8d30: Difference between revisions

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'''Unreleased structure'''


The entry 8d30 is ON HOLD
==Crystal structure of the human COPB2 WD-domains==
 
<StructureSection load='8d30' size='340' side='right'caption='[[8d30]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
Authors: Zeng, H., Dong, A., Hutchinson, A., Seitova, A., Loppnau, P., Arrowsmith, C.H., Edwards, A.M., Halabelian, L., Structural Genomics Consortium (SGC)
== Structural highlights ==
 
<table><tr><td colspan='2'>[[8d30]] 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=8D30 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8D30 FirstGlance]. <br>
Description: Crystal structure of the human COPB2 WD-domains
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.4&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene></td></tr>
[[Category: Loppnau, P]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8d30 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8d30 OCA], [https://pdbe.org/8d30 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8d30 RCSB], [https://www.ebi.ac.uk/pdbsum/8d30 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8d30 ProSAT]</span></td></tr>
[[Category: Hutchinson, A]]
</table>
[[Category: Arrowsmith, C.H]]
== Disease ==
[[Category: Seitova, A]]
[https://www.uniprot.org/uniprot/COPB2_HUMAN COPB2_HUMAN] Autosomal recessive primary microcephaly. The disease may be caused by variants affecting the gene represented in this entry.
[[Category: Dong, A]]
== Function ==
[[Category: Halabelian, L]]
[https://www.uniprot.org/uniprot/COPB2_HUMAN COPB2_HUMAN] The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. In mammals, the coatomer can only be recruited by membranes associated to ADP-ribosylation factors (ARFs), which are small GTP-binding proteins; the complex also influences the Golgi structural integrity, as well as the processing, activity, and endocytic recycling of LDL receptors (By similarity). This coatomer complex protein, essential for Golgi budding and vesicular trafficking, is a selective binding protein (RACK) for protein kinase C, epsilon type. It binds to Golgi membranes in a GTP-dependent manner (By similarity).
[[Category: Zeng, H]]
__TOC__
[[Category: Edwards, A.M]]
</StructureSection>
[[Category: Structural Genomics Consortium (Sgc)]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Arrowsmith CH]]
[[Category: Dong A]]
[[Category: Edwards AM]]
[[Category: Halabelian L]]
[[Category: Hutchinson A]]
[[Category: Loppnau P]]
[[Category: Seitova A]]
[[Category: Zeng H]]

Latest revision as of 20:24, 18 October 2023

Crystal structure of the human COPB2 WD-domainsCrystal structure of the human COPB2 WD-domains

Structural highlights

8d30 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 2.4Å
Ligands:
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Disease

COPB2_HUMAN Autosomal recessive primary microcephaly. The disease may be caused by variants affecting the gene represented in this entry.

Function

COPB2_HUMAN The coatomer is a cytosolic protein complex that binds to dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles, which further mediate biosynthetic protein transport from the ER, via the Golgi up to the trans Golgi network. Coatomer complex is required for budding from Golgi membranes, and is essential for the retrograde Golgi-to-ER transport of dilysine-tagged proteins. In mammals, the coatomer can only be recruited by membranes associated to ADP-ribosylation factors (ARFs), which are small GTP-binding proteins; the complex also influences the Golgi structural integrity, as well as the processing, activity, and endocytic recycling of LDL receptors (By similarity). This coatomer complex protein, essential for Golgi budding and vesicular trafficking, is a selective binding protein (RACK) for protein kinase C, epsilon type. It binds to Golgi membranes in a GTP-dependent manner (By similarity).

8d30, resolution 2.40Å

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