7e5v

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(New page: '''Unreleased structure''' The entry 7e5v is ON HOLD Authors: Description: Category: Unreleased Structures)
Current revision (07:11, 3 April 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 7e5v is ON HOLD
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==Crystal structure of Phm7 in complex with inhibitor==
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<StructureSection load='7e5v' size='340' side='right'caption='[[7e5v]], [[Resolution|resolution]] 1.61&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7e5v]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Pyrenochaetopsis_sp. Pyrenochaetopsis sp.]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7E5V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7E5V FirstGlance]. <br>
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Description:
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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]] 1.61&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=HZC:[(1S,2S,5R)-5-methyl-2-propan-2-yl-cyclohexyl]methanamine'>HZC</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</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=7e5v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7e5v OCA], [https://pdbe.org/7e5v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7e5v RCSB], [https://www.ebi.ac.uk/pdbsum/7e5v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7e5v ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/PHM7_PYRSX PHM7_PYRSX] Diels-Alderase; part of the gene cluster that mediates the biosynthesis of the trans-fused decalin-containing tetramic acid phomasetin, the stereochemical opposite of the HIV-1 integrase inhibitor equisetin (PubMed:29972614). The PKS module of phm1 together with the enoylreductase phm4 catalyze the formation of the polyketide unit which is then conjugated to L-serine by the condensation domain of the phm1 NRPS module (PubMed:29972614). Activity of the Dieckmann cyclase domain (RED) of phm1 results in release of the Dieckmann product intermediate (PubMed:29972614). The Diels-Alderase phm7 then uses the Dieckmann product of phm1 as substrate and catalyzes the Diels-Alder cycloaddition to form the decalin ring of N-desmethylphomasetin (PubMed:29972614, PubMed:34121297). N-desmethylphomasetin is further methylated to phomasetin by the methyltransferase phm5 (PubMed:29972614).<ref>PMID:29972614</ref> <ref>PMID:34121297</ref>
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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: Pyrenochaetopsis sp]]
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[[Category: Fujiyama K]]
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[[Category: Hino T]]
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[[Category: Kato N]]
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[[Category: Kinugasa K]]
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[[Category: Nagano S]]
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[[Category: Takahashi S]]

Current revision

Crystal structure of Phm7 in complex with inhibitor

PDB ID 7e5v

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