4icu
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[4icu]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ICU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ICU FirstGlance]. <br> | <table><tr><td colspan='2'>[[4icu]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ICU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ICU FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4icv|4icv]]</td></tr> | + | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4icv|4icv]]</td></tr> |
| - | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4icu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4icu OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4icu RCSB], [http://www.ebi.ac.uk/pdbsum/4icu 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=4icu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4icu OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4icu RCSB], [http://www.ebi.ac.uk/pdbsum/4icu PDBsum]</span></td></tr> |
| - | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/TBCE_HUMAN TBCE_HUMAN]] Sanjad-Sakati syndrome;Autosomal recessive Kenny-Caffey syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | [[http://www.uniprot.org/uniprot/TBCE_HUMAN TBCE_HUMAN]] Sanjad-Sakati syndrome;Autosomal recessive Kenny-Caffey syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: Boutin, M | + | [[Category: Boutin, M]] |
| - | [[Category: Coll, M | + | [[Category: Coll, M]] |
| - | [[Category: Janowski, R | + | [[Category: Janowski, R]] |
| - | [[Category: Zabala, J C | + | [[Category: Zabala, J C]] |
[[Category: Alpha tubulin]] | [[Category: Alpha tubulin]] | ||
[[Category: Chaperone]] | [[Category: Chaperone]] | ||
Revision as of 13:22, 4 January 2015
Ubiquitin-like domain of human tubulin folding cofactor E - crystal from A
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