8xtp: Difference between revisions

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New page: '''Unreleased structure''' The entry 8xtp is ON HOLD Authors: Wang, L., Xie, J.H., Zhang, C., Zou, J., Huang, Z.R., Chen, X.Y., Yang, Y., Dong, H.H., Huang, D.M., Su, Z.M. Description:...
 
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'''Unreleased structure'''


The entry 8xtp is ON HOLD
==Comamonas testosteroni KF-1 circularly permuted group II intron Post-2S state==
<StructureSection load='8xtp' size='340' side='right'caption='[[8xtp]], [[Resolution|resolution]] 2.90&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[8xtp]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Comamonas_testosteroni_KF-1 Comamonas testosteroni KF-1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8XTP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8XTP FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.9&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=SPD:SPERMIDINE'>SPD</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8xtp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xtp OCA], [https://pdbe.org/8xtp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xtp RCSB], [https://www.ebi.ac.uk/pdbsum/8xtp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xtp ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Circularly permuted group II introns (CP introns) consist of rearranged structural domains separated by two tethered exons, generating branched introns and circular exons via back-splicing. Structural and mechanistic understanding of circular RNA (circRNA) generation by CP introns remains elusive. We resolve cryo-electron microscopy structures of a natural CP intron in different states during back-splicing at a resolution of 2.5-2.9 A. Domain 6 (D6) undergoes a conformational change of 65 degrees after branching, to facilitate 3'-exon recognition and circularization. Previously unseen tertiary interactions compact the catalytic triad and D6 for splicing without protein, whereas a metal ion, M(35), is observed to stabilize the 5'-exon during splicing. While these unique features were not observed in canonical group II introns and spliceosomes, they are common in CP introns, as demonstrated by the cryo-EM structure of another CP intron discovered by comparative genomics analysis. Our results elucidate the mechanism of CP intron back-splicing dynamics, with potential applications in circRNA research and therapeutics.


Authors: Wang, L., Xie, J.H., Zhang, C., Zou, J., Huang, Z.R., Chen, X.Y., Yang, Y., Dong, H.H., Huang, D.M., Su, Z.M.
Structural basis of circularly permuted group II intron self-splicing.,Wang L, Xie J, Zhang C, Zou J, Huang Z, Shang S, Chen X, Yang Y, Liu J, Dong H, Huang D, Su Z Nat Struct Mol Biol. 2025 Jan 31. doi: 10.1038/s41594-025-01484-x. PMID:39890981<ref>PMID:39890981</ref>


Description: CryoEM Structure of intron 4
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Wang, L]]
<div class="pdbe-citations 8xtp" style="background-color:#fffaf0;"></div>
[[Category: Dong, H.H]]
== References ==
[[Category: Huang, Z.R]]
<references/>
[[Category: Su, Z.M]]
__TOC__
[[Category: Yang, Y]]
</StructureSection>
[[Category: Chen, X.Y]]
[[Category: Comamonas testosteroni KF-1]]
[[Category: Zou, J]]
[[Category: Large Structures]]
[[Category: Zhang, C]]
[[Category: Chen XY]]
[[Category: Xie, J.H]]
[[Category: Dong HH]]
[[Category: Huang, D.M]]
[[Category: Huang DM]]
[[Category: Huang ZR]]
[[Category: Liu J]]
[[Category: Shang ST]]
[[Category: Su ZM]]
[[Category: Wang L]]
[[Category: Xie JH]]
[[Category: Yang Y]]
[[Category: Zhang C]]
[[Category: Zou J]]

Latest revision as of 09:17, 12 February 2025

Comamonas testosteroni KF-1 circularly permuted group II intron Post-2S stateComamonas testosteroni KF-1 circularly permuted group II intron Post-2S state

Structural highlights

8xtp is a 2 chain structure with sequence from Comamonas testosteroni KF-1. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:Electron Microscopy, Resolution 2.9Å
Ligands:, ,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Publication Abstract from PubMed

Circularly permuted group II introns (CP introns) consist of rearranged structural domains separated by two tethered exons, generating branched introns and circular exons via back-splicing. Structural and mechanistic understanding of circular RNA (circRNA) generation by CP introns remains elusive. We resolve cryo-electron microscopy structures of a natural CP intron in different states during back-splicing at a resolution of 2.5-2.9 A. Domain 6 (D6) undergoes a conformational change of 65 degrees after branching, to facilitate 3'-exon recognition and circularization. Previously unseen tertiary interactions compact the catalytic triad and D6 for splicing without protein, whereas a metal ion, M(35), is observed to stabilize the 5'-exon during splicing. While these unique features were not observed in canonical group II introns and spliceosomes, they are common in CP introns, as demonstrated by the cryo-EM structure of another CP intron discovered by comparative genomics analysis. Our results elucidate the mechanism of CP intron back-splicing dynamics, with potential applications in circRNA research and therapeutics.

Structural basis of circularly permuted group II intron self-splicing.,Wang L, Xie J, Zhang C, Zou J, Huang Z, Shang S, Chen X, Yang Y, Liu J, Dong H, Huang D, Su Z Nat Struct Mol Biol. 2025 Jan 31. doi: 10.1038/s41594-025-01484-x. PMID:39890981[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Wang L, Xie J, Zhang C, Zou J, Huang Z, Shang S, Chen X, Yang Y, Liu J, Dong H, Huang D, Su Z. Structural basis of circularly permuted group II intron self-splicing. Nat Struct Mol Biol. 2025 Jan 31. PMID:39890981 doi:10.1038/s41594-025-01484-x

8xtp, resolution 2.90Å

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