6xjo
From Proteopedia
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==Human atlastin-3 (residues 1-334) bound to GDP-Mg2+ exhibits an ordered amino terminus== | ==Human atlastin-3 (residues 1-334) bound to GDP-Mg2+ exhibits an ordered amino terminus== | ||
| - | <StructureSection load='6xjo' size='340' side='right'caption='[[6xjo]]' scene=''> | + | <StructureSection load='6xjo' size='340' side='right'caption='[[6xjo]], [[Resolution|resolution]] 2.10Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6XJO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6XJO FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6xjo]] 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=6XJO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6XJO FirstGlance]. <br> |
| - | </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=6xjo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6xjo OCA], [https://pdbe.org/6xjo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6xjo RCSB], [https://www.ebi.ac.uk/pdbsum/6xjo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6xjo ProSAT]</span></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr> |
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GDP:GUANOSINE-5-DIPHOSPHATE'>GDP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene></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=6xjo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6xjo OCA], [https://pdbe.org/6xjo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6xjo RCSB], [https://www.ebi.ac.uk/pdbsum/6xjo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6xjo ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Disease == | ||
| + | [https://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 == | ||
| + | [https://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> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Atlastin (ATL) GTPases catalyze homotypic membrane fusion of the peripheral endoplasmic reticulum (ER). GTP-hydrolysis-driven conformational changes and membrane tethering are prerequisites for proper membrane fusion. However, the molecular basis for regulation of these processes is poorly understood. Here we establish intrinsic and extrinsic modes of ATL1 regulation that involve the N-terminal hypervariable region (HVR) of ATLs. Crystal structures of ATL1 and ATL3 exhibit the HVR as a distinct, isoform-specific structural feature. Characterizing the functional role of ATL1's HVR uncovered its positive effect on membrane tethering and on ATL1's cellular function. The HVR is post-translationally regulated through phosphorylation-dependent modification. A kinase screen identified candidates that modify the HVR site specifically, corresponding to the modifications on ATL1 detected in cells. This work reveals how the HVR contributes to efficient and potentially regulated activity of ATLs, laying the foundation for the identification of cellular effectors of ATL-mediated membrane processes. | ||
| + | |||
| + | The hypervariable region of atlastin-1 is a site for intrinsic and extrinsic regulation.,Kelly CM, Byrnes LJ, Neela N, Sondermann H, O'Donnell JP J Cell Biol. 2021 Nov 1;220(11). pii: 212648. doi: 10.1083/jcb.202104128. Epub, 2021 Sep 21. PMID:34546351<ref>PMID:34546351</ref> | ||
| + | |||
| + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| + | </div> | ||
| + | <div class="pdbe-citations 6xjo" style="background-color:#fffaf0;"></div> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Atlastin 3D structures|Atlastin 3D structures]] | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: O'Donnell JP]] | [[Category: O'Donnell JP]] | ||
[[Category: Sondermann H]] | [[Category: Sondermann H]] | ||
Current revision
Human atlastin-3 (residues 1-334) bound to GDP-Mg2+ exhibits an ordered amino terminus
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