36ad: Difference between revisions

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'''Unreleased structure'''


The entry 36ad is ON HOLD
==Fumarate hydratase (human mitochondrial)==
 
<StructureSection load='36ad' size='340' side='right'caption='[[36ad]], [[Resolution|resolution]] 2.11&Aring;' scene=''>
Authors: Weaver, T.M., May, J.F., Bhattacharyya, B., Strauss, L.A.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[36ad]] 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=36AD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=36AD FirstGlance]. <br>
Description: Fumarate hydratase (human mitochondria)
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.11&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=TLA:L(+)-TARTARIC+ACID'>TLA</scene></td></tr>
[[Category: Bhattacharyya, B]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=36ad FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=36ad OCA], [https://pdbe.org/36ad PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=36ad RCSB], [https://www.ebi.ac.uk/pdbsum/36ad PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=36ad ProSAT]</span></td></tr>
[[Category: Weaver, T.M]]
</table>
[[Category: May, J.F]]
== Disease ==
[[Category: Strauss, L.A]]
[https://www.uniprot.org/uniprot/FUMH_HUMAN FUMH_HUMAN] Defects in FH are the cause of fumarase deficiency (FHD) [MIM:[https://omim.org/entry/606812 606812]; also known as fumaricaciduria. FHD is characterized by progressive encephalopathy, developmental delay, hypotonia, cerebral atrophy and lactic and pyruvic acidemia.[:]<ref>PMID:9635293</ref>  Defects in FH are the cause of hereditary leiomyomatosis and renal cell cancer (HLRCC) [MIM:[https://omim.org/entry/150800 150800]. A disorder characterized by predisposition to cutaneous and uterine leiomyomas, and papillary type 2 renal cancer which occurs in about 20% of patients.<ref>PMID:11865300</ref>
== Function ==
[https://www.uniprot.org/uniprot/FUMH_HUMAN FUMH_HUMAN] Also acts as a tumor suppressor.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Bhattacharyya B]]
[[Category: May JF]]
[[Category: Strauss LA]]
[[Category: Weaver TM]]

Latest revision as of 15:02, 10 June 2026

Fumarate hydratase (human mitochondrial)

36ad, resolution 2.11Å

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