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Search Count: 23

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9AXA image
Cryoem Structure Of Activated Craf/Mek/14-3-3 Complex With Nst-628

9AXC image
Activated Craf/Mek Heterotetramer From Focused Refinement Of Craf/Mek/14-3-3 Complex

9AXH image
Crystal Structure Of Ksr1/Mek1 Complex Heterotetramer With Nst-628
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.81 Å Release Date: 2024-04-17
Classification: TRANSFERASE
Ligands: A1AHE, ANP, MG, EDO, CL

9AXM image
Crystal Structure Of Araf/Mek1 Complex With Nst-628 And A Raf Dimer

9AXX image
Crystal Structure Of Braf/Mek1 Complex With Nst-628 And An Active Raf Dimer

9AXY image
Crystal Structure Of Braf/Mek Complex With Nst-628 And Inactive Raf

9AY7 image
Crystal Structure Of Craf/Mek1 Complex With Nst-628 And Inactive Raf
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.41 Å Release Date: 2024-04-17
Classification: TRANSFERASE
Ligands: ANP, MG, NI, ACT, EDO, A1AHE

9AYA image
Crystal Structure Of Craf/Mek Complex With Nst-628 And Active Raf Dimer

6B16 image
P21-Activated Kinase 1 In Complex With A 4-Azaindole Inhibitor

5IME image
Crystal Structure Of P21-Activated Kinase 1 (Pak1) In Complex With Compound 9

5DEY image
Crystal Structure Of Pak1 In Complex With An Inhibitor Compound G-5555

5DFP image
Crystal Structure Of Pak1 In Complex With An Inhibitor Compound Frax1036

4ZY4 image
Crystal Structure Of P21 Activated Kinase 1 In Complex With An Inhibitor Compound 4

4ZY5 image
Crystal Structure Of P21-Activated Kinase 1 In Complex With An Inhibitor Compound 17

4ZY6 image
Crystal Structure Of P21-Activated Kinase 1 In Complex With An Inhibitor Compound 29

5BMS image
Crystal Structure Of P21-Activated Kinase 4 In Complex With An Inhibitor Compound 29

4O0R image
Back Pocket Flexibility Provides Group-Ii Pak Selectivity For Type 1 Kinase Inhibitors

4O0T image
Back Pocket Flexibility Provides Group-Ii Pak Selectivity For Type 1 Kinase Inhibitors

4O0V image
Back Pocket Flexibility Provides Group-Ii Pak Selectivity For Type 1 Kinase Inhibitors

4O0X image
Back Pocket Flexibility Provides Group-Ii Pak Selectivity For Type 1 Kinase Inhibitors
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