M. S. Matta

发表

Parallel behavior in kinetic and NMR effects: secondary deuterium isotope effects on the alkaline hydrolysis of esters

M. S. Matta, D. Broadway, M. K. Stroot, 1987 .

Proton inventory of the second step of ribonuclease catalysis

M. S. Matta, Diep Thi Vo, 1986 .

Geometric Configuration of the isomeric 2-amino--2-decalincarboxylic acids

M. Rohde, M. S. Matta, 1972 .

Residual esterase activity of lima bean inhibitor-binding anhydrochymotrypsin preparations.

P. Henderson, M. S. Matta, J. Benitez, 1977, The Journal of biological chemistry.

Preparation and 13C NMR characterization of [[epsilon-13C] methionine-192]-alpha-chymotrypsin. The demethylation of [S-[13C] methylmethionine-192]-alpha-chymotrypsin by an active site-directed thiol.

T. Patrick, P. Henderson, M. S. Matta, 1981, Journal of Biological Chemistry.

Alpha-chymotrypsin: effects of bicyclic substrate geometry and hydrophobicity on reactivity.

M. Rohde, M. S. Matta, 1973, Archives of biochemistry and biophysics.

A comparison of the utilization of methyl and p-nitrophenyl esters in determining the specificity of -chymotrypsin.

M. Silver, M. S. Matta, 1972, Archives of biochemistry and biophysics.

Alpha-chymotrypsin. The use of substrates of restricted geometry to define the reactive conformation of methyl N-acetyl-l-phenylalaninate.

M. Silver, M. S. Matta, M. Stoddard, 1970, Journal of the American Chemical Society.

Specificities of α-Chymotrypsin and Subtilisin Carlsberg THE α-ACYLAMIDO EFFECT IN β-PHENYLPROPIONATES AND THEIR RIGID ANALOGS

M. S. Matta, D. D. Staley, 1974 .

Acylation of subtilisin A by aryl esters: contribution to rate limitation by a physical step preceding general acid-base catalysis.

M. S. Matta, M. Andracki, 1988, Biochemistry.