Search Count: 19
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Structures Of The Two-Chain Human Plasma Factor Xiia Co-Crystallized With Potent Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.32 Å Release Date: 2018-03-21 Classification: BLOOD CLOTTING Ligands: BEN, IOD, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: BEN, IOD, SO4, GOL
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Structures Of The Two-Chain Human Plasma Factor Xiia Co-Crystallized With Potent Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.37 Å Release Date: 2018-03-21 Classification: BLOOD CLOTTING Ligands: CWV, IOD, SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: CWV, IOD, SO4, GOL
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Crystal Structure Of Carbonmonoxy Hemoglobin S (Liganded Sickle Cell Hemoglobin) Complexed With Gbt Compound 31
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2017-02-22 Classification: OXYGEN TRANSPORT Ligands: HEM, CMO, 7SJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: HEM, CMO, 7SJ
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Crystal Structure Of Carbonmonoxy Hemoglobin S (Liganded Sickle Cell Hemoglobin) Complexed With Gbt Compound 6
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2017-02-22 Classification: OXYGEN TRANSPORT Ligands: HEM, CMO, 86M |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: HEM, CMO, 86M
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Crystal Structure Of Jak3 Kinase Domain In Complex With A Pyrrolopyrazine-2-Phenyl Ether Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2013-12-11 Classification: TRANSFERASE Ligands: 1NX, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-11
Ligands: 1NX, GOL
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Jak3 Kinase Domain In Complex With 2-Phenoxy-5H-Pyrrolo[2,3-B]Pyrazine-7-Carboxylic Acid ((S)-1-Cyclopropyl-Ethyl)-Amide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2013-10-16 Classification: Transferase/Transferase Inhibitor Ligands: PHU, 1DT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-16
Ligands: PHU, 1DT
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Crystal Structure Of Jak3 Kinase Domain In Complex With An Indazole Substituted Pyrrolopyrazine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.42 Å Release Date: 2013-09-25 Classification: TRANSFERASE Ligands: VFC, PEG, CL, PG4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-25
Ligands: VFC, PEG, CL, PG4
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Crystal Structure Of Spleen Tyrosine Kinase Complexed With 6-((1R,2S)-2-Amino-Cyclohexylamino)-4-(6-Ethyl-Pyridin-2-Ylamino)-Pyridazine-3-Carboxylic Acid Amide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2013-07-10 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0VH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-07-10
Ligands: 0VH
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Jak3 Kinase Domain In Complex With 2-Cyclopropyl-5H-Pyrrolo[2,3-B]Pyrazine-7-Carboxylic Acid ((S)-1,2,2-Trimethyl-Propyl)-Amide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2013-01-16 Classification: Transferase/Transferase Inhibitor Ligands: PHU, 933 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: PHU, 933
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Jak3 Kinase Domain In Complex With 2-Cyclopropyl-5H-Pyrrolo[2,3-B]Pyrazine-7-Carboxylic Acid ((S)-2-Hydroxy-1,2-Dimethyl-Propyl)-Amide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2013-01-16 Classification: Transferase/Transferase Inhibitor Ligands: 19Q |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: 19Q
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Jak3 Kinase Domain In Complex With 2-Cyclopropyl-5H-Pyrrolo[2,3-B]Pyrazine-7-Carboxylic Acid ((R)-2-Hydroxy-1,2-Dimethyl-Propyl
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-01-16 Classification: Transferase/Transferase Inhibitor Ligands: 19R |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: 19R
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Jak3 Kinase Domain In Complex With 2-Cyclopropyl-5H-Pyrrolo[2,3-B]Pyrazine-7-Carboxylic Acid ((R)-1-Methyl-2-Oxo-2-Piperidin-1-Yl-Ethyl)-Amide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2013-01-16 Classification: Transferase/Transferase Inhibitor Ligands: 19S |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-01-16
Ligands: 19S
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Hepatitis C Virus Polymerase Ns5B (Bk) With Amide Bioisostere Thumb Site Inhibitor
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2010-07-28 Classification: TRANSFERASE Ligands: HJZ, GOL |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2010-07-28
Ligands: HJZ, GOL
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Hepatitis C Virus Polymerase Ns5B (Bk 1-570) With Thiazine Inhibitor
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2009-09-08 Classification: TRANSFERASE Ligands: T18, NI |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2009-09-08
Ligands: T18, NI
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Hepatitis C Virus Polymerase Ns5B With Thiazine Inhibitor 2
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2009-09-08 Classification: TRANSFERASE Ligands: H59 |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2009-09-08
Ligands: H59
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Hepatitis C Virus Polymerase Ns5B With Saccharin Inhibitor
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2009-09-08 Classification: TRANSFERASE Ligands: H5S |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2009-09-08
Ligands: H5S
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Hepatitis C Virus Polymerase Ns5B With Saccharin Inhibitor 1
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2009-09-08 Classification: TRANSFERASE Ligands: H5U |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2009-09-08
Ligands: H5U
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Targeting Tuberculosis And Malaria Through Inhibition Of Enoyl Reductase: Compound Activity And Structural Data
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2003-09-16 Classification: OXIDOREDUCTASE Ligands: NAD, GEQ |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2003-09-16
Ligands: NAD, GEQ
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Targeting Tuberculosis And Malaria Through Inhibition Of Enoyl Reductase: Compound Activity And Structural Data
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2003-09-16 Classification: OXIDOREDUCTASE Ligands: NAD, TCL |
Organism: Mycobacterium tuberculosis
Method: X-RAY DIFFRACTION
Release Date: 2003-09-16
Ligands: NAD, TCL