Isopeptidases have also been identified in prokaryotes that express lasso peptides, or peptides with a knotted conformation established by the presence of a non-main-chain linkage between an acidic amino acid and the peptide's N-terminus to form the knot. (Some lasso peptides also have topological complexity conferred by disulfide bonds.) Isopeptidase enzymes linearize the peptides by cleaving the isopeptide bond.[5][6]
References
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^Wilkinson, KD; Tashayev, VL; O'Connor, LB; Larsen, CN; Kasperek, E; Pickart, CM (7 November 1995). "Metabolism of the polyubiquitin degradation signal: structure, mechanism, and role of isopeptidase T.". Biochemistry. 34 (44): 14535–46. doi:10.1021/bi00044a032. PMID7578059.
^Clague, Michael J.; Heride, Claire; Urbé, Sylvie (July 2015). "The demographics of the ubiquitin system". Trends in Cell Biology. 25 (7): 417–426. doi:10.1016/j.tcb.2015.03.002. PMID25906909.
^Maksimov, Mikhail O.; Link, A. James (14 August 2013). "Discovery and Characterization of an Isopeptidase That Linearizes Lasso Peptides". Journal of the American Chemical Society. 135 (32): 12038–12047. doi:10.1021/ja4054256. PMID23862624.
^Hegemann, Julian D.; Zimmermann, Marcel; Xie, Xiulan; Marahiel, Mohamed A. (21 July 2015). "Lasso Peptides: An Intriguing Class of Bacterial Natural Products". Accounts of Chemical Research. 48 (7): 1909–1919. doi:10.1021/acs.accounts.5b00156. PMID26079760.