View source for 8xxq


==Structural of methylmalonate semialdehyde dehydrogenase ALDH6A1==
<StructureSection load='8xxq' size='340' side='right'caption='[[8xxq]], [[Resolution|resolution]] 2.75&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8xxq]] is a 4 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=8XXQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8XXQ FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.75&#8491;</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=8xxq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xxq OCA], [https://pdbe.org/8xxq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xxq RCSB], [https://www.ebi.ac.uk/pdbsum/8xxq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xxq ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/MMSA_HUMAN MMSA_HUMAN] Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency. The disease may be caused by variants affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/MMSA_HUMAN MMSA_HUMAN] Malonate and methylmalonate semialdehyde dehydrogenase involved in the catabolism of valine, thymine, and compounds catabolized by way of beta-alanine, including uracil and cytidine.<ref>PMID:23835272</ref> 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Luan X]]
[[Category: Su G]]
[[Category: Xu Y]]