ライフサイエンスコーパス: glutathione transferase

1 s 1 (ABA-1), Asc l 3 (tropomyosin) and GST (glutathione transferase).

2 rium lacks yliJ, a gene encoding a predicted glutathione transferase.

3 e design of selective inhibitors of class pi glutathione transferases.

4 ccharomyces cerevisiae genes, GTT1 and GTT2 (glutathione transferase 1 and 2), coding for functional

5 Microsomal glutathione transferase-1 (MGST1) is a trimeric, membran

6 The detoxication enzyme glutathione transferase A1-1 (GSTA1-1), exploits a molte

7 e C-terminal region of the human class alpha glutathione transferase A1-1 have been investigated with

8 teroid Delta(5)-androstene-3,17-dione by the glutathione transferase A3-3 in mammals was investigated

9 he Marcus formalism indicates that the human glutathione transferase A3-3 lowers the intrinsic kineti

10 Conjugation to glutathione (GSH) by glutathione transferase A4-4 (GSTA4-4) is a major route

11 colon mucosal biopsies revealed increases in glutathione transferase activity at the lower dose level

12 This glutathione transferase activity of MMACHC is reminiscen

13 CblC is the first example of an enzyme with glutathione transferase activity that has a sequence and

14 ow epoxide hydrolase activity and even lower glutathione transferase activity toward 1 and does not c

15 CblC, a B12 trafficking protein, exhibits glutathione transferase and reductive decyanase activiti

16 mportant in the monomer-dimer equilibrium of glutathione transferase and that, although GST M1-1 may

17 The extracts induced glutathione transferases and heat shock protein 70, sugg

18 ajor enzyme families- the carboxylesterases, glutathione transferases, and cytochrome P450s-that are

19 s (GS- HQRs) are a newly identified group of glutathione transferases, and they are widely distribute

20 cytochromes P450 (P450s), sulfotransferases, glutathione transferases, and UDP-glucuronosyltransferas

21 Glutathione transferases are a multigene family of prote

22 Glutathione transferases are detoxification enzymes that

23 elated to the FosA class of Mn(2+)-dependent glutathione transferases but with a preference for Mg(2+

24 he low expression allele may be deficient in glutathione transferase catalyzed biological functions.

25 The fact that pi-glutathione transferase catalyzes the acyl-interchange r

26 channel 2 (CLIC2) protein is a member of the glutathione transferase class of proteins.

27 Glutathione transferases comprise a large family of cell

28 The cytosolic glutathione transferase (cytGST) superfamily comprises m

29 have characterized a Drosophila melanogaster glutathione transferase (DmGSTE6) which has activity tow

30 otective enzymes such as the Phase II enzyme glutathione transferase (EC 2.5.1.18).

31 ction of phase 2 detoxication enzymes [e.g., glutathione transferases, epoxide hydrolase, NAD(P)H: qu

32 perfamily, we identified two novel mammalian glutathione transferase families that were recognized pr

33 nd identification of a thiol reductase and a glutathione transferase from soybean seedling cotyledons

34 The crystal structure of the sigma class glutathione transferase from squid digestive gland in co

35 MAP4 was expressed in Escherichia coli as a glutathione transferase fusion protein and was injected

36 ombinant HGE-44, expressed and purified as a glutathione transferase fusion protein, was used as the

37 mouse and human nardilysin were expressed as glutathione transferase fusion proteins.

38 Induction of hepatic glutathione transferase genes and elevated total glutath

39 The specificity of human glutathione transferase (GST) A1-1 is drastically altere

40 Glutathione transferase (GST) A4-4 is a key component in

41 ssion in Escherichia coli of a tau (U) class glutathione transferase (GST) from maize (Zea mays L.),

42 the ability of purified arrestins to bind to glutathione transferase (GST) fusion proteins containing

43 Arrestin 3 bound to glutathione transferase (GST) fusion proteins of the D(2

44 Negative cooperativity occurs in human glutathione transferase (GST) GSTP1-1 when it binds and

45 The phase II detoxification system glutathione transferase (GST) is associated with the est

46 ne (GSNO)-mediated transnitrosation of human glutathione transferase (GST) P1-1, a major detoxificati

