5vgr: Difference between revisions

Line 1:

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

The entry ~~5vgr is ON HOLD~~ ~~until Paper Publication~~

==Human Atlastin-3, GDP-bound==

~~Authors~~:

== Structural highlights ==

<table><tr><td colspan='2'>[[5vgr]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5VGR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5VGR FirstGlance]. <br>

~~Description~~:

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GDP:GUANOSINE-5-DIPHOSPHATE'>GDP</scene></td></tr>

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

<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=5vgr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vgr OCA], [http://pdbe.org/5vgr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5vgr RCSB], [http://www.ebi.ac.uk/pdbsum/5vgr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5vgr ProSAT]</span></td></tr>

</table>

== Disease ==

[[http://www.uniprot.org/uniprot/ATLA3_HUMAN ATLA3_HUMAN]] Hereditary sensory and autonomic neuropathy type 1. The disease is caused by mutations affecting the gene represented in this entry.

== Function ==

[[http://www.uniprot.org/uniprot/ATLA3_HUMAN ATLA3_HUMAN]] GTPase tethering membranes through formation of trans-homooligomers and mediating homotypic fusion of endoplasmic reticulum membranes. Functions in endoplasmic reticulum tubular network biogenesis.<ref>PMID:18270207</ref> <ref>PMID:19665976</ref>

== References ==

__TOC__

</StructureSection>

[[Category: Donnell, J P.O]]

[[Category: Sondermann, H]]

[[Category: G protein]]

[[Category: Gtpase]]

[[Category: Hydrolase]]

[[Category: Membrane fusion]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 5vgr is ON HOLD  until Paper Publication
+==Human Atlastin-3, GDP-bound==
+<StructureSection load='5vgr' size='340' side='right' caption='[[5vgr]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
-Authors:
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5vgr]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5VGR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5VGR FirstGlance]. <br>
-Description:
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GDP:GUANOSINE-5-DIPHOSPHATE'>GDP</scene></td></tr>
-[[Category: Unreleased Structures]]
+<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=5vgr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vgr OCA], [http://pdbe.org/5vgr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5vgr RCSB], [http://www.ebi.ac.uk/pdbsum/5vgr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5vgr ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[http://www.uniprot.org/uniprot/ATLA3_HUMAN ATLA3_HUMAN]] Hereditary sensory and autonomic neuropathy type 1. The disease is caused by mutations affecting the gene represented in this entry.
+== Function ==
+[[http://www.uniprot.org/uniprot/ATLA3_HUMAN ATLA3_HUMAN]] GTPase tethering membranes through formation of trans-homooligomers and mediating homotypic fusion of endoplasmic reticulum membranes. Functions in endoplasmic reticulum tubular network biogenesis.<ref>PMID:18270207</ref> <ref>PMID:19665976</ref>
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Donnell, J P.O]]
+[[Category: Sondermann, H]]
+[[Category: G protein]]
+[[Category: Gtpase]]
+[[Category: Hydrolase]]
+[[Category: Membrane fusion]]