View source for 6k71


==eIF2 - eIF2B complex==
<SX load='6k71' size='340' side='right' viewer='molstar' caption='[[6k71]], [[Resolution|resolution]] 4.30&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6k71]] is a 13 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=6jlw 6jlw]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6K71 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6K71 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]] 4.3&#8491;</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=6k71 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6k71 OCA], [https://pdbe.org/6k71 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6k71 RCSB], [https://www.ebi.ac.uk/pdbsum/6k71 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6k71 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]]
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</SX>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ito T]]
[[Category: Kashiwagi K]]
[[Category: Yokoyama T]]