7d46

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====
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==eIF2B apo==
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<StructureSection load='7d46' size='340' side='right'caption='[[7d46]]' scene=''>
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<StructureSection load='7d46' size='340' side='right'caption='[[7d46]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id= OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol= FirstGlance]. <br>
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<table><tr><td colspan='2'>[[7d46]] 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=7D46 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7D46 FirstGlance]. <br>
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</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=7d46 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7d46 OCA], [https://pdbe.org/7d46 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7d46 RCSB], [https://www.ebi.ac.uk/pdbsum/7d46 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7d46 ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 4&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7d46 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7d46 OCA], [https://pdbe.org/7d46 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7d46 RCSB], [https://www.ebi.ac.uk/pdbsum/7d46 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7d46 ProSAT]</span></td></tr>
</table>
</table>
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== Disease ==
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[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.
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== Function ==
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[https://www.uniprot.org/uniprot/EI2BA_HUMAN EI2BA_HUMAN] Catalyzes the exchange of eukaryotic initiation factor 2-bound GDP for GTP.
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==See Also==
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*[[Eukaryotic initiation factor 3D structures|Eukaryotic initiation factor 3D structures]]
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Z-disk]]
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[[Category: Ito T]]
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[[Category: Kashiwagi K]]

Revision as of 10:52, 27 March 2024

eIF2B apo

PDB ID 7d46

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