戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 near the extracellular surface of the second putative transmembrane domain.
2 minK, a 130-amino-acid protein with a single putative transmembrane domain.
3 otropic salt wash, consistent with lack of a putative transmembrane domain.
4  codon following the first amino acid in the putative transmembrane domain.
5 e first transmembrane domain or in the 4(th) putative transmembrane domain.
6 tion of the TfR2-alpha protein including the putative transmembrane domain.
7 ) encodes the LMBD1 protein that possesses 9 putative transmembrane domains.
8 y 65.2 kDa predicted molecular mass) with 12 putative transmembrane domains.
9 und that lin-17 encodes a protein with seven putative transmembrane domains.
10  reading frame encoding a protein with seven putative transmembrane domains.
11 lypeptide containing 541 amino acids with 10 putative transmembrane domains.
12 ontains a conserved ATP-binding site and six putative transmembrane domains.
13  with N-terminal coiled-coil regions and two putative transmembrane domains.
14 roteins contain putative signal peptides and putative transmembrane domains.
15 2 is a 101-amino acid protein containing two putative transmembrane domains.
16 EJ, a GPS, a LH2/PLAT, a coiled-coil, and 11 putative transmembrane domains.
17 , TEM5, TEM7, and TEM8, all of which contain putative transmembrane domains.
18 des for a protein of 701 amino acids with 11 putative transmembrane domains.
19 mily) consists of 487 amino acids and has 12 putative transmembrane domains.
20 s encoding a 253-amino acid protein with two putative transmembrane domains.
21 r a protein of 497 amino acids containing 12 putative transmembrane domains.
22 r a protein of 551 amino acids containing 12 putative transmembrane domains.
23 s a 610-amino acid protein that contains two putative transmembrane domains.
24 of 578 amino acids and contains 12 conserved putative transmembrane domains.
25 of Lys-20 in the NH2 terminus, just prior to putative transmembrane domain 1 (TMD1).
26 indicate the important role of the conserved putative transmembrane domain 1 in interactions with the
27 ighly conserved regions, particularly in the putative transmembrane domains 1 and 2.
28       Three consecutive residues adjacent to putative transmembrane domain 10 (TM10) were demonstrate
29 on, Gly-499 to Arg (G499R) is located in the putative transmembrane domain 10 of the ClC-1 protein.
30 n four consensus glycosylation sites between putative transmembrane domains 3 and 4.
31 o highly conserved aspartate residues within putative transmembrane domains 4 and 10 are essential fo
32 erminant for homoligomerization lies between putative transmembrane domain 5 and the C terminus.
33                              Residues within putative transmembrane domain 8 (TMD8) of anion exchange
34 ary structure analysis of GLUT10 predicts 12 putative transmembrane domains, a hallmark structure of
35    The primary structures of Nirs reveal six putative transmembrane domains, a region homologous to p
36 of G protein-coupled receptors, having seven putative transmembrane domains, an extracellular amino t
37  of TRPM1 dimers is characterized by a small putative transmembrane domain and a larger domain with a
38 he N-terminal 337 residues, which included a putative transmembrane domain and a region relatively ri
39   The N-terminal half of RET-RGS1 contains a putative transmembrane domain and a string of nine cyste
40                                  A30.5 has a putative transmembrane domain and colocalized with marke
41                      Amino acids in both the putative transmembrane domain and extracytoplasmic carbo
42  unusual member of the PKC family that has a putative transmembrane domain and pleckstrin homology do
43         This additional sequence contained a putative transmembrane domain and two potential tryptic
44                           The enzyme has six putative transmembrane domains and a hydrophilic region
45  of molecular weight 85,000, containing four putative transmembrane domains and an ATP binding domain
46 ted KAM3 encodes a novel protein with twelve putative transmembrane domains and contains limited sequ
47 amino acid residues (63.4 kDa) with 11 to 14 putative transmembrane domains and exhibits approximatel
48 rane protein 74 (TMEM74), which contains two putative transmembrane domains and exhibits high levels
49  appears to be genes encoding MMPs that have putative transmembrane domains and may be membrane-tethe
50 odes a protein of 436 amino acids with seven putative transmembrane domains and shares common ancestr
51 n identified that encode proteins with seven putative transmembrane domains and that are expressed se
52                          The protein has six putative transmembrane domains and the two signature mot
53                           SadA contains nine putative transmembrane domains and three conserved EGF-l
54 the primary amino acid sequence include four putative transmembrane domains and, unlike other cloned
55 isting of a hydrophobic region (encoding six putative transmembrane domains) and an ATP-binding site.
