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7aba

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'''Unreleased structure'''
 
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The entry 7aba is ON HOLD
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==The structure of the Bottromycin biosynthetic protein SalCYP==
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<StructureSection load='7aba' size='340' side='right'caption='[[7aba]], [[Resolution|resolution]] 1.85&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7aba]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Salinispora_tropica Salinispora tropica]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7ABA OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ABA 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]] 1.8500232&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=HEC:HEME+C'>HEC</scene></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=7aba FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7aba OCA], [https://pdbe.org/7aba PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7aba RCSB], [https://www.ebi.ac.uk/pdbsum/7aba PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7aba ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Bottromycins are ribosomally synthesized and post-translationally modified peptide natural product antibiotics that are effective against high-priority human pathogens such as methicillin-resistant Staphylococcus aureus. The total synthesis of bottromycins involves at least 17 steps, with a poor overall yield. Here, we report the characterization of the cytochrome P450 enzyme BotCYP from a bottromycin biosynthetic gene cluster. We determined the structure of a close BotCYP homolog and used our data to conduct the first large-scale survey of P450 enzymes associated with RiPP biosynthetic gene clusters. We demonstrate that BotCYP converts a C-terminal thiazoline to a thiazole via an oxidative decarboxylation reaction and provides stereochemical resolution for the pathway. Our data enable the two-pot in vitro production of the bottromycin core scaffold and may allow the rapid generation of bottromycin analogues for compound development.
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Authors: Adam, S., Koehnke, J.
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Characterization of the Stereoselective P450 Enzyme BotCYP Enables the In Vitro Biosynthesis of the Bottromycin Core Scaffold.,Adam S, Franz L, Milhim M, Bernhardt R, Kalinina OV, Koehnke J J Am Chem Soc. 2020 Dec 9;142(49):20560-20565. doi: 10.1021/jacs.0c10361. Epub, 2020 Nov 28. PMID:33249843<ref>PMID:33249843</ref>
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Description: The structure of the Bottromycin biosynthetic protein SalCYP
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Adam, S]]
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<div class="pdbe-citations 7aba" style="background-color:#fffaf0;"></div>
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[[Category: Koehnke, J]]
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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: Large Structures]]
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[[Category: Salinispora tropica]]
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[[Category: Adam S]]
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[[Category: Koehnke J]]

Current revision

The structure of the Bottromycin biosynthetic protein SalCYP

PDB ID 7aba

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