7oqf

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Current revision (09:03, 17 October 2024) (edit) (undo)
 
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7oqf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7oqf OCA], [https://pdbe.org/7oqf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7oqf RCSB], [https://www.ebi.ac.uk/pdbsum/7oqf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7oqf 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=7oqf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7oqf OCA], [https://pdbe.org/7oqf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7oqf RCSB], [https://www.ebi.ac.uk/pdbsum/7oqf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7oqf ProSAT]</span></td></tr>
</table>
</table>
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== Disease ==
 
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[https://www.uniprot.org/uniprot/UMPS_HUMAN UMPS_HUMAN] Defects in UMPS are the cause of orotic aciduria type 1 (ORAC1) [MIM:[https://omim.org/entry/258900 258900]. A disorder of pyrimidine metabolism resulting in megaloblastic anemia and orotic acid crystalluria that is frequently associated with some degree of physical and mental retardation. A minority of cases have additional features, particularly congenital malformations and immune deficiencies.<ref>PMID:9042911</ref>
 
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== Function ==
 
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[https://www.uniprot.org/uniprot/UMPS_HUMAN UMPS_HUMAN]
 
==See Also==
==See Also==
*[[Uridine 5'-monophosphate synthase 3D structures|Uridine 5'-monophosphate synthase 3D structures]]
*[[Uridine 5'-monophosphate synthase 3D structures|Uridine 5'-monophosphate synthase 3D structures]]
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== References ==
 
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<references/>
 
__TOC__
__TOC__
</StructureSection>
</StructureSection>

Current revision

Human OMPD-domain of UMPS in complex with OMP at 1.05 Angstrom resolution, 5 minutes soaking

PDB ID 7oqf

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