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Search Count: 35

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9RD5 image
Phi3T Srof Bound To Dna

9RGL image
Crystal Structure Of The Srof-Sar Complex, Repressor And Antirepressor Of Phage Phi3T.


9FKU image
Crystal Structure Of Aimr From Katmira Phage

9F82 image
Arbitrium Receptor From Atcc13952 Phage In Complex With Gvvrga Peptide

9F36 image
Crystal Estructure Of Aimr From Atcc13952 Phage

9F17 image
Crystal Structure Of N Term His-Tag Adenylosuccinate Synthetase From Helicobacter Pylori

8Q5B image
Characterization Of The Zinc Finger U-Protein Hvo_0758 From Haloferax Volcanii: Biological Roles, Zinc Binding, And Nmr Solution Structure

7ROA image
Crystal Structure Of Entv136 From Enterococcus Faecalis

7NQQ image
Discovery Of Astx029, A Clinical Candidate Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

7NQW image
Discovery Of Astx029, A Clinical Candidate Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

7NR3 image
Discovery Of Astx029, A Clinical Candidate Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

7NR5 image
Discovery Of Astx029, A Clinical Candidate Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

7NR8 image
Discovery Of Astx029, A Clinical Candidate Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

7NR9 image
Discovery Of Astx029, A Clinical Candidate Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

6G8X image
Fragment-Based Discovery Of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

6G91 image
Fragment-Based Discovery Of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

6G92 image
Fragment-Based Discovery Of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

6G93 image
Fragment-Based Discovery Of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2

6G97 image
Fragment-Based Discovery Of A Highly Potent, Orally Bioavailable Inhibitor Which Modulates The Phosphorylation And Catalytic Activity Of Erk1/2
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