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4YT6

Factor VIIa in complex with the inhibitor 4-{[(R)-[5-ethoxy-2-fluoro-3-(propan-2-yloxy)phenyl](4-phenyl-1H-imidazol-2-yl)methyl]amino}benzenecarboximidamide

Summary for 4YT6
Entry DOI10.2210/pdb4yt6/pdb
Related4YT7
DescriptorCoagulation factor VII (heavy chain), Coagulation factor VII (light chain), 4-[[(R)-(5-ethoxy-2-fluoranyl-3-propan-2-yloxy-phenyl)-(4-phenyl-1H-imidazol-2-yl)methyl]amino]benzenecarboximidamide, ... (7 entities in total)
Functional Keywordsglycoprotein, hydrolase, serine protease, plasma, blood coagulation factor, protein inhibitor complex, calcium-binding, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
More
Cellular locationSecreted: P08709 P08709
Total number of polymer chains2
Total formula weight35563.55
Authors
Wei, A. (deposition date: 2015-03-17, release date: 2015-04-29, Last modification date: 2023-09-27)
Primary citationGlunz, P.W.,Cheng, X.,Cheney, D.L.,Weigelt, C.A.,Wei, A.,Luettgen, J.M.,Wong, P.C.,Wexler, R.R.,Priestley, E.S.
Design and synthesis of potent, selective phenylimidazole-based FVIIa inhibitors.
Bioorg.Med.Chem.Lett., 25:2169-2173, 2015
Cited by
PubMed: 25881820
DOI: 10.1016/j.bmcl.2015.03.062
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.07 Å)
Structure validation

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