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5ao5

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Revision as of 17:10, 18 August 2017

Endo180 D1-4, monoclinic form

Structural highlights

5ao5 is a 2 chain structure. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Ligands:	,
Related:	5ao6
Resources:	FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

[MRC2_HUMAN] May play a role as endocytotic lectin receptor displaying calcium-dependent lectin activity. Internalizes glycosylated ligands from the extracellular space for release in an endosomal compartment via clathrin-mediated endocytosis. May be involved in plasminogen activation system controlling the extracellular level of PLAUR/PLAU, and thus may regulate protease activity at the cell surface. May contribute to cellular uptake, remodeling and degradation of extracellular collagen matrices. May play a role during cancer progression as well as in other chronic tissue destructive diseases acting on collagen turnover. May participate in remodeling of extracellular matrix cooperating with the matrix metalloproteinases (MMPs).^[1] ^[2]

Publication Abstract from PubMed

The C-type mannose receptor and its homolog Endo180 (or uPARAP, for urokinase plasminogen activator receptor-associated protein) mediate the endocytic uptake of collagen by macrophages and fibroblasts. This process is required for normal tissue remodeling, but also facilitates the growth and dissemination of tumors. We have determined the crystal structure at 2.5 A resolution of the N-terminal region of Endo180, consisting of a ricin-like domain, a fibronectin type II (FN2) domain, and two C-type lectin (CTL) domains. The L-shaped arrangement of these domains creates a shallow trench spanning the FN2 and CTL1 domains, which was shown by mutagenesis to bind triple-helical and denatured collagen. Small-angle X-ray scattering showed that the L-shaped structure is maintained in solution at neutral and acidic pH, irrespective of calcium ion loading. Collagen binding was equally unaffected by acidic pH, suggesting that collagen release in endosomes is not regulated by changes within the Endo180 N-terminal region.

Insights into Collagen Uptake by C-type Mannose Receptors from the Crystal Structure of Endo180 Domains 1-4.,Paracuellos P, Briggs DC, Carafoli F, Loncar T, Hohenester E Structure. 2015 Nov 3;23(11):2133-42. doi: 10.1016/j.str.2015.09.004. Epub 2015, Oct 15. PMID:26481812^[3]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

↑ Sheikh H, Yarwood H, Ashworth A, Isacke CM. Endo180, an endocytic recycling glycoprotein related to the macrophage mannose receptor is expressed on fibroblasts, endothelial cells and macrophages and functions as a lectin receptor. J Cell Sci. 2000 Mar;113 ( Pt 6):1021-32. PMID:10683150
↑ Wienke D, MacFadyen JR, Isacke CM. Identification and characterization of the endocytic transmembrane glycoprotein Endo180 as a novel collagen receptor. Mol Biol Cell. 2003 Sep;14(9):3592-604. Epub 2003 Jul 25. PMID:12972549 doi:http://dx.doi.org/10.1091/mbc.E02-12-0814
↑ Paracuellos P, Briggs DC, Carafoli F, Loncar T, Hohenester E. Insights into Collagen Uptake by C-type Mannose Receptors from the Crystal Structure of Endo180 Domains 1-4. Structure. 2015 Nov 3;23(11):2133-42. doi: 10.1016/j.str.2015.09.004. Epub 2015, Oct 15. PMID:26481812 doi:http://dx.doi.org/10.1016/j.str.2015.09.004

1 Structural highlights
2 Function
3 Publication Abstract from PubMed
4 References

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/5ao5"

@@ Line 1: / Line 1: @@
 ==Endo180 D1-4, monoclinic form==
 <StructureSection load='5ao5' size='340' side='right' caption='[[5ao5]], [[Resolution|resolution]] 2.48&Aring;' scene=''>
@@ Line 5: / Line 6: @@
 </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
 <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5ao6|5ao6]]</td></tr>
-<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=5ao5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ao5 OCA], [http://pdbe.org/5ao5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5ao5 RCSB], [http://www.ebi.ac.uk/pdbsum/5ao5 PDBsum]</span></td></tr>
+<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=5ao5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ao5 OCA], [http://pdbe.org/5ao5 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5ao5 RCSB], [http://www.ebi.ac.uk/pdbsum/5ao5 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5ao5 ProSAT]</span></td></tr>
 </table>
 == Function ==

5ao5

From Proteopedia

Revision as of 17:10, 18 August 2017

Endo180 D1-4, monoclinic form

Structural highlights

Function

Publication Abstract from PubMed

References

Contents

Proteopedia Page Contributors and Editors (what is this?)

Views

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