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6BQJ

CRYSTAL STRUCTURE OF HEPATIS C VIRUS PROTEASE (NS3) COMPLEXED WITH TRIPEPTIDIC ACYL SULFONAMIDE INHIBITOR (COMPOUND 16)

Summary for 6BQJ
Entry DOI10.2210/pdb6bqj/pdb
DescriptorNS3 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 Keywordsserine protease, viral protein, hydrolase
Biological sourceHepatitis C virus
Total number of polymer chains3
Total formula weight72846.49
Authors
Klei, H.E.,Sack, J.S. (deposition date: 2017-11-28, release date: 2018-03-21, Last modification date: 2024-03-13)
Primary citationZheng, 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: 29456803
DOI: 10.1021/acsmedchemlett.7b00503
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.69 Å)
Structure validation

218853

數據於2024-04-24公開中

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