ライフサイエンスコーパス: periplasmic binding protein

1 hydrolyze ATP and also phosphorylate the two periplasmic binding proteins.

2 s close structural similarities to bacterial periplasmic binding proteins.

3 tent with the sequence homology to bacterial periplasmic binding proteins.

4 e a common architecture typical of Class III periplasmic binding proteins.

5 cholerae, and other bacteria with homologous periplasmic binding proteins.

6 olitica, showing identities of 84% for YfuA (periplasmic binding protein), 87% for YfuB (inner membra

7 of four HisGS catalytic subunits related to periplasmic binding proteins and four HisZ regulatory su

8 cess is unique among the family of bacterial periplasmic binding proteins and has interesting implica

9 structure shows that THI5p is a mix between periplasmic binding proteins and pyridoxal 5'-phosphate-

10 R0 structures reveal homology with bacterial periplasmic binding proteins and the rat GluR2 AMPA subt

11 e shows very high structural homology to the periplasmic binding proteins and the transferrins.

12 ed using three biological examples, namely a periplasmic binding protein, aspartate carbamoyltransfer

13 The protein is homologous with periplasmic-binding proteins associated with ABC transpo

14 (GenBank L34009) predicts that it encodes a periplasmic binding protein based on the presence of a l

15 Frommer laboratory, which combine bacterial periplasmic-binding protein-based specificity for ligand

16 hat the monosaccharides require binding to a periplasmic binding protein before they can interact wit

17 crystal structures of BtuCD and its cognate periplasmic binding protein BtuF have been recently dete

18 cluster with similarities to genes encoding periplasmic binding proteins (BztA), integral membrane p

19 was synthesized and co-crystallized with the periplasmic binding protein CeuE of Campylobacter jejuni

20 Here, we show that the periplasmic binding protein CeuE of Campylobacter jejuni

21 In Campylobacter jejuni the periplasmic binding protein CeuE, an integral part of th

22 PEB1a is also the periplasmic binding protein component of an aspartate/gl

23 The structure of the periplasmic binding protein component of this transporte

24 constitutive synthesis of OppA and DppA, the periplasmic-binding protein components of the two major

25 Periplasmic binding proteins comprise a superfamily that

26 ce that do not align with those of bacterial periplasmic-binding proteins correspond to four loops wi

27 In Gram-negative bacteria, periplasmic-binding proteins deliver ions or molecules s

28 o other structurally characterized Class III periplasmic binding proteins, demonstrates that PhuT/Shu

29 g proteins (potB and potH; potC and potI) of periplasmic binding protein-dependent (ABC) transport sy

30 tPDGC, which are linked to vctA and encode a periplasmic binding protein-dependent ABC transport syst

31 rted across the inner membrane by one of two periplasmic binding protein-dependent ABC transporters,

32 mologue of the ferrous transporter Feo and a periplasmic binding protein-dependent ATP binding casset

33 her with chvE, encode putative proteins of a periplasmic binding protein-dependent sugar uptake syste

34 mbrane of Escherichia coli is catalyzed by a periplasmic binding protein-dependent transport system a

35 ED genes encode components of a conventional periplasmic binding protein-dependent transport system c

36 tion of arginine is mediated by two distinct periplasmic binding protein-dependent transport systems,

37 terial cells is mediated by a large class of periplasmic binding protein-dependent transport systems,

38 ystems are ABC transporters, of which 44 are periplasmic-binding protein-dependent uptake systems and

39 The fbpABC operon encodes a periplasmic-binding-protein-dependent ABC transport syst

40 lE, aglF, aglG, and aglK) appear to encode a periplasmic-binding-protein-dependent sugar transport sy

41 inding to maltose-binding protein (MBP), the periplasmic binding protein, does not fully account for

42 The ABC-type transporter had a periplasmic-binding protein (EppA) that should confer th

43 ing protein (MBP), a member of the bacterial periplasmic binding protein family, provides a model sys

44 re reveals that ThiY belongs to the group II periplasmic binding protein family.

45 ture shows that TbpA belongs to the group II periplasmic-binding protein family.

46 The gene encoding Neisseria gonorrhoeae periplasmic binding protein FbpA contains two regions wh

47 ding the previously identified Fur-regulated periplasmic binding protein (FbpA) in a metal ion-depend

48 amino-acid mutation in the gene encoding the periplasmic binding protein, FbpA(Y196I), resulted in a

49 encodes an outer membrane protein (FitA), a periplasmic binding protein (FitE), two permease protein

50 four HisG(S) catalytic subunits based on the periplasmic binding protein fold and four HisZ regulator

51 lation, and into the remarkable usage of the periplasmic binding protein fold in multi-domain recepto

52 ed by alpha-helices, and exhibits the type I periplasmic binding protein fold.

53 rom the usual small molecule binding site in periplasmic binding protein folds.

54 esults finally establish the identity of the periplasmic binding protein for Cbl uptake, which is one

55 A), that is about 46% identical to OppA, the periplasmic binding protein for Opp.

56 nomic sequence is related in sequence to the periplasmic binding proteins for iron-siderophore comple

57 o as GcvB) that regulates OppA and DppA, two periplasmic binding proteins for the oligopeptide and di

58 ble to predict one conformational state of a periplasmic binding protein from another conformational

59 structures and ligand binding affinities of periplasmic binding proteins from bacterial phosphite an

60 echniques, the ligand-binding pockets of two periplasmic binding proteins, glucose-binding protein an

61 No periplasmic binding protein has been demonstrated for th

62 the histidine and lysine-arginine-ornithine periplasmic binding proteins (HisJ and LAO, respectively

63 The soluble periplasmic binding protein, HisJ, creates a signal that

64 revious structural models based on bacterial periplasmic binding protein homology.

