2e6p: Difference between revisions

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OCA

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 ==Solution structure of the Ig-like domain (714-804) from human Obscurin-like protein 1==
-<StructureSection load='2e6p' size='340' side='right'caption='[[2e6p]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
+<StructureSection load='2e6p' size='340' side='right'caption='[[2e6p]]' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[2e6p]] 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=2E6P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2E6P FirstGlance]. <br>
+<table><tr><td colspan='2'>[[2e6p]] 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=2E6P OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2E6P FirstGlance]. <br>
-</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">OBSL1, KIAA0657 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2e6p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2e6p OCA], [https://pdbe.org/2e6p PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2e6p RCSB], [https://www.ebi.ac.uk/pdbsum/2e6p PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2e6p ProSAT], [https://www.topsan.org/Proteins/RSGI/2e6p TOPSAN]</span></td></tr>
 </table>
 == Disease ==
-[[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[https://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>
+[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[https://omim.org/entry/612921 612921]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>
+== Function ==
+[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]
 == Evolutionary Conservation ==
 [[Image:Consurf_key_small.gif|200px|right]]
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 __TOC__
 </StructureSection>
-[[Category: Human]]
+[[Category: Homo sapiens]]
 [[Category: Large Structures]]
-[[Category: Hayashi, F]]
+[[Category: Hayashi F]]
-[[Category: Qin, X R]]
+[[Category: Qin XR]]
-[[Category: Structural genomic]]
+[[Category: Suetake T]]
-[[Category: Suetake, T]]
+[[Category: Yokoyama S]]
-[[Category: Yokoyama, S]]
-[[Category: Ig-like domain]]
-[[Category: National project on protein structural and functional analyse]]
-[[Category: Nppsfa]]
-[[Category: Obscurin-like protein 1]]
-[[Category: Rsgi]]
-[[Category: Structural protein]]