3nfr

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==Casimiroin analog inhibitor of quinone reductase 2==
==Casimiroin analog inhibitor of quinone reductase 2==
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<StructureSection load='3nfr' size='340' side='right' caption='[[3nfr]], [[Resolution|resolution]] 1.57&Aring;' scene=''>
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<StructureSection load='3nfr' size='340' side='right'caption='[[3nfr]], [[Resolution|resolution]] 1.57&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[3nfr]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3NFR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3NFR FirstGlance]. <br>
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<table><tr><td colspan='2'>[[3nfr]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3NFR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3NFR FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=EWQ:6,8-DIMETHOXY-1,4-DIMETHYLQUINOLIN-2(1H)-ONE'>EWQ</scene>, <scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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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]] 1.57&#8491;</td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3g5m|3g5m]], [[3gam|3gam]]</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=EWQ:6,8-DIMETHOXY-1,4-DIMETHYLQUINOLIN-2(1H)-ONE'>EWQ</scene>, <scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">NQO2, NMOR2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=3nfr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3nfr OCA], [https://pdbe.org/3nfr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3nfr RCSB], [https://www.ebi.ac.uk/pdbsum/3nfr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3nfr ProSAT]</span></td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Ribosyldihydronicotinamide_dehydrogenase_(quinone) Ribosyldihydronicotinamide dehydrogenase (quinone)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.10.99.2 1.10.99.2] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3nfr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3nfr OCA], [http://pdbe.org/3nfr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3nfr RCSB], [http://www.ebi.ac.uk/pdbsum/3nfr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3nfr ProSAT]</span></td></tr>
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</table>
</table>
== Function ==
== Function ==
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[[http://www.uniprot.org/uniprot/NQO2_HUMAN NQO2_HUMAN]] The enzyme apparently serves as a quinone reductase in connection with conjugation reactions of hydroquinones involved in detoxification pathways as well as in biosynthetic processes such as the vitamin K-dependent gamma-carboxylation of glutamate residues in prothrombin synthesis.<ref>PMID:18254726</ref>
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[https://www.uniprot.org/uniprot/NQO2_HUMAN NQO2_HUMAN] The enzyme apparently serves as a quinone reductase in connection with conjugation reactions of hydroquinones involved in detoxification pathways as well as in biosynthetic processes such as the vitamin K-dependent gamma-carboxylation of glutamate residues in prothrombin synthesis.<ref>PMID:18254726</ref>
==See Also==
==See Also==
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*[[Quinone reductase|Quinone reductase]]
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*[[Quinone reductase 3D structures|Quinone reductase 3D structures]]
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Human]]
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[[Category: Homo sapiens]]
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[[Category: Cushman, M]]
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[[Category: Large Structures]]
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[[Category: Jermihov, K]]
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[[Category: Cushman M]]
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[[Category: Maiti, A]]
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[[Category: Jermihov K]]
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[[Category: Mesecar, A D]]
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[[Category: Maiti A]]
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[[Category: Sturdy, M]]
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[[Category: Mesecar AD]]
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[[Category: Nq02]]
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[[Category: Sturdy M]]
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[[Category: Oxidoreductase-oxidoreductase inhibitor complex]]
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[[Category: Qr2]]
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[[Category: Quinone reductase 2]]
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Current revision

Casimiroin analog inhibitor of quinone reductase 2

PDB ID 3nfr

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