7lxf: Difference between revisions

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<StructureSection load='7lxf' size='340' side='right'caption='[[7lxf]], [[Resolution|resolution]] 1.65&Aring;' scene=''>
<StructureSection load='7lxf' size='340' side='right'caption='[[7lxf]], [[Resolution|resolution]] 1.65&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[7lxf]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7LXF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7LXF FirstGlance]. <br>
<table><tr><td colspan='2'>[[7lxf]] 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=7LXF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7LXF FirstGlance]. <br>
</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=7lxf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7lxf OCA], [https://pdbe.org/7lxf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7lxf RCSB], [https://www.ebi.ac.uk/pdbsum/7lxf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7lxf ProSAT]</span></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.65&#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=7lxf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7lxf OCA], [https://pdbe.org/7lxf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7lxf RCSB], [https://www.ebi.ac.uk/pdbsum/7lxf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7lxf ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/PCARE_HUMAN PCARE_HUMAN] Retinitis pigmentosa. The disease is caused by variants affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/PCARE_HUMAN PCARE_HUMAN] Plays an essential role for normal photoreceptor cell maintenance and vision.<ref>PMID:20398886</ref>
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
== Publication Abstract from PubMed ==
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Grant, R A]]
[[Category: Grant RA]]
[[Category: Hwang, T]]
[[Category: Hwang T]]
[[Category: Keating, A E]]
[[Category: Keating AE]]
[[Category: Complex]]
[[Category: Cytoskeleton]]
[[Category: Protein binding]]