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1 cholerae, and other bacteria with homologous periplasmic binding proteins.
2 hydrolyze ATP and also phosphorylate the two periplasmic binding proteins.
3 s close structural similarities to bacterial periplasmic binding proteins.
4 tent with the sequence homology to bacterial periplasmic binding proteins.
5 e a common architecture typical of Class III 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 he first atomic-scale structures of liganded periplasmic binding protein-based biosensors, accelerati
16  Frommer laboratory, which combine bacterial periplasmic-binding protein-based specificity for ligand
17 hat the monosaccharides require binding to a periplasmic binding protein before they can interact wit
18  crystal structures of BtuCD and its cognate periplasmic binding protein BtuF have been recently dete
19  cluster with similarities to genes encoding periplasmic binding proteins (BztA), integral membrane p
20 was synthesized and co-crystallized with the periplasmic binding protein CeuE of Campylobacter jejuni
21                       Here, we show that the periplasmic binding protein CeuE of Campylobacter jejuni
22                  In Campylobacter jejuni the periplasmic binding protein CeuE, an integral part of th
23                            PEB1a is also the periplasmic binding protein component of an aspartate/gl
24                         The structure of the periplasmic binding protein component of this transporte
25 constitutive synthesis of OppA and DppA, the periplasmic-binding protein components of the two major
26                                              Periplasmic binding proteins comprise a superfamily that
27 ce that do not align with those of bacterial periplasmic-binding proteins correspond to four loops wi
28                   In Gram-negative bacteria, periplasmic-binding proteins deliver ions or molecules s
29 o other structurally characterized Class III periplasmic binding proteins, demonstrates that PhuT/Shu
30 g proteins (potB and potH; potC and potI) of periplasmic binding protein-dependent (ABC) transport sy
31 tPDGC, which are linked to vctA and encode a periplasmic binding protein-dependent ABC transport syst
32 rted across the inner membrane by one of two periplasmic binding protein-dependent ABC transporters,
33 mologue of the ferrous transporter Feo and a periplasmic binding protein-dependent ATP binding casset
34 her with chvE, encode putative proteins of a periplasmic binding protein-dependent sugar uptake syste
35 mbrane of Escherichia coli is catalyzed by a periplasmic binding protein-dependent transport system a
36 ED genes encode components of a conventional periplasmic binding protein-dependent transport system c
37 tion of arginine is mediated by two distinct periplasmic binding protein-dependent transport systems,
38 terial cells is mediated by a large class of periplasmic binding protein-dependent transport systems,
39 ystems are ABC transporters, of which 44 are periplasmic-binding protein-dependent uptake systems and
40                  The fbpABC operon encodes a periplasmic-binding-protein-dependent ABC transport syst
41 lE, aglF, aglG, and aglK) appear to encode a periplasmic-binding-protein-dependent sugar transport sy
42 inding to maltose-binding protein (MBP), the periplasmic binding protein, does not fully account for
43               The ABC-type transporter had a periplasmic-binding protein (EppA) that should confer th
44 ing protein (MBP), a member of the bacterial periplasmic binding protein family, provides a model sys
45 re reveals that ThiY belongs to the group II periplasmic binding protein family.
46 ture shows that TbpA belongs to the group II periplasmic-binding protein family.
47      The gene encoding Neisseria gonorrhoeae periplasmic binding protein FbpA contains two regions wh
48 ding the previously identified Fur-regulated periplasmic binding protein (FbpA) in a metal ion-depend
49 amino-acid mutation in the gene encoding the periplasmic binding protein, FbpA(Y196I), resulted in a
50  encodes an outer membrane protein (FitA), a periplasmic binding protein (FitE), two permease protein
51 four HisG(S) catalytic subunits based on the periplasmic binding protein fold and four HisZ regulator
52 lation, and into the remarkable usage of the periplasmic binding protein fold in multi-domain recepto
53 ed by alpha-helices, and exhibits the type I periplasmic binding protein fold.
