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1  correlated with the methylation of FrzCD (a methyl-accepting chemotaxis protein).
2 omain has high homology with the eubacterial methyl-accepting chemotaxis protein.
3 the S signal using SscL and SscS, homologous methyl-accepting chemotaxis proteins.
4 main that controls input-output signaling in methyl-accepting chemotaxis proteins.
5  is bioinformatically indistinguishable from methyl-accepting chemotaxis proteins.
6 ses, cyclic-di-GMP synthases/hydrolases, and methyl-accepting chemotaxis proteins.
7 eptad stutter adjacent to the HAMP domain in methyl-accepting chemotaxis proteins.
8 e residues within the cytoplasmic domains of methyl-accepting chemotaxis proteins.
9  fused through a membrane-spanning region to methyl-accepting chemotaxis proteins.
10 ethylation changes, methylation enzymes, and methyl-accepting chemotaxis proteins.
11 s well as two genes, mcpA and mcpB, encoding methyl-accepting chemotaxis proteins.
12 lassical two-component histidine kinases and methyl-accepting chemotaxis proteins.
13 o contains a homolog of E. coli Trg or other methyl-accepting chemotaxis proteins.
14 ylated FrzCD protein, the Frz homolog of the methyl-accepting chemotaxis proteins.
15 ts with defects in any one of the four known methyl-accepting chemotaxis proteins also retained the a
16 rane signal transduction proteins, including methyl-accepting chemotaxis proteins and histidine kinas
17 ignal-transducing regulatory systems include methyl-accepting chemotaxis proteins and membrane-bound,
18 n inosine/xanthosine triphosphatase, GidA, a methyl-accepting chemotaxis protein, and a PIN domain pr
19 equires the activity of FrzCD, a cytoplasmic methyl-accepting chemotaxis protein, and FrzF, a methylt
20    HAMP (histidine kinase, adenylyl cyclase, methyl-accepting chemotaxis protein, and phosphatase) li
21 c HAMP (histidine kinase, adenylyl cyclases, methyl-accepting chemotaxis proteins, and phosphatases)
22 HAMP (histidine kinases, adenylate cyclases, methyl-accepting chemotaxis proteins, and phosphatases)
23 ied in histidine kinases, adenylyl cyclases, methyl-accepting chemotaxis proteins, and phosphatases,
24 ing in histidine kinases, adenylyl cyclases, methyl-accepting chemotaxis proteins, and some phosphata
25                                          The methyl-accepting chemotaxis proteins are a family of rec
26 nisms, such as sensory histidine kinases and methyl-accepting chemotaxis proteins, are molecular devi
27 gutted" mutant that was deleted for all four methyl-accepting chemotaxis proteins, as well as for Che
28 ent signal transduction pathway proteins and methyl-accepting chemotaxis proteins, but will be expand
29 serine/threonine protein kinases (CHASE2) or methyl-accepting chemotaxis proteins (CHASE3).
30 brane proteins (PilQ, MshO, MshP, and CapK), methyl-accepting chemotaxis proteins, chemotaxis and mot
31 s of the bacterial chemotaxis proteins MCPs (methyl-accepting chemotaxis proteins), CheW, CheY and Ch
32  and difE, encoding respective homologs of a methyl-accepting chemotaxis protein, CheW, and CheA, are
33 The characterized phototaxis systems rely on methyl-accepting chemotaxis proteins containing bilin-bi
34                                          The methyl-accepting chemotaxis protein, DcrH, from the anae
35                 This gene encodes a putative methyl-accepting chemotaxis protein, DcrH.
36 eR (DeltacheR(3)), CheA (DeltacheA(3)) and a methyl-accepting chemotaxis protein (Deltamcp(3)) are de
37                                          The methyl-accepting chemotaxis protein, DifA, has two diffe
38             The BdlA protein harbors an MCP (methyl-accepting chemotaxis protein) domain and two PAS
39  a mutant strain of F1 in which the putative methyl-accepting chemotaxis protein-encoding gene Pput_0
40                        Chemoreceptors of the methyl-accepting chemotaxis protein family form clusters
41          Periplasmic sensor domains from two methyl-accepting chemotaxis proteins from Geobacter sulf
42 ant, hyper-reversal mutant in the M. xanthus methyl accepting chemotaxis protein homolog, frzCD224, f
43        These results suggest that a specific methyl-accepting chemotaxis protein is involved in multi
44                                          The methyl-accepting chemotaxis protein-like chemosensor Pil
45 omal or a plasmid-encoded allele displayed a methyl-accepting chemotaxis protein localization pattern
46 therefore be considered a marker for general methyl-accepting chemotaxis protein (MCP) clustering.
47 ost strain lacking all chemoreceptors of the methyl-accepting chemotaxis protein (MCP) family.