65 receptor; TonB and ExbBD; HugB, the putative periplasmic binding protein; HugCD, the putative inner m

66 that hutBCD, which are predicted to encode a periplasmic binding protein (HutB) and cytoplasmic membr

67 Here we present how a gene duplication of a periplasmic binding protein in a mannose ATP-binding cas

68 MppA is a periplasmic binding protein in Escherichia coli essentia

69 d adaptive advantage for the presence of two periplasmic-binding proteins in ATP-binding cassette tra

70 NikA is a periplasmic binding protein involved in nickel uptake in

71 he closest structural homologues of ThiY are periplasmic binding proteins involved in alkanesulfonate

72 in E. coli K-12, the phosphorylation of the periplasmic binding protein is not related to the functi

73 as been well characterized and its role as a periplasmic binding protein is well defined, little is k

74 ructural motifs of GlnBP with those of other periplasmic binding proteins is discussed.

75 Last, the expression of ArtJ, an arginine periplasmic binding protein, is increased a mean of 16.6

76 Periplasmic binding protein ligand-binding sites have di

77 A leucine binding periplasmic binding protein (LivK) of Escherichia coli K

78 tegral membrane receptor LuxPQ, comprised of periplasmic binding protein (LuxP) and histidine sensor

79 the TonB-dependent transporter MbnT and the periplasmic binding protein MbnE.

80 n-dependent transport system consisting of a periplasmic binding protein (NasF), a homodimeric intrin

81 in with sequence similarity to the family of periplasmic binding proteins necessary for transporting

82 e pathogenicity and are mediated through the periplasmic binding protein NspS and the transmembrane b

83 component VirB5; and BMEII 0691, a predicted periplasmic binding protein of a peptide transport syste

84 regulates this locus, and accA codes for the periplasmic binding protein of the agrocinopine transpor

85 oding a homolog of the Escherichia coli LivJ periplasmic binding protein of the leucine, isoleucine,

86 nsertion mutation of sitA, which encodes the periplasmic binding protein of the putative iron/mangane

87 hermal titration calorimetry of the purified periplasmic binding proteins of each system revealed tha

88 ing protein (MBP), a member of the family of periplasmic binding proteins of Gram-negative bacteria.

89 tein has a signal sequence and resembles the periplasmic binding proteins of several other ABC transp

90 This periplasmic binding protein, part of the oligopeptide pe

91 The periplasmic binding protein (PBP) FepB plays a key role

92 crystal structure of YclQ reveals a bilobal periplasmic binding protein (PBP) fold consisting of two

93 BtuF is the periplasmic binding protein (PBP) for the vitamin B12 tr

94 The periplasmic binding protein (PBP) IbpA mediates the upta

95 transport mechanisms involve members of the periplasmic binding protein (PBP) superfamily that bind

96 As an alternative, we demonstrate use of a periplasmic binding protein (PBP) to provide high affini

97 e ligand binding domain is that of a bilobal periplasmic binding protein (PBP) very similar to that o

98 A periplasmic binding protein (PBP) was investigated as a

99 -terminal d-xylose-binding domain contains a periplasmic-binding protein (PBP) fold with structural h

100 The bacterial periplasmic-binding protein (PBP) superfamily members, i

101 Periplasmic binding proteins (PBPs) comprise a protein s

102 Periplasmic binding proteins (PBPs) constitute a protein

103 ential for the substrate-binding function of periplasmic binding proteins (PBPs), which are indispens

104 nts and imported into the bacterial cell via periplasmic-binding proteins (PBPs) and ABC-transporters

105 nsferase ScrA; signal reception required the periplasmic binding protein ScrB and the membrane-bound

106 TP hydrolysis and transport of heme from the periplasmic binding protein, ShuT, to the cytoplasmic bi

107 The sitA gene encodes a putative periplasmic binding protein, sitB encodes an ATP-binding

108 -bending motions, intrinsic to the bacterial periplasmic binding protein superfamily, to establish al

109 h-throughput method relies upon the thiamine periplasmic binding protein (TBP) from Escherichia coli

110 Escherichia coli HisJ is a type II periplasmic binding protein that functions to reversibly

111 The fepB gene encodes a periplasmic binding protein that is essential for the up

112 This gene, referred to as agpA, encodes a periplasmic binding protein that is most similar to prot

113 hromosomal virulence gene E (chvE) encodes a periplasmic-binding protein that binds several neutral s

114 Each of these systems includes a specific periplasmic binding protein, the AO-binding protein for

115 ating the bound ("closed") conformation of a periplasmic binding protein, the glutamine-binding prote

116 whose protein products have homology to the periplasmic binding protein, the two integral cytoplasmi

117 d sequence of the CaR with that of bacterial periplasmic-binding proteins, the first approximately 53

118 yrosine to phenylalanine substitution in the periplasmic binding protein VctP did not alter enterobac

119 reduced levels of phosphorylation of the two periplasmic binding proteins, was isolated and character

120 amino acid transport, only the LivJ and LivK periplasmic binding proteins were required for wild-type

121 ed light on the binding mechanism of type II periplasmic binding proteins where ligand is initially b

122 tumefaciens virulence determinant ChvE is a periplasmic binding protein which participates in chemot

123 e (ABC) family of transporters and include a periplasmic binding protein (YfeA), an ATP-binding prote