54 rom the usual small molecule binding site in periplasmic binding protein folds.
55 esults finally establish the identity of the periplasmic binding protein for Cbl uptake, which is one
56 A), that is about 46% identical to OppA, the periplasmic binding protein for Opp.
57 nomic sequence is related in sequence to the periplasmic binding proteins for iron-siderophore comple
58 o as GcvB) that regulates OppA and DppA, two periplasmic binding proteins for the oligopeptide and di
59                          The contribution of periplasmic binding proteins forming part of amino acid
60 ble to predict one conformational state of a periplasmic binding protein from another conformational
61 orescence spectroscopy showed that MatC, the periplasmic binding protein from this system, binds to l
62  structures and ligand binding affinities of periplasmic binding proteins from bacterial phosphite an
63  X-ray crystal structure of the maltodextrin periplasmic-binding protein from Thermotoga maritima (tm
64 echniques, the ligand-binding pockets of two periplasmic binding proteins, glucose-binding protein an
65                                           No periplasmic binding protein has been demonstrated for th
66                                     However, periplasmic binding proteins have been investigated exte
67  the histidine and lysine-arginine-ornithine periplasmic binding proteins (HisJ and LAO, respectively
68                                  The soluble periplasmic binding protein, HisJ, creates a signal that
69 revious structural models based on bacterial periplasmic binding protein homology.
70 receptor; TonB and ExbBD; HugB, the putative periplasmic binding protein; HugCD, the putative inner m
71 that hutBCD, which are predicted to encode a periplasmic binding protein (HutB) and cytoplasmic membr
72  Here we present how a gene duplication of a periplasmic binding protein in a mannose ATP-binding cas
73 his study, we examine an operon containing a periplasmic binding protein in Actinobacillus for its po
74                                    MppA is a periplasmic binding protein in Escherichia coli essentia
75 d adaptive advantage for the presence of two periplasmic-binding proteins in ATP-binding cassette tra
76                                    NikA is a periplasmic binding protein involved in nickel uptake in
77 he closest structural homologues of ThiY are periplasmic binding proteins involved in alkanesulfonate
78  in E. coli K-12, the phosphorylation of the periplasmic binding protein is not related to the functi
79 as been well characterized and its role as a periplasmic binding protein is well defined, little is k
80 ructural motifs of GlnBP with those of other periplasmic binding proteins is discussed.
81    Last, the expression of ArtJ, an arginine periplasmic binding protein, is increased a mean of 16.6
82                                              Periplasmic binding protein ligand-binding sites have di
83 re, composed of two related domains from the periplasmic-binding protein-like II domain family, have
84                            A leucine binding periplasmic binding protein (LivK) of Escherichia coli K
85 tegral membrane receptor LuxPQ, comprised of periplasmic binding protein (LuxP) and histidine sensor
86  the TonB-dependent transporter MbnT and the periplasmic binding protein MbnE.
87 ransporter in conjunction with a PG-specific periplasmic binding protein, MppA.
88 n-dependent transport system consisting of a periplasmic binding protein (NasF), a homodimeric intrin
89 in with sequence similarity to the family of periplasmic binding proteins necessary for transporting
90 e pathogenicity and are mediated through the periplasmic binding protein NspS and the transmembrane b
91 component VirB5; and BMEII 0691, a predicted periplasmic binding protein of a peptide transport syste
92 regulates this locus, and accA codes for the periplasmic binding protein of the agrocinopine transpor
93 oding a homolog of the Escherichia coli LivJ periplasmic binding protein of the leucine, isoleucine,
94 nsertion mutation of sitA, which encodes the periplasmic binding protein of the putative iron/mangane
95 hermal titration calorimetry of the purified periplasmic binding proteins of each system revealed tha
96 ing protein (MBP), a member of the family of periplasmic binding proteins of Gram-negative bacteria.
