6BQJ
CRYSTAL STRUCTURE OF HEPATIS C VIRUS PROTEASE (NS3) COMPLEXED WITH TRIPEPTIDIC ACYL SULFONAMIDE INHIBITOR (COMPOUND 16)
Summary for 6BQJ
Entry DOI | 10.2210/pdb6bqj/pdb |
Descriptor | NS3 protease, N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-N-{(2S)-1-[(cyclopropylsulfonyl)amino]-4,4-difluoro-1-oxobutan-2-yl}-4-[(7-methoxy-2-phenylquinolin-4-yl)oxy]-L-prolinamide, ZINC ION, ... (6 entities in total) |
Functional Keywords | serine protease, viral protein, hydrolase |
Biological source | Hepatitis C virus |
Total number of polymer chains | 3 |
Total formula weight | 72846.49 |
Authors | Klei, H.E.,Sack, J.S. (deposition date: 2017-11-28, release date: 2018-03-21, Last modification date: 2024-03-13) |
Primary citation | Zheng, B.,D'Andrea, S.V.,Sun, L.Q.,Wang, A.X.,Chen, Y.,Hrnciar, P.,Friborg, J.,Falk, P.,Hernandez, D.,Yu, F.,Sheaffer, A.K.,Knipe, J.O.,Mosure, K.,Rajamani, R.,Good, A.C.,Kish, K.,Tredup, J.,Klei, H.E.,Paruchuri, M.,Ng, A.,Gao, Q.,Rampulla, R.A.,Mathur, A.,Meanwell, N.A.,McPhee, F.,Scola, P.M. Potent Inhibitors of Hepatitis C Virus NS3 Protease: Employment of a Difluoromethyl Group as a Hydrogen-Bond Donor. ACS Med Chem Lett, 9:143-148, 2018 Cited by PubMed: 29456803DOI: 10.1021/acsmedchemlett.7b00503 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.69 Å) |
Structure validation
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