3k46

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'''Unreleased structure'''
 
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The entry 3k46 is ON HOLD until Paper Publication
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==Crystal structure of full-length E. coli beta-glucuronidase==
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<StructureSection load='3k46' size='340' side='right'caption='[[3k46]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3k46]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Escherichia_coli_K-12 Escherichia coli K-12]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3K46 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3K46 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.5&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3k46 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3k46 OCA], [https://pdbe.org/3k46 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3k46 RCSB], [https://www.ebi.ac.uk/pdbsum/3k46 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3k46 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/BGLR_ECOLI BGLR_ECOLI]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The dose-limiting side effect of the common colon cancer chemotherapeutic CPT-11 is severe diarrhea caused by symbiotic bacterial beta-glucuronidases that reactivate the drug in the gut. We sought to target these enzymes without killing the commensal bacteria essential for human health. Potent bacterial beta-glucuronidase inhibitors were identified by high-throughput screening and shown to have no effect on the orthologous mammalian enzyme. Crystal structures established that selectivity was based on a loop unique to bacterial beta-glucuronidases. Inhibitors were highly effective against the enzyme target in living aerobic and anaerobic bacteria, but did not kill the bacteria or harm mammalian cells. Finally, oral administration of an inhibitor protected mice from CPT-11-induced toxicity. Thus, drugs may be designed to inhibit undesirable enzyme activities in essential microbial symbiotes to enhance chemotherapeutic efficacy.
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Authors: Wallace, B.D., Lane, K.T., Redinbo, M.R.
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Alleviating cancer drug toxicity by inhibiting a bacterial enzyme.,Wallace BD, Wang H, Lane KT, Scott JE, Orans J, Koo JS, Venkatesh M, Jobin C, Yeh LA, Mani S, Redinbo MR Science. 2010 Nov 5;330(6005):831-5. PMID:21051639<ref>PMID:21051639</ref>
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Description: Crystal structure of full-length E. coli beta-glucuronidase
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 3k46" style="background-color:#fffaf0;"></div>
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 21 10:00:32 2009''
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==See Also==
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*[[Glucuronisidase 3D structures|Glucuronisidase 3D structures]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Escherichia coli K-12]]
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[[Category: Large Structures]]
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[[Category: Lane KT]]
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[[Category: Redinbo MR]]
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[[Category: Wallace BD]]

Current revision

Crystal structure of full-length E. coli beta-glucuronidase

PDB ID 3k46

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