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- W3136308129 abstract "Inteins are intervening polypeptides that interrupt the functional domains of several important proteins across the three domains of life. Inteins excise themselves from the precursor protein, ligating concomitant extein residues in a process called protein splicing. Post-translational auto-removal of inteins remain critical for the generation of active proteins. The perspective of inteins in science is a robust field of research, however fundamental studies centralized upon splicing regulatory mechanism are imperative for addressing more intricate issues. Controlled engineering of intein splicing has many applications; intein inhibition can facilitate novel drug design, while activation of intein splicing is exploited in protein purification. This paper provides a comprehensive review of the past and recent advances in the splicing regulation via metal-intein interaction. We compare the behavior of different metal ions on diverse intein systems. Though metals such as Zn, Cu, Pt, Cd, Co, Ni exhibit intein inhibitory effect heterogeneously on different inteins, divalent metal ions such as Ca and Mg fail to do so. The observed diversity in the metal-intein interaction arises mostly due to intein polymorphism and variations in atomic structure of metals. A mechanistic understanding of intein regulation by metals in native as well as synthetically engineered intein systems may yield potent intein inhibitors via direct or indirect approach." @default.
- W3136308129 created "2021-03-29" @default.
- W3136308129 creator A5003086112 @default.
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- W3136308129 creator A5055211583 @default.
- W3136308129 creator A5060776562 @default.
- W3136308129 creator A5066532759 @default.
- W3136308129 creator A5087498525 @default.
- W3136308129 date "2021-06-01" @default.
- W3136308129 modified "2023-09-27" @default.
- W3136308129 title "Metal effect on intein splicing: A review" @default.
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