STEREOCHEMISTRY OF THE PHOSPHORYLATION REACTION OF alpha -CHYMOTRYPSIN BY A CYCLIC PHOSPHATE TRIESTER.

DOI: 10.1021/ja00361a033

Source and publish data:

Journal of the American Chemical Society p. 6942 - 6943 (1983)

Update date:2022-09-26

Topics:

Authors:

Shah Shah

Kallick Kallick

Rowell Rowell

Chen Chen

Gorenstein

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Article abstract of DOI:10.1021/ja00361a033

The reaction of alpha -chymotrypsin with the axial triester -(2,4-dinitrophenoxy)-2-oxo-trans-5,6-tetramethylene-1,3,2-dioxaphos phorinane yields a stable serine ester enzyme complex. The **3**1P NMR spectrum of the native and denatured triester complex s

Full text of DOI:10.1021/ja00361a033

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Product name:2-(N-carbobenzoxy-L-serine methyl ester)-2-oxo-trans-5,6-tetramethylene-1,3,2-dioxaphosphorinane

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