Search Count: 109
![]() |
Heat Shock Protein 90 Bound To Cs301
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.91 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4EO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4EO
![]() |
Heat Shock Protein 90 Bound To Cs302
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.61 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4EP, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4EP, GOL
![]() |
Heat Shock Protein 90 Bound To Cs307
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4EQ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4EQ
![]() |
Heat Shock Protein 90 Bound To Cs311
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4ER |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4ER
![]() |
Heat Shock Protein 90 Bound To Cs312
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4ES |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4ES
![]() |
Heat Shock Protein 90 Bound To Cs318
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4ET, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4ET, GOL
![]() |
Heat Shock Protein 90 Bound To Cs319
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.78 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4EU, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4EU, GOL
![]() |
Heat Shock Protein 90 Bound To Cs320
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2016-03-09 Classification: CHAPERONE/Inhibitor Ligands: 4EV |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-03-09
Ligands: 4EV
![]() |
Crystal Structure Of The Lpxc In Complex With N-[(2S)-3-Amino-1-(Hydroxyamino)-1-Oxopropan-2-Yl]-4-(4-Phenylbuta-1,3-Diyn-1-Yl)Benzamide Inhibitor
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2013-05-15 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, L52, GOL |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: ZN, L52, GOL
![]() |
Crystal Structure Of The Lpxc In Complex With N-[(1S,2R)-2-Hydroxy-1-(Hydroxycarbamoyl)Propyl]-4-(4-Phenylbuta-1,3-Diyn-1-Yl)Benzamide Inhibitor
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:2.19 Å Release Date: 2013-05-15 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, 3P3, GOL, ACT |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: ZN, 3P3, GOL, ACT
![]() |
Crystal Structure Of The Lpxc In Complex With 4'-Bromo-N-[(2S,3R)-3-Hydroxy-1-(Hydroxyamino)-1-Oxobutan-2-Yl]Biphenyl-4-Carboxamide Inhibitor
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2013-05-15 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, L58, ACT, GOL |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: ZN, L58, ACT, GOL
![]() |
Crystal Structure Of The Lpxc In Complex With N-[(2S,3R)-3-Hydroxy-1-(Hydroxyamino)-1-Oxobutan-2-Yl]-4-(Phenylethynyl)Benzamide Inhibitor
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:1.83 Å Release Date: 2013-05-15 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, L59, GOL, ACT, PEG, NA |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: ZN, L59, GOL, ACT, PEG, NA
![]() |
Crystal Structure Of The Lpxc In Complex With N-[(2S,3R)-3-Hydroxy-1-(Hydroxyamino)-1-Oxobutan-2-Yl]Biphenyl-4-Carboxamide Inhibitor
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2013-05-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, L63, GOL, ACT |
Organism: Pseudomonas aeruginosa
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: ZN, L63, GOL, ACT
![]() |
Crystal Structure Of The Cdk2/Cyclin A Complex With Oxindole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.75 Å Release Date: 2013-05-15 Classification: transferase/transferase inhibitor Ligands: 60K, DTT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-15
Ligands: 60K, DTT
![]() |
Crystal Structure Of The Cdk2 In Complex With Aminopyrazole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.51 Å Release Date: 2013-05-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 4CK |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-08
Ligands: 4CK
![]() |
Crystal Structure Of The Cdk2 In Complex With Aminopyrazole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2013-05-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 09K |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-08
Ligands: 09K
![]() |
Crystal Structure Of The Cdk2 In Complex With Aminopyrazole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.63 Å Release Date: 2013-05-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 11K, ACT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-08
Ligands: 11K, ACT
![]() |
Crystal Structure Of The Cdk2 In Complex With Thiazolylpyrimidine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.26 Å Release Date: 2013-05-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: CK2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-08
Ligands: CK2
![]() |
Crystal Structure Of The Cdk2 In Complex With Thiazolylpyrimidine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2013-05-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 20K, ACT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-08
Ligands: 20K, ACT
![]() |
Crystal Structure Of The Cdk2 In Complex With Oxindole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2013-05-08 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: LS5, NA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-08
Ligands: LS5, NA
