ライフサイエンスコーパス: catabolic enzyme

1 ular xanthine and hypoxanthine by the purine catabolic enzyme.

2 tional repressor to a membrane-bound proline catabolic enzyme.

3 uster whose products have homology to purine catabolic enzymes.

4 changing the activity of local synthetic and catabolic enzymes.

5 ion of numerous genes which specify nitrogen catabolic enzymes.

6 tion and activities of both its anabolic and catabolic enzymes.

7 ripts encoding the relevant biosynthetic and catabolic enzymes.

8 s is substrate for a variety of anabolic and catabolic enzymes.

9 ions also depend upon the levels of the PGE2 catabolic enzyme 15-hydroxyprostaglandin dehydrogenase (

10 nown about the role of the key prostaglandin catabolic enzyme 15-hydroxyprostaglandin dehydrogenase (

11 to cancer progression, is inactivated by the catabolic enzyme, 15-hydroxyprostaglandin dehydrogenase

12 Mutation of alh-6, a conserved proline catabolic enzyme, accelerates fat mobilization, enhances

13 t, be related to inhibition of prostaglandin catabolic enzyme activities.

14 Recently, we showed that catabolic enzyme activity could be assessed by substrate

15 ctions both as a membrane-associated proline catabolic enzyme and as a transcriptional repressor of t

16 ic growth of Escherichia coli, expression of catabolic enzymes and envelope and periplasmic proteins

17 osis enabled induction of several additional catabolic enzymes and sugar transporters at the high pH,

18 ethylglycine, sarcosine, glycine, and serine catabolic enzymes and the BetX and CbcXWV quaternary ami

19 se provides curated information on microbial catabolic enzymes and their organization into metabolic

20 ehydrogenase (15-PGDH, the key prostaglandin catabolic enzyme) and the cell cycle inhibitor p21.

21 s and is expressed in tissues in which these catabolic enzymes are expressed.

22 The structural genes that encode nitrogen catabolic enzymes are subject to nitrogen metabolite rep

23 rter, and nanA and nanE, predicted to encode catabolic enzymes, are essential for growth on Neu5Ac.

24 he administration of a pegylated form of the catabolic enzyme arginase I (peg-Arg I) has shown some p

25 The Neurospora crassa catabolic enzyme, arginase (L-arginine amidinohydrolase,

26 g submergence in the SUB1A rice through a GA catabolic enzyme as part of an early response and may re

27 uman chondrocytes promoted the expression of catabolic enzymes associated with OA.

28 d and genes encoding many of the chlorophyll catabolic enzymes been identified.

29 Here we demonstrate that SOD1 is not just a catabolic enzyme, but can also directly regulate NADPH o

30 kdown, STAY-GREEN1 (SGR1) interacts with Chl catabolic enzymes (CCEs) and light-harvesting complex II

31 d Ile content, suggesting that these two Thr catabolic enzymes compete for a common substrate pool.

32 iated with the known overexpression of lipid catabolic enzymes, could be detected through metabolomic

33 idermis, as were the activities of two lipid catabolic enzymes critical to stratum corneum function,

34 pecifically examined the effect of its major catabolic enzyme, CYP24A1, in prostate cancer.

35 120% increase in the expression of the ATRA catabolic enzyme Cyp26a1 in Dhrs3(-/-) embryos vs. contr

36 dh ortholog, rdh1, and a major retinoic acid catabolic enzyme, cyp26a1, suggesting coordinate modulat

37 ation (by knocking out the gene encoding the catabolic enzyme CYP7B1) decreased estrogen-dependent ex

38 Deficiency of the pyrimidine catabolic enzyme, dihydropyrimidine dehydrogenase (DPD),

39 f ADMA are controlled by two isoforms of its catabolic enzyme dimethylarginine dimethylaminohydrolase

40 The Pdu MCP consists of catabolic enzymes encased within a protein shell, and it

41 is consumed by this microorganism using the catabolic enzymes encoded by genes hpdH, hbdH and mmsA.

