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Ligands
Code Name Style Show Link
ACT Acetate ion
C1P N~2~-(morpholin-4-ylcarbonyl)-N-[(3s)-1-phenyl-5-(phenylsulfonyl)pentan-3-yl]-L-leucinamide
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Code : 3S3Q   PDBj   RCSB PDB   PDBe
Header : HYDROLASE/HYDROLASE INHIBITOR
Title : Structure of cathepsin B1 from Schistosoma mansoni in complex with K11017 inhibitor
Release Data : 2011-08-10
Compound :
mol_id molecule chains synonym
1 Cathepsin B-like peptidase (C01 family) A Cathepsin B1 isotype 1
ec: 3.4.22.1
fragment: UNP residues 87-340
mutation: T168A, T283A
Source :
mol_id organism_scientific organism_common expression_system
1 Schistosoma mansoni  (taxid:6183) Blood fluke Pichia pastoris  (taxid:4922)
gene: cb1.1, Smp_103610
expression_system_strain: X33
expression_system_vector_type: plasmid
expression_system_plasmid: pPICZalphaA
Authors : Rezacova, P., Jilkova, A., Brynda, J., Horn, M., Mares, M.
Keywords : peptidase, digestive tract, HYDROLASE-HYDROLASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.80 Å )
Citation :

Structural Basis for Inhibition of Cathepsin B Drug Target from the Human Blood Fluke, Schistosoma mansoni.

Jilkova, A.,Rezacova, P.,Lepsik, M.  et al.
(2011)  J.Biol.Chem.  286 : 35770 - 35781

PubMed: 21832058
DOI: 10.1074/jbc.M111.271304

Chain : A
UniProt : Q8MNY2 (Q8MNY2_SCHMA)
Reaction : -