6dzr

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'''Unreleased structure'''
 
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The entry 6dzr is ON HOLD until Paper Publication
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==Crystal structure of h38C2 K99R mutation==
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<StructureSection load='6dzr' size='340' side='right'caption='[[6dzr]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6dzr]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DZR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DZR FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FLC:CITRATE+ANION'>FLC</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6dzr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dzr OCA], [http://pdbe.org/6dzr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6dzr RCSB], [http://www.ebi.ac.uk/pdbsum/6dzr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6dzr ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Homogeneous antibody-drug conjugates (ADCs) that use a highly reactive buried lysine (Lys) residue embedded in a dual variable domain (DVD)-IgG1 format can be assembled with high precision and efficiency under mild conditions. Here we show that replacing the Lys with an arginine (Arg) residue affords an orthogonal ADC assembly that is site-selective and stable. X-ray crystallography confirmed the location of the reactive Arg residue at the bottom of a deep pocket. As the Lys-to-Arg mutation is confined to a single residue in the heavy chain of the DVD-IgG1, heterodimeric assemblies that combine a buried Lys in one arm, a buried Arg in the other arm, and identical light chains, are readily assembled. Furthermore, the orthogonal conjugation chemistry enables the loading of heterodimeric DVD-IgG1s with two different cargos in a one-pot reaction and thus affords a convenient platform for dual-warhead ADCs and other multifaceted antibody conjugates.
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Authors: Park, H., Rader, C.
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Site-Selective Antibody Functionalization via Orthogonally Reactive Arginine and Lysine Residues.,Hwang D, Nilchan N, Nanna AR, Li X, Cameron MD, Roush WR, Park H, Rader C Cell Chem Biol. 2019 Jun 11. pii: S2451-9456(19)30179-5. doi:, 10.1016/j.chembiol.2019.05.010. PMID:31231031<ref>PMID:31231031</ref>
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Description: Crystal structure of h38C2 K99R mutation
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Rader, C]]
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<div class="pdbe-citations 6dzr" style="background-color:#fffaf0;"></div>
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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: Large Structures]]
[[Category: Park, H]]
[[Category: Park, H]]
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[[Category: Rader, C]]
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[[Category: Antibody]]
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[[Category: Immune system]]

Revision as of 05:40, 10 July 2019

Crystal structure of h38C2 K99R mutation

PDB ID 6dzr

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