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3CS7

FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-(4-methoxyphenyl)-6-(4-(1-(pyrrolidin-1-ylmethyl)cyclopropyl)phenyl)-3-(trifluoromethyl)-5,6-dihydro-1H-pyrazolo[3,4-c]pyridin-7(4H)-one

Summary for 3CS7
Entry DOI10.2210/pdb3cs7/pdb
DescriptorCoagulation factor X, CALCIUM ION, 1-(4-methoxyphenyl)-6-(4-(1-(pyrrolidin-1-ylmethyl)cyclopropyl)phenyl)-3-(trifluoromethyl)-5,6-dihydro-1H-pyrazolo[3,4-c]pyridin-7(4H)-one, ... (5 entities in total)
Functional Keywordsglycoprotein, hydrolase, serine protease, plasma, blood coagulation factor, protein inhibitor complex, calcium-binding, cleavage on pair of basic residues, egf-like domain, gamma-carboxyglutamic acid, hydroxylation, polymorphism, zymogen, blood coagulation, calcium, protease
Biological sourceHomo sapiens (Human)
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Cellular locationSecreted: P00742 P00742
Total number of polymer chains2
Total formula weight32586.97
Authors
Alexander, R.S. (deposition date: 2008-04-09, release date: 2008-07-08, Last modification date: 2011-07-13)
Primary citationQiao, J.X.,Cheney, D.L.,Alexander, R.S.,Smallwood, A.M.,King, S.R.,He, K.,Rendina, A.R.,Luettgen, J.M.,Knabb, R.M.,Wexler, R.R.,Lam, P.Y.
Achieving structural diversity using the perpendicular conformation of alpha-substituted phenylcyclopropanes to mimic the bioactive conformation of ortho-substituted biphenyl P4 moieties: discovery of novel, highly potent inhibitors of Factor Xa.
Bioorg.Med.Chem.Lett., 18:4118-4123, 2008
Cited by
PubMed: 18550370
DOI: 10.1016/j.bmcl.2008.05.095
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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