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-Structure paper
Title | Exploration of the P1 residue in 3CL protease inhibitors leading to the discovery of a 2-tetrahydrofuran P1 replacement. |
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Journal, issue, pages | Bioorg. Med. Chem., Vol. 100, Page 117618-117618, Year 2024 |
Publish date | Oct 9, 2023 (structure data deposition date) |
Authors | Barton, L.S. / Callahan, J.F. / Cantizani, J. / Concha, N.O. / Cotillo Torrejon, I. / Goodwin, N.C. / Joshi-Pangu, A. / Kiesow, T.J. / McAtee, J.J. / Mellinger, M. ...Barton, L.S. / Callahan, J.F. / Cantizani, J. / Concha, N.O. / Cotillo Torrejon, I. / Goodwin, N.C. / Joshi-Pangu, A. / Kiesow, T.J. / McAtee, J.J. / Mellinger, M. / Nixon, C.J. / Padron-Barthe, L. / Patterson, J.R. / Pearson, N.D. / Pouliot, J.J. / Rendina, A.R. / Buitrago Santanilla, A. / Schneck, J.L. / Sanz, O. / Thalji, R.K. / Ward, P. / Williams, S.P. / King, B.W. |
External links | Bioorg. Med. Chem. / PubMed:38309201 |
Methods | X-ray diffraction |
Resolution | 1.75 - 2.02 Å |
Structure data | PDB-8uho: PDB-8uia: PDB-8uif: PDB-8uld: |
Chemicals |
ChemComp-WTE: ChemComp-HOH:
ChemComp-WTV: ChemComp-GOL: ChemComp-CL: PDB-1ads:
ChemComp-WYR: ChemComp-EDO: |
Source |
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Keywords | HYDROLASE / 3CL protease / SARS / viral protein / SARS CoV-2 / protease / inhibitor |