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9DU2

SARS-CoV-2 Mpro in complex with compound 7

This is a non-PDB format compatible entry.
Summary for 9DU2
Entry DOI10.2210/pdb9du2/pdb
Descriptor3C-like proteinase nsp5, N-[(2S)-3-cyclopropyl-1-{[(1Z,2S)-1-imino-4-(methanesulfonyl)butan-2-yl]amino}-1-oxopropan-2-yl]-4-methoxy-1H-indole-2-carboxamide (3 entities in total)
Functional Keywordssars-cov-2 mpro hydrolase, compound 7, corona virus, aldehyde and nitrile based inhibitors, viral protein, hydrolase-inhibitor complex, hydrolase/inhibitor
Biological sourceSevere acute respiratory syndrome coronavirus 2
Total number of polymer chains2
Total formula weight70952.84
Authors
Bigelow, L.,Tang, H.,Boguslaw, N.,Duda, D.M. (deposition date: 2024-10-02, release date: 2025-04-30)
Primary citationPadmanabha Das, K.M.,Chen, J.,Charifson, P.S.,Green, J.,Tang, H.,Panchal, S.,Pu, F.,Korepanova, A.,Afanador, G.,Stojkovic, V.,Nocek, B.,Bigelow, L.,Stubbs, S.,Davey, R.A.,DeGoey, D.A.,Arthanari, H.,Namchuk, M.N.
Inhibition of Dimeric SARS-CoV-2 Mpro by Aldehyde and Nitrilebased Inhibitors Displays Positive Cooperativity and a Mixture of Covalent and Non-covalent Binding.
To Be Published,
Experimental method
X-RAY DIFFRACTION (1.86 Å)
Structure validation

237423

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