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1Z4U

hepatitis C virus NS5B RNA-dependent RNA polymerase complex with inhibitor PHA-00799585

Summary for 1Z4U
Entry DOI10.2210/pdb1z4u/pdb
Related1YVF
DescriptorHCV NS5B POLYMERASE, CHLORIDE ION, PHOSPHATE ION, ... (6 entities in total)
Functional Keywordsns5b, polymerase, hcv, fingers, palm, thumb, transferase
Biological sourceHepatitis C virus
Total number of polymer chains1
Total formula weight65287.17
Authors
Pfefferkorn, J.A.,Greene, M.,Nugent, R.,Gross, R.J.,Mitchell, M.A.,Finzel, B.C.,Harris, M.S.,Wells, P.A.,Shelly, J.A.,Anstadt, R. (deposition date: 2005-03-16, release date: 2005-06-07, Last modification date: 2024-04-03)
Primary citationPfefferkorn, J.A.,Nugent, R.,Gross, R.J.,Greene, M.,Mitchell, M.A.,Reding, M.T.,Funk, L.A.,Anderson, R.,Wells, P.A.,Shelly, J.A.,Anstadt, R.,Finzel, B.C.,Harris, M.S.,Kilkuskie, R.E.,Kopta, L.A.,Schwende, F.J.
Inhibitors of HCV NS5B polymerase. Part 2: Evaluation of the northern region of (2Z)-2-benzoylamino-3-(4-phenoxy-phenyl)-acrylic acid
Bioorg.Med.Chem.Lett., 15:2812-2818, 2005
Cited by
PubMed Abstract: A novel series of non-nucleoside HCV NS5B polymerase inhibitors was prepared from a (2Z)-2-benzoylamino-3-(4-phenoxy-phenyl)-acrylic acid template. Solution and solid phase analog synthesis focused on the northern region of the template combined with structure based design led to the discovery of several potent and orally bioavailable lead compounds.
PubMed: 15911260
DOI: 10.1016/j.bmcl.2005.03.106
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.8 Å)
Structure validation

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