This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
7l70
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 7l70 is ON HOLD Authors: Description: Category: Unreleased Structures) |
|||
| (2 intermediate revisions not shown.) | |||
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | The | + | ==The eukaryotic translation initiation factor 2B from Homo sapiens in its apo form== |
| + | <StructureSection load='7l70' size='340' side='right'caption='[[7l70]], [[Resolution|resolution]] 2.80Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[7l70]] is a 10 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7L70 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7L70 FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.8Å</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=7l70 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7l70 OCA], [https://pdbe.org/7l70 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7l70 RCSB], [https://www.ebi.ac.uk/pdbsum/7l70 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7l70 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/EI2BA_HUMAN EI2BA_HUMAN] Cree leukoencephalopathy;Late infantile CACH syndrome;Ovarioleukodystrophy. The disease is caused by mutations affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/EI2BA_HUMAN EI2BA_HUMAN] Catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP. | ||
| - | + | ==See Also== | |
| - | + | *[[Eukaryotic initiation factor 3D structures|Eukaryotic initiation factor 3D structures]] | |
| - | + | __TOC__ | |
| - | [[Category: | + | </StructureSection> |
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Boone M]] | ||
| + | [[Category: Frost A]] | ||
| + | [[Category: Lawrence R]] | ||
| + | [[Category: Schoof M]] | ||
| + | [[Category: Walter P]] | ||
| + | [[Category: Wang L]] | ||
Current revision
The eukaryotic translation initiation factor 2B from Homo sapiens in its apo form
| |||||||||||
Categories: Homo sapiens | Large Structures | Boone M | Frost A | Lawrence R | Schoof M | Walter P | Wang L