47 vered small protein distantly related to the glutathione transferase (GST) structural family, is high

48 m uroporphyrinogen and the induction of a mu-glutathione transferase (GST) were consistent with the o

49 greatly elevated levels of a specific type I glutathione transferase (GST), termed AmGST2, but simila

50 Since the 1960s, the multiple forms of glutathione transferase (GST), the GSTome, were isolated

51 A that V(max) was stimulated 3- to 4-fold by glutathione transferase (GST)-Galpha(12) with little eff

52 h huntingtin and P150 selectively bound to a glutathione transferase (GST)-HAP1 fusion protein.

53 H) is added to a mixture containing RBCs and glutathione transferase (GST).

54 Here, two structurally similar glutathione transferase (GST, glutathione S-transferase)

55 cytochrome P450s (CYP), esterases (EST), or glutathione transferases (GST) and at 12 previously mapp

56 Theta class glutathione transferases (GST) from various species exhi

57 A1, we created a bacterial fusion protein of glutathione-transferase (GST) and BRCA1 zinc finger doma

58 his study we discovered that the Omega class glutathione transferase GSTO1-1 plays a significant role

59 s linked to the overexpression of a pi class glutathione transferase (GSTP1), which has both detoxifi

60 ption-PCR was used to measure mRNA levels of glutathione transferases (GSTs) and glutathione peroxida

61 Glutathione transferases (GSTs) are protection enzymes c

62 Glutathione transferases (GSTs) are ubiquitous scavenger

63 The glutathione transferases (GSTs) from maize (Zea mays L.)

64 Six phi (F) class glutathione transferases (GSTs) were cloned from bread w

65 Here, we demonstrate the importance of two glutathione transferases (GSTs), GST-U24 and GST-U25, fr

66 erse superfamilies (amidohydrolase, enolase, glutathione transferase, haloalkanoic acid dehalogenase,

67 Continuing work with glutathione transferases has resulted in the identificat

68 e transferase (rGSTT2) and the human theta 1 glutathione transferase (hGSTT1) genes (63% DNA sequence

69 SH) bound in the active site of the class mu glutathione transferase M1-1 from rat involves a hydroge

70 Although rat glutathione transferase M1-1 is crystallized as a homodi

71 CYP2D6, CYP2E1, NAD(P)H-menadione reductase, glutathione transferases M1 and T1, and N-acetyltransfer

72 Phase 2 enzymes (e.g., glutathione transferases, NAD(P)H:quinone reductase) and

73 Induction of phase 2 enzymes (e.g., glutathione transferases, NAD(P)H:quinone reductase, glu

74 Glutathione transferase Omega 1 (GSTO1-1) is an atypical

75 Human glutathione transferase pi (GST pi) has been crystallize

76 Glutathione transferase pi (GSTP) catalyzes the detoxifi

77 Glutathione transferase Pi (GSTP) is commonly overexpres

78 These regions are attributed to the glutathione transferase portion of the fusion protein be

79 Here, the glutathione transferase pull-down assay was used to inve

80 Glutathione transferase pull-down assays and site-direct

81 Glutathione transferase pulldown assays demonstrate that

82 highly reactive cob(I)alamin product of the glutathione transferase reaction.

83 Glutathione transferase rGSTM1-1 catalyzes the addition

84 tructed such a library using the rat theta 2 glutathione transferase (rGSTT2) and the human theta 1 g

85 Using query sequences from known mammalian glutathione transferase subfamilies, we identified new c

86 Using query sequences from the glutathione transferase superfamily, we identified two n

87 Unlike many glutathione transferases, the reaction catalysed by MPI

88 A marked increase in serum alpha-glutathione transferase, TNF-alpha, IL-6, IL-10, MCP-1,

89 down assay, with cpSRP43 or cpSRP54 fused to glutathione-transferase, to study interactions between c

90 none reductases (GS-HQRs) are a new class of glutathione transferases, widely present in bacteria, ha

91 ification of fragments of carbon-13-enriched glutathione transferase within a complex mixture of unla

92 MAAI is also known as glutathione transferase zeta (GSTZ1).