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1 located 18 amino acids or more away from the membrane spanning domain.
2 , even though both proteins lack any obvious membrane spanning domain.
3 ted to encode an ICAM-4 isoform, lacking the membrane-spanning domain.
4 A, has structural features indicative of the membrane-spanning domain.
5 this conserved groove and is distal from the membrane-spanning domain.
6 ptic plasma membrane via a single C-terminal membrane-spanning domain.
7 residues (Pro(595)-Gly(596)) near the second membrane-spanning domain.
8 al N-linked glycosylation sites and a single membrane-spanning domain.
9 within a region immediately adjacent to the membrane-spanning domain.
10 envelope proteins with substitutions in the membrane-spanning domain.
11 SIV) or 59-70 (HIV-1) residues from the gp41 membrane-spanning domain.
12 e linked to a large hydrophobic, potentially membrane-spanning domain.
13 ucine near the center of the presumed second membrane-spanning domain.
14 op is tempered by residue F162 in the second membrane-spanning domain.
15 rface between the cytoplasmic domain and the membrane-spanning domain.
16 132-amino-acid protein containing a putative membrane-spanning domain.
17 lope glycoprotein topology includes a single membrane-spanning domain.
18 n a region predicted to lie within the sixth membrane-spanning domain.
19 tes, predominantly at Leu34-Met35 within the membrane-spanning domain.
20 PSS1 contains a predicted single membrane-spanning domain.
21 are anchored to a lipid surface by their own membrane-spanning domain.
22 Both subunits contain a single predicted membrane-spanning domain.
23 he lack of a recognizable signal sequence or membrane-spanning domain.
24 of the small Tim proteins to the hydrophobic membrane spanning domains.
25 itoylation and myristoylation) as opposed to membrane spanning domains.
26 %) were identified as containing two or more membrane spanning domains.
27 loop, between the third (M3) and fourth (M4) membrane spanning domains.
28 ce on calnexin for proper assembly of CFTR's membrane spanning domains.
29 all missense mutations were in the putative membrane-spanning domains.
30 red to a membrane by two adjacent N-terminal membrane-spanning domains.
31 bility of the interface between NBD1 and the membrane-spanning domains.
32 suggests a model in which FATP1 has multiple membrane-spanning domains.
33 teins by the absence of putative hydrophobic membrane-spanning domains.
34 n the 114-residue loop between the M3 and M4 membrane-spanning domains.
35 ed to a membrane by two adjacent N-terminal, membrane-spanning domains.
36 he hypothetical proteins possess one or more membrane-spanning domains.
37 a 1214-residue polypeptide with 12 putative membrane-spanning domains.
38 erminal domain which contains nine potential membrane-spanning domains.
39 encode novel proteins, one of which has five membrane-spanning domains.
40 ins a sugar transport motif and 12 potential membrane-spanning domains.
41 egral membrane protein with 9 to 10 putative membrane-spanning domains.
42 el has been proposed which features multiple membrane-spanning domains.
43 ino acid residues and possessing 12 putative membrane-spanning domains.
44 agonists that activate receptors with seven membrane-spanning domains.
45 gral cytoplasmic membrane protein with eight membrane-spanning domains.
46 ,035 amino acids long with several potential membrane-spanning domains.
47 amino acids that is predicted to contain two membrane-spanning domains.
48 in (Vma12p) that is predicted to contain two membrane-spanning domains.
49 a 1D-subtype amino acid sequences within the membrane-spanning domains.
50 ature virions, consistent with two potential membrane-spanning domains.
51 an 181 amino acid protein with two putative membrane-spanning domains.
52 uding the conserved hydrophilic and terminal membrane-spanning domains.
53 surface exposed, despite a lack of classical membrane-spanning domains.
54 omains (TMDs) and three loops connecting the membrane-spanning domains.
55 of RLIP76, despite the lack of identifiable membrane-spanning domains.
56 at 7 of the 12 TM domains tested function as membrane-spanning domains.
