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1 for the hydrolysis of mNBP, consistent with general acid catalysis.
2 yl substrates and a His-Glu pair involved in general acid catalysis.
3 ve charge on the leaving group and efficient general acid catalysis.
4 cates that these reactions involve only weak general acid catalysis.
5 roles in transition state stabilization and general acid catalysis.
6 n a Bronsted plot that was characteristic of general acid catalysis.
7 he active phosphatase conformation, enabling general acid catalysis.
8 ism of PPT is likely to involve general base-general acid catalysis.
9 ge residue Trp354 to Ala completely disables general acid catalysis.
10 ntermediate is subject to both specific- and general-acid catalysis.
11 l acetate ester was studied with and without general-acid catalysis.
12 ed MKP3 clearly indicated the involvement of general acid catalysis, a hallmark of protein-tyrosine p
13 olves transition-state stabilization through general-acid catalysis and freeing of three water molecu
15 gainst other enzymatic KIEs with and without general acid catalysis, are consistent with a loose tran
16 g against a role for rescuing nucleobases in general acid catalysis, because a nucleobase that contri
17 he transition state for cleavage of 1-F from general acid catalysis by 0.80 M cyanoacetate buffer at
20 s, provide support for a mechanism involving general-acid catalysis by a conserved adenine residue in
21 o estimate the individual rate constants for general-acid catalysis by the diacid and monoacid forms
22 rom Yersinia, we have examined the effect on general acid catalysis caused by mutations to two conser
24 hydroxide ion on the scissile phosphate, and general acid catalysis for protonation of the leaving 3'
25 s from previous studies that Cdc25A utilizes general acid catalysis for substrates with a leaving gro
26 acidic system reacted by means of concerted general acid catalysis (found to be a so-called D(N)A(N)
28 lysis, because a nucleobase that contributes general acid catalysis in the cleavage pathway should pr
29 suggest a general base mechanism with likely general acid catalysis in the oxidative decarboxylation
36 ion provides an explanation for the impaired general acid catalysis observed in kinetic experiments w
37 f acetic acid and the imidazolium ion showed general acid catalysis of 18.5 and 1.5 M-1 sec-1, respec
38 nt with the conclusion that Glu-461 provides general acid catalysis of leaving group departure, which
39 bond fission with the alkyl substrate, while general acid catalysis of pNPP by YopH is more synchrono
41 e Tyr-274 on the scissile phosphodiester and general-acid catalysis of the expulsion of the 5'-deoxyr
42 N (CHI.CHN) and CHI.TS, we found: (i) Lys-97-general-acid catalysis of the O2'(-) nucleophilic additi
43 ired for phosphodiester cleavage, either for general acid catalysis or for electrostatic stabilizatio
45 rformed to study the proton-transfer step in general acid catalysis that is facilitated by the cataly
47 rimental data that points to a novel mode of general acid catalysis through the N3 position of an ade
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