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6t7b
From Proteopedia
(Difference between revisions)
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<StructureSection load='6t7b' size='340' side='right'caption='[[6t7b]], [[Resolution|resolution]] 5.10Å' scene=''> | <StructureSection load='6t7b' size='340' side='right'caption='[[6t7b]], [[Resolution|resolution]] 5.10Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[6t7b]] is a 11 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[6t7b]] is a 11 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6T7B OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6T7B FirstGlance]. <br> |
| - | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 5.1Å</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=6t7b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6t7b OCA], [https://pdbe.org/6t7b PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6t7b RCSB], [https://www.ebi.ac.uk/pdbsum/6t7b PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6t7b ProSAT]</span></td></tr> | |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
| - | == Disease == | ||
| - | [[http://www.uniprot.org/uniprot/SOX2_HUMAN SOX2_HUMAN]] Defects in SOX2 are the cause of microphthalmia syndromic type 3 (MCOPS3) [MIM:[http://omim.org/entry/206900 206900]]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS3 is characterized by the rare association of malformations including uni- or bilateral anophthalmia or microphthalmia, and esophageal atresia with trachoesophageal fistula.<ref>PMID:12612584</ref> | ||
== Function == | == Function == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/H32_HUMAN H32_HUMAN] |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 6t7b" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 6t7b" style="background-color:#fffaf0;"></div> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Histone 3D structures|Histone 3D structures]] | ||
| + | *[[OCT4 and SOX2 transcription factors|OCT4 and SOX2 transcription factors]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Cramer | + | [[Category: Synthetic construct]] |
| - | [[Category: Dienemann | + | [[Category: Cramer P]] |
| - | [[Category: Dodonova | + | [[Category: Dienemann C]] |
| - | [[Category: Taipale | + | [[Category: Dodonova SO]] |
| - | [[Category: Zhu | + | [[Category: Taipale J]] |
| - | + | [[Category: Zhu F]] | |
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Current revision
Structure of human Sox2 transcription factor in complex with a nucleosome
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