Search Count: 19
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Co-Crystal Structure Of Human Nicotinamide N-Methyltransferase (Nnmt) With Tricyclic Small Molecule Inhibitor Jbsnf-000028
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.61 Å Release Date: 2022-05-18 Classification: TRANSFERASE Ligands: SAH, JCU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-05-18
Ligands: SAH, JCU
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Co-Crystal Structure Of Human Nicotinamide N-Methyltransferase (Nnmt) With Tricyclic Small Molecule Inhibitor Jbsnf-000107
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.73 Å Release Date: 2022-05-18 Classification: TRANSFERASE Ligands: SAH, JDL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-05-18
Ligands: SAH, JDL
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Modulating The Interaction Between Cdk2 And Cyclin A With A Quinoline-Based Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2013-11-27 Classification: transferase/transferase inhibitor Ligands: 2KD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-27
Ligands: 2KD
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Recognition Of The Bg-H Antigen By A Lamprey Variable Lymphocyte Receptor
Organism: Petromyzon marinus
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2013-06-26 Classification: IMMUNE SYSTEM Ligands: GAL |
Organism: Petromyzon marinus
Method: X-RAY DIFFRACTION
Release Date: 2013-06-26
Ligands: GAL
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Recognition Of The Thomsen-Friedenreich Antigen By A Lamprey Variable Lymphocyte Receptor
Organism: Petromyzon marinus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2013-06-26 Classification: IMMUNE SYSTEM |
Organism: Petromyzon marinus
Method: X-RAY DIFFRACTION
Release Date: 2013-06-26
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Synthesis And Sar Studies Of Imidazo-[1,2-A]-Pyrazine Aurora Kinase Inhibitors With Improved Off Target Kinase Selectivity
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.66 Å Release Date: 2012-05-02 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-05-02
Ligands: 0FY
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Crystal Structure Of Catalytic Domain Of Tace With 2-(2-Aminothiazol-4-Yl)Pyrrolidine-Based Tartrate Diamides
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2011-04-20 Classification: hydrolase/hydrolase inhibitor Ligands: IPA, INN, ZN, CA, 786 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-04-20
Ligands: IPA, INN, ZN, CA, 786
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Crystal Structure Of The Catalytic Domain Of Tace With Indazolinone-Phenyl-Hydantoin Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2010-12-08 Classification: HYDROLASE Ligands: ZN, 727, IPA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-08
Ligands: ZN, 727, IPA
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Crystal Structure Of The Catalytic Domain Of Tace With Isoindolinone-Biphenyl-Hydantoin Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2010-12-08 Classification: HYDROLASE Ligands: Z93, ZN, IPA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-08
Ligands: Z93, ZN, IPA
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X-Ray Crystal Structure Of Compound 70 Bound To Human Chk1 Kinase Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2010-12-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: C70 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-08
Ligands: C70
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X-Ray Crystal Structure Of Compound 2A Bound To Human Chk1 Kinase Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.59 Å Release Date: 2010-12-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: C72, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-08
Ligands: C72, GOL
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X-Ray Crystal Structure Of Compound 1 Bound To Human Chk1 Kinase Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2010-12-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: C73, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-08
Ligands: C73, GOL
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Imidazo[1,2-A]Pyrazine-Based Aurora Kinase Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.05 Å Release Date: 2010-08-18 Classification: TRANSFERASE Ligands: NRM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-08-18
Ligands: NRM
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Crystal Structure Of Catalytic Domain Of Tace With Benzimidazolyl-Thienyl-Tartrate Based Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2010-07-28 Classification: HYDROLASE Ligands: ZN, 50X |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-07-28
Ligands: ZN, 50X
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Aurora A Kinase Complexed With Sch 1473759
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2010-07-21 Classification: TRANSFERASE Ligands: PG4, EML |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-07-21
Ligands: PG4, EML
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Crystal Structure Of Catalytic Domain Of Tace With Hydantoin Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.92 Å Release Date: 2010-03-02 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, INN, IPA, Z94 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-03-02
Ligands: ZN, INN, IPA, Z94
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Crystal Structure Of Catalytic Domain Of Tace With The First Hydantoin Inhibitor Occupying The S1' Pocket
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2010-03-02 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 724 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-03-02
Ligands: ZN, 724
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Crystal Structure Of Thrombin In Complex With A Novel Bicyclic Lactam Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2002-02-27 Classification: HYDROLASE Ligands: BLI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-02-27
Ligands: BLI
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Crystal Structure Of Human Alpha-Thrombin Complexed With Bch-10556 And Exosite-Directed Peptide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2001-04-21 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 110 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2001-04-21
Ligands: 110