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1 1 functions as both the general acid and the general base catalyst.
2 rt of a water molecule serving as the direct general base catalyst.
3 Q, R, and M to probe its possible role as a general base catalyst.
4 K(a) of 4.4 indicate that it cannot act as a general base catalyst.
5 the imidazole group of histidine serves as a general base catalyst.
6 and tautomerically stabilized to serve as a general base catalyst.
7 ween the nucleophile and G12, the implicated general base catalyst.
8 nce of solvent water, which itself acts as a general base catalyst.
9 aminoacyl-tRNA probably replaces water as a general base catalyst.
10 s assigned to Glu-570, which is the proposed general base catalyst, abstracting a proton from the eps
11 cular they support the role of Arg(297) as a general base catalyst accepting a proton in the dehydrog
12 tify the best arrangement of a pyridine as a general base catalyst and an alcohol nucleophile to acce
13 the side chain of Asp-15 functioning as the general base catalyst and His-144 serving as the general
14 l-based ligand plays the essential role of a general base catalyst and selectively accelerates the cy
17 dependence argues against a role for G8 as a general base catalyst, because G8 deprotonation could no
18 an essential catalytic residue, acting as a general base catalyst by deprotonating the histone subst
19 (2)(-).H-OCH(3) is in a position to act as a general base catalyst for hydride equivalent transfer to
20 It has been proposed that His447 acts as the general base catalyst for oxidation, and that the result
21 ith D302 mutants suggest D302 functions as a general base catalyst in activation of the 3-hydroxyl of
22 e thus suggest that Glu171 plays the role of general base catalyst in PQQ reduction rather than Asp29
23 44 is consistent with its proposed roll as a general base catalyst in the addition of water to the an
25 rotonate tautomerase (4-OT) functions as the general base catalyst in the enzyme-catalyzed isomerizat
26 tion, it is concluded that Pro-1 acts as the general base catalyst in the MIF-catalyzed reaction.
27 glutamate-166 in its functional role as the general base catalyst in the wild-type enzyme for hydrol
28 (2)(-)) have been considered as the required general base catalysts in the bacterial o-quinoprotein m
29 e, suggesting that this residue may act as a general-base catalyst in the phosphoryl transfer reactio
30 he proton transfer from Ser278 to Glu78 (the general base catalyst) is synchronous with the nucleophi
31 ODI, hydrogen peroxide, imidazole (ImH), the general-base catalysts lutidine and collidine, and tempe
35 cks Asp38-hereby implicated as the essential general base catalyst that abstracts a proton from the 5
37 9 by sT-CoA and is proposed to function as a general base catalyst to activate the hydroxyl of HBCoA
39 e gamma-phosphate oxygen atoms to serve as a general base catalyst to induce an "associative" phospho
40 n important role in catalysis by acting as a general base catalyst toward the zinc-bound water molecu
42 ariant glutamate residue (Glu-243) acts as a general base catalyst, which activates the hydroxyl grou
43 ds and Gly-l-Xaa dipeptides do not include a general base catalyst, while such catalysis is essential
44 data do not support a mechanism involving a general-base catalyst whose pK(a) is greater than 5 or l
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