6ev3: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The entry 6ev3 is ON HOLD until Paper Publication~~

==Structure of wild type A. niger Fdc1 that has been illuminated with UV light, with prFMN in the iminium and ketimine form==

~~Authors: Bailey, S.S., David, L., Payne, K.A.P.~~

== Structural highlights ==

<table><tr><td colspan='2'>[[6ev3]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EV3 OCA]. For a guided tour on the structure components use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EV3 FirstGlance].

~~Description:~~ Structure of wild type A. niger Fdc1 that has been illuminated with UV light, with prFMN in the iminium and ketimine form

</td></tr><tr id='ligand'><td class="sblockLbl">[[Ligand|Ligands:]]</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=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>

[[~~Category~~: ~~Unreleased Structures~~]]

<tr id='activity'><td class="sblockLbl">Activity:</td><td class="sblockDat">[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] </td></tr>

[[~~Category~~: ~~Payne~~, K.A.P]]

<tr id='resources'><td class="sblockLbl">Resources:</td><td class="sblockDat">[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6ev3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ev3 OCA], [http://pdbe.org/6ev3 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ev3 RCSB], [http://www.ebi.ac.uk/pdbsum/6ev3 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ev3 ProSAT]</td></tr>

[[Category: Bailey, S.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 ==

__TOC__

</StructureSection>

[[Category: Phenacrylate decarboxylase]]

[[Category: Bailey, S S]]

[[Category: David, L]]

[[Category: Payne, K A.P]]

[[Category: Lyase]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 6ev3 is ON HOLD  until Paper Publication
+==Structure of wild type A. niger Fdc1 that has been illuminated with UV light, with prFMN in the iminium and ketimine form==
+<StructureSection load='6ev3' size='340' side='right' caption='[[6ev3]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
-Authors: Bailey, S.S., David, L., Payne, K.A.P.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6ev3]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EV3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6EV3 FirstGlance]. <br>
-Description: Structure of wild type A. niger Fdc1 that has been illuminated with UV light, with prFMN in the iminium and ketimine form
+</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=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>
-[[Category: Unreleased Structures]]
+<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: Payne, K.A.P]]
+<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=6ev3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ev3 OCA], [http://pdbe.org/6ev3 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6ev3 RCSB], [http://www.ebi.ac.uk/pdbsum/6ev3 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6ev3 ProSAT]</span></td></tr>
-[[Category: Bailey, S.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: Payne, K A.P]]
+[[Category: Lyase]]