48                   A gene, dmcA, expressing a methyl-accepting chemotaxis protein (MCP) from the oral
49 8 amino acids of Tar4 (TtTar4H), a predicted methyl-accepting chemotaxis protein (MCP) from the stric
50               We identified large numbers of methyl-accepting chemotaxis protein (MCP) homologs that
51                                    A soluble methyl-accepting chemotaxis protein (MCP) of Pseudomonas
52 eric bacteria shuttles between transmembrane methyl-accepting chemotaxis protein (MCP) receptor compl
53 nd severely reduced in mutants with impaired methyl-accepting chemotaxis protein (MCP) signaling acti
54 pG, we examined the targeting of this single methyl-accepting chemotaxis protein (MCP) under differen
55 fied were two adjacent genes, one encoding a methyl-accepting chemotaxis protein (MCP), presumably re
56                                    DifA is a methyl-accepting chemotaxis protein (MCP)-like sensory t
57 rom CNB-1 and genetic complementation of the methyl-accepting chemotaxis protein (MCP)-null mutant CN
58 rolled by the cytoplasmic receptor, FrzCD, a methyl-accepting chemotaxis protein (MCP).
59 tilis is mediated by the PTS as well as by a methyl-accepting chemotaxis protein (MCP).
60 behavior, possibly through interactions with methyl-accepting chemotaxis proteins (MCP).
61    It was demonstrated previously that DifA (methyl-accepting chemotaxis protein [MCP]-like), DifC (C
62                                          The methyl-accepting chemotaxis protein, McpB, is the sole r
63 of which encodes modular cyanobacteriochrome-methyl-accepting chemotaxis proteins (MCPs) and other pr
64                                          The methyl-accepting chemotaxis proteins (MCPs) are concentr
65 lis CheR-mediated methylation of B. subtilis methyl-accepting chemotaxis proteins (MCPs) but not of E
66       The serine chemoreceptor Tsr and other methyl-accepting chemotaxis proteins (MCPs) control the
67                                              Methyl-accepting chemotaxis proteins (MCPs) detect speci
68 important model for transmembrane signaling, methyl-accepting chemotaxis proteins (MCPs) have been ex
69            We found that polar clustering of methyl-accepting chemotaxis proteins (MCPs) is not depen
70 , the che3 cluster, encoding homologs to two methyl-accepting chemotaxis proteins (MCPs), a CheW, a h
71  manner similar to that observed earlier for methyl-accepting chemotaxis proteins (MCPs), but only if
72 in product shows strong sequence identity to methyl-accepting chemotaxis proteins (MCPs), followed by
73 ergy taxis mechanism and mediated by several methyl-accepting chemotaxis proteins (MCPs), rather than
74 ng one of the genes encoding the 18 putative methyl-accepting chemotaxis proteins (MCPs), revealed th
75  Transmembrane chemoreceptors, also known as methyl-accepting chemotaxis proteins (MCPs), translate e
76 f closely resembles the signaling domains of methyl-accepting chemotaxis proteins (MCPs), which under
77 ipeptides, and the responses are mediated by methyl-accepting chemotaxis proteins (MCPs).
78 e residues within the cytoplasmic domains of methyl-accepting chemotaxis proteins (MCPs).
79 utamate residues in the signaling domains of methyl-accepting chemotaxis proteins (MCPs).
80 highly conserved domains (HCDs) of bacterial methyl-accepting chemotaxis proteins (MCPs).
81 logy with the C-terminal region of bacterial methyl-accepting chemotaxis proteins (MCPs).
82 d with sensory transduction events involving methyl-accepting chemotaxis proteins (MCPs).
83 sms of transmembrane chemoreceptors known as methyl-accepting chemotaxis proteins (MCPs).
84 ins a conserved C-terminal module present in methyl-accepting chemotaxis proteins (MCPs); but, in con
85 In bacterial chemotaxis, the chemoreceptors [methyl-accepting chemotaxis proteins (MCPs)] transduce c
86                       Thus, the mechanism of methyl-accepting chemotaxis protein-mediated chemotaxis
87 identified B burgdorferi peptides, only 1, a methyl-accepting chemotaxis protein peptide Mcp4442-462,
88 poly-HAMP (histidine kinase-adenylyl cyclase-methyl-accepting chemotaxis protein-phosphatase) domain
89  of two components of the CheIV cluster, the methyl-accepting chemotaxis protein PilJ and the PilJ de
90 portant role in chemotaxis by deamidation of methyl-accepting chemotaxis protein receptors (MCPs) and
91 tic analysis of the HAMP domain from the Tsr methyl-accepting chemotaxis protein resulted in a distin
92 w, potential flagellar genes, three putative methyl-accepting chemotaxis proteins, STM3138 (McpA), ST
93 ically similar sensory proteins, such as the methyl-accepting chemotaxis proteins, the transmembrane
94  element observed in many sensor kinases and methyl-accepting chemotaxis proteins, transmits signals
95 4 operon, which encodes homologues to a MCP (methyl-accepting chemotaxis protein), two CheWs, a hybri
96                                     FrzCD, a methyl-accepting chemotaxis protein, was predominantly l