ライフサイエンスコーパス: heme-binding protein

1 -like proteins (gb|ADZ24001.1), is in fact a heme-binding protein.

2 that HrtR expressed as a fusion protein is a heme-binding protein.

3 We furthermore demonstrate that BdlA is a heme-binding protein.

4 rhythms in mammals, has been identified as a heme-binding protein.

5 haride was suppressed by hemopexin, a plasma heme-binding protein.

6 HemQ is a multimeric heme-binding protein.

7 n-1 (NRAMP-1), transferrin, lactoferrin, and heme-binding proteins.

8 nd was not detectable when the medium lacked heme-binding proteins.

9 he availability and avidity of extracellular heme-binding proteins.

10 ng cassette (ABC) transporter made by GAS as heme-binding proteins.

11 We show that one of these markers, heme-binding protein 1 (Hebp1), is elevated in the brain

12 Pap31, a homolog of the Bartonella quintana heme-binding protein A (HbpA), defined the high-density

13 synthetic agonists due to the wide range of heme binding proteins and potential pleotropic effects.

14 ctional heme transfer between a cell surface heme-binding protein and the lipoprotein of a heme-speci

15 r results provide a structural framework for heme-binding proteins and add IL-1 cytokines to the grou

16 . gingivalis for the extraction of heme from heme-binding proteins and for iron transport are poorly

17 tionships within this multilineage family of heme-binding proteins and presents new molecular players

18 cation to a range of other systems including heme-binding proteins and proteins to which a covalently

19 inimal amino acid sequence identity to these heme-binding proteins and the structure of Shp(180) reve

20 we showed that MF6p/FhHDM-1 is a transitory heme-binding protein as protein.heme complexes can be di

21 The cytoplasmic heme-binding proteins belong to a structurally related f

22 ShuS is a heme binding protein, but its role in heme utilization i

23 ass of proteins that includes esterases, the heme-binding protein ChaN, and an uncharacterized domain

24 Cytochrome b562 is a heme-binding protein consisting of four helices folded i

25 rovide further evidence that the cytoplasmic heme-binding proteins, contrary to previous reports, are

26 vo protein design, we design a high-affinity heme-binding protein, dnHEM1, with an axial histidine li

27 PhuS is a cytoplasmic heme binding protein encoded within the phu operon and h

28 -family proteins) are a widespread family of heme-binding proteins for which chemical and biological

29 PhuS is a cytoplasmic, 39 kDa heme-binding protein from Pseudomonas aeruginosa.

30 ggest the possibility that these cytoplasmic heme-binding proteins have multiple functions that are t

31 The lipoprotein-anchored heme binding protein (HBP) of this transporter is SiaA (

32 enzyme, resulting from the combination of a heme binding protein, heme oxygenase, with cobalt-protop

33 An increase in the heme-binding protein hemopexin (Hpx) 3 months after anth

34 ng agent methylene blue, haptoglobin, or the heme-binding protein hemopexin.

35 receptor membrane component 1 (PGRMC1) is a heme-binding protein implicated in a wide range of cellu

36 We propose that the targets are the heme binding proteins in the pathways (CcmC, CcmE, and C

37 NikA was identified as a heme-binding protein in the periplasm of anaerobically g

38 owever, the comprehensive annotation of such heme-binding proteins in the human proteome remains inco

39 xpression, and an increase in haptoglobin, a heme binding protein, in leukocytes in vivo and in vitro

40 We also identified phuS, encoding a heme binding protein involved in heme acquisition, and v

41 ochemical level, the role of the cytoplasmic heme binding proteins is not yet clear.

42 derived from the amino-terminal cleavage of heme-binding protein, is a potent chemoattractant for hu

43 y, several Gram-negative pathogens secrete a heme binding protein known as HasA to scavenge heme from

44 a hepatica that belongs to a broad family of heme-binding proteins (MF6p/helminth defense molecules (

45 thin common subfields of bioinorganic study: heme binding proteins, monometal- and dimetal-containing

46 onal study of the first purified periplasmic heme-binding protein (PBP), ShuT from Shigella dysenteri

47 functional characterization of a cytoplasmic heme-binding protein PhuS from the opportunistic pathoge

48 The cytoplasmic heme-binding protein PhuS, encoded within the Fur-regula

49 al rearrangement of the C-terminal domain of heme binding protein (PhuS) is required for interaction

50 eletion of the gene encoding the cytoplasmic heme-binding protein, PhuS, homologs of which have been

51 id-lipid-associated protein-fibrillins, SOUL heme-binding proteins, phytyl ester synthases, beta-caro

52 Dap1 is a heme-binding protein related to cytochrome b5 that activ

53 ide, mRNA II is suppressed suggesting that a heme-binding protein (responsive to oxygen) may suppress

54 ally, this organism produces a hemolymphatic heme-binding protein (RHBP) that transports heme to peri

55 The heme-binding proteins Shp and HtsA are part of the heme

56 The heme-binding proteins Shp and HtsA of Streptococcus pyog

57 The Shigella dysenteriae cytoplasmic heme binding protein, ShuS, has previously been shown to

58 A mutant in the hemoglobin/heme-binding protein Spbhp-37 was impaired for growth on

59 d in other pathogenic bacterial cell surface heme-binding proteins, suggesting that the mechanisms of

60 as heme-regulated inhibitor (HRI), is a key heme-binding protein that senses intracellular heme conc

61 heme, we characterize two new intracellular heme-binding proteins that are distinct from the previou

62 Cig1 exhibited the absorbance spectrum of a heme-binding protein upon heme titration, and Cig1 may t

63 which are found in all putative periplasmic heme-binding proteins, were subjected to UV-visible, res

64 DGCR8 is the first example of a heme-binding protein with two endogenous cysteine side c