PDB ID: 2BXT
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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C2D | 6-chloro-1-(2-{[(5-chloro-1-benzothien-3-yl)methyl]amino}ethyl)-3-[(2-pyridin-2-ylethyl)amino]-1,4-dihydropyrazin-2-ol | PoSSuM |
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TYS | O-sulfo-L-tyrosine |
Code | Name | Emphasize |
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Code | Name | Show |
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Download interaction data: 2BXT
Structure summary
Code : | 2BXT PDBj RCSB PDB PDBe | ||||||||||||||||||||||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||||||||||||||||||||||
Title : | Design and Discovery of Novel, Potent Thrombin Inhibitors with a Solubilizing Cationic P1-P2-Linker | ||||||||||||||||||||||||||||||||
Release Data : | 2006-10-26 | ||||||||||||||||||||||||||||||||
Compound : |
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Source : |
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Authors : | Bulat, S., Bosio, S., Grabowski, E., Papadopoulos, M.A., Cerezo-Galvez, S., Rosenbaum, C., Matassa, V.G., Ott, I., Metz, G., Schamberger, J., Sekul, R., Feurer, A. | ||||||||||||||||||||||||||||||||
Keywords : | SERINE PROTEINASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX | ||||||||||||||||||||||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.83 Å ) | ||||||||||||||||||||||||||||||||
Citation : |
Design and Discovery of Novel, Potent Pyrazinone-Based Thrombin Inhibitors with a Solubilizing P1-P2-Linker
Bulat, S.,Bosio, S.,Papadopoulos, M.A.
et al.
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Reaction
Chain : | L | ||||||||
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UniProt : | P00734 (THRB_HUMAN) | ||||||||
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Chain : | I |
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UniProt : | P09945 (HIRV2_HIRME) |
Reaction : | - |