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-Structure paper
Title | Structure Based Design of a Grp94-Selective Inhibitor: Exploiting a Key Residue in Grp94 To Optimize Paralog-Selective Binding. |
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Journal, issue, pages | J. Med. Chem., Vol. 61, Page 2793-2805, Year 2018 |
Publish date | May 26, 2017 (structure data deposition date) |
![]() | Que, N.L.S. / Crowley, V.M. / Duerfeldt, A.S. / Zhao, J. / Kent, C.N. / Blagg, B.S.J. / Gewirth, D.T. |
![]() | ![]() ![]() |
Methods | X-ray diffraction |
Resolution | 1.792 - 2.895 Å |
Structure data | ![]() PDB-5vyy: ![]() PDB-5wmt: ![]() PDB-6baw: ![]() PDB-6c91: ![]() PDB-6ceo: |
Chemicals | ![]() ChemComp-9QY: ![]() ChemComp-FMT: ![]() ChemComp-EDO: ![]() ChemComp-MG: ![]() ChemComp-NA: ![]() ChemComp-HOH: ![]() ChemComp-D57: ![]() ChemComp-PO4: ![]() ChemComp-SO4: ![]() ChemComp-EQD: |
Source |
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![]() | CHAPERONE/INHIBITOR / chaperone / chaperone-inhibitor / CHAPERONE-INHIBITOR complex / Inhibitor / Complex / endoplasmin |