6hcf: Difference between revisions

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New page: '''Unreleased structure''' The entry 6hcf is ON HOLD Authors: Juszkiewicz, S., Chandrasekaran, V., Lin, Z., Kraatz, S., Ramakrishnan, V., Hegde, R.S. Description: Structure of the rabb...
 
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'''Unreleased structure'''


The entry 6hcf is ON HOLD
==Structure of the rabbit 80S ribosome stalled on globin mRNA at the stop codon==
<SX load='6hcf' size='340' side='right' viewer='molstar' caption='[[6hcf]], [[Resolution|resolution]] 3.90&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6hcf]] is a 10 chain structure with sequence from [https://en.wikipedia.org/wiki/Oryctolagus_cuniculus Oryctolagus cuniculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6HCF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6HCF 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]] 3.9&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=6hcf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6hcf OCA], [https://pdbe.org/6hcf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6hcf RCSB], [https://www.ebi.ac.uk/pdbsum/6hcf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6hcf ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/RL5_RABIT RL5_RABIT] Component of the ribosome, a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:26245381, PubMed:27863242). The small ribosomal subunit (SSU) binds messenger RNAs (mRNAs) and translates the encoded message by selecting cognate aminoacyl-transfer RNA (tRNA) molecules (PubMed:26245381, PubMed:27863242). The large subunit (LSU) contains the ribosomal catalytic site termed the peptidyl transferase center (PTC), which catalyzes the formation of peptide bonds, thereby polymerizing the amino acids delivered by tRNAs into a polypeptide chain (PubMed:26245381, PubMed:27863242). The nascent polypeptides leave the ribosome through a tunnel in the LSU and interact with protein factors that function in enzymatic processing, targeting, and the membrane insertion of nascent chains at the exit of the ribosomal tunnel (By similarity). As part of the 5S RNP/5S ribonucleoprotein particle it is an essential component of the LSU, required for its formation and the maturation of rRNAs (By similarity). It also couples ribosome biogenesis to p53/TP53 activation. As part of the 5S RNP it accumulates in the nucleoplasm and inhibits MDM2, when ribosome biogenesis is perturbed, mediating the stabilization and the activation of TP53 (By similarity).[UniProtKB:P46777]<ref>PMID:26245381</ref> <ref>PMID:27863242</ref>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Aberrantly slow translation elicits quality control pathways initiated by the ubiquitin ligase ZNF598. How ZNF598 discriminates physiologic from pathologic translation complexes and ubiquitinates stalled ribosomes selectively is unclear. Here, we find that the minimal unit engaged by ZNF598 is the collided di-ribosome, a molecular species that arises when a trailing ribosome encounters a slower leading ribosome. The collided di-ribosome structure reveals an extensive 40S-40S interface in which the ubiquitination targets of ZNF598 reside. The paucity of 60S interactions allows for different ribosome rotation states, explaining why ZNF598 recognition is indifferent to how the leading ribosome has stalled. The use of ribosome collisions as a proxy for stalling allows the degree of tolerable slowdown to be tuned by the initiation rate on that mRNA; hence, the threshold for triggering quality control is substrate specific. These findings illustrate how higher-order ribosome architecture can be exploited by cellular factors to monitor translation status.


Authors: Juszkiewicz, S., Chandrasekaran, V., Lin, Z., Kraatz, S., Ramakrishnan, V., Hegde, R.S.
ZNF598 Is a Quality Control Sensor of Collided Ribosomes.,Juszkiewicz S, Chandrasekaran V, Lin Z, Kraatz S, Ramakrishnan V, Hegde RS Mol Cell. 2018 Oct 1. pii: S1097-2765(18)30697-X. doi:, 10.1016/j.molcel.2018.08.037. PMID:30293783<ref>PMID:30293783</ref>


Description: Structure of the rabbit 80S ribosome stalled on globin mRNA at the stop codon
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Juszkiewicz, S]]
<div class="pdbe-citations 6hcf" style="background-color:#fffaf0;"></div>
[[Category: Lin, Z]]
 
[[Category: Chandrasekaran, V]]
==See Also==
[[Category: Hegde, R.S]]
*[[Ribosome 3D structures|Ribosome 3D structures]]
[[Category: Kraatz, S]]
*[[3D sructureseceptor for activated protein kinase C 1|3D sructureseceptor for activated protein kinase C 1]]
[[Category: Ramakrishnan, V]]
== References ==
<references/>
__TOC__
</SX>
[[Category: Large Structures]]
[[Category: Oryctolagus cuniculus]]
[[Category: Chandrasekaran V]]
[[Category: Hegde RS]]
[[Category: Juszkiewicz S]]
[[Category: Kraatz S]]
[[Category: Lin Z]]
[[Category: Ramakrishnan V]]

Latest revision as of 18:27, 8 September 2026

Structure of the rabbit 80S ribosome stalled on globin mRNA at the stop codon

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