-Indol-4-Yl)Methyl)Piperidin-2-Yl)Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.70 Å Release Date: 2020-03-04
Classification: HYDROLASE
Ligands: SO4, MVW, ZN

6RAV image
Complement Factor B Protease Domain In Complex With The Reversible Inhibitor 4-((2S,4S)-4-Ethoxy-1-((5-Methoxy-7-Methyl-1H-Indol-4-Yl)Methyl)Piperidin-2-Yl)Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.70 Å Release Date: 2019-04-17
Classification: HYDROLASE
Ligands: SO4, JGQ, ZN

6QSW image
Complement Factor B Protease Domain In Complex With The Reversible Inhibitor N-(2-Bromo-4-Methylnaphthalen-1-Yl)-4,5-Dihydro-1H-Imidazol-2-Amine.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.64 Å Release Date: 2019-03-27
Classification: HYDROLASE
Ligands: SO4, JGT

6QSX image
Complement Factor B Protease Domain In Complex With The Reversible Inhibitor ((2S,4S)-1-((5,7-Dimethyl-1H-Indol-4-Yl)Methyl)-4-Methoxypiperidin-2-Yl)Methanol.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.77 Å Release Date: 2019-03-27
Classification: HYDROLASE
Ligands: SO4, JGN, ZN

6FFN image
Structure-Based Design And Synthesis Of Macrocyclic Human Rhinovirus 3C Protease Inhibitors

6FFS image
Structure-Based Design And Synthesis Of Macrocyclic Human Rhinovirus 3C Protease Inhibitors

3GMD image
Structure-Based Design Of 7-Azaindole-Pyrrolidines As Inhibitors Of 11Beta-Hydroxysteroid-Dehydrogenase Type I
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