7zbp

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==Unspecific peroxygenase from Marasmius rotula==
==Unspecific peroxygenase from Marasmius rotula==
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<StructureSection load='7zbp' size='340' side='right'caption='[[7zbp]]' scene=''>
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<StructureSection load='7zbp' size='340' side='right'caption='[[7zbp]], [[Resolution|resolution]] 1.45&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7ZBP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZBP FirstGlance]. <br>
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<table><tr><td colspan='2'>[[7zbp]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7ZBP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZBP FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7zbp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zbp OCA], [https://pdbe.org/7zbp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zbp RCSB], [https://www.ebi.ac.uk/pdbsum/7zbp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zbp ProSAT]</span></td></tr>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Unspecific_peroxygenase Unspecific peroxygenase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.2.1 1.11.2.1] </span></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=7zbp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zbp OCA], [https://pdbe.org/7zbp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zbp RCSB], [https://www.ebi.ac.uk/pdbsum/7zbp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zbp ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Unspecific peroxygenases (UPOs) are extracellular fungal enzymes of biotechnological interest as self-sufficient (and more stable) counterparts of cytochrome P450 monooxygenases, the latter being present in most living cells. Expression hosts and structural information are crucial for exploiting UPO diversity (over eight thousand UPO-type genes were identified in sequenced genomes) in target reactions of industrial interest. However, while many thousands of entries in the Protein Data Bank include molecular coordinates of P450 enzymes, only 19 entries correspond to UPO enzymes, and UPO structures from only two species (Agrocybe aegerita and Hypoxylon sp.) have been published to date. In the present study, two UPOs from the basidiomycete Marasmius rotula (rMroUPO) and the ascomycete Collariella virescens (rCviUPO) were crystallized after sequence optimization and Escherichia coli expression as active soluble enzymes. Crystals of rMroUPO and rCviUPO were obtained at sufficiently high resolution (1.45 and 1.95 A, respectively) and the corresponding structures were solved by molecular replacement. The crystal structures of the two enzymes (and two mutated variants) showed dimeric proteins. Complementary biophysical and molecular biology studies unveiled the diverse structural bases of the dimeric nature of the two enzymes. Intermolecular disulfide bridge and parallel association between two alpha-helices, among other interactions, were identified at the dimer interfaces. Interestingly, one of the rCviUPO variants incorporated the ability to produce fatty acid diepoxides-reactive compounds with valuable cross-linking capabilities-due to removal of the enzyme C-terminal tail located near the entrance of the heme access channel. In conclusion, different dimeric arrangements could be described in (short) UPO crystal structures.
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Structural Characterization of Two Short Unspecific Peroxygenases: Two Different Dimeric Arrangements.,Linde D, Santillana E, Fernandez-Fueyo E, Gonzalez-Benjumea A, Carro J, Gutierrez A, Martinez AT, Romero A Antioxidants (Basel). 2022 Apr 30;11(5). pii: antiox11050891. doi:, 10.3390/antiox11050891. PMID:35624755<ref>PMID:35624755</ref>
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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 7zbp" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Romero A]]
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[[Category: Unspecific peroxygenase]]
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[[Category: Santillana E]]
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[[Category: Romero, A]]
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[[Category: Santillana, E]]
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[[Category: Fatty acid epoxidation]]
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[[Category: Marasmius rotula]]
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[[Category: Molecular structure]]
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[[Category: Oxidoreductase]]
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[[Category: Short upo family]]

Revision as of 05:38, 8 June 2022

Unspecific peroxygenase from Marasmius rotula

PDB ID 7zbp

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