2022
DOI: 10.3389/fphys.2022.913063
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Counting Degrons: Lessons From Multivalent Substrates for Targeted Protein Degradation

Abstract: E3s comprise a structurally diverse group of at least 800 members, most of which target multiple substrates through specific and regulated protein-protein interactions. These interactions typically rely on short linear motifs (SLiMs), called “degrons”, in an intrinsically disordered region (IDR) of the substrate, with variable rules of engagement governing different E3-docking events. These rules of engagement are of importance to the field of targeted protein degradation (TPD), where substrate ubiquitination … Show more

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Cited by 10 publications
(16 citation statements)
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“…In addition, the same model predicts a hydrogen bond forming between EXO1’s T824 (mutated to E824 to mimic the phosphorylated residue) and cyclin F’s Y387, indicating a potential second valence mediating the cyclin F-EXO1 interaction. The results above suggest a multivalent binding mechanism similar to that used by other ligases 35 and they outline a possible multi-step procedure to prevent uncontrolled degradation of CDK/cyclin substrates by SCF cyclin F at the G2 and M transition.…”
Section: Resultsmentioning
confidence: 62%
“…In addition, the same model predicts a hydrogen bond forming between EXO1’s T824 (mutated to E824 to mimic the phosphorylated residue) and cyclin F’s Y387, indicating a potential second valence mediating the cyclin F-EXO1 interaction. The results above suggest a multivalent binding mechanism similar to that used by other ligases 35 and they outline a possible multi-step procedure to prevent uncontrolled degradation of CDK/cyclin substrates by SCF cyclin F at the G2 and M transition.…”
Section: Resultsmentioning
confidence: 62%
“…Moreover, we also envision the strategy as expandable. Though dlg1[4K] includes an epitope tag, this can be modified to include a fluorescent reporter, any kind of general effector, or even a degron (Okoye et al, 2022) to study the targeted function of DLG1. Moreover, by adjusting the homology arms of the construct (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The importance of residues 56-60 in the 1a-2b interaction and residues 39-60 in the AGO1-2b interaction (which overlaps with the sequence needed for 1a-2b complex formation) suggests that larger regions of the 2b protein structure are required for these interactions. Such effects can occur when two or more proteins with intrinsically disordered structures interact (Okoye et al, 2022) and may also explain 1a-2b protein complex formation in P-bodies (Wallmann and Kesten, 2020).…”
Section: In Silico Prediction Of Intrinsic Disorder In the 2b Proteinmentioning
confidence: 99%
“…Although the mechanism has not been investigated, it is not based on the formation of disulfide bridges and another explanation is required. This could be the emergence of structure from the interactions of intrinsically disordered domains within the interaction partners (Dunker et al, 1998(Dunker et al, , 2005Wright and Dyson, 1999;Tompa and Fuxreiter, 2008;Ulrich et al, 2008;Okoye et al, 2022).…”
Section: New Questions On the CMV 2b Protein Secondary Structure And ...mentioning
confidence: 99%