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{{STRUCTURE_3hon|  PDB=3hon  |  SCENE=  }}
===Crystal Structure of Human Collagen XVIII Trimerization Domain (cubic form)===
{{ABSTRACT_PUBMED_19631658}}


==Disease==
==Crystal Structure of Human Collagen XVIII Trimerization Domain (cubic form)==
[[http://www.uniprot.org/uniprot/COIA1_HUMAN COIA1_HUMAN]] Defects in COL18A1 are a cause of Knobloch syndrome type 1 (KNO1) [MIM:[http://omim.org/entry/267750 267750]]. An autosomal recessive disorder defined by the occurrence of high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipital encephalocele.<ref>PMID:10942434</ref>  
<StructureSection load='3hon' size='340' side='right'caption='[[3hon]], [[Resolution|resolution]] 3.00&Aring;' scene=''>
 
== Structural highlights ==
==Function==
<table><tr><td colspan='2'>[[3hon]] is a 1 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=3HON OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3HON FirstGlance]. <br>
[[http://www.uniprot.org/uniprot/COIA1_HUMAN COIA1_HUMAN]] COLA18A probably plays a major role in determining the retinal structure as well as in the closure of the neural tube.  Endostatin potently inhibits endothelial cell proliferation and angiogenesis. May inhibit angiogenesis by binding to the heparan sulfate proteoglycans involved in growth factor signaling.  
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3&#8491;</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=3hon FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3hon OCA], [https://pdbe.org/3hon PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3hon RCSB], [https://www.ebi.ac.uk/pdbsum/3hon PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3hon ProSAT]</span></td></tr>
==About this Structure==
</table>
[[3hon]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3HON OCA].  
== Disease ==
[https://www.uniprot.org/uniprot/COIA1_HUMAN COIA1_HUMAN] Defects in COL18A1 are a cause of Knobloch syndrome type 1 (KNO1) [MIM:[https://omim.org/entry/267750 267750]. An autosomal recessive disorder defined by the occurrence of high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipital encephalocele.<ref>PMID:10942434</ref>  
== Function ==
[https://www.uniprot.org/uniprot/COIA1_HUMAN COIA1_HUMAN] COLA18A probably plays a major role in determining the retinal structure as well as in the closure of the neural tube.  Endostatin potently inhibits endothelial cell proliferation and angiogenesis. May inhibit angiogenesis by binding to the heparan sulfate proteoglycans involved in growth factor signaling.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/ho/3hon_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=3hon ConSurf].
<div style="clear:both"></div>


==See Also==
==See Also==
*[[Collagen|Collagen]]
*[[Collagen 3D structures|Collagen 3D structures]]
 
== References ==
==Reference==
<references/>
<ref group="xtra">PMID:019631658</ref><references group="xtra"/><references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Bachinger, H P.]]
[[Category: Large Structures]]
[[Category: Boudko, S P.]]
[[Category: Bachinger HP]]
[[Category: Alternative promoter usage]]
[[Category: Boudko SP]]
[[Category: Cell adhesion]]
[[Category: Collagen]]
[[Category: Collagen triple helix]]
[[Category: Collagen xviii]]
[[Category: Disulfide bond]]
[[Category: Extracellular matrix]]
[[Category: Glycoprotein]]
[[Category: Hydroxylation]]
[[Category: Metal-binding]]
[[Category: Multiplexin]]
[[Category: Protein binding]]
[[Category: Secreted]]
[[Category: Trimerization domain]]

Latest revision as of 10:01, 21 February 2024

Crystal Structure of Human Collagen XVIII Trimerization Domain (cubic form)

3hon, resolution 3.00Å

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