56 z domains within a 170-residue ectodomain, a putative transmembrane domain, and a 31-residue hydrophi
57 ns and three fibronectin III-like domains, a putative transmembrane domain, and a distinct intracellu
58 a protein with two Ig-like domains, a single putative transmembrane domain, and a short region C term
59 as a predicted molecular mass of 18.3 kDa, a putative transmembrane domain, and limited sequence simi
60 o tetratricopeptide repeat (TPR) motifs, two putative transmembrane domains, and an extended carboxyl
61                                  ACER2 has 7 putative transmembrane domains, and its amino (N) and ca
62 ar to most members of MFS, PIC30 contains 12 putative transmembrane domains, and PIC30-GFP fusion pro
63 the fz encodes a membrane protein with seven putative transmembrane domains, and that it has a comple
64 t adaptive emerging sequences tend to encode putative transmembrane domains, and that thymine-rich in
65 main, a potential furin cleavage site, and a putative transmembrane domain are located in the C-termi
66 p, a 919-amino acid membrane protein with 14 putative transmembrane domains, as a participant in gluc
67 ceptor proteolytic site, an LH2/PLAT, and 11 putative transmembrane domains, as well as a number of r
68      Consistent with prior observations, the putative transmembrane domain at the C terminus of mZP2
69 The solution structure of Bax, including the putative transmembrane domain at the C terminus, was det
70                      All five UGTs contain a putative transmembrane domain at their C terminus as is
71 uence and is very hydrophobic, with 10 to 12 putative transmembrane domains, both typical characteris
72               The translated product has two putative transmembrane domains but no clear matches in c
73  deduced amino acid sequence identified five putative transmembrane domains but no significant homolo
74 y plots of HvCBT1 showed the presence of six putative transmembrane domains, but sequence alignment i
75 ntains 592 amino acids and appears to have a putative transmembrane domain close to the N terminus.
76         The 63-amino acid p7 monomer has two putative transmembrane domains connected by a cytosolic
77  mutants and a truncation mutant lacking the putative transmembrane domain (DeltaTM) were generated.
78                                   The fourth putative transmembrane domain does not appear to play a
79 located in the intracellular loop connecting putative transmembrane domains eight and nine.
80                                 Coupled with putative transmembrane domains flanking the variable reg
81                         Six out of the seven putative transmembrane domains had membrane insertion si
82 lar, possessing cytosolic active sites, with putative transmembrane domains immediately N-terminal to
83 ed histidyl residue is located in the fourth putative transmembrane domain in hPEPT1 as well as in hP
84  helices reveal the presence of at least one putative transmembrane domain in the TMEM2 protein.
85 ns, these two soybean thioredoxins contain a putative transmembrane domain in their N-terminal region
86 ignal in the amino-terminal region, and five putative transmembrane domains in the carboxyl-terminal
87 ion includes the P region and half of the S6 putative transmembrane domain, including sites not previ
88 ed arrangement of 16 cysteine residues and a putative transmembrane domain, indicating a similar arch
89                                            A putative transmembrane domain is conserved in some, but
90            A mutant Wsc1 protein lacking the putative transmembrane domain is not functional and part
91 consists of 1715 amino acids containing four putative transmembrane domains, multiple ankyrin repeats
92 ce and N-glycosylation sites, but contains a putative transmembrane domain near its carboxy terminus.
93           Like ScPex17p, PpPex17p contains a putative transmembrane domain near the amino terminus an
94   The deduced amino acid sequence contains a putative transmembrane domain near the N-terminus.
95 re also isolated that encode proteins with a putative transmembrane domain near their C termini.
96  amino acids 480-504, representing the fifth putative transmembrane domain of ACAT2.
