Search Count: 1,143
All
Selected
 |
Crystal Structure Of The Catalytic Domain Of The Inosine Monophosphate Dehydrogenase From Bacillus Anthracis In The Complex With Imp And The Inhibitor P200
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2017-03-08 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: IMP, 8L4, K |
 |
Crystal Structure Of The Catalytic Domain Of The Inosine Monophosphate Dehydrogenase From Bacillus Anthracis In The Complex With Imp And The Inhibitor P221
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.34 Å Release Date: 2021-06-09 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: IMP, GOL, ZO7, K, EDO |
 |
Crystal Structure Of 11Beta-Hsd1 Double Mutant (L262R, F278E) Complexed With 1-(3-Hydroxyazetidin-1-Yl)-2-[(2S,5R)-2-(4-Fluorophenyl)-5-Methoxyadamantan-2-Yl]Ethan-1-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2017-11-01 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: NAP, 8K7 |
 |
Crystal Structure Of 11Beta-Hsd1 Double Mutant (L262R, F278E) Complexed With 2-[(5R,7S)-6-Hydroxy-2-Phenyladamantan-2-Yl]-1-(3-Hydroxyazetidin-1-Yl)Ethan-1-One (Bms-816336)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.07 Å Release Date: 2017-11-01 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: NAP, 8KG |
 |
Crystal Structure Of 11Beta-Hsd1 Double Mutant (L262R, F278E) Complexed With 2-[2-(4-Fluorophenyl)-2-Adamantyl]-1-(3-Methoxyazetidin-1-Yl)Ethanone
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2017-11-01 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: NAP, 8K4 |
 |
Crystal Structure Of 11Beta-Hsd1 Double Mutant (L262R, F278E) Complexed With 2-(2-Benzyl-6-Hydroxyadamantan-2-Yl)-1-(3-Hydroxyazetidin-1-Yl)Ethan-1-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2017-11-01 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: NAP, 8KD |
 |
Crystal Structure Of 11Beta-Hsd1 Double Mutant (L262R, F278E) Complexed With 2-[(1R,3S,5R,7S)-2-[4-(4-Fluorophenyl)Phenyl]-6-Hydroxyadamantan-2-Yl]-1-(3- Hydroxyazetidin-1-Yl)Ethan-1-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.37 Å Release Date: 2017-11-01 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: NAP, 8KA |
 |
Crystal Structure Of The Inosine 5'-Monophosphate Dehydrogenase With An Internal Deletion Of The Cbs Domain From Bacillus Anthracis Str. Ames Complexed With Inhibitor C91
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.59 Å Release Date: 2014-06-11 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: IMP, C91, MLI |
 |
Crystal Structure Of 11Beta-Hsd1 Double Mutant (L262R, F278E) Complexed With 2-(3-(1-(4-Chlorophenyl)Cyclopropyl) -[1,2,4]Triazolo[4,3-A]Pyridin-8-Yl)Propan-2-Ol
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.45 Å Release Date: 2018-12-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: NAP, HJG |
 |
Crystal Structure Of The Inosine 5'-Monophosphate Dehydrogenase, With A Internal Deletion Of Cbs Domain From Bacillus Anthracis Str. Ame Complexed With P32
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2014-07-23 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: IMP, 2F0, FMT, GOL, MLI, EDO, SO4 |
 |
Crystal Structure Of The Inosine 5'-Monophosphate Dehydrogenase, With A Internal Deletion Of Cbs Domain From Bacillus Anthracis Str. Ames Complexed With P68
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2014-01-01 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: IMP, P68 |
 |
Structure Of Pycr1 Complexed With The Allosteric Inhibitor 7-Benzamido-4-Hydroxynaphthalene-2-Sulfonic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.66 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: SO4, PEG, A1CFH, PGE |
 |
Structure Of Pycr1 Complexed With The Allosteric Inhibitor 4-Hydroxy-7-(Phenylamino)Naphthalene-2-Sulfonic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.58 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: A1CFI, SO4, PGE |
 |
Structure Of Pycr1 Complexed With The Allosteric Inhibitor 1-Benzyl-1H-1,3-Benzodiazole-2-Sulfonic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.74 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: A1CFK, SO4 |
 |
Structure Of Pycr1 Complexed With The Allosteric Inhibitor 7-Benzamido-4-Hydroxynaphthalene-2-Sulfonic Acid In A Remote Site And Nadh And (S)-(-)-2-Hydroxy-3,3-Dimethylbutyric Acid In The Active Site
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: G8I, A1CFH, NAI |
 |
Quaternary Complex Of Pycr1 With The Allosteric Inhibitor 1-Benzyl-1H-1,3-Benzodiazole-2-Sulfonic Acid In A Remote Site And Nadh And (S)-Tetrahydrofuran-2-Carboxylic Acid In The Active Site
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: TFB, NAI, A1CFK, PEG |
 |
Structure Of Pycr1 Complexed With The Allosteric Inhibitor 4-Hydroxy-7-(Phenylamino)Naphthalene-2-Sulfonic Acid In A Remote Site And Nadh And (S)-(-)-2-Hydroxy-3,3-Dimethylbutyric Acid In The Active Site
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: G8I, A1CFI, NAI, PEG |
 |
Ternary Complex Of Pycr1 With The Allosteric Inhibitor 2-[(2,6-Dichlorophenyl)Amino]Pyridine-3-Sulfonic Acid In Two Remote Sites And The Active Site, And (S)-(-)-2-Hydroxy-3,3-Dimethylbutyric Acid In The Active Site
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2026-02-04 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: G8I, A1CFJ, SO4 |
 |
Structure Of Human Endothelial Nitric Oxide Synthase Heme Domain Bound With 6-((5-(2-(Diethylamino)Ethyl)-2,3-Difluorophenxy)Methyl)-4-Methylpyridin-2-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2025-09-10 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: HEM, H4B, A1COA, BTB, GOL, CL, GD, ZN, CA |
 |
Structure Of Human Endothelial Nitric Oxide Synthase Heme Domain Bound With 6-((5-(2-(Azetidin-1-Yl)Ethyl)-2,3-Difluorophenxy)Methyl)-4-Methylpyridin-2-Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2025-09-10 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: HEM, H4B, A1CN5, BTB, GOL, CL, GD, ZN |