7q1q

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(New page: '''Unreleased structure''' The entry 7q1q is ON HOLD Authors: Description: Category: Unreleased Structures)
Current revision (13:54, 6 November 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 7q1q is ON HOLD
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==De novo designed homo-dimeric antiparallel helices Homomer-S==
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<StructureSection load='7q1q' size='340' side='right'caption='[[7q1q]], [[Resolution|resolution]] 1.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7q1q]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7Q1Q OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7Q1Q 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]] 1&#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=ACE:ACETYL+GROUP'>ACE</scene>, <scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene>, <scene name='pdbligand=NH2:AMINO+GROUP'>NH2</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=7q1q FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7q1q OCA], [https://pdbe.org/7q1q PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7q1q RCSB], [https://www.ebi.ac.uk/pdbsum/7q1q PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7q1q 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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Increasingly, it is possible to design peptide and protein assemblies de novo from first principles or computationally. This approach provides new routes to functional synthetic polypeptides, including designs to target and bind proteins of interest. Much of this work has been developed in vitro. Therefore, a challenge is to deliver de novo polypeptides efficiently to sites of action within cells. Here we describe the design, characterisation, intracellular delivery, and subcellular localisation of a de novo synthetic peptide system. This system comprises a dual-function basic peptide, programmed both for cell penetration and target binding, and a complementary acidic peptide that can be fused to proteins of interest and introduced into cells using synthetic DNA. The designs are characterised in vitro using biophysical methods and X-ray crystallography. The utility of the system for delivery into mammalian cells and subcellular targeting is demonstrated by marking organelles and actively engaging functional protein complexes.
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Authors:
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De novo designed peptides for cellular delivery and subcellular localisation.,Rhys GG, Cross JA, Dawson WM, Thompson HF, Shanmugaratnam S, Savery NJ, Dodding MP, Hocker B, Woolfson DN Nat Chem Biol. 2022 Sep;18(9):999-1004. doi: 10.1038/s41589-022-01076-6. Epub , 2022 Jul 14. PMID:35836017<ref>PMID:35836017</ref>
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Description:
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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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<div class="pdbe-citations 7q1q" 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]]
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[[Category: Synthetic construct]]
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[[Category: Dawson WM]]
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[[Category: Hocker B]]
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[[Category: Rhys GG]]
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[[Category: Shanmugaratnam S]]
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[[Category: Woolfson DN]]

Current revision

De novo designed homo-dimeric antiparallel helices Homomer-S

PDB ID 7q1q

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