Search Count: 28
 |
G-925 Bound To The Smarca4 (Brg1) Bromodomain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.16 Å Release Date: 2022-08-17 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: GGU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-08-17
Ligands: GGU
 |
G-059 Bound To The Smarca4 (Brg1) Bromodomain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.61 Å Release Date: 2022-08-17 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: GJN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-08-17
Ligands: GJN
 |
Crystal Structure Of Hepatis C Virus Protease (Ns3) Complexed With Tripeptidic Acyl Sulfonamide Inhibitor (Compound 16)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2018-03-21 Classification: HYDROLASE Ligands: Z1B, ZN, CL, ACT |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: Z1B, ZN, CL, ACT
 |
Crystal Structure Of Hepatis C Virus Protease (Ns3) Complexed With Tripeptidic Acyl Sulfonamide Inhibitor (Compound 18)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:1.97 Å Release Date: 2018-03-21 Classification: HYDROLASE Ligands: Z1E, ZN |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: Z1E, ZN
 |
Structure Of Human Polycomb Repressive Complex 2 (Prc2) With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.47 Å Release Date: 2017-02-22 Classification: Transferase/Inhibitor Ligands: ZN, 74D |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-02-22
Ligands: ZN, 74D
 |
Brd9 In Complex With Cpd1 (6-Methyl-1,6-Dihydro-7H-Pyrrolo[2,3-C]Pyridin-7-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.04 Å Release Date: 2016-10-12 Classification: RNA BINDING PROTEIN Ligands: EDO, PEG, 67N |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-10-12
Ligands: EDO, PEG, 67N
 |
Brd9 In Complex With Cpd2 (N,N-Dimethyl-3-(6-Methyl-7-Oxo-6,7-Dihydro-1H-Pyrrolo[2,3-C]Pyridin-4-Yl)Benzamide)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.18 Å Release Date: 2016-10-12 Classification: RNA BINDING PROTEIN Ligands: 67B |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-10-12
Ligands: 67B
 |
Brd9 In Complex With Cpd4 ((E)-3-(6-(But-2-En-1-Yl)-7-Oxo-6,7-Dihydro-1H-Pyrrolo[2,3-C]Pyridin-4-Yl)-N,N-Dimethylbenzamide)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2016-10-12 Classification: TRANSCRIPTION Ligands: 69G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-10-12
Ligands: 69G
 |
Brd4 In Complex With Cpd2 (N,N-Dimethyl-3-(6-Methyl-7-Oxo-6,7-Dihydro-1H-Pyrrolo[2,3-C]Pyridin-4-Yl)Benzamide)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2016-10-12 Classification: TRANSCRIPTION Ligands: 67B, EDO, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-10-12
Ligands: 67B, EDO, DMS
 |
Brd4 In Complex With Cpd4 ((E)-3-(6-(But-2-En-1-Yl)-7-Oxo-6,7-Dihydro-1H-Pyrrolo[2,3-C]Pyridin-4-Yl)-N,N-Dimethylbenzamide)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2016-10-12 Classification: TRANSCRIPTION Ligands: PGE, EDO, DMS, 69G, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-10-12
Ligands: PGE, EDO, DMS, 69G, GOL
 |
Second Bromodomain Of Taf1 Bound To A Pyrrolopyridone Compound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2016-06-08 Classification: PROTEIN BINDING/INHIBITOR Ligands: 67C |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-06-08
Ligands: 67C
 |
Taf1(2) Bound To A Pyrrolopyridone Compound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.21 Å Release Date: 2016-06-08 Classification: PROTEIN BINDING/INHIBITOR Ligands: 67B, CA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-06-08
Ligands: 67B, CA
 |
Crystal Structure Of Hepatis C Virus Protease (Ns3) Complexed With Bms-605339 Aka N-(Tert-Butoxycarbonyl)-3-Me Thyl-L-Valyl-(4R)-N-((1R,2S)-1-((Cyclopropylsulfonyl)Carba Moyl)-2-Vinylcyclopropyl)-4-((6-Methoxy-1-Isoquinolinyl)Ox Y)-L-Prolinamide
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:1.62 Å Release Date: 2014-03-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 2R8, ZN, SO4, GOL |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2014-03-26
Ligands: 2R8, ZN, SO4, GOL
 |
Crystal Structure Of Hepatis C Virus Protease (Ns3) Complexed With Bms-650032 Aka N-(Tert-Butoxycarbonyl)-3-Me Thyl-L-Valyl-(4R)-4-((7-Chloro-4-Methoxy-1-Isoquinolinyl)O Xy)-N-((1R,2S)-1-((Cyclopropylsulfonyl)Carbamoyl)-2-Vinylc Yclopropyl)-L-Prolinamide
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2014-03-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 2R9, ZN |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2014-03-26
Ligands: 2R9, ZN
 |
Crystal Structure Of Beta-Site App-Cleaving Enzyme 1 (Bace-Wt) Complex With N-(N-(4-Amino-3,5- Dichlorobenzyl)Carbamimidoyl)-3-(4-Methoxyphenyl)-5- Methyl-4-Isothiazolecarboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2012-10-10 Classification: HYDROLASE/INHIBITOR Ligands: 0VA, IOD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: 0VA, IOD
 |
Crystal Structure Of Beta-Site App-Cleaving Enzyme 1 (Bace-Db-Mut) Complex With N-(N-(4- Acetamido-3-Chloro-5-Methylbenzyl)Carbamimidoyl)-3-(4- Methoxyphenyl)-5-Methyl-4-Isothiazolecarboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2012-10-10 Classification: HYDROLASE/INHIBITOR Ligands: 0VB, IOD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: 0VB, IOD
 |
Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0F5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0F5
 |
Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.23 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0F9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0F9
 |
Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.08 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FK |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0FK
 |
Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.48 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0FN