4g31: Difference between revisions

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[[Image:4g31.png|left|200px]]


{{STRUCTURE_4g31|  PDB=4g31  |  SCENE=  }}
==Crystal Structure of GSK6414 Bound to PERK (R587-R1092, delete A660-T867) at 2.28 A Resolution==
 
<StructureSection load='4g31' size='340' side='right'caption='[[4g31]], [[Resolution|resolution]] 2.28&Aring;' scene=''>
===Crystal Structure of GSK6414 Bound to PERK (R587-R1092, delete A660-T867) at 2.28 A Resolution===
== Structural highlights ==
 
<table><tr><td colspan='2'>[[4g31]] is a 1 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=4G31 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4G31 FirstGlance]. <br>
{{ABSTRACT_PUBMED_22827572}}
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.28&#8491;</td></tr>
 
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0WH:1-[5-(4-AMINO-7-METHYL-7H-PYRROLO[2,3-D]PYRIMIDIN-5-YL)-2,3-DIHYDRO-1H-INDOL-1-YL]-2-[3-(TRIFLUOROMETHYL)PHENYL]ETHANONE'>0WH</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
==About this Structure==
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4g31 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4g31 OCA], [https://pdbe.org/4g31 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4g31 RCSB], [https://www.ebi.ac.uk/pdbsum/4g31 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4g31 ProSAT]</span></td></tr>
[[4g31]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4G31 OCA].  
</table>
 
== Disease ==
==Reference==
[https://www.uniprot.org/uniprot/E2AK3_HUMAN E2AK3_HUMAN] Wolcott-Rallison syndrome. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:10932183</ref>  
<ref group="xtra">PMID:022827572</ref><references group="xtra"/>
== Function ==
[https://www.uniprot.org/uniprot/E2AK3_HUMAN E2AK3_HUMAN] Phosphorylates the alpha subunit of eukaryotic translation-initiation factor 2 (EIF2), leading to its inactivation and thus to a rapid reduction of translational initiation and repression of global protein synthesis. Serves as a critical effector of unfolded protein response (UPR)-induced G1 growth arrest due to the loss of cyclin-D1 (CCND1) (By similarity).
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Large Structures]]
[[Category: Axten, J M.]]
[[Category: Axten JM]]
[[Category: Gampe, R T.]]
[[Category: Gampe RT]]
[[Category: Catalytic domain]]
[[Category: Deletion mutant]]
[[Category: Synthetic inhibitor]]
[[Category: Transferase-transferase inhibitor complex]]
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