97                   This Cys is located in the putative transmembrane domain of E1 and was shown to be
98 sitively charged arginine residue within the putative transmembrane domain of E1 would be expected to
99 dings suggest that a localized region of the putative transmembrane domain of Ost4p mediates in stabi
100 in a region close to the luminal face of the putative transmembrane domain of Ost4p were changed into
101  18-25) is localized to only one half of the putative transmembrane domain of Ost4p.
102  acid(s) within or immediately adjacent to a putative transmembrane domain of the transporter.
103 carboxyl-terminal 338 amino acids within the putative transmembrane domain of the type 2 ryanodine re
104          A construct encoding only the first putative transmembrane domain of the type I isoform was
105 show that the positions in the core of the 3 putative transmembrane domains of lambda S are protected
106                             First, the seven putative transmembrane domains of the CCK-A receptor wer
107 the coding sequence for the first and second putative transmembrane domains of the G-protein-coupled
108 ne NPC1 protein has sequence homology to the putative transmembrane domains of the Hedgehog signaling
109 hin exons 1, 2, 3, and 6 in conserved and/or putative transmembrane domains of the protein.
110 tations was distributed throughout the three putative transmembrane domains of the SUR1 protein.
111 ys or Asp residues at other positions in the putative transmembrane domain or at the N or C terminus
112 foci, whereas PcfC deleted of its N-terminal putative transmembrane domain (PcfCDelta N103) distribut
113 lation of the RNA templates encoding all the putative transmembrane domains present in the C-terminal
114  an EPCR construct truncated just before the putative transmembrane domain produced only soluble EPCR
115          In addition, we have identified two putative transmembrane domain residues, phenylalanine 18
116                       Mutations in the three putative transmembrane domains resulted in mislocalizati
117 This protein contains five CUB domains and a putative transmembrane domain suggesting that p160 is an
118  N- and O-glycosylated followed by a pair of putative transmembrane domains surrounding a short hydro
119 ch contains a basic amino acid cluster and a putative transmembrane domain, targeted the protein to t
120  we describe two regions on either side of a putative transmembrane domain that are required for the
121 show that ESyt2 is directed to the ER by its putative transmembrane domain, that the ESyts hetero- an
122  terminating the deduced sequence prior to a putative transmembrane domain, thereby truncating the pr
123 port domain (interfacial helix 2, hairpin 1, putative transmembrane domain (TM) 7, and TM8), as well
124 subtypes with a splice site within the first putative transmembrane domain (TM).
125 in [OTU], the hypervariable domain [HV], the putative transmembrane domain [TM], and the C-terminal r
126    We examined the involvement of the second putative transmembrane domain (TM2) of the P2X2 subunit
127  affected by amino acid alterations within a putative transmembrane domain (TMD) ligand pocket.
128  11 highly conserved W, Y, and F residues in putative transmembrane domains (TMDs) of rat VAChT was m
129 oles of 7 conserved ionic residues in the 12 putative transmembrane domains (TMDs) of vesicular acety
130             TMEM16 channels consist of eight putative transmembrane domains (TMs) with TM5-TM6 flanki
131 rms, we have utilized RNA templates encoding putative transmembrane domains to program a cell-free tr
132                            These include two putative transmembrane domains, two sequences rich in Pr
133 a mutant in which asparagine177 of the third putative transmembrane domain was replaced by glycine, s
134 uence (amino acids [aa] 181 to 323), and the putative transmembrane domain were critical for replicat
135 nd an alternative splice variant lacking the putative transmembrane domain were encoded by the PMEPA1
136 ted against amino acids 42-59 near the first putative transmembrane domain, whereas [125I]RTI 82 was
137 ernatively spliced isoforms: Ser5-001 has 10 putative transmembrane domains, whereas Ser5-004, -005,
138  sequence indicates that the Tc-1 gene has a putative transmembrane domain with multiple cytoplasmic
139     Analysis of the PMT sequence predicted a putative transmembrane domain with predicted hydrophobic
140               MAR1 encodes a protein with 11 putative transmembrane domains with low similarity to fe
141                            It contains seven putative transmembrane domains with the amino and carbox
142  containing a zinc binding active site and a putative transmembrane domain, with signal peptides in t
143  first proton using homologous aspartates in putative transmembrane domain X (ten), but they transloc

 
Page Top