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It has low biological activity and needs to be converted to a more active form by the liver

We found that Ser2035-Cys and Ser2035-Phe completely abolished binding of rapamycin-FKBP12 to mTORC1 and dramatically decreased the binding of bi-steric mTORC1 inhibitor-FKBP12, whereas Ser2035-Pro had smaller effects on these binding events, as assessed in co-IP experiments (Figure 1F

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c , Expression of Agxt , Grhpr , Prodh2 , Hoga1 , Hao1 , and Ldha relative to Gapdh , ( d, e ) protein abundance and quantification of AGXT, and ( f, g ) LDHA relative to -Actin, ( h ) LDH activity, and ( i ) oxalate concentrations normalized to tissue weight in liver samples from mice with (n=6) or without early MASH (12 weeks, n=6)