ライフサイエンスコーパス: chloroperoxidase

1 und I derivative of the heme-thiolate enzyme chloroperoxidase.

2 rom the two-electron oxidations catalyzed by chloroperoxidase.

3 the chlorination and dismutation activity of chloroperoxidase.

4 t essential for the chlorination activity of chloroperoxidase.

5 nd had significant overlap with complexes of chloroperoxidase.

6 for compound I of horseradish peroxidase and chloroperoxidase.

7 f which putatively encode vanadium-dependent chloroperoxidases.

8 ve-site alignment of the vanadium-containing chloroperoxidase and G6Pases predicts that Arg-83, His-1

9 nplay the importance of a thiolate ligand in chloroperoxidase and suggest that the distal environment

10 Genes for non-heme, no-metal chloroperoxidases and haloalkane dehalogenases were the

11 se, soybean peroxidase, Caldariomyces fumago chloroperoxidase, and mushroom polyphenol oxidase-is muc

12 te NMR spectroscopy of the 67.5-kDa vanadium chloroperoxidase, at 14.1 T.

13 t investigation, ferric and ferrous alkaline chloroperoxidase (C420) have been characterized by elect

14 dase (MPO), eosinophil peroxidase (EPO), and chloroperoxidase can oxidize iodide, bromide, and chlori

15 investigate the role of glutamic acid 183 in chloroperoxidase catalysis.

16 dative dehalogenation catalyzed by C. fumago chloroperoxidase (CCPO) involves two consecutive one-ele

17 f suitable amounts of peroxide and chloride, chloroperoxidase chlorinates thionin and bleaches the in

18 r spectrum of CYP119-I is similar to that of chloroperoxidase compound I, although its electron param

19 roscopy, we have found that the Fe-O bond in chloroperoxidase compound II (CPO-II) is much longer tha

20 Resonance Raman measurements on chloroperoxidase compound II (CPO-II) reveal an isotope

21 and Mossbauer spectroscopy, we have examined chloroperoxidase compound II (CPO-II).

22 n explicitly solvated cis-beta-methylstyrene/chloroperoxidase-Compound I complex are performed to det

23 ymatic natural halogenation: chlorination by chloroperoxidase (CPO) and flavin-dependent halogenases

24 dependent peroxidatic reactions catalyzed by chloroperoxidase (CPO) are extended to CPO-catalyzed hal

25 Cytochrome P450 (P450) and chloroperoxidase (CPO) are thiolate-ligated haem protein

26 Chloroperoxidase (CPO) catalyzes the enantioselective ox

27 g x-ray absorption spectroscopy, we examined chloroperoxidase (CPO) compound I (CPO-I).

28 Chloroperoxidase (CPO) is suspected to play an important

29 py to study a heme-N-alkylated derivative of chloroperoxidase (CPO) prepared by mechanism-based inact

30 The heme active site structure of chloroperoxidase (CPO), a glycoprotein that displays ver

31 e rebinding kinetics of Caldariomyces fumago chloroperoxidase (CPO).

32 o those observed in cytochrome P450(cam) and chloroperoxidase (CPO).

33 cid residue supplying the thiolate ligand in chloroperoxidase, Cys-29 has been replaced with a histid

34 two algal bromoperoxidases and the vanadium chloroperoxidase from the fungus Curvularia inaequalis.

35 Since chloroperoxidase functions normally through the ferric a

36 Mutant clones of the chloroperoxidase genome have been expressed in a Caldari

37 d on the x-ray crystallographic structure of chloroperoxidase, Glu-183 is postulated to function on d

38 The presence of a thiolate ligand in chloroperoxidase has long been thought to play an essent

39 on by representative soil enzymes (C. fumago chloroperoxidase, horseradish peroxidase, and laccase fr

40 eAPO-I (361, 694 nm) are similar to those of chloroperoxidase-I and the recently described cytochrome

41 Chloroperoxidase, in addition to catalyzing classical pe

42 Chloroperoxidase is a versatile fungal heme-thiolate pro

43 Chloroperoxidase is a versatile heme enzyme which can cr

44 ism by which the heme-containing peroxidase, chloroperoxidase, is able to chlorinate substrates is po

45 e spectroscopically related inactive form of chloroperoxidase lead to the conclusion that a sulfur-de

46 As eNOS and chloroperoxidase lie closer than do eNOS and P450cam on

47 The vanadium-dependent chloroperoxidase Mcl24 was discovered to mediate a compl

48 he distal heme environment in eNOS resembles chloroperoxidase more than P450cam.

49 The multiple functions of chloroperoxidase must be derived from its unique active

50 terization of a bacterial vanadium-dependent chloroperoxidase, NapH1 from Streptomyces sp. CNQ-525, w

51 The haloperoxidase Notomastus lobatus chloroperoxidase (NCPO) is unusual in requiring a flavop

52 Chloroperoxidase possesses a proximal cysteine thiolate

53 tochromes; however, unlike the P450 enzymes, chloroperoxidase possesses a very polar environment dist

54 ponents of the global chlorine cycle because chloroperoxidase-producing fungi are ubiquitous in decay

55 to the heme iron may be weaker, as found in chloroperoxidase, than in cytochrome P-450 enzymes.

56 ntained a previously described C. inaequalis chloroperoxidase that very likely catalyzed lignin chlor

57 C. fumago produces wild-type chloroperoxidase, thus requiring gene replacement of the

58 This finding biochemically links a vanadium chloroperoxidase to microbial natural product biosynthes

59 In particular, under alkaline conditions, chloroperoxidase undergoes a transition to a new, spectr

60 r in the resting state of vanadium-dependent chloroperoxidases (VCPO).

61 acid phosphatases, and a vanadium-containing chloroperoxidase (whose tertiary structure is known) sha