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1NM6

thrombin in complex with selective macrocyclic inhibitor at 1.8A

Summary for 1NM6
Entry DOI10.2210/pdb1nm6/pdb
Related1NT1
Descriptorthrombin, Hirudin, (11S)-11-BENZYL-6-CHLORO-1,2,10,11,12,13,14,15,16,17,18,19-DODECAHYDRO-5,9-METHANO-2,5,8,10,13,17-BENZOHEXAAZACYCLOHENICOSINE-3,24-DIONE, ... (4 entities in total)
Functional Keywordsthrombin inhibitor complex, blood clotting-hydrolase inhibitor complex, blood clotting/hydrolase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationSecreted, extracellular space: P00734
Secreted: P28504
Total number of polymer chains2
Total formula weight35023.48
Authors
Nantermet, P.G.,Barrow, J.C.,Newton, C.L.,Pellicore, J.M.,Young, M.,Lewis, S.D.,Lucas, B.J.,Krueger, J.A.,McMasters, D.R.,Yan, Y.,Kuo, L.C.,Vacca, J.P.,Selnick, H.G. (deposition date: 2003-01-09, release date: 2003-09-02, Last modification date: 2017-10-11)
Primary citationNantermet, P.G.,Barrow, J.C.,Newton, C.L.,Pellicore, J.M.,Young, M.,Lewis, S.D.,Lucas, B.J.,Krueger, J.A.,McMasters, D.R.,Yan, Y.,Kuo, L.C.,Vacca, J.P.,Selnick, H.G.
Design and synthesis of potent and selective macrocyclic thrombin inhibitors
Bioorg.Med.Chem.Lett., 13:2781-2784, 2003
Cited by
PubMed: 12873514
DOI: 10.1016/S0960-894X(03)00506-7
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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