97 tein has a signal sequence and resembles the periplasmic binding proteins of several other ABC transp
98                                         This periplasmic binding protein, part of the oligopeptide pe
99                                          The periplasmic binding protein (PBP) FepB plays a key role
100  crystal structure of YclQ reveals a bilobal periplasmic binding protein (PBP) fold consisting of two
101                                  BtuF is the periplasmic binding protein (PBP) for the vitamin B12 tr
102 membrane receptor (OMR) protein FvtA and the periplasmic binding protein (PBP) FvtB, both of which mu
103                                          The periplasmic binding protein (PBP) IbpA mediates the upta
104  transport mechanisms involve members of the periplasmic binding protein (PBP) superfamily that bind
105   As an alternative, we demonstrate use of a periplasmic binding protein (PBP) to provide high affini
106 e ligand binding domain is that of a bilobal periplasmic binding protein (PBP) very similar to that o
107                                            A periplasmic binding protein (PBP) was investigated as a
108 d within the sequence of a mutated bacterial periplasmic binding protein (PBP).
109 -terminal d-xylose-binding domain contains a periplasmic-binding protein (PBP) fold with structural h
110                                The bacterial periplasmic-binding protein (PBP) superfamily members, i
111                                              Periplasmic binding proteins (PBPs) are bacterial protei
112              Numerous studies have shown how periplasmic binding proteins (PBPs) bind substrates with
113                                              Periplasmic binding proteins (PBPs) comprise a protein s
114                                              Periplasmic binding proteins (PBPs) constitute a protein
115       Uptake is facilitated by high-affinity periplasmic binding proteins (PBPs) that bind cargo in t
116                                  We focus on periplasmic binding proteins (PBPs), a superfamily of dy
117 ential for the substrate-binding function of periplasmic binding proteins (PBPs), which are indispens
118 nts and imported into the bacterial cell via periplasmic-binding proteins (PBPs) and ABC-transporters
119 s belonging to the well-known superfamily of periplasmic binding proteins, PotF and PotD.
120 nsferase ScrA; signal reception required the periplasmic binding protein ScrB and the membrane-bound
121 TP hydrolysis and transport of heme from the periplasmic binding protein, ShuT, to the cytoplasmic bi
122             The sitA gene encodes a putative periplasmic binding protein, sitB encodes an ATP-binding
123  the potential for using genetically encoded periplasmic binding proteins such as RBP to measure meta
124 -bending motions, intrinsic to the bacterial periplasmic binding protein superfamily, to establish al
125 h-throughput method relies upon the thiamine periplasmic binding protein (TBP) from Escherichia coli
126           Escherichia coli HisJ is a type II periplasmic binding protein that functions to reversibly
127                      The fepB gene encodes a periplasmic binding protein that is essential for the up
128    This gene, referred to as agpA, encodes a periplasmic binding protein that is most similar to prot
129 hromosomal virulence gene E (chvE) encodes a periplasmic-binding protein that binds several neutral s
130    Each of these systems includes a specific periplasmic binding protein, the AO-binding protein for
131 ating the bound ("closed") conformation of a periplasmic binding protein, the glutamine-binding prote
132  whose protein products have homology to the periplasmic binding protein, the two integral cytoplasmi
133 d sequence of the CaR with that of bacterial periplasmic-binding proteins, the first approximately 53
134 yrosine to phenylalanine substitution in the periplasmic binding protein VctP did not alter enterobac
135 n obtained from the crystal structure of the periplasmic binding protein was best fit with a molecula
136        The identity of the P5P bound to this periplasmic binding protein was verified by isothermal t
137 reduced levels of phosphorylation of the two periplasmic binding proteins, was isolated and character
138 amino acid transport, only the LivJ and LivK periplasmic binding proteins were required for wild-type
139 ed light on the binding mechanism of type II periplasmic binding proteins where ligand is initially b
140  tumefaciens virulence determinant ChvE is a periplasmic binding protein which participates in chemot
141 e (ABC) family of transporters and include a periplasmic binding protein (YfeA), an ATP-binding prote

 
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