9v34: Difference between revisions

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'''Unreleased structure'''


The entry 9v34 is ON HOLD  until Paper Publication
==Crystal structure of DHODH inhibitor HL6 in complex with DHODH==
 
<StructureSection load='9v34' size='340' side='right'caption='[[9v34]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
Authors: Jun, L., Xi, L., Zhaomin, X., Caiyue, C., Yuanyuan, Z.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9v34]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9V34 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9V34 FirstGlance]. <br>
Description: Crystal structure of DHODH inhibitor HL6 in complex with DHODH
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1EZL:(4~{R})-2-[[2-(cyclobutylmethoxy)-3-phenyl-phenyl]amino]-4,5,6,7-tetrahydro-1,3-benzothiazol-4-ol'>A1EZL</scene>, <scene name='pdbligand=FMN:FLAVIN+MONONUCLEOTIDE'>FMN</scene>, <scene name='pdbligand=ORO:OROTIC+ACID'>ORO</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
[[Category: Jun, L]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9v34 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9v34 OCA], [https://pdbe.org/9v34 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9v34 RCSB], [https://www.ebi.ac.uk/pdbsum/9v34 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9v34 ProSAT]</span></td></tr>
[[Category: Xi, L]]
</table>
[[Category: Caiyue, C]]
== Disease ==
[[Category: Zhaomin, X]]
[https://www.uniprot.org/uniprot/PYRD_HUMAN PYRD_HUMAN] Defects in DHODH are the cause of postaxial acrofacial dysostosis (POADS) [MIM:[https://omim.org/entry/263750 263750]; also known as Miller syndrome. POADS is characterized by severe micrognathia, cleft lip and/or palate, hypoplasia or aplasia of the posterior elements of the limbs, coloboma of the eyelids and supernumerary nipples. POADS is a very rare disorder: only 2 multiplex families, each consisting of 2 affected siblings born to unaffected, nonconsanguineous parents, have been described among a total of around 30 reported cases.<ref>PMID:19915526</ref>
[[Category: Yuanyuan, Z]]
== Function ==
[https://www.uniprot.org/uniprot/PYRD_HUMAN PYRD_HUMAN] Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Caiyue C]]
[[Category: Jun L]]
[[Category: Xi L]]
[[Category: Yuanyuan Z]]
[[Category: Zhaomin X]]
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