4ud8: Difference between revisions

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4ud8]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Arabidopsis_thaliana Arabidopsis thaliana]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UD8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4UD8 FirstGlance]. <br>
<table><tr><td colspan='2'>[[4ud8]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Arabidopsis_thaliana Arabidopsis thaliana]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UD8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4UD8 FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=PE5:3,6,9,12,15,18,21,24-OCTAOXAHEXACOSAN-1-OL'>PE5</scene></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.088&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=PE5:3,6,9,12,15,18,21,24-OCTAOXAHEXACOSAN-1-OL'>PE5</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4ud8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ud8 OCA], [https://pdbe.org/4ud8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4ud8 RCSB], [https://www.ebi.ac.uk/pdbsum/4ud8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4ud8 ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4ud8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ud8 OCA], [https://pdbe.org/4ud8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4ud8 RCSB], [https://www.ebi.ac.uk/pdbsum/4ud8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4ud8 ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
[https://www.uniprot.org/uniprot/BBE15_ARATH BBE15_ARATH] Required for endosperm development and polar nuclei fusion (PubMed:15634699). Mediates oxidation of cinnamyl alcohol and of p-hydroxylated derivatives of cinnamyl alcohol (i.e. the monolignols p-coumaryl-, coniferyl-, and sinapyl alcohol) to their corresponding aldehydes. Can use cinnamyl alcohol and derivatives, as well as beta-O-glycosylated form of coniferyl alcohol (coniferin) as substrate (PubMed:26037923).<ref>PMID:15634699</ref> <ref>PMID:26037923</ref>  
[https://www.uniprot.org/uniprot/BBE15_ARATH BBE15_ARATH] Required for endosperm development and polar nuclei fusion (PubMed:15634699). Mediates oxidation of p-hydroxylated derivatives of cinnamyl alcohol (i.e. the monolignols p-coumaryl-, coniferyl-, and sinapyl alcohol) to their corresponding aldehydes. Can also use the beta-O-glycosylated form of coniferyl alcohol (coniferin) as substrate, but is much less efficient towards cinnamyl alcohol. The electron acceptor required for these reactions is not known, but does not seem to be dioxygen (PubMed:26037923).<ref>PMID:15634699</ref> <ref>PMID:26037923</ref>  
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== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==

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