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Ligands
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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
CO3 Carbonate ion
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Glycosylation
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Code : 3V7T   PDBj   RCSB PDB   PDBe
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 :
mol_id molecule chains
1 TPSB2 protein A,B,C,D
fragment: unp residues 38-282
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Komagataella pastoris  (taxid:4922)
gene: TPSB2
expression_system_common: Pichia pastoris
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.
(2012)  Bioorg.Med.Chem.Lett.  22 : 1606 - 1610

PubMed: 22264487
DOI: 10.1016/j.bmcl.2011.12.127

Chain : A, B, C, D
UniProt : Q6NZY1 (Q6NZY1_HUMAN)
Reaction : -