5zrv
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | The entry | + | ==Structure of human mitochondrial trifunctional protein, octamer== |
| - | + | <StructureSection load='5zrv' size='340' side='right' caption='[[5zrv]], [[Resolution|resolution]] 7.70Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5zrv]] is a 8 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5ZRV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5ZRV FirstGlance]. <br> | |
| - | + | </td></tr><tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Acetyl-CoA_C-acyltransferase Acetyl-CoA C-acyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.16 2.3.1.16] </span></td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5zrv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5zrv OCA], [http://pdbe.org/5zrv PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5zrv RCSB], [http://www.ebi.ac.uk/pdbsum/5zrv PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5zrv ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Disease == | ||
| + | [[http://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. [[http://www.uniprot.org/uniprot/ECHB_HUMAN ECHB_HUMAN]] Mitochondrial trifunctional protein deficiency. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/ECHA_HUMAN ECHA_HUMAN]] Bifunctional subunit. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Acetyl-CoA C-acyltransferase]] | ||
| + | [[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]] | ||
| + | [[Category: Cryo-em single-particle reconstruction]] | ||
| + | [[Category: Fatty acid beta-oxidation]] | ||
| + | [[Category: Liase]] | ||
| + | [[Category: Mitochondrial trifunctional protein]] | ||
| + | [[Category: Oxidoreductase-transferase complex]] | ||
Revision as of 05:45, 20 June 2018
Structure of human mitochondrial trifunctional protein, octamer
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