-
1
-
-
0042653155
-
-
note
-
The original name of the enzyme was ethanol deaminase (see ref 3), but later it was changed to ethanolamine ammonia lyase (EC 4.3.1.7).
-
-
-
-
2
-
-
0042653158
-
-
note
-
While the actual substrate is 2-aminoethanol, for the sake of shortness, it is abbreviated in the text as aminoethanol.
-
-
-
-
4
-
-
0035830318
-
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46
-
-
0042653149
-
-
note
-
The QCISD enthalpies at 298 K were computed as fallows: ΔH (QCISD; 298 K) = ΔH (QCISD; 0 K) + ΔH (B3LYP; 298K) - ΔH (B3LYP; 0 K), where enthalpies at 0 K include the sum of the electronic energy and ZPE corrections scaled by 0.9806.
-
-
-
-
47
-
-
84962348955
-
-
For the sake of shortness, it is the pH of the reaction environment around the enzyme's active site which is meant when the phrase "pH in the active site" is used. For a superb discussion of this and related aspects, see: Barril, X.; Alemán, C.; Orozco, M.; Luque, F. J. Proteins 1998, 32, 67.
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54
-
-
0042152088
-
-
note
-
a (Glu) = 4.1, taken from ref 45.
-
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-
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55
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0003464216
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Linstrom P.J., Mallard W.G., Eds.; Nist Standard Reference Database Number 69; National Institute of Standards and Technology, Gaithersburg, MD, July
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63
-
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0033603034
-
-
For a study on neutral aminoethanol, see: Silva, C. F. P.; Duarte, M. L. T. S.; Fausto, R. J. Mol. Struct. 1999, 482-483, 591.
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Silva, C.F.P.1
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64
-
-
0041651183
-
-
note
-
- will not be included due to the very high activation enthalpy associated with the migration pathway.
-
-
-
-
65
-
-
0042152084
-
-
note
-
In ref 8 this type of rearrangement is described as " dissociation-association mechanism".
-
-
-
-
66
-
-
0041651185
-
-
note
-
2 or, equivalently, calculating the activation enthalpy for the dissociation starting from the conformer in which the H-bond interaction does not exist and adding the energy difference between the two reactant conformers. Here, the latter method was used.
-
-
-
-
67
-
-
0042152083
-
-
note
-
3) = 204.0 kcal/mol. All data taken from ref 47.
-
-
-
-
68
-
-
0041651184
-
-
note
-
For example, the optimal pH for catalytic activity of related glutamate mutase falls into the range 7.5-8; see ref 28.
-
-
-
-
69
-
-
0037899473
-
-
For recent review articles on this and related topics, see: (a) Banerjee, R. Chem. Rev. 2003, 103, 2083;
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Banerjee, R.1
|