4gqi

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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=4gqi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gqi OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4gqi RCSB], [http://www.ebi.ac.uk/pdbsum/4gqi PDBsum]</span></td></tr>
<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=4gqi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gqi OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4gqi RCSB], [http://www.ebi.ac.uk/pdbsum/4gqi PDBsum]</span></td></tr>
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== 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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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==

Revision as of 01:47, 25 December 2014

Synthesis of novel MT3 receptor ligands via unusual Knoevenagel condensation

4gqi, resolution 1.95Å

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