ライフサイエンスコーパス: ferric reductase

1 not catalyzed by the expected membrane-bound ferric reductase.

2 e b, and is thus predicted to be active as a ferric reductase.

3 ing four independent loci, with dysregulated ferric reductase.

4 sumably was dependent upon the cell membrane ferric reductase.

5 duced activity of the heme-containing enzyme ferric reductase.

6 diheme protein, characteristic of eukaryotic ferric reductases.

7 -containing parasite enzyme LFR1 (Leishmania Ferric Reductase 1).

8 and RBT7, encode, respectively, an apparent ferric reductase, a plant pathogenesis-related protein (

9 ived receptor 2 is a catecholamine-regulated ferric reductase active in the brain.

10 The hypothesis that aberrant ferric reductase activities are involved in the progress

11 ms, including secreted glutathione-dependent ferric reductase activity (GSH-FeR).

12 Here we show that YqjH has ferric reductase activity and is required for iron homeo

13 Y1F and S2A cells had increased levels of ferric reductase activity and were hypersensitive to phl

14 rivation and accounts for all the detectable ferric reductase activity exposed on the surface of Leis

15 B. japonicum cells showed inducible ferric reductase activity in iron-limited cells that was

16 NADH-dependent ferric reductase activity increased approximately 100-fo

17 the frcB gene in Escherichia coli conferred ferric reductase activity on those cells.

18 ith the nature of HGA-melanins, the secreted ferric reductase activity was positively influenced by t

19 embrane of duodenal enterocytes, and induced ferric reductase activity when expressed in Xenopus oocy

20 eumophila-secreted HGA-melanin has intrinsic ferric reductase activity, converting Fe(3+) to Fe(2+),

21 he E. coli CymA orthologue NapC also carried ferric reductase activity.

22 time, that wild-type L. pneumophila secretes ferric reductase activity.

23 Ferric reductase also reduces FMN and FAD, but not ribof

24 ransferrin served both as substrates for the ferric reductase and as iron sources for yeast-phase gro

25 in a host, we studied the regulation of the ferric reductase and ferrous uptake system of this organ

26 xpression by H. capsulatum of both enzymatic ferric reductase and nonproteinaceous ferric reductant,

27 hodotorulic acid acted as substrates for the ferric reductase, and rhodotorulic acid removed Fe(III)

28 ed by copper starvation or inhibition of the ferric reductase by Pt, indicating that Fe solubilized b

29 SDS-polyacrylamide gel electrophoresis, the ferric reductase consists of a single subunit with a M(r

30 opsis, but did not complement an Arabidopsis ferric reductase defective 3 (FRD3) mutant.

31 The ferric reductase defective3 (frd3) mutant of Arabidopsis

32 ediated by duodenal cytochrome b (Cybrd1), a ferric reductase enzyme resident on the luminal surface

33 ophores, extracellular glutathione-dependent ferric reductase enzyme, extracellular nonproteinaceous

34 1), which is necessary for GB03-induction of ferric reductase FRO2 and the iron transporter IRT1.

35 igen of the prostate 3 (Steap3) is the major ferric reductase in developing erythrocytes.

36 s and a potential role for the extracellular ferric reductase in utilization of environmental and hos

37 of which have been functionally assigned as ferric reductases involved in iron ion transport.

38 aphy to be 40,000 suggesting that the native ferric reductase is a homodimer.

39 c reductases suggesting that the A. fulgidus ferric reductase is a novel enzyme.

40 ormation of the unsaturated lactone; and the ferric-reductase-like enzyme RbtH, which regioselectivel

41 igher values were achieved by a constitutive ferric reductase mutant in high concentrations of Fe(III

42 red whether Fe(II) generated by the external ferric reductase of fungi might have the physiologic fun

43 one of the eight members of the Arabidopsis ferric reductase oxidase (FRO) family, FRO7, localizes t

44 In response to Cu deficiency, FERRIC REDUCTASE OXIDASE5 (FRO5) and FRO4 transcript lev

45 uggests that membrane-bound, heme-containing ferric reductase proteins are not confined to eukaryotes

46 N-terminal sequence analysis of the purified ferric reductase resulted in the identification of the h

47 The A. fulgidus ferric reductase shares amino acid sequence similarity w

48 NAD(P)H:FMN oxidoreductases but not with any ferric reductases suggesting that the A. fulgidus ferric

49 We also demonstrated that the ferric reductase was regulated by copper and could act a

50 ioxamine B also acted as a substrate for the ferric reductase, while the foreign siderophore ferrichr