9n1s: Difference between revisions

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'''Unreleased structure'''


The entry 9n1s is ON HOLD  until Paper Publication
==Crystal structure of the Transport and Golgi Organization protein 2 Homolog (TANGO2) tetragonal form==
 
<StructureSection load='9n1s' size='340' side='right'caption='[[9n1s]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
Authors: Lovell, S., Cooper, A., Powers, A., Battaile, K.P., Moshen, A.W., Ghaloul-Gonzalez, L.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9n1s]] is a 1 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=9N1S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9N1S FirstGlance]. <br>
Description: Crystal structure of the Transport and Golgi Organization protein 2 Homolog (TANGO2) tetragonal form
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3&#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=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=OCS:CYSTEINESULFONIC+ACID'>OCS</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
[[Category: Battaile, K.P]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9n1s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9n1s OCA], [https://pdbe.org/9n1s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9n1s RCSB], [https://www.ebi.ac.uk/pdbsum/9n1s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9n1s ProSAT]</span></td></tr>
[[Category: Ghaloul-Gonzalez, L]]
</table>
[[Category: Cooper, A]]
== Disease ==
[[Category: Moshen, A.W]]
[https://www.uniprot.org/uniprot/TNG2_HUMAN TNG2_HUMAN] Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome. The disease is caused by variants affecting the gene represented in this entry.
[[Category: Powers, A]]
== Function ==
[[Category: Lovell, S]]
[https://www.uniprot.org/uniprot/TNG2_HUMAN TNG2_HUMAN] May be involved in lipid homeostasis.<ref>PMID:36961129</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Battaile KP]]
[[Category: Cooper A]]
[[Category: Ghaloul-Gonzalez L]]
[[Category: Lovell S]]
[[Category: Moshen AW]]
[[Category: Powers A]]
Retrieved from "https://proteopedia.org/9n1s"