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

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

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

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

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

11 The Escherichia coli protein Ada specifically repairs the S(

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

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

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

15 These Escherichia coli proteins are encoded on the same operon

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

17 The Escherichia coli protein BirA undergoes a switch between

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

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

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

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

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

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

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

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

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

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

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

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

30 The Escherichia coli protein Fis is remarkable for its abili

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

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

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

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

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

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

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

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

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

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

41 The Escherichia coli protein IscU serves as the scaffold for

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

43 The Escherichia coli protein LptD is an integral outer membr

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

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

46 The Escherichia coli proteins MoeB and MoaD are involved in

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

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

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

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

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

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

53 The Escherichia coli protein regulator of RNase E activity A

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

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

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

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

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

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

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

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

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

63 The Escherichia coli protein targets branched DNA substrates

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

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

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

67 SecA ATPase promotes Escherichia coli protein translocation by its associatio

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

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

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

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

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

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

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

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

76 In Escherichia coli, proteins with LytM domains also partic

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

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

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

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