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Moreover, the amino acid sequence of this new protein included a Cyclin homology domain, similar to that found in the previously identified Cyclins A, B, D, and E

The chemical modifications that were made at the N- and C-terminals of the AngIV molecule and the resultant improvement in metabolic stability highlight the critical role played by exopeptidases in the metabolism of AngIV-derived molecules

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Researchers have identified elevated levels of ATF4 expression in GS-deficient cells, which has been shown to result in increased expression of aminoacyl-tRNA synthetase (ARS) [214]

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