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Ligands
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28G 1-{5-[2-(morpholin-4-yl)ethoxy]-6-(pyridin-3-yl)[1,3]thiazolo[5,4-B]pyridin-2-yl}-3-prop-2-en-1-ylurea
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Code : 4MBC   PDBj   RCSB PDB   PDBe
Header : ISOMERASE/ISOMERASE INHIBITOR
Title : Structure of Streptococcus pneumonia ParE in complex with AZ13053807
Release Data : 2013-10-16
Compound :
mol_id molecule chains
1 DNA topoisomerase IV, B subunit A
ec: 5.99.1.-
fragment: ATPase domain (UNP residues 1-226)
Source :
mol_id organism_scientific expression_system
1 Streptococcus pneumoniae  (taxid:760835) Escherichia coli  (taxid:469008)
strain: GA47373
gene: SPAR94_0831
expression_system_strain: Bl21(de3)
expression_system_vector_type: Plasmid
Authors : Ogg, D., Tucker, J.
Keywords : ATP binding, structure-based drug design, antimicrobial, ISOMERASE-ISOMERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.75 Å )
Citation :

Thiazolopyridine Ureas as Novel Antitubercular Agents Acting through Inhibition of DNA Gyrase B.

Kale, M.G.,Raichurkar, A.,Hameed, S.P.  et al.
(2013)  J.Med.Chem.  56 : 8834 - 8848

PubMed: 24088190
DOI: 10.1021/jm401268f

Chain : A
UniProt : G6TGY9
Reaction : -