6drf: Difference between revisions

← Older edit

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

@@ Line 1: / Line 1: @@
 ==Structure of human Retinal Degeneration 3(RD3) Protein==
-<StructureSection load='6drf' size='340' side='right'caption='[[6drf]], [[NMR_Ensembles_of_Models | 10 NMR models]]' scene=''>
+<StructureSection load='6drf' size='340' side='right'caption='[[6drf]]' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[6drf]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DRF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DRF FirstGlance]. <br>
+<table><tr><td colspan='2'>[[6drf]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DRF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DRF FirstGlance]. <br>
-</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">RD3, C1orf36 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
+</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=6drf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6drf OCA], [https://pdbe.org/6drf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6drf RCSB], [https://www.ebi.ac.uk/pdbsum/6drf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6drf ProSAT]</span></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=6drf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6drf OCA], [https://pdbe.org/6drf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6drf RCSB], [https://www.ebi.ac.uk/pdbsum/6drf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6drf ProSAT]</span></td></tr>
 </table>
 == Disease ==
-[[https://www.uniprot.org/uniprot/RD3_HUMAN RD3_HUMAN]] Leber congenital amaurosis. The disease is caused by mutations affecting the gene represented in this entry.
+[https://www.uniprot.org/uniprot/RD3_HUMAN RD3_HUMAN] Leber congenital amaurosis. The disease is caused by mutations affecting the gene represented in this entry.
+== Function ==
+[https://www.uniprot.org/uniprot/RD3_HUMAN RD3_HUMAN]
 <div style="background-color:#fffaf0;">
 == Publication Abstract from PubMed ==
@@ Line 22: / Line 23: @@
 __TOC__
 </StructureSection>
-[[Category: Human]]
+[[Category: Homo sapiens]]
 [[Category: Large Structures]]
-[[Category: Ames, J B]]
+[[Category: Ames JB]]
-[[Category: Cudia, D]]
+[[Category: Cudia D]]
-[[Category: Dizhoor, A M]]
+[[Category: Dizhoor AM]]
-[[Category: Lim, S]]
+[[Category: Lim S]]
-[[Category: Peshenko, I]]
+[[Category: Peshenko I]]
-[[Category: Yu, Q]]
+[[Category: Yu Q]]
-[[Category: Sensory transduction]]
-[[Category: Signaling protein]]
-[[Category: Vision]]