5v3f

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Current revision (14:30, 6 March 2024) (edit) (undo)
 
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<StructureSection load='5v3f' size='340' side='right'caption='[[5v3f]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
<StructureSection load='5v3f' size='340' side='right'caption='[[5v3f]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[5v3f]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5V3F OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5V3F FirstGlance]. <br>
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<table><tr><td colspan='2'>[[5v3f]] 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=5V3F OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5V3F FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=74G:4-{[(2S)-3-{2,16-DIOXO-20-[(3AS,4S,6AR)-2-OXOHEXAHYDRO-1H-THIENO[3,4-D]IMIDAZOL-4-YL]-6,9,12-TRIOXA-3,15-DIAZAICOSAN-1-YL}-2,3-DIHYDRO-1,3-BENZOTHIAZOL-2-YL]METHYL}-1-METHYLQUINOLIN-1-IUM'>74G</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
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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]] 1.7&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=5v3f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5v3f OCA], [http://pdbe.org/5v3f PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5v3f RCSB], [http://www.ebi.ac.uk/pdbsum/5v3f PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5v3f ProSAT]</span></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=74G:4-{[(2S)-3-{2,16-DIOXO-20-[(3AS,4S,6AR)-2-OXOHEXAHYDRO-1H-THIENO[3,4-D]IMIDAZOL-4-YL]-6,9,12-TRIOXA-3,15-DIAZAICOSAN-1-YL}-2,3-DIHYDRO-1,3-BENZOTHIAZOL-2-YL]METHYL}-1-METHYLQUINOLIN-1-IUM'>74G</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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=5v3f FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5v3f OCA], [https://pdbe.org/5v3f PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5v3f RCSB], [https://www.ebi.ac.uk/pdbsum/5v3f PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5v3f ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
 
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== Publication Abstract from PubMed ==
 
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Genetically encoded fluorescent protein tags have revolutionized proteome studies, whereas the lack of intrinsically fluorescent RNAs has hindered transcriptome exploration. Among several RNA-fluorophore complexes that potentially address this problem, RNA Mango has an exceptionally high affinity for its thiazole orange (TO)-derived fluorophore, TO1-Biotin (Kd approximately 3 nM), and, in complex with related ligands, it is one of the most redshifted fluorescent macromolecular tags known. To elucidate how this small aptamer exhibits such properties, which make it well suited for studying low-copy cellular RNAs, we determined its 1.7-A-resolution co-crystal structure. Unexpectedly, the entire ligand, including TO, biotin and the linker connecting them, abuts one of the near-planar faces of the three-tiered G-quadruplex. The two heterocycles of TO are held in place by two loop adenines and form a 45 degrees angle with respect to each other. Minimizing this angle would increase quantum yield and further improve this tool for in vivo RNA visualization.
 
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Structural basis for high-affinity fluorophore binding and activation by RNA Mango.,Trachman RJ 3rd, Demeshkina NA, Lau MWL, Panchapakesan SSS, Jeng SCY, Unrau PJ, Ferre-D'Amare AR Nat Chem Biol. 2017 Jul;13(7):807-813. doi: 10.1038/nchembio.2392. Epub 2017 May , 29. PMID:28553947<ref>PMID:28553947</ref>
 
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
 
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</div>
 
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<div class="pdbe-citations 5v3f" style="background-color:#fffaf0;"></div>
 
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== References ==
 
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<references/>
 
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Amare, A R.Ferre-D]]
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[[Category: Synthetic construct]]
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[[Category: Trachman, R J]]
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[[Category: Ferre-D'Amare AR]]
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[[Category: Quadruplex fluorescent rna]]
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[[Category: Trachman RJ]]
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[[Category: Rna]]
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Current revision

Co-crystal structure of the fluorogenic RNA Mango

PDB ID 5v3f

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