3w7r: Difference between revisions
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{{STRUCTURE_3w7r| PDB=3w7r | SCENE= }} | |||
===Structure of Human dihydroorotate dehydrogenase in complex with mii-4-097=== | |||
==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== | |||
[[3w7r]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3W7R OCA]. | |||
==Reference== | |||
<references group="xtra"/><references/> | |||
[[Category: Aoki, T.]] | |||
[[Category: Balogun, E O.]] | |||
[[Category: Harada, S.]] | |||
[[Category: Hashimoto, S.]] | |||
[[Category: Honma, T.]] | |||
[[Category: Iida, M.]] | |||
[[Category: Inaoka, D K.]] | |||
[[Category: Inoue, M.]] | |||
[[Category: Kita, K.]] | |||
[[Category: Kuranaga, T.]] | |||
[[Category: Lee, N.]] | |||
[[Category: Matsuoka, S.]] | |||
[[Category: Nara, T.]] | |||
[[Category: Sakamoto, K.]] | |||
[[Category: Shiba, T.]] | |||
[[Category: Suzuki, S.]] | |||
[[Category: Tabuchi, T.]] | |||
[[Category: Tanaka, A.]] | |||
[[Category: Dihydroorotate/orotate and ubiquinone/ubiquinol]] | |||
[[Category: Mitochondrial inner membrane]] | |||
[[Category: Oxidoreductase]] | |||
[[Category: Oxidoreductase-oxidoreductase inhibitor complex]] | |||
[[Category: Rossmann fold]] | |||