8w15: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The entry~~ 8w15 is ~~ON HOLD~~

==HTT in complex with HAP40 in the apo state.==

~~Authors~~: ~~Poweleit~~, N., ~~Boudet~~, J., ~~Doherty~~, E.

== Structural highlights ==

<table><tr><td colspan='2'>[[8w15]] 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=8W15 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8W15 FirstGlance]. <br>

~~Description~~: ~~HTT~~ in ~~complex with HAP40~~ in ~~the apo state~~.

</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.72Å</td></tr>

[[Category: ~~Unreleased~~ Structures]]

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8w15 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8w15 OCA], [https://pdbe.org/8w15 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8w15 RCSB], [https://www.ebi.ac.uk/pdbsum/8w15 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8w15 ProSAT]</span></td></tr>

[[Category: Boudet, J]]

</table>

[[Category: Doherty, E]]

== Disease ==

[[Category: Poweleit, N]]

[https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] Juvenile Huntington disease;Huntington disease. The disease is caused by mutations affecting the gene represented in this entry.

== Function ==

[https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] May play a role in microtubule-mediated transport or vesicle function.

__TOC__

</StructureSection>

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Boudet J]]

[[Category: Doherty E]]

[[Category: Poweleit N]]

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-'''Unreleased structure'''
-The entry 8w15 is ON HOLD
+==HTT in complex with HAP40 in the apo state.==
+<StructureSection load='8w15' size='340' side='right'caption='[[8w15]], [[Resolution|resolution]] 2.72&Aring;' scene=''>
-Authors: Poweleit, N., Boudet, J., Doherty, E.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8w15]] 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=8W15 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8W15 FirstGlance]. <br>
-Description: HTT in complex with HAP40 in the apo state.
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.72&#8491;</td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8w15 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8w15 OCA], [https://pdbe.org/8w15 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8w15 RCSB], [https://www.ebi.ac.uk/pdbsum/8w15 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8w15 ProSAT]</span></td></tr>
-[[Category: Boudet, J]]
+</table>
-[[Category: Doherty, E]]
+== Disease ==
-[[Category: Poweleit, N]]
+[https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] Juvenile Huntington disease;Huntington disease. The disease is caused by mutations affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/HD_HUMAN HD_HUMAN] May play a role in microtubule-mediated transport or vesicle function.
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Boudet J]]
+[[Category: Doherty E]]
+[[Category: Poweleit N]]