57 (119) because a chimera that contained GIRK4 membrane-spanning domain 1 significantly reduced the add
60 ed maturation defect, and substituting mouse membrane-spanning domain-2 or its intracellular loops (I
61 flux) in overall topology in that it has six membrane-spanning domains, a histidine-rich intracellula
62 (Gly430) that lies N-terminal to the second membrane-spanning domain activates BNC1 and converts it
63 in modulating the conformation of the first membrane spanning domain (Aleksandrov et al., 2012; Ren
64 ural models for these proteins predict eight membrane-spanning domains alternating with hydrophilic i
65 are predominantly located in or adjacent to membrane-spanning domains, although no significant bias
66 e fourth identified molecule having multiple membrane spanning domains among mammalian type C oncoret
67 idopsis; second, to search for proteins with membrane-spanning domains among the predicted plastidial
68 These findings suggest that distal to the membrane-spanning domain, an interaction of the gp41 LLP
71 structed that contained the CD4 external and membrane spanning domains and a SIV TM cytoplasmic tail
72 Both clones contained two copies each of the membrane spanning domains and nucleotide-binding folds d
73 has 634 amino acid residues with 12 putative membrane spanning domains and shows a low level of ident
74 es were predicted to encode proteins with 14 membrane spanning domains and were from 26 to 53% identi
75 P1 and TAP2, each of which has an N-terminal membrane-spanning domain and a C-terminal ABC ATPase dom
76 in that they both contain an amino-terminal membrane-spanning domain and a carboxy-terminal ATPase.
77 els, having a voltage sensor and pore as the membrane-spanning domain and a cytosolic domain containi
78 gene, which encodes a protein with a single membrane-spanning domain and a large presumptive extrace
79 t Hrd1p interacts with substrate through its membrane-spanning domain and discriminates misfolded fro
80 truncate the NaP(i)-IIc protein in the first membrane-spanning domain and thus likely results in a co
81 sed of proteins that are predicted to have a membrane-spanning domain and to be localized at the plas
82 type Ia transmembrane protein with a single membrane-spanning domain and without any extracellular l
83 predicted to encode a protein with multiple membrane-spanning domains and a COOH-terminal glycosylph
85 des two tandem repeats each containing three membrane-spanning domains and a pore-forming loop with t
86 these regions are separated by two putative membrane-spanning domains and are 150 residues apart in
87 lated by a receptor that does not have seven membrane-spanning domains and does not employ G-proteins
89 e encoded by these genes contain up to eight membrane-spanning domains and four 'U-motifs' with conse
90 encodes a novel protein with seven putative membrane-spanning domains and homology to the Saccharomy
91 agonism for a chimeric receptor in which the membrane-spanning domains and intervening linkers of the
92 mino-acid integral membrane protein with six membrane-spanning domains and intracellular NH2 and COOH
93 ral amino acid transporters with 11 putative membrane-spanning domains and is a potential target to m
94 n integral membrane protein with six to nine membrane-spanning domains and is expressed in neurons th
96 id receptor (LTB(4)-R2) that possesses seven membrane-spanning domains and is homologous (42%) and ge
97 is a 561-amino-acid protein with 12 putative membrane-spanning domains and is ubiquitously expressed,
98 that encodes a protein with seven predicted membrane-spanning domains and other features characteris
100 vely, we demonstrate that VirB3 contains two membrane-spanning domains and that both the N and C term
102 uggests that PRP does not have any prominent membrane-spanning domains and thus is not typical of ABC
104 taining the intracellular N terminus, the S1 membrane-spanning domain, and a portion of the S1/S2 loo
105 Ig-like extracellular domains (D1 and D2), a membrane-spanning domain, and a short cytoplasmic tail.
106 ch pilI is an integral membrane protein with membrane-spanning domains, and pilG is an accessory fact
107 e observation that both cysteines within the membrane-spanning domain are accessible for acylation ha
110 cells indicates that two of CAML's putative membrane-spanning domains are necessary and sufficient f
111 ggest that sequence differences in the first membrane-spanning domains are responsible for the differ
112 ss the intermembrane space by binding to the membrane spanning domains as shown by Tim23p peptide sca
114 uence predicts that the peptide contains two membrane-spanning domains as well as a cytochrome b5-lik
115 that the PrrB polypeptide could contain six membrane-spanning domains at its amino terminus and a hy
116 features of Mcp1 included (i) six potential membrane-spanning domains at the N terminus, (ii) two pr
117 A form of BarA lacking the two N-terminal membrane-spanning domains, BarA198, autophosphorylates i
119 rotein of 458 amino acids containing 9 or 10 membrane-spanning domains but has no significant similar
120 complements a mutant of LMP-1 with wild-type membrane-spanning domains but no carboxy-terminal signal
