PDB ID: 3V7T
Hetero Atom Contents
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0GX | {(3-exo)-3-[5-(aminomethyl)-2-fluorophenyl]-8-azabicyclo[3.2.1]oct-8-yl}(4-bromo-3-methyl-5-propoxythiophen-2-yl)methanone | PoSSuM | |||
CO3 | Carbonate ion | PoSSuM |
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Download interaction data: 3V7T
Structure summary
Code : | 3V7T PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | Crystal Structure of Human Beta-Tryptase Complexed with a Synthetic Inhibitor with a Tropanylamide Scaffold | ||||||||||||
Release Data : | 2012-03-14 | ||||||||||||
Compound : |
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Authors : | Zhang, Y., Colonna, C., Michot, N. | ||||||||||||
Keywords : | tryptase, serine protease, tetramer, protein-ligand complex, HYDROLASE-HYDROLASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.0900 Å ) | ||||||||||||
Citation : |
A beta-tryptase inhibitor with a tropanylamide scaffold to improve in vitro stability and to lower hERG channel binding affinity
Liang, G.,Choi-Sledeski, Y.M.,Shum, P.
et al.
PubMed: 22264487 |
Reaction
Chain : | A, B, C, D |
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UniProt : | Q6NZY1 (Q6NZY1_HUMAN) |
Reaction : | - |