4kr3

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(New page: '''Unreleased structure''' The entry 4kr3 is ON HOLD until Paper Publication Authors: Qin, X., Hao, Z., Tian, Q., Zhang, Z., Zhou, C., Xie, W. Description: Glycyl-tRNA synthetase mutan...)
Current revision (08:54, 20 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 4kr3 is ON HOLD until Paper Publication
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==Glycyl-tRNA synthetase mutant E71G in complex with tRNA-Gly==
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<StructureSection load='4kr3' size='340' side='right'caption='[[4kr3]], [[Resolution|resolution]] 3.23&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4kr3]] is a 2 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=4KR3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4KR3 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.235&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ANP:PHOSPHOAMINOPHOSPHONIC+ACID-ADENYLATE+ESTER'>ANP</scene>, <scene name='pdbligand=GLY:GLYCINE'>GLY</scene>, <scene name='pdbligand=GTP:GUANOSINE-5-TRIPHOSPHATE'>GTP</scene></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=4kr3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4kr3 OCA], [https://pdbe.org/4kr3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4kr3 RCSB], [https://www.ebi.ac.uk/pdbsum/4kr3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4kr3 ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/GARS_HUMAN GARS_HUMAN] Autosomal dominant Charcot-Marie-Tooth disease type 2D;Distal hereditary motor neuropathy type 5. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry.
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== Function ==
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[https://www.uniprot.org/uniprot/GARS_HUMAN GARS_HUMAN] Catalyzes the ATP-dependent ligation of glycine to the 3'-end of its cognate tRNA, via the formation of an aminoacyl-adenylate intermediate (Gly-AMP) (PubMed:17544401, PubMed:28675565, PubMed:24898252). Also produces diadenosine tetraphosphate (Ap4A), a universal pleiotropic signaling molecule needed for cell regulation pathways, by direct condensation of 2 ATPs. Thereby, may play a special role in Ap4A homeostasis (PubMed:19710017).<ref>PMID:17544401</ref> <ref>PMID:19710017</ref> <ref>PMID:24898252</ref> <ref>PMID:28675565</ref>
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Authors: Qin, X., Hao, Z., Tian, Q., Zhang, Z., Zhou, C., Xie, W.
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==See Also==
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*[[Aminoacyl tRNA synthetase 3D structures|Aminoacyl tRNA synthetase 3D structures]]
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Description: Glycyl-tRNA synthetase mutant E71G in complex with tRNA-Gly
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*[[Transfer RNA (tRNA)|Transfer RNA (tRNA)]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Hao Z]]
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[[Category: Qin X]]
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[[Category: Tian Q]]
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[[Category: Xie W]]
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[[Category: Zhang Z]]
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[[Category: Zhou C]]

Current revision

Glycyl-tRNA synthetase mutant E71G in complex with tRNA-Gly

PDB ID 4kr3

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