42 nant proteins we characterized four inositol catabolic enzymes encoded in the TM0412-TM0416 chromosom

43 e of a RA sink in the form of the CYP26B1 RA catabolic enzyme expressed in deeper regions of the brai

44 r-2.1(0) and older wild-type males, enhanced catabolic enzymes expression, coupled with the reduced e

45 r proteins that mediate AEA transport to its catabolic enzyme fatty acid amide hydrolase (FAAH).

46 ndocannabinoid anandamide is degraded by the catabolic enzyme fatty acid amide hydrolase (FAAH).

47 type 1 (CRF1) potentiation of the anandamide catabolic enzyme fatty acid amide hydrolase.

48 x 10(-53)), a gene that encodes the primary catabolic enzyme for 1,25-dihydroxyvitamin D and 25-dihy

49 Adenosine deaminase (ADA) is the principal catabolic enzyme for adenosine in vivo, and its deficien

50 of ethanolamine ammonia lyase (EA-lyase), a catabolic enzyme for ethanolamine.

51 rolase (FAAH) (C385A; rs324420), the primary catabolic enzyme for the endocannabinoid anandamide.

52 ce deficient in both CD73 and AMPD3, the key catabolic enzymes for extracellular and intra-erythrocyt

53 on acetate, Methanosarcina barkeri expresses catabolic enzymes for other methanogenic substrates such

54 information exists on the quinate/shikimate catabolic enzymes found in these organisms.

55 These evolved catabolic enzymes have application for improving biodegr

56 st likely due to reduced activity of the HDL-catabolic enzyme hepatic lipase (Lipc) and increased exp

57 e (IDE, insulysin) is the best characterized catabolic enzyme implicated in proteolysis of insulin.

58 cond, phenylethylamine oxidase is an unusual catabolic enzyme in that it is localized in the periplas

59 resis demonstrated downregulation of several catabolic enzymes in 8-month-old offspring of NR ewes.

60 s are reflected in expression levels of BCAA catabolic enzymes in both mice and humans.

61 arkness regulates the gene expression of fat catabolic enzymes in mice.

62 ased on the loss of essential amino acids by catabolic enzymes in the microenvironment is a critical

63 deacetylation steps, whereas the downstream catabolic enzymes in the pathway were largely conserved.

64 To examine the role of the catabolic enzymes in the response of breast cancer cells

65 The operon encoding catabolic enzymes in the utilization of L-ascorbate (ula

66 Overexpression of SSAT (polyamine catabolic enzyme) in female mice results in impaired ova

67 a is provided with a focus on the tryptophan catabolic enzyme indoleamine 2,3-dioxygenase (IDO) and i

68 -molecule inhibitors of the tryptophan (Trp) catabolic enzyme indoleamine 2,3-dioxygenase (IDO) repre

69 s are the first to show that endocannabinoid catabolic enzyme inhibitors reduce abrupt withdrawal in

70 the transcription of genes encoding several catabolic enzymes is increased.

71 covery of impaired branched chain amino acid catabolic enzyme isovaleryl-CoA dehydrogenase (encoded b

72 gene that encodes a rate-limiting polyamine catabolic enzyme, leads to lower intracellular polyamine

73 embers of the cytochrome P450 superfamily of catabolic enzymes, localized in the endoplasmic reticulu

74 s indicated by upregulated expression of the catabolic enzymes LYPLA1, LYPLA2, and GPCPD1.

75 The mannitol catabolic enzyme mannitol dehydrogenase (MTD) is a prime

76 Conversely, we show that the catabolic enzyme mannitol dehydrogenase is induced in a

77 Inhibition of the endocannabinoid catabolic enzymes, monoacylglycerol lipase (MAGL) or fat

78 The catabolic enzyme myo-inositol oxygenase (MIOX) is expres

79 king PMA-induced expression of the polyamine catabolic enzyme N(1)-spermidine/spermine acetyltransfer

80 n level of the gene that encodes the primary catabolic enzyme of active vitamin D [25(OH)D-24-hydroxy

81 omocysteine has been proposed to inhibit the catabolic enzyme of ADMA, dimethylarginine dimethylamino

82 DDAH1 is a key catabolic enzyme of asymmetric dimethylarginine (ADMA),

83 Catabolic enzymes of the ceramide and glycolipid pathway

84 s, type 1 and 2, as well as biosynthetic and catabolic enzymes of the endocannabinoids N-arachidonoyl

85 ytes and combined it with the specificity of catabolic enzymes of the sphingolipid pathway.

