5vnf
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 5vnf is ON HOLD Authors: Ma, W., Goldberg, J. Description: Crystal structure of Sec23a/Sec24a/Sec22 complexed with a C-terminal VV sorting motif [[...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of Sec23a/Sec24a/Sec22 complexed with a C-terminal VV sorting motif== | |
| - | + | <StructureSection load='5vnf' size='340' side='right'caption='[[5vnf]], [[Resolution|resolution]] 2.41Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5vnf]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5VNF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5VNF 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]] 2.407Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5vnf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5vnf OCA], [https://pdbe.org/5vnf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5vnf RCSB], [https://www.ebi.ac.uk/pdbsum/5vnf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5vnf ProSAT]</span></td></tr> |
| - | [[Category: Goldberg | + | </table> |
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/SC23A_HUMAN SC23A_HUMAN] Defects in SEC23A are the cause of craniolenticulosutural dysplasia (CLSD) [MIM:[https://omim.org/entry/607812 607812]; also known as cranio-lenticulo-sutural dysplasia. CLSD is an autosomal recessive syndrome characterized by late-closing fontanels, sutural cataracts, facial dysmorphisms and skeletal defects.<ref>PMID:16980979</ref> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/SC23A_HUMAN SC23A_HUMAN] Component of the COPII coat, that covers ER-derived vesicles involved in transport from the endoplasmic reticulum to the Golgi apparatus. COPII acts in the cytoplasm to promote the transport of secretory, plasma membrane, and vacuolar proteins from the endoplasmic reticulum to the Golgi complex. | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Mus musculus]] | ||
| + | [[Category: Goldberg J]] | ||
| + | [[Category: Ma W]] | ||
Current revision
Crystal structure of Sec23a/Sec24a/Sec22 complexed with a C-terminal VV sorting motif
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