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Search Count: 22

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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

6IBB image
Crystal Structure Of The Rat Isoform Of The Succinate Receptor Sucnr1 (Gpr91) In Complex With A Nanobody

6RNK image
Crystal Structure Of A Humanized (K18E, K269N) Rat Succinate Receptor Sucnr1 (Gpr91) In Complex With A Nanobody And Antagonist Nf-56-Ej40.

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

4WX4 image
Crystal Structure Of Adenovirus 8 Protease In Complex With A Nitrile Inhibitor

4WX6 image
Crystal Structure Of Human Adenovirus 8 Protease With An Irreversible Vinyl Sulfone Inhibitor

4WX7 image
Crystal Structure Of Adenovirus 8 Protease With A Nitrile Inhibitor

4PID image
Crystal Structure Of Human Adenovirus 2 Protease With A Weak Pyrimidine Nitrile Inhibitor

4PIE image
Crystal Structure Of Human Adenovirus 2 Protease A Substrate Based Nitrile Inhibitor

4PIQ image
Crystal Structure Of Human Adenovirus 8 Protease With A Nitrile Inhibitor

4PIS image
Crystal Structure Of Human Adenovirus 8 Protease In Complex With A Nitrile Inhibitor

4N8D image
Dpp4 Complexed With Syn-7Aa
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.65 Å Release Date: 2014-02-12
Classification: HYDROLASE
Ligands: NAG, SO4, 2KS

4N8E image
Dpp4 Complexed With Compound 12A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.30 Å Release Date: 2014-02-12
Classification: HYDROLASE
Ligands: NAG, SO4, 2KV

4A5S image
Crystal Structure Of Human Dpp4 In Complex With A Noval Heterocyclic Dpp4 Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.62 Å Release Date: 2012-02-08
Classification: HYDROLASE
Ligands: N7F, NAG, SO4
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