6g74

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m (Protected "6g74" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 6g74 is ON HOLD
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==Structure of the Y21F variant of quinolinate synthase in complex with phthalate==
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<StructureSection load='6g74' size='340' side='right' caption='[[6g74]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6g74]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6G74 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6G74 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=PHT:PHTHALIC+ACID'>PHT</scene>, <scene name='pdbligand=SF4:IRON/SULFUR+CLUSTER'>SF4</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6f48|6f48]], [[6f4d|6f4d]], [[6f4l|6f4l]]</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/Quinolinate_synthase Quinolinate synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.5.1.72 2.5.1.72] </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=6g74 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6g74 OCA], [http://pdbe.org/6g74 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6g74 RCSB], [http://www.ebi.ac.uk/pdbsum/6g74 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6g74 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/NADA_THEMA NADA_THEMA]] Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity).
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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NadA is a multifunctional enzyme that condenses dihydroxyacetone phosphate (DHAP) with iminoaspartate (IA) to generate quinolinic acid (QA), the universal precursor of the nicotinamide adenine dinucleotide (NAD(P)) cofactor. Using X-ray crystallography, we have (i) characterized two of the reaction intermediates of QA synthesis using a "pH-shift" approach and a slowly reacting Thermotoga maritima NadA variant and (ii) observed the QA product, resulting from the degradation of an intermediate analogue, bound close to the entrance of a long tunnel leading to the solvent medium. We have also used molecular docking to propose a condensation mechanism between DHAP and IA based on two previously published Pyrococcus horikoshi NadA structures. The combination of reported data and our new results provide a structure-based complete catalytic sequence of QA synthesis by NadA.
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Authors: Volbeda, A., Fontecilla-Camps, J.C.
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Crystallographic Trapping of Reaction Intermediates in Quinolinic Acid Synthesis by NadA.,Volbeda A, Saez Cabodevilla J, Darnault C, Gigarel O, Han TH, Renoux O, Hamelin O, Ollagnier-de-Choudens S, Amara P, Fontecilla-Camps JC ACS Chem Biol. 2018 Apr 19. doi: 10.1021/acschembio.7b01104. PMID:29641168<ref>PMID:29641168</ref>
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Description: Structure of the Y21F variant of quinolinate synthase in complex with phthalate
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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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<div class="pdbe-citations 6g74" style="background-color:#fffaf0;"></div>
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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: Quinolinate synthase]]
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[[Category: Fontecilla-Camps, J C]]
[[Category: Volbeda, A]]
[[Category: Volbeda, A]]
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[[Category: Fontecilla-Camps, J.C]]
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[[Category: Iron sulfur cluster]]
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[[Category: Nad biosynthesis]]
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[[Category: Transferase]]

Revision as of 05:39, 25 April 2018

Structure of the Y21F variant of quinolinate synthase in complex with phthalate

6g74, resolution 2.00Å

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