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Significantly, as shown in Figure 6 in their Extended Data ( only to the inactive M pro C145A mutant, and concluded it was a likely M pro substrate, because they were able to identify a putative M pro cleavage site in the TRMT1 protein sequence (PRLQ/ANFT), where the slash (/) represents the cleavage site
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We performed a frequentist network meta-analysis to measure network estimates for the relative outcomes
We thus explain the enzymatic inactivity of ROXY9 by a poor scaffold site for standard glutathionylated substrates
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TimperKDel Rio-MartinACremerALBremserSAlberJGiavaliscoPet al
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