Structural Entry Filters:

Search Count: 17

Download
7N2A image
Human Pxr Lbd Bound To Compound 2

7RIO image
Human Pxr Lbd Bound To Gsk003

7RIU image
Human Pxr Lbd Bound To Gsk002

7RIV image
Human Pxr Lbd Bound To Gsk001

6SZJ image
Rip2 Kinase Catalytic Domain Complex With 5Amino1Tertbutyl3(3Methoxyphenyl)1H Pyrazole4Carboxamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.53 Å Release Date: 2019-12-04
Classification: TRANSFERASE
Ligands: M5W, CA

6UL8 image
Rip2 Kinase Catalytic Domain Complex With (5S,6S,8R)-2-(Benzo[D]Thiazol-5-Yl)-6-Hydroxy-4,5,6,7,8,9-Hexahydro-5,8-Methanopyrazolo[1,5-A][1,3]Diazocine-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.68 Å Release Date: 2019-12-04
Classification: TRANSFERASE
Ligands: Q9J, CA

6SZE image
Rip2 Kinase Catalytic Domain Complex With 5-Amino-1-Phenylpyrazole-4-Carboxamide.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.94 Å Release Date: 2019-10-23
Classification: TRANSFERASE
Ligands: M2B, CA

6QMC image
Small Molecule Inhibitor Of The Keap1-Nrf2 Protein-Protein Interaction

6QMD image
Small Molecule Inhibitor Of The Keap1-Nrf2 Protein-Protein Interaction

6QME image
Small Molecule Inhibitor Of The Keap1-Nrf2 Protein-Protein Interaction

6QMJ image
Small Molecule Inhibitor Of The Keap1-Nrf2 Protein-Protein Interaction

6QMK image
Small Molecule Inhibitor Of The Keap1-Nrf2 Protein-Protein Interaction

6HMX image
Rip2 Kinase Catalytic Domain Complex With N(4,5Dimethyl1Hpyrazol3Yl)7Methoxy6(2Methylpropane2Sulfonyl)Quinolin4Amine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.53 Å Release Date: 2018-11-07
Classification: TRANSFERASE
Ligands: GEZ

5J79 image
The Identification And Pharmacological Characterization Of 6-(Tert-Butylsulfonyl)-N-(5-Fluoro-1H-Indazol-3-Yl)Quinolin-4-Amine (Gsk583), A Highly Potent And Selective Inhibitor Of Rip2 Kinase, Compound 3 Complex

5J7B image
The Identification And Pharmacological Characterization Of 6-(Tert-Butylsulfonyl)-N-(5-Fluoro-1H-Indazol-3-Yl)Quinolin-4-Amine (Gsk583), A Highly Potent And Selective Inhibitor Of Rip2 Kinase, Gsk583 Complex

5HX6 image
Crystal Structure Of Rip1 Kinase With A Benzo[B][1,4]Oxazepin-4-One

2FB8 image
Structure Of The B-Raf Kinase Domain Bound To Sb-590885
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.90 Å Release Date: 2006-12-12
Classification: TRANSFERASE
Ligands: 215
Protein Functional Filters:
Feedback Form
Name
Email
Institute
Feedback