Structural Entry Filters:

Search Count: 34

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9S3A image
Tagst-10 In Complex With Deoxynivalenol-13-Glutathione

8UPS image
Structure Of Sars-Cov2 3Clpro In Complex With Compound 5

8UPV image
Structure Of Sars-Cov2 3Clpro In Complex With Compound 33

8UPW image
Structure Of Sars-Cov2 3Clpro In Complex With Compound 34

8UTE image
Structure Of Sars-Cov2 3Clpro In Complex With Compound 27

8CLQ image
Zearalenone Lactonase Of Streptomyces Coelicoflavus Mutant H286Y In Complex With Hydrolyzed Zearalenone

8CLV image
Zearalenone Lactonase Of Rhodococcus Erythropolis In Complex With Hydrolyzed Zearalenone

8CLN image
Zearalenone Lactonase From Streptomyces Coelicoflavus, Semet Derivative For Sad Phasing

8CLO image
Zearalenone Lactonase From Streptomyces Coelicoflavus

8CLP image
Zearalenone Lactonase From Streptomyces Coelicoflavus Mutant H286Y

8CLT image
Zearalenone Lactonase Of Rhodococcus Erythropolis

8CLU image
Zearalenone Lactonase From Rhodococcus Erythropolis In Complex With Zearalactamenone

7SVL image
Dpp9 In Complex With Ligand Iced-2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.46 Å Release Date: 2022-10-05
Classification: HYDROLASE
Ligands: D06

7SVM image
Dpp8 In Complex With Ligand Iced-2
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.69 Å Release Date: 2022-10-05
Classification: HYDROLASE
Ligands: D06, TMO

7SVN image
Dpp9 In Complex With Ligand Iced-1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.78 Å Release Date: 2022-10-05
Classification: HYDROLASE
Ligands: CW8

7SVO image
Dpp8 In Complex With Ligand Iced-1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.58 Å Release Date: 2022-10-05
Classification: HYDROLASE
Ligands: CW8, TMO

7RN5 image
Discovery Of An Anion-Dependent Farnesyltransferase Inhibitor From A Phenotypic Screen

7RNI image
Discovery Of An Anion-Dependent Farnesyltransferase Inhibitor From A Phenotypic Screen

7LTG image
Structure Of Human Hdac2 In Complex With Apicidin

7LTK image
Structure Of Human Hdac2 In Complex With An Inhibitor That Lacks A Zinc Binding Group (Compound 12)
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