Search Count: 14
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Crystal Structure Of Irak4-Hsa Complexed With N-[(2R)-2-Fluoro-3-Hydroxy-3-Methylbutyl]-6-[(5-Fluoropyri-Yl)Amino]-4-[(Propan-2-Yl)Amino]Pyridine-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.89 Å Release Date: 2025-02-12 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZVD, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-02-12
Ligands: ZVD, SO4
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Crystal Structure Of Irak4-Hsa Complexed With Bms-986126; 6-((5-Cyano-2-Pyrimidinyl)Amino)-N-((2R)-2-Fluoro-3-Hydroxhylbutyl)-4-(Isopropylamino)Nicotinamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.69 Å Release Date: 2025-02-12 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZVG, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-02-12
Ligands: ZVG, SO4
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Crystal Structure Of Irak4-Hsa Complexed With Bms-986147; 6-{5-Cyano-1H-Pyrazolo[3,4-B]Pyridin-1-Yl}-N-[(2R)-2-Fluorroxy-3-Methylbutyl]-4-[(Propan-2-Yl)Amino]Pyridine-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.76 Å Release Date: 2025-02-12 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: SO4, ZVA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-02-12
Ligands: SO4, ZVA
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Discovery Of Bms-986144, A Third Generation, Pan Genotype Ns3/4A Protease Inhibitor For The Treatment Of Hepatitis C Virus Infection
Organism: Hepacivirus c
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2020-12-16 Classification: VIRAL PROTEIN Ligands: ZN, GXO |
Organism: Hepacivirus c
Method: X-RAY DIFFRACTION
Release Date: 2020-12-16
Ligands: ZN, GXO
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Factor Viia In Complex With The Inhibitor (2R)-2-[(1-Aminoisoquinolin-6-Yl)Amino]-2-[3-Ethoxy-4-(Propan-2-Yloxy)Phenyl]-N-(3-Sulfamoylbenzyl)Ethanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2014-01-08 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 2KE, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-01-08
Ligands: 2KE, CA, SO4, GOL
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Factor Viia In Complex With The Inhibitor (2R)-2-[(1-Aminoisoquinolin-6-Yl)Amino]-2-[3-Ethoxy-4-(Propan-2-Yloxy)Phenyl]-N-[2-(Propan-2-Ylsulfonyl)Benzyl]Ethanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2014-01-08 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 2KF, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-01-08
Ligands: 2KF, CA, SO4, GOL
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Ratintestinal Ap Expressed In E. Coli
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.21 Å Release Date: 2013-10-16 Classification: HYDROLASE Ligands: MG, GOL |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-16
Ligands: MG, GOL
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Structure Of Rat Intestinal Alkaline Phosphatase Expressed In Insect Cell
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.38 Å Release Date: 2013-10-16 Classification: HYDROLASE Ligands: ZN, MG, 4NP, NAG |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-16
Ligands: ZN, MG, 4NP, NAG
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Structure Of Factor Viia In Complex With The Inhibitor 2-{2-[(4-Carbamimidoylphenyl)Carbamoyl]-6-Methoxypyridin-3-Yl}-5-{[(2S)-1-Hydroxy-3,3-Dimethylbutan-2-Yl]Carbamoyl}Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2013-08-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1NJ, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-21
Ligands: 1NJ, CA, SO4, GOL
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Structure Of Factor Viia In Complex With The Inhibitor 2-{2-[(1-Aminoisoquinolin-6-Yl)Carbamoyl]-6-Methoxypyridin-3-Yl}-5-{[(2S)-1-Hydroxy-3,3-Dimethylbutan-2-Yl]Carbamoyl}Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.52 Å Release Date: 2013-08-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1NK, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-21
Ligands: 1NK, CA, SO4, GOL
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Structure Of Factor Viia In Complex With The Inhibitor 2-{2-[(3-Carbamoylphenyl)Carbamoyl]-6-Methoxypyridin-3-Yl}-5-{[(2S)-1-Hydroxy-3,3-Dimethylbutan-2-Yl]Carbamoyl}Benzoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2013-08-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1NL, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-21
Ligands: 1NL, CA, SO4, GOL
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Structure Of Factor Viia In Complex With The Inhibitor (2R)-2-[(1-Aminoisoquinolin-6-Yl)Amino]-2-[3-Ethoxy-4-(Propan-2-Yloxy)Phenyl]-N-(Phenylsulfonyl)Ethanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2013-07-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1OK, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-07-24
Ligands: 1OK, CA, SO4, GOL
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Structure Of Factor Viia In Complex With The Inhibitor (2R)-2-[3-Ethoxy-4-(Propan-2-Yloxy)Phenyl]-2-(Isoquinolin-6-Ylamino)-N-[(3-Sulfamoylphenyl)Sulfonyl]Ethanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.19 Å Release Date: 2013-07-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1OJ, CA, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-07-24
Ligands: 1OJ, CA, SO4, GOL
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Human Beta-Glucuronidase At 1.7 A Resolution
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2009-12-01 Classification: HYDROLASE Ligands: NAG, MRD, MPD, BMA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-12-01
Ligands: NAG, MRD, MPD, BMA