Search Count: 24
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Crystal Structure Of Hca Ii In Complex With 1-Aryl-6,7-Dimethoxy-3,4-Dihydroisoquinoline-2(1H)-Sulfonamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.05 Å Release Date: 2026-08-05 Classification: LYASE Ligands: ZN, MBO, A1J8Z |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-08-05
Ligands: ZN, MBO, A1J8Z
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Crystal Structure Of Hca Ii In Complex With An 1-Aryl-6,7-Dimethoxy-3,4-Dihydroisoquinoline-2(1H)-Sulfonamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.15 Å Release Date: 2026-08-05 Classification: LYASE Ligands: ZN, A1J8Y, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-08-05
Ligands: ZN, A1J8Y, GOL
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Crystal Structure Of Human Carbonic Anhydrase Vii (Hca Vii) In Complex With A 4-(4-Aroylpiperazine-1-Carbonyl)Benzenesulfonamide Derivative.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2021-07-14 Classification: LYASE Ligands: ZN, U7Z, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-07-14
Ligands: ZN, U7Z, GOL
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The Crystal Structure Of Hca Ii In Complex With A 4-(4-Aroylpiperazine-1-Carbonyl)Benzenesulfonamide Derivative.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.05 Å Release Date: 2020-06-03 Classification: LYASE Ligands: ZN, O42, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-06-03
Ligands: ZN, O42, GOL
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Crystal Structure Of Tyrosinase From Bacillus Megaterium With Jkb Inhibitor In The Active Site.
Organism: Bacillus megaterium
Method: X-RAY DIFFRACTION Resolution:2.32 Å Release Date: 2019-06-19 Classification: OXIDOREDUCTASE Ligands: CU, JKB |
Organism: Bacillus megaterium
Method: X-RAY DIFFRACTION
Release Date: 2019-06-19
Ligands: CU, JKB
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The Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With 4-(4-Phenylpiperidine-1-Carbonyl)Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2018-12-19 Classification: LYASE Ligands: ZN, FKE, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-12-19
Ligands: ZN, FKE, GOL
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The Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With 4-(4-Phenyl)-4-Hydroxy-1-Piperidine-1-Carbonyl)Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.58 Å Release Date: 2018-12-19 Classification: LYASE Ligands: ZN, FKQ, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-12-19
Ligands: ZN, FKQ, GOL
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The Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With 4-[(4-Fluorophenyl)Methyl]-1-Piperazinyl]Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2018-12-19 Classification: LYASE Ligands: ZN, FKK, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-12-19
Ligands: ZN, FKK, GOL
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The Crystal Structure Of Human Carbonic Anhydrase Vii In Complex With 4-(4-Phenylpiperidine-1-Carbonyl)Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2018-12-19 Classification: LYASE Ligands: ZN, FKE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-12-19
Ligands: ZN, FKE
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The Crystal Structure Of Human Carbonic Anhydrase Vii In Complex With 4-(4-Phenyl)-4-Hydroxy-1-Piperidine-1-Carbonyl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2018-12-19 Classification: LYASE Ligands: ZN, FKQ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-12-19
Ligands: ZN, FKQ
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The Crystal Structure Of Human Carbonic Anhydrase Vii In Complex With 4-[(4-Fluorophenyl)Methyl]-1-Piperazinyl]Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2018-12-19 Classification: LYASE Ligands: ZN, FKK, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-12-19
Ligands: ZN, FKK, GOL
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Crystal Structure Of Tyrosinase From Bacillus Megaterium With Svf Inhibitor In The Active Site
Organism: Bacillus megaterium
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2018-04-25 Classification: OXIDOREDUCTASE Ligands: CU, SVF |
Organism: Bacillus megaterium
Method: X-RAY DIFFRACTION
Release Date: 2018-04-25
Ligands: CU, SVF
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Crystal Structure Of Tyrosinase From Bacillus Megaterium With B5N Inhibitor In The Active Site
Organism: Bacillus megaterium
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2018-04-25 Classification: OXIDOREDUCTASE Ligands: B5N, CU |
Organism: Bacillus megaterium
Method: X-RAY DIFFRACTION
Release Date: 2018-04-25
Ligands: B5N, CU
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Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With (R)-4-(6,7-Dihydroxy-1-Phenyl-3,4-Tetrahydroisoquinoline-1H-2-Carbonyl)Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2017-05-10 Classification: LYASE Ligands: ZN, 8F2, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-10
Ligands: ZN, 8F2, GOL
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Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With (S)-4-(6,7-Dihydroxy-1-Phenyl-3,4-Tetrahydroisoquinoline-1H-2-Carbonyl)Benzenesulfonamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2017-05-10 Classification: LYASE Ligands: ZN, 8F3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-10
Ligands: ZN, 8F3
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2009 H1N1 Pa Endonuclease Domain In Complex With An N-Acylhydrazone Inhibitor
Organism: Influenza a virus
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2016-08-31 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MN, GK0 |
Organism: Influenza a virus
Method: X-RAY DIFFRACTION
Release Date: 2016-08-31
Ligands: MN, GK0
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Carbonic Anhydrase Inhibitors: Design And Synthesis Of New Heteroaryl-N-Carbonylbenzenesulfonamides Targeting Druggable Human Carbonic Anhydrase Isoforms (Hca Vii, Hca Ix, And Hca Xiv)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2015-08-26 Classification: LYASE Ligands: ZN, 4K9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-08-26
Ligands: ZN, 4K9
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Carbonic Anhydrase Inhibitors: Design And Synthesis Of New Heteroaryl-N-Carbonylbenzenesulfonamides Targeting Druggable Human Carbonic Anhydrase Isoforms (Hca Vii, Hca Ix, And Hca Xiv)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.01 Å Release Date: 2015-08-26 Classification: LYASE Ligands: ZN, DF5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-08-26
Ligands: ZN, DF5
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Carbonic Anhydrase Inhibitors: Design And Synthesis Of New Heteroaryl-N-Carbonylbenzenesulfonamides Targeting Druggable Human Carbonic Anhydrase Isoforms (Hca Vii, Hca Ix, And Hca Xiv)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.27 Å Release Date: 2015-08-26 Classification: LYASE Ligands: ZN, 4KC |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-08-26
Ligands: ZN, 4KC
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Carbonic Anhydrase Inhibitors: Design And Synthesis Of New Heteroaryl-N-Carbonylbenzenesulfonamides Targeting Druggable Human Carbonic Anhydrase Isoforms (Hca Vii, Hca Ix, And Hca Xiv)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.35 Å Release Date: 2015-08-26 Classification: LYASE Ligands: ZN, 4KB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-08-26
Ligands: ZN, 4KB