View source for 6hq9


==Crystal structure of the Tudor domain of human ERCC6-L2==
<StructureSection load='6hq9' size='340' side='right'caption='[[6hq9]], [[Resolution|resolution]] 1.98&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6hq9]] is a 2 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=6HQ9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6HQ9 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.982&#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=6hq9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6hq9 OCA], [https://pdbe.org/6hq9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6hq9 RCSB], [https://www.ebi.ac.uk/pdbsum/6hq9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6hq9 ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/ER6L2_HUMAN ER6L2_HUMAN] Pancytopenia-developmental delay syndrome. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/ER6L2_HUMAN ER6L2_HUMAN] May be involved in early DNA damage response.<ref>PMID:24507776</ref> 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Arrowsmith CH]]
[[Category: Bountra C]]
[[Category: Edwards A]]
[[Category: Gavard AE]]
[[Category: Gileadi O]]
[[Category: Nathan WJ]]
[[Category: Newman JA]]
[[Category: Pinkas DM]]
[[Category: Von Delft F]]