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- W1963599527 abstract "Propionic acid and isobutyric acid, which are structural analogues of N-carbamoyl-beta-alanine and N-carbamoyl-beta-aminoisobutyric acid, respectively, acted as an allosteric activator as well as a competitive inhibitor of purified rat liver beta-ureidopropionase. Propionic acid and isobutyric acid had a Ki value of approx. 0.3 mM at pH 7.0. The Hill coefficient for N-carbamoyl-beta-alanine was 2.0, but the cooperatively decreased to 1.0 in the presence of 1 mM propionic acid. The K1/2 value towards N-carbamoyl-beta-alanine was calculated to be 0.17 mM from Hill plots and the Km value was determined to be 0.06 mM from replots of the apparent Km vs propionic acid." @default.
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- W1963599527 date "1988-03-14" @default.
- W1963599527 modified "2023-09-27" @default.
- W1963599527 title "Bisfunction of propionic acid on purified rat liver β-ureidopropionase" @default.
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- W1963599527 doi "https://doi.org/10.1016/0014-5793(88)81153-0" @default.
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