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9DW6 image
Crystal Structure Of Sars-Cov-2 Main Protease (Mpro) C145A Mutant In Complex With Peptide From Human Trna Methyltransferase Trmt1

7M6T image
Crystal Structure Of Socs2/Elonginb/Elonginc Bound To A Non-Canonical Peptide That Enhances Phospho-Peptide Binding

6DN5 image
Spry Domain-Containing Socs Box Protein 2 Complexed With Wdinnn(Bal) Cyclic Peptide Inhibitor

6DN6 image
Spry Domain-Containing Socs Box Protein 2 Complexed With Innn(Abu) Cyclic Peptide Inhibitor

6DN7 image
Spry Domain-Containing Socs Box Protein 2 Complexed With Wdinnn(Bal) Cyclic Peptide Inhibitor

6DN8 image
Spry Domain-Containing Socs Box Protein 2 Complexed With (Gzj)Vdinnn(Cy3) Cyclic Peptide Inhibitor

6BZH image
Structure Of Mouse Rig-I Tandem Cards
Organism: Mus musculus
Method: X-RAY DIFFRACTION
Resolution:2.50 Å Release Date: 2018-01-17
Classification: HYDROLASE
Ligands: EDO, CL

2N34 image
Nmr Assignments And Solution Structure Of The Jak Interaction Region Of Socs5

4QOC image
Crystal Structure Of Compound 16 Bound To Mdm2(17-111), {(3R,5R,6S)-5-(3-Chlorophenyl)-6-(4-Chlorophenyl)-1-[(1S)-1-Cyclopropyl-2-(Pyrrolidin-1-Ylsulfonyl)Ethyl]-3-Methyl-2-Oxopiperidin-3-Yl}Acetic Acid

4WT2 image
Co-Crystal Structure Of Mdm2 In Complex With Am-7209

4QO4 image
Co-Crystal Structure Of Mdm2 (17-111) With Compound 16, {(3R,5R,6S)-5-(3-Chlorophenyl)-6-(4-Chlorophenyl)-1-[(1S)-1-(6-Cyclopropylpyridin-2-Yl)Propyl]-3-Methyl-2-Oxopiperidin-3-Yl}Acetic Acid

4OCC image
Co-Crystal Structure Of Mdm2(17-111) In Complex With Compound 48

4ODE image
Co-Crystal Structure Of Mdm2 With Inhibitor Compound 4

4ODF image
Co-Crystal Structure Of Mdm2 With Inhibitor Compound 47

4OGN image
Co-Crystal Structure Of Mdm2 With Inhbitor Compound 3

4OGT image
Co-Crystal Structure Of Mdm2 With Inhbitor Compound 46

4OGV image
Co-Crystal Structure Of Mdm2 With Inhibitor Compound 49

4OBA image
Co-Crystal Structure Of Mdm2 With Inhibitor Compound 4

4OAS image
Co-Crystal Structure Of Mdm2 (17-111) In Complex With Compound 25

4JLJ image
Human Dck C4S-S74E Mutant In Complex With Udp And The F2.1.1 Inhibitor (2-[({2-[3-(2-Fluoroethoxy)-4-Methoxyphenyl]-1,3-Thiazol-4-Yl}Methyl)Sulfanyl]Pyrimidine-4,6-Diamine)
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