8UE0

Crystal structure of SARS-CoV-2 3CL protease with inhibitor 47

Summary for 8UE0

• Entry DOI: 10.2210/pdb8ue0/pdb
• Descriptor: 3C-like proteinase nsp5, 2,4-dichloro-Nalpha-[(2R)-2-chloro-3-(2-cyanophenyl)propanoyl]-N-[(2S)-4-{[4-(dimethylamino)butyl]amino}-1-(4-fluorophenyl)-4-oxobutan-2-yl]-D-phenylalaninamide, SODIUM ION, ... (5 entities in total)
• Functional Keywords: 3cl protease, hydrolase-inhibitor complex, hydrolase/inhibitor
• Biological source: Severe acute respiratory syndrome coronavirus 2
• Total number of polymer chains: 1
• Total formula weight: 34610.05

Authors

Forouhar, F.,Liu, H.,Zack, A.,Iketani, S.,Williams, A.,Vaz, D.R.,Habashi, D.L.,Choi, K.,Resnick, S.J.,Chavez, A.,Ho, D.D.,Stockwell, B.R. (deposition date: 2023-09-29, release date: 2025-01-15)

Primary citation

Liu, H.,Zask, A.,Forouhar, F.,Iketani, S.,Williams, A.,Vaz, D.R.,Habashi, D.,Choi, K.,Resnick, S.J.,Hong, S.J.,Lovett, D.H.,Bai, T.,Chavez, A.,Ho, D.D.,Stockwell, B.R.
Development of small molecule non-covalent coronavirus 3CL protease inhibitors from DNA-encoded chemical library screening.
Nat Commun, 16:152-152, 2025

PubMed Abstract: Variants of SARS-CoV-2 have continued to emerge across the world and cause hundreds of deaths each week. Due to the limited efficacy of vaccines against SARS-CoV-2 and resistance to current therapies, additional anti-viral therapeutics with pan-coronavirus activity are of high interest. Here, we screen 2.8 billion compounds from a DNA-encoded chemical library and identify small molecules that are non-covalent inhibitors targeting the conserved 3CL protease of SARS-CoV-2 and other coronaviruses. We perform structure-based optimization, leading to the creation of a series of potent, non-covalent SARS-CoV-2 3CL protease inhibitors, for coronavirus infections. To characterize their binding mechanism to the 3CL protease, we determine 16 co-crystal structures and find that optimized inhibitors specifically interact with both protomers of the native homodimer of 3CL protease. Since 3CL protease is catalytically competent only in the dimeric state, these data provide insight into the design of drug-like inhibitors targeting the native homodimer state. With a binding mode different from the covalent 3CL inhibitor nirmatrelvir, the protease inhibitor in the COVID drug Paxlovid, these compounds may overcome resistance reported for nirmatrelvir and complement its clinical utility.

PubMed: 39747827
DOI: 10.1038/s41467-024-55421-5

Experimental method

X-RAY DIFFRACTION (2.16 Å)