6ev4
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure of wild type A. niger Fdc1 purified in the dark with prFMN in the iminium form== | |
| - | + | <StructureSection load='6ev4' size='340' side='right' caption='[[6ev4]], [[Resolution|resolution]] 1.14Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6ev4]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EV4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EV4 FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=4LU:1-DEOXY-5-O-PHOSPHONO-1-(3,3,4,5-TETRAMETHYL-9,11-DIOXO-2,3,8,9,10,11-HEXAHYDRO-7H-QUINOLINO[1,8-FG]PTERIDIN-12-IUM-7-YL)-D-RIBITOL'>4LU</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=MN:MANGANESE+(II)+ION'>MN</scene></td></tr> | |
| - | [[ | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Phenacrylate_decarboxylase Phenacrylate decarboxylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.1.1.102 4.1.1.102] </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=6ev4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ev4 OCA], [http://pdbe.org/6ev4 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ev4 RCSB], [http://www.ebi.ac.uk/pdbsum/6ev4 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ev4 ProSAT]</span></td></tr> |
| - | [[Category: Bailey, S | + | </table> |
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/FDC1_ASPNC FDC1_ASPNC]] Catalyzes the reversible decarboxylation of aromatic carboxylic acids like ferulic acid, p-coumaric acid or cinnamic acid, producing the corresponding vinyl derivatives 4-vinylphenol, 4-vinylguaiacol, and styrene, respectively, which play the role of aroma metabolites.[HAMAP-Rule:MF_03196]<ref>PMID:26083754</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Phenacrylate decarboxylase]] | ||
| + | [[Category: Bailey, S S]] | ||
[[Category: David, L]] | [[Category: David, L]] | ||
| + | [[Category: Payne, K A.P]] | ||
| + | [[Category: Lyase]] | ||
Revision as of 08:44, 27 December 2017
Structure of wild type A. niger Fdc1 purified in the dark with prFMN in the iminium form
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