4f3j: Difference between revisions

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==Crystal Structure of Trimeric gC1q Domain of Human C1QTNF5 associated with Late-onset Retinal Macular Degeneration==
==Crystal Structure of Trimeric gC1q Domain of Human C1QTNF5 associated with Late-onset Retinal Macular Degeneration==
<StructureSection load='4f3j' size='340' side='right' caption='[[4f3j]], [[Resolution|resolution]] 1.34&Aring;' scene=''>
<StructureSection load='4f3j' size='340' side='right' caption='[[4f3j]], [[Resolution|resolution]] 1.34&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4f3j]] 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=4F3J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4F3J FirstGlance]. <br>
<table><tr><td colspan='2'>[[4f3j]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4F3J OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4F3J FirstGlance]. <br>
</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">C1QTNF5, CTRP5, UNQ303/PRO344 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr>
</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">C1QTNF5, CTRP5, UNQ303/PRO344 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=4f3j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4f3j OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4f3j RCSB], [http://www.ebi.ac.uk/pdbsum/4f3j 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=4f3j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4f3j OCA], [http://pdbe.org/4f3j PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4f3j RCSB], [http://www.ebi.ac.uk/pdbsum/4f3j PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4f3j ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
[[http://www.uniprot.org/uniprot/C1QT5_HUMAN C1QT5_HUMAN]] Late-onset retinal degeneration. The disease is caused by mutations affecting the gene represented in this entry.
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
</div>
<div class="pdbe-citations 4f3j" style="background-color:#fffaf0;"></div>
== References ==
== References ==
<references/>
<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Human]]
[[Category: Palczewski, K]]
[[Category: Palczewski, K]]
[[Category: Tu, X]]
[[Category: Tu, X]]