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3zxi

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(New page: '''Unreleased structure''' The entry 3zxi is ON HOLD Authors: Bonnefond, L., Frugier, M., Rudinger-Thirion, J., Balg, C., Chenevert, R., Lorber, B., Giege, R., Sauter, C. Description: ...)
Current revision (11:15, 20 December 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 3zxi is ON HOLD
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==Crystal structure of human mitochondrial tyrosyl-tRNA synthetase in complex with a tyrosyl-adenylate analog==
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<StructureSection load='3zxi' size='340' side='right'caption='[[3zxi]], [[Resolution|resolution]] 2.75&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3zxi]] 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=3ZXI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3ZXI 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]] 2.75&#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=TYA:PHOSPHORIC+ACID+2-AMINO-3-(4-HYDROXY-PHENYL)-PROPYL+ESTER+ADENOSIN-5YL+ESTER'>TYA</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=3zxi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3zxi OCA], [https://pdbe.org/3zxi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3zxi RCSB], [https://www.ebi.ac.uk/pdbsum/3zxi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3zxi ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/SYYM_HUMAN SYYM_HUMAN] Defects in YARS2 are the cause of myopathy with lactic acidosis and sideroblastic anemia type 2 (MLASA2) [MIM:[https://omim.org/entry/613561 613561]. MLASA2 is a rare oxidative phosphorylation disorder specific to skeletal muscle and bone marrow. Affected individuals manifest sideroblastic anemia, progressive lethargy, muscle weakness, and exercise intolerance associated with persistent lactic acidemia.<ref>PMID:20598274</ref> <ref>PMID:22504945</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/SYYM_HUMAN SYYM_HUMAN] Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction: tyrosine is first activated by ATP to form Tyr-AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity).<ref>PMID:15779907</ref>
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Authors: Bonnefond, L., Frugier, M., Rudinger-Thirion, J., Balg, C., Chenevert, R., Lorber, B., Giege, R., Sauter, C.
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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: Crystal structure of human mitochondrial tyrosyl-tRNA synthetase in complex with a tyrosyl-adenylate analog
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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: Balg C]]
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[[Category: Bonnefond L]]
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[[Category: Chenevert R]]
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[[Category: Frugier M]]
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[[Category: Giege R]]
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[[Category: Lorber B]]
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[[Category: Rudinger-Thirion J]]
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[[Category: Sauter C]]

Current revision

Crystal structure of human mitochondrial tyrosyl-tRNA synthetase in complex with a tyrosyl-adenylate analog

PDB ID 3zxi

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