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4icv

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[4icv]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ICV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ICV FirstGlance]. <br>
<table><tr><td colspan='2'>[[4icv]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4ICV OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4ICV FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=PR:PRASEODYMIUM+ION'>PR</scene><br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=PR:PRASEODYMIUM+ION'>PR</scene></td></tr>
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<tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4icu|4icu]]</td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4icu|4icu]]</td></tr>
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<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=4icv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4icv OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4icv RCSB], [http://www.ebi.ac.uk/pdbsum/4icv PDBsum]</span></td></tr>
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<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=4icv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4icv OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4icv RCSB], [http://www.ebi.ac.uk/pdbsum/4icv PDBsum]</span></td></tr>
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<table>
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</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>
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[[Category: Boutin, M.]]
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[[Category: Boutin, M]]
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[[Category: Coll, M.]]
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[[Category: Coll, M]]
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[[Category: Janowski, R.]]
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[[Category: Janowski, R]]
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[[Category: Zabala, J C.]]
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[[Category: Zabala, J C]]
[[Category: Alpha tubulin]]
[[Category: Alpha tubulin]]
[[Category: Chaperone]]
[[Category: Chaperone]]

Revision as of 14:19, 4 January 2015

Ubiquitin-like domain of human tubulin folding cofactor E - crystal form B

4icv, resolution 1.45Å

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