86 nephosphotransferase (PAF-CPT), and its main catabolic enzyme (PAF acetylhydrolase; PAF-AH), on U937

87 oleamine 2,3-dioxygenase (IDO), a tryptophan catabolic enzyme previously shown to have regulatory act

88 osis factor alpha [TNFalpha], and IL-6), and catabolic enzymes (procathepsin B and neutrophil elastas

89 atrix deposition, whilst enhancing selective catabolic enzyme production, suggesting its potential fo

90 te phosphotransferase system (PTS) and other catabolic enzymes responsible for transport and cataboli

91 on of the operon that encodes the L-rhamnose catabolic enzymes, rhaBAD, as well as the operon that en

92 Examination of chondroitin/dermatan sulfate catabolic enzymes showed that heparan sulfate and hepari

93 n nature have evolved new genes which encode catabolic enzymes specific for chlorinated aromatic subs

94 Maximal induction of the polyamine catabolic enzyme spermidine/spermine N(1)-acetyltransfer

95 enzymes and potently inducing the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas

96 nsive to analogue induction of the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas

97 sults in the superinduction of the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas

98 hesis and potently upregulates the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas

99 Rapid synthesis of the polyamine catabolic enzyme spermidine/spermine-N(1)-acetyltransfer

100 To test this, the responses of the polyamine catabolic enzymes spermidine/spermine acetyltransferase

101 ion of polyamines by overexpression of a key catabolic enzyme, spermidine/spermine N(1)-acetyltransfe

102 e most potent known inducer of the polyamine catabolic enzyme, spermidine/spermine N1-acetyltransfera

103 The polyamine catabolic enzyme spermine oxidase (SMOX) is induced in c

104 pression levels of the gibberellic acid (GA) catabolic enzyme StGA2ox1.

105 for biochemically undefined observations in catabolic enzyme substrate specificity, the interplay be

106 of only two operons, both encoding pyruvate catabolic enzymes, suggesting an intimate relationship b

107 discovery of a novel IDO-related tryptophan catabolic enzyme termed IDO2 that is preferentially inhi

108 protein 43% identical to a mammalian valine catabolic enzyme that hydrolyzes beta-hydroxyisobutyryl-

109 Indoleamine 2,3 dioxygenase (IDO) is a catabolic enzyme that initiates the kynurenine pathway o

110 Spermine oxidase (SMO) is a polyamine catabolic enzyme that is highly inducible by inflammator

111 Adenosine deaminase (ADA) is a purine catabolic enzyme that manages levels of the biologically

112 ism by which bFGF controls the production of catabolic enzymes that are associated with excessive deg

113 ceutical Co.'s KH-1060 (3), is recognized by catabolic enzymes, the selective biological profile of s

114 Targeting a catabolic enzyme to buy time for recombination is an ama

115 denitrificans did not produce extracellular catabolic enzymes to transform cholesterol.

116 ed to concentrate low levels of ethanolamine catabolic enzymes, to keep the level of toxic acetaldehy

117 genes that encode the tbu pathway's initial catabolic enzyme, toluene-3-monooxygenase, as well as Tb

118 uggests that coordinate targeting of the Trp catabolic enzymes tryptophan 2,3-dioxygenase (TDO) and I

119 peron contains three genes encoding probable catabolic enzymes, two of which (AgaF and AgaG) are thou

120 erase (SSAT) gene, which encodes a polyamine catabolic enzyme, was induced by clinically relevant sul

121 expression of CYP26A1, a major retinoic acid catabolic enzyme, was up-regulated in Apc(MIN) mouse ade

122 atous degeneration by excessive secretion of catabolic enzymes, we examined the functional characteri

123 However, key polyamine anabolic and catabolic enzymes were upregulated, and there were corre

124 atch a broad specificity of hydroxycinnamate catabolic enzymes while responding to toxic thioester in

125 osine deaminase (ADA) is a ubiquitous purine catabolic enzyme whose expression is subject to developm

126 ofibroblasts and express excessive levels of catabolic enzymes, without altered levels of interstitia