Structural Entry Filters:

Search Count: 51

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9Q8R image
Human Rock1 In Complex With A Dihydropyrazolo-Pyrimidine Inhibitor

9SI2 image
Human Ddr1 In Complex With A Pyrrolidine Inhibitor

9SP9 image
Human Ddr1 In Complex With A Indoline Inhibitor

9Q9T image
Human Rock2 In Complex With A Dihydropyrazolo-Pyrimidine Inhibitor

9S89 image
N-Terminal 40Kda Fragment Of Human Pms2 With Covalent Ligand Np1867

9PRP image
N-Terminal Domain Of E. Coli Mutl Bound To Np660

9MVX image
Crystal Structure Of Knob-In-Hole Immunoglobulin G1 Fc Heterodimer With P374A

9N8Q image
Crystal Structure Of Trastuzumab Fab With P151A

9EP8 image
Crystal Structure Of Rock2 In Complex With A 8-(Azaindolyl)-Benzoazepinone Inhibitor

8FBC image
Crystal Structure Of P450T2

7UOR image
Crystal Structure Of Cytochrome P450 Enzyme Cyp119 In Complex With Methyliridium(Iii) Mesoporphyrin.

7T82 image
Crystal Structure Of Leukocidin E/Centyrin S26/Fab B438

7T86 image
Crystal Structure Of Fab Cr5133 / Phospho-Sd Peptide Complex

7T87 image
Crystal Structure Of Leukocidin Ab/Centyrin S17/Fab 214F Complex

7PZX image
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria

7PZS image
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria

7PZU image
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria

7PZV image
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria

7PZW image
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria

7Q01 image
Lpxc Inhibitors With Fluoroproline As A Novel Zinc-Binding Group Can Serve As A Novel Class Of Antibiotic With Activity Against Multidrug-Resistant Gram-Negative Bacteria
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