4js3: Difference between revisions

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'''Unreleased structure'''
{{STRUCTURE_4js3|  PDB=4js3  |  SCENE=  }}
===Crystal structure of human dihydroorotate dehydrogenase (DHODH) with 057===


The entry 4js3 is ON HOLD until Paper Publication
==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>  


Authors: Zhu, L.,, Li, H.,, Zhu, J.,, Ren, X.,
==Function==
[[http://www.uniprot.org/uniprot/PYRD_HUMAN PYRD_HUMAN]] Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.  


Description: Crystal structure of human dihydroorotate dehydrogenase (DHODH) with 057
==About this Structure==
[[4js3]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4JS3 OCA].
 
==Reference==
<references group="xtra"/><references/>
[[Category: Li, H.]]
[[Category: Ren, X.]]
[[Category: Zhu, J.]]
[[Category: Zhu, L.]]
[[Category: Fmn binding]]
[[Category: Mitochondrion inner membrane]]
[[Category: Oxidoreductase]]
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