3fj6: Difference between revisions
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{{STRUCTURE_3fj6| PDB=3fj6 | SCENE= }} | {{STRUCTURE_3fj6| PDB=3fj6 | SCENE= }} | ||
===Human dihydroorotate dehydrogenase in complex with a leflunomide derivative inhibitor 2=== | |||
{{ABSTRACT_PUBMED_19351152}} | |||
=== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/PYRD_HUMAN PYRD_HUMAN]] Defects in DHODH are the cause of postaxial acrofacial dysostosis (POADS) [MIM:[http://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> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/PYRD_HUMAN PYRD_HUMAN]] Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor. | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:019351152</ref><references group="xtra"/> | <ref group="xtra">PMID:019351152</ref><references group="xtra"/><references/> | ||
[[Category: Dihydroorotate oxidase]] | [[Category: Dihydroorotate oxidase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
