Search Count: 17
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Crystal Structure Of Bcl-2 In Complex With Prodrug Abbv-167
Organism: Homo sapiens, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:2.07 Å Release Date: 2021-04-14 Classification: APOPTOSIS Ligands: XZD |
Organism: Homo sapiens, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2021-04-14
Ligands: XZD
 |
Bcl_2-Navitoclax Analog (With Indole) Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.07 Å Release Date: 2014-01-29 Classification: APOPTOSIS REGULATOR/INHIBITOR Ligands: 1Y1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-01-29
Ligands: 1Y1
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Bcl_2-Navitoclax (Abt-263) Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2013-08-14 Classification: APOPTOSIS REGULATOR/INHIBITOR Ligands: 1XJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-14
Ligands: 1XJ
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Bcl_2-Navitoclax Analog (Without Thiophenyl) Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-08-14 Classification: APOPTOSIS REGULATOR/INHIBITOR Ligands: 1XV |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-14
Ligands: 1XV
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Discovery Of New Hiv Protease Inhibitors With Potential For Convenient Dosing And Reduced Side Effects: A-790742 And A-792611.
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2012-04-11 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: LK0 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2012-04-11
Ligands: LK0
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Parp Complexed With A927929
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2010-06-23 Classification: TRANSFERASE Ligands: A92 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-06-23
Ligands: A92
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Hiv Protease Inhibitors With Pseudo-Symmetric Cores
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2009-05-26 Classification: HYDROLASE Ligands: GGW |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2009-05-26
Ligands: GGW
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Hiv Protease, Pseudo-Symmetric Inhibitors
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:3.09 Å Release Date: 2009-05-26 Classification: HYDROLASE Ligands: GGV |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2009-05-26
Ligands: GGV
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Hiv Protease, Pseudo-Symmetric Inhibitors
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2009-05-26 Classification: HYDROLASE Ligands: GGX |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2009-05-26
Ligands: GGX
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Pka Structures Of Akt, Indazole-Pyridine Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: SS3 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: SS3
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Pka Structures Of Indazole-Pyridine Series Of Akt Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: L20 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: L20
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Pka Structures Of Indazole-Pyridine Series Of Akt Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: SS5 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: SS5
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Pka Structures Of Indazole-Pyridine Series Of Akt Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: SS4 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: SS4
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Protein Kinase A Bound To (S)-2-(1H-Indol-3-Yl)-1-[5-((E)-2-Pyridin-4-Yl-Vinyl)-Pyridin-3-Yloxymethyl]-Ethylamine
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2006-06-27 Classification: TRANSFERASE Ligands: 4EA |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: 4EA
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Synthesis And Activity Of N-Axyl Azacyclic Urea Hiv-1 Protease Inhibitors With High Potency Against Multiple Drug Resistant Viral Strains.
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2005-09-20 Classification: HYDROLASE Ligands: AAU |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2005-09-20
Ligands: AAU
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Hiv-1 Protease Dimer Complexed With A-84538
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1998-02-04 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: RIT |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1998-02-04
Ligands: RIT
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Hiv-1 Protease Dimer Complexed With A-98881
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1996-08-17 Classification: HYDROLASE (ASPARTIC PROTEASE) Ligands: A88 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1996-08-17
Ligands: A88