6ev6
From Proteopedia
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- | '''Unreleased structure''' | ||
- | + | ==Structure of E282Q A. niger Fdc1 with prFMN in the hydroxylated and ketimine forms== | |
- | + | <StructureSection load='6ev6' size='340' side='right' caption='[[6ev6]], [[Resolution|resolution]] 1.10Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[6ev6]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EV6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EV6 FirstGlance]. <br> | |
- | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BYN:hydroxylated+prenyl-FMN'>BYN</scene>, <scene name='pdbligand=FZZ:1-DEOXY-5-O-PHOSPHONO-1-[(10AR)-2,2,3,4-TETRAMETHYL-8,10-DIOXO-1,2,8,9,10,10A-HEXAHYDRO-6H-INDENO[1,7-EF]PYRIMIDO[4,5-B][1,4]DIAZEPIN-6-YL]-D-RIBITOL'>FZZ</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> | |
- | [[Category: | + | <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=6ev6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ev6 OCA], [http://pdbe.org/6ev6 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ev6 RCSB], [http://www.ebi.ac.uk/pdbsum/6ev6 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ev6 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 06:27, 20 December 2017
Structure of E282Q A. niger Fdc1 with prFMN in the hydroxylated and ketimine forms
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