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1 and calcium content as thermally inactivated manganese peroxidase.
2        CdII alters the heme Soret on binding manganese peroxidase and exhibits a Kd approximately 8 m
3 y emphasis on the enzymes lignin peroxidase, manganese peroxidase and laccase.
4             Versatile peroxidase shares with manganese peroxidase and lignin peroxidase the ability t
5 f calcium to prevent thermal inactivation of manganese peroxidase and the rate of calcium binding dec
6 site with both compound I and compound II of manganese peroxidase and to determine whether phenolic s
7   The 16 encoded enzymes include 13 putative manganese peroxidases and one generic peroxidase but mos
8 me c peroxidase, horseradish peroxidase, and manganese peroxidase, and (d) examination of the crystal
9  conformational changes proposed to occur in manganese peroxidase as a result of the binding and rele
10                                Inhibition of manganese peroxidase by cadmium was studied under steady
11 s that occurred during thermal incubation of manganese peroxidase could be explained by the loss of t
12 stal heme environment, thermally inactivated manganese peroxidase did not react with hydrogen peroxid
13              We previously demonstrated that manganese peroxidase from Phanerochaete chrysosporiumwas
14 igates whether compound I and compound II of manganese peroxidase from the white-rot fungus Phaneroch
15              We previously demonstrated that manganese peroxidase from the white-rot fungus Phaneroch
16 and 55 degrees C, MnII and CdII both protect manganese peroxidase from thermal denaturation more effi
17 inactivation and the release of calcium from manganese peroxidase have now been characterized.
18                                A recombinant manganese peroxidase, in which the distal calcium bindin
19 ulfonic acid, dipotassium salt (bis-ANS), to manganese peroxidase indicated that the active, calcium-
20 tations R177A and R177K in the gene encoding manganese peroxidase isozyme 1 (mnp1) from Phanerochaete
21 190L, F190I, and F190A, in the gene encoding manganese peroxidase isozyme 1 (mnp1) from Phanerochaete
22 , E39Q, and E35Q-D179N, in the gene encoding manganese peroxidase isozyme 1 (mnp1) from Phanerochaete
23  in MnII binding at the MnII binding site of manganese peroxidase isozyme 1 (MnP1) of Phanerochaete c
24 esis that the synergy of Fenton reaction and manganese peroxidase might play an important role in DR5
25                  Phanerochaete chrysosporium manganese peroxidase (MnP) [isoenzyme H4] was engineered
26 nce CcP contains both Trp51 and Trp191 while manganese peroxidase (MnP) contains phenylalanine residu
27                                              Manganese peroxidase (MnP) from Phanerochaete chrysospor
28                                     Purified manganese peroxidase (MnP) from Phanerochaete chrysospor
29  cytochrome c peroxidase that closely mimics manganese peroxidase (MnP) has been characterized by bot
30                                              Manganese peroxidase (MnP) is a heme-containing enzyme p
31                                              Manganese peroxidase (MnP) is an extracellular heme enzy
32 f a series of functionally active models for manganese peroxidase (MnP) is described.
33                                              Manganese peroxidase (MnP), an extracellular heme enzyme
34 ases, including the lignin degrading enzymes manganese peroxidase (MnP), lignin peroxidase (LiP), and
35  detectable values of 7.9% for free laccase, manganese peroxidase (MnP), lignin peroxidase (LiP), res
36  an efficiency that is comparable to that of manganese peroxidase (MnP).
37 ated by purified lignin peroxidase (LiP) and manganese peroxidase (MnP).
38                                   The mutant manganese peroxidases (MnPs) were purified and character
39 on of these genes together with a lignolytic manganese peroxidase, multiple copper radical oxidases,
40                               Genes encoding manganese peroxidase numbered 13 and five in C. subvermi
41                                          The manganese peroxidase variants (MnPs) were purified and c
42                                              Manganese peroxidase was expressed from its cDNA in Esch
43 oposed that, at lower pH, calcium binding to manganese peroxidase was more thermodynamically favorabl
44 hat the heme iron of the inactivated form of manganese peroxidase was predominantly in a low-spin sta
45       The absorption spectrum of inactivated manganese peroxidase was similar to that of low-spin fer
46 alcium to the distal calcium binding site of manganese peroxidase was studied by optical absorption s
47 idized by the radical products of lignin and manganese peroxidases, whereas cellulose and hemicellulo

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