ライフサイエンスコーパス: heme enzyme

1 re of a thioether inhibitor complexed to any heme enzyme.

2 sm of regulation of the activity of this key heme enzyme.

3 or the understanding of O-O bond cleavage in heme enzymes.

4 onding that is important for the function of heme enzymes.

5 idation of hydrocarbons by both heme and non-heme enzymes.

6 , ligand, and metal modulate the function of heme enzymes.

7 M(IV)(O)(porph(*+)) (M = Mn or Fe) found in heme enzymes.

8 Heme enzymes activate oxygen through formation of transi

9 ts add new features to SA's interaction with heme enzymes and its in vivo redox properties.

10 [Fe(IV)O] intermediate is important in many heme enzymes, and thus, the precise nature of the Fe(IV)

11 Heme enzymes are capable of catalyzing a range of oxidat

12 a and the properties of other well-described heme enzymes are proposed.

13 II)-O(2)*(-) intermediates are well known in heme enzymes, but none have been characterized in the no

14 MCS)+ are higher than the ones obtained with heme enzymes, but the chemoselectivity is lesser affecte

15 at fine-tuning E degrees ' in HCOs and other heme enzymes can modulate their substrate affinity, ET r

16 ins, demonstrating that non-thiolate-ligated heme enzymes can perform this function.

17 ial life processes, nature has had to evolve heme enzymes capable of synthesizing and manipulating co

18 Catalytic heme enzymes carry out a wide range of oxidations in bio

19 Catalase activity of the dual-function heme enzyme catalase-peroxidase (KatG) depends on severa

20 tuberculosis catalase-peroxidase (KatG) is a heme enzyme considered important for virulence, which is

21 We conclude that both new heme enzymes contain histidine as their proximal heme ir

22 (a) approximately 12 in the thiolate-ligated heme enzyme cytochrome P450, this result provides insigh

23 In exponentially growing yeast, the heme enzyme, cytochrome c peroxidase (Ccp1) is targeted

24 orphyrin IX (Mn-PGHS) to those of the native heme enzyme (Fe-PGHS).

25 Manganese peroxidase (MnP), an extracellular heme enzyme from the lignin-degrading basidiomycetous fu

26 ereoselectivity of P4H and many non-heme and heme enzymes in general, and insight into this matter ma

27 of metal-organic materials (MOMs) that mimic heme enzymes in terms of both structure and reactivity.

28 The heme enzyme indoleamine 2,3-dioxygenase (IDO) is a key r

29 The heme enzyme indoleamine 2,3-dioxygenase (IDO) plays an i

30 The heme enzyme indoleamine 2,3-dioxygenase (IDO) was found

31 The heme enzyme is shown to follow the halogenation cycle th

32 yrin intermediates, inadequate activation of heme enzymes, low catalase activity, defective clearance

33 que has been used to study copper complexes, hemes, enzyme mechanisms, micellar water content, and wa

34 DHP I is a heme enzyme (Mr = 30,790) composed of two identical subu

35 The heme enzyme myeloperoxidase (MPO) participates in innate

36 e oxygen species that are generated by their heme enzyme myeloperoxidase.

37 Heme enzymes provide a striking example of this complexi

38 tudies it was reported that thiolate-ligated heme enzymes react with peroxynitrite to form a ferryl i

39 Eosinophil peroxidase, a heme enzyme released by eosinophils, generates hypobromo

40 Myeloperoxidase, a heme enzyme released by polymorphonuclear neutrophils, a

41 erium tuberculosis KatG is a multifunctional heme enzyme responsible for activation of the antibiotic

42 Myeloperoxidase, the heme enzyme secreted by activated neutrophils and monocy

43 The pathway begins with myeloperoxidase, a heme enzyme secreted by activated neutrophils.

44 Myeloperoxidase (MPO), a heme enzyme secreted by activated phagocytes, generates

45 Myeloperoxidase, a heme enzyme secreted by activated phagocytes, uses H(2)O

46 nflammation that involves myeloperoxidase, a heme enzyme secreted by activated phagocytes.

47 es and is also an essential cofactor for non-heme enzymes such as ribonucleotide reductase, the limit

48 This presents the first example for a heme enzyme that catalyzes the enantioselective oxidatio

49 nganese peroxidase (MnP) is an extracellular heme enzyme that catalyzes the peroxide-dependent oxidat

50 talase is a luminal thylakoid membrane-bound heme enzyme that has not been identified previously.

51 DO) and tryptophan 2,3-dioxygenase (TDO) are heme enzymes that catalyze the O(2)-dependent oxidation

52 NOS) are catalytically self-sufficient flavo-heme enzymes that generate NO from arginine (Arg) and di

53 and diverse superfamily of mononuclear, non-heme enzymes that perform a variety of oxidative transfo

54 Nitric oxide synthases (NOSs) are flavo-heme enzymes that require (6R)-tetrahydrobiopterin (H(4)

55 (NO), is biosynthesized by a group of flavo-heme enzymes, the nitric oxide synthases.

56 on chaperones, delivering iron to target non-heme enzymes through direct protein-protein interactions

57 a plethora of metalloporphyrin complexes and heme enzymes used as electrocatalysts for small-molecule

58 The heme enzyme was shown to release hypobromous acid that m

59 Chloroperoxidase is a versatile heme enzyme which can cross over the catalytic boundarie

60 ure can be catalyzed by phenol-coupling P450 heme enzymes, which might also apply to the plant kingdo

61 Nitric-oxide synthases (NOSs) are flavo-heme enzymes whose electron transfer reactions are contr

62 atalase-peroxidases (KatGs) are bifunctional heme enzymes widely spread in archaea, bacteria, and low

63 mphitrite ornata dehaloperoxidase (DHP) is a heme enzyme with a globin structure, which is capable of