6dv2
From Proteopedia
(Difference between revisions)
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal Structure of Human Mitochondrial Trifunctional Protein== | |
| - | + | <StructureSection load='6dv2' size='340' side='right' caption='[[6dv2]], [[Resolution|resolution]] 3.60Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6dv2]] is a 12 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DV2 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DV2 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=6dv2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dv2 OCA], [http://pdbe.org/6dv2 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6dv2 RCSB], [http://www.ebi.ac.uk/pdbsum/6dv2 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6dv2 ProSAT]</span></td></tr> |
| - | [[Category: Battaile, K | + | </table> |
| + | == Disease == | ||
| + | [[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. [[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. | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/ECHA_HUMAN ECHA_HUMAN]] Bifunctional subunit. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Acetyl-CoA C-acyltransferase]] | ||
| + | [[Category: Battaile, K P]] | ||
[[Category: Fu, Z]] | [[Category: Fu, Z]] | ||
| + | [[Category: Kim, J P]] | ||
[[Category: Xia, C]] | [[Category: Xia, C]] | ||
| - | [[Category: | + | [[Category: Fatty acid beta-oxidation]] |
| + | [[Category: Transferase]] | ||
| + | [[Category: Transferase-oxidoreductase complex]] | ||
Revision as of 08:05, 26 September 2018
Crystal Structure of Human Mitochondrial Trifunctional Protein
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