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2G00

Factor Xa in complex with the inhibitor 3-(6-(2'-((dimethylamino)methyl)-4-biphenylyl)-7-oxo-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-1-yl)benzamide

Summary for 2G00
Entry DOI10.2210/pdb2g00/pdb
DescriptorCoagulation factor X, 3-[6-{2'-[(DIMETHYLAMINO)METHYL]BIPHENYL-4-YL}-7-OXO-3-(TRIFLUOROMETHYL)-4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN-1-YL]BENZAMIDE (3 entities in total)
Functional Keywordsglycoprotein, hydrolase, serine protease, plasma, blood coagulation factor, protein inhibitor complex, calcium-binding
Biological sourceHomo sapiens (human)
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Cellular locationSecreted: P00742 P00742
Total number of polymer chains2
Total formula weight32569.88
Authors
Alexander, R.S. (deposition date: 2006-02-10, release date: 2006-10-03, Last modification date: 2017-10-18)
Primary citationPinto, D.J.,Galemmo, R.A.,Quan, M.L.,Orwat, M.J.,Clark, C.,Li, R.,Wells, B.,Woerner, F.,Alexander, R.S.,Rossi, K.A.,Smallwood, A.,Wong, P.C.,Luettgen, J.M.,Rendina, A.R.,Knabb, R.M.,He, K.,Wexler, R.R.,Lam, P.Y.
Discovery of potent, efficacious, and orally bioavailable inhibitors of blood coagulation factor Xa with neutral P1 moieties.
Bioorg.Med.Chem.Lett., 16:5584-5589, 2006
Cited by
PubMed: 16963264
DOI: 10.1016/j.bmcl.2006.08.027
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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