View source for 5zqz


==Structure of human mitochondrial trifunctional protein, tetramer==
<SX load='5zqz' size='340' side='right' viewer='molstar' caption='[[5zqz]], [[Resolution|resolution]] 4.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[5zqz]] 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=5ZQZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5ZQZ 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]] 4.2&#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=5zqz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5zqz OCA], [https://pdbe.org/5zqz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5zqz RCSB], [https://www.ebi.ac.uk/pdbsum/5zqz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5zqz ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/ECHA_HUMAN ECHA_HUMAN] Mitochondrial trifunctional protein deficiency;Acute fatty liver of pregnancy;Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/ECHA_HUMAN ECHA_HUMAN] Bifunctional subunit.
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</SX>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Chen X]]
[[Category: Dai J]]
[[Category: Gao N]]
[[Category: Li N]]
[[Category: Liang K]]
[[Category: Liu P]]
[[Category: Wang C]]
[[Category: Wang X]]
[[Category: Xiao J]]