ライフサイエンスコーパス: Escherichia coli protein

1 is analogous to the S506F derivative of the Escherichia coli protein.

2 LysRS (LysRS2), we studied the lysS-encoded Escherichia coli protein.

3 in the genomic data base by homology to the Escherichia coli protein.

4 conformational change similar to that of the Escherichia coli protein.

5 d only a small region of similarity with the Escherichia coli protein.

6 en for marine natural products that bound to Escherichia coli proteins.

7 at high purity via removal of contaminating Escherichia coli proteins.

8 association than that observed for the same Escherichia coli proteins.

9 majority of these loci across more than 500 Escherichia coli proteins.

10 del proteins, human hemoglobin variants, and Escherichia coli proteins.

11 , allowing for continuing expression of some Escherichia coli proteins.

12 The Escherichia coli protein Ada specifically repairs the S(

13 chaperone holdase, which protects essential Escherichia coli proteins against HOCl-induced aggregati

14 ensive information available on functions of Escherichia coli proteins, analysis of sequence-related

15 ces showed 61% identity to the corresponding Escherichia coli proteins and 41% identity to each other

16 By individually purifying 19 Escherichia coli proteins and reconstituting them in vit

17 These Escherichia coli proteins are encoded on the same operon

18 The ability of the Escherichia coli protein BirA to function as both a meta

19 The Escherichia coli protein BirA undergoes a switch between

20 A related Escherichia coli protein bound only a single zinc ion, v

21 seria BamD and BamE share overall folds with Escherichia coli proteins but contain differences that m

22 Through a blind search of thousands of Escherichia coli proteins, CF-random suggests that up to

23 In contrast to the Bacillus subtilis and Escherichia coli proteins, CgtA(C) does not fractionate

24 Unlike most DEAD/H proteins, the purified Escherichia coli protein DbpA demonstrates high specific

25 Using a component of the Escherichia coli protein degradation machinery, we have

26 timized and applied for analysis of 1-100 ng Escherichia coli protein digests in a single run (single

27 The Escherichia coli proteins DksA, GreA, and GreB are all s

28 The Escherichia coli protein DnaA and the plasmid RK2-encode

29 menal stretch of Sec63p with homology to the Escherichia coli protein DnaJ is the likely region of in

30 ilar to the AFM images of the stress-induced Escherichia coli protein, Dps, when complexed with DNA;

31 vity, as it could prevent the aggregation of Escherichia coli proteins during thermal stress.

32 ect to translational frameshift repair in an Escherichia coli protein expression system.

33 uld reconstitute OL synthesis in a cell-free Escherichia coli protein extract.

34 The Escherichia coli protein Fis is remarkable for its abili

35 hese relationships, we show that the need of Escherichia coli proteins for the chaperonin GroEL can b

36 esions and inhibitors when compared with the Escherichia coli protein (for which the structure has al

37 an example of a fine filter on a test set of Escherichia coli protein fragmentation spectra, the top

38 rase eta (Poleta) in plants, we expressed in Escherichia coli proteins from Arabidopsis thaliana (At)

39 majority of bacteria possess homologs of the Escherichia coli proteins FtsL, FtsB, and FtsQ, three pr

40 ing motif near their amino terminus, and the Escherichia coli protein has been found to be a weak ATP

41 stallography and the structure of the intact Escherichia coli protein has been studied by NMR.

42 Studies of the Escherichia coli protein in vitro have been hampered by

43 globally monitor the structures of refolding Escherichia coli proteins in the cytosolic medium and wi

44 UvrA is one of the key Escherichia coli proteins involved in removing DNA damag

45 CPS containing a biotinylation site from an Escherichia coli protein is accumulated in a vps27 yeast

46 The Escherichia coli protein IscU serves as the scaffold for

47 e sequence space of four key residues in the Escherichia coli protein kinase PhoQ that drive recognit

48 The Escherichia coli protein LptD is an integral outer membr

49 ignal peptide influence the targeting of two Escherichia coli proteins, maltose binding protein and O

50 d with a mixture of protein standards and an Escherichia coli protein mixture.

51 domains (E and G) that are homologous to the Escherichia coli proteins MoeA and MogA, the atomic stru

52 The Escherichia coli proteins MoeB and MoaD are involved in

53 ntional 'on-bead' approach, we reconstituted Escherichia coli proteins MsbA and MscS and find that pe

54 uires the participation of a large number of Escherichia coli proteins (Nus factors), as well as an R

55 A structural survey of the Escherichia coli proteins occurring in metabolic network

56 e localized the potential sulfation sites of Escherichia coli proteins on a proteome microarray by us

57 Display of affinity-purified Escherichia coli proteins on two-dimensional gels reveal

58 In the present study, fusions to the Escherichia coli proteins PhoA and LacZ and analysis of

59 lish its DNA strand exchange activities, the Escherichia coli protein RecA polymerizes onto DNA to fo

60 The Escherichia coli protein regulator of RNase E activity A

61 nding sites overlap with those of homologous Escherichia coli proteins, revealing conservation in ass

62 The Escherichia coli protein RhlB is an ATP-dependent motor

63 lude the cytosolic ATPase Get3 in yeast, the Escherichia coli protein RidA, and the mammalian protein

64 intended to be similar to that found in the Escherichia coli protein ROP.

65 uble-stranded DNA fragments encoding defined Escherichia coli protein secondary structural elements (

66 current human, mouse, Drosophila, yeast, and Escherichia coli protein sequence data bases and identif

67 Using available data for Escherichia coli protein solubility in a cell-free expre

68 The Escherichia coli protein SufI (FtsP) has recently been p

69 plasm, we screened a genome-scale library of Escherichia coli proteins tagged with green fluorescent

70 The Escherichia coli protein targets branched DNA substrates

71 A chloroplast homologue of FtsY, an Escherichia coli protein that is critical for the functi

72 gration host factor (IHF) is a heterodimeric Escherichia coli protein that plays essential roles in a

73 SdiA is an Escherichia coli protein that regulates cell division in

74 SecA ATPase promotes Escherichia coli protein translocation by its associatio

75 Uniformly (13)C-labeled Escherichia coli protein was used to test the developed

76 Here, using Escherichia coli proteins, we present the first X-ray cr

77 ber of known functional associations for the Escherichia coli proteins when compared with earlier imp

78 mino acids that displays 41% identity to the Escherichia coli protein, which provides an important fu

79 mixture of fluorescence-labeled thrombin and Escherichia coli proteins with an aptamer microarray, we

80 In this study, we set out to identify Escherichia coli proteins with RNS-sensitive cysteines.

81 A 3.3 MDa macromolecular cage between two Escherichia coli proteins with seemingly incompatible sy

82 ing this technique, we identified a group of Escherichia coli proteins with significantly (30-90%) ox

83 he three-dimensional structures of human and Escherichia coli proteins with their mRNA sequences.

84 In Escherichia coli, proteins with LytM domains also partic

85 Escherichia coli protein Y (pY) binds to the small ribos

86 The Escherichia coli protein YajL (ThiJ) is a member of the

87 The Escherichia coli protein YbbN is a Trx-like protein that

88 Here, we identify the uncharacterized Escherichia coli protein YcaQ as an ICL repair glycosyla

89 Escherichia coli protein YicC belongs to the well-conser

90 hows significant sequence relatedness to the Escherichia coli protein YidC, an inner membrane protein