121 f a truncated RocA derivative, harboring the membrane-spanning domains but not the dimerization or HA
122 located in the cytoplasmic loops (C loops), membrane-spanning domain, C/N terminus, and nonmissense
123 eas the exchange of amino acids in predicted membrane-spanning domains caused loss of function or sho
124 acellular amino and carboxyl termini and two membrane-spanning domains connected by large extracellul
125 e Golgi, the leucine heptad within the first membrane-spanning domain contributes to its trafficking,
127 d that the structure of both hydrophilic and membrane-spanning domains determines the degree to which
129 we show that the protein CaT1, which has six membrane-spanning domains, exhibits the unique biophysic
130 g4 proteins lacking the predicted C-terminal membrane-spanning domain fail to assemble into oligomers
132 fused to GFP demonstrate that the N-terminal membrane-spanning domain flanked by a few positively cha
133 e range of eukaryotes and are defined by two membrane-spanning domains flanking a conserved hydrophil
134 y as a spacer between the IgV domain and the membrane-spanning domain for efficient Tvc receptor acti
135 within a region immediately adjacent to the membrane-spanning domain for their effect on the outcome
136 plasmic and membrane-spanning domains with a membrane-spanning domain from MalG restored subcellular
138 ructed chimeras containing extracellular and membrane-spanning domains from CD25 (Tac) and cytoplasmi
141 stitution of seven leucines in LMP-1's sixth membrane-spanning domain has no effect on its function,
142 proteins and membrane proteins with multiple membrane-spanning domains has so far been observed only
143 atpB, which encodes the a subunit of the F0 membrane-spanning domain, has a similar effect on transf
145 mplete enzyme, conformational changes in the membrane-spanning domain II, which result from proton tr
146 aspase activation, along with the absence of membrane spanning domains in bcl-X(s), may, therefore, r
147 ests a significant involvement of the second membrane-spanning domain in antagonist binding in the bi
148 antly abrogated by peptides derived from the membrane-spanning domain in gp41 and coreceptor binding
149 sites for two hemes, and a three contiguous membrane-spanning domain in the photosynthetic reaction
150 5th and 6th alpha-helices (thought to be the membrane-spanning domains in bcl-2, bcl-X(L), and bax) a
152 oducts were similar and showed four putative membrane-spanning domains in the molecules' C-terminal h
153 milar to that of mammalian NCKX, having five membrane-spanning domains in the NH(2) terminus separate
155 se behavior, and may explain one role of the membrane-spanning domains in the proteins that mediate m
156 esolutive three-dimensional structure of AE1 membrane-spanning domain, in silico modeling combined wi
158 D2 appears to be anchored with an N-terminal membrane-spanning domain into the inner envelope membran
159 similar to Int and Inv in that the proposed membrane-spanning domain is followed by several 90-amino
160 , that the actual amino acid sequence of the membrane-spanning domain is not critical for the activit
164 -1 that contains only its amino-terminal and membrane-spanning domains is sufficient to inhibit repor
165 oduced in yeast that, lacking the C-terminal membrane-spanning domain, is secreted directly into the
166 n, consisting almost entirely of an apparent membrane-spanning domain, it contributed significantly t
167 % identity) and contained a single potential membrane-spanning domain located near its amino terminus
169 revices penetrating into the interior of the membrane-spanning domain may allow anesthetics and alcoh
170 ves a substrate encoding the first predicted membrane-spanning domain (MP1) of the replicase polyprot
171 domain (residues approximately 1-395) and a membrane-spanning domain (MSD) (residues approximately 3
172 on of one amino acid (+1 leucine) within the membrane-spanning domain (MSD) abolished protein functio
173 larly W127 and W137, and the residues in the membrane-spanning domain (MSD) and also immediately flan
174 truncations at the carboxyl terminus of the membrane-spanning domain (MSD) have been characterized.
175 s with one nucleotide-binding domain and one membrane-spanning domain (MSD) likely work as dimers, wh
180 ein, Env-mu26, with an L165R mutation in the membrane-spanning domain (MSD) of TM, that exhibited dra
181 ution of the hydrophobicity of the F-MLV Env membrane-spanning domain (MSD) to its incorporation into
182 MRP1 and four other MRPs have an additional membrane-spanning domain (MSD) with a putative extracell
184 ator (CFTR) is a Cl- channel composed of two membrane-spanning domains (MSD), two nucleotide-binding
187 nd ZmMRP1 contained an additional N-terminal membrane-spanning domain (MSD0) that is typical of MRP t
188 er ABC transporters, ABCC1 has an additional membrane-spanning domain (MSD0) with a putative extracel
189 Different from Pgp, MRP1 contains an extra membrane-spanning domain (MSD1) with a putative extracel
190 minal neighbors, most essentially the second membrane-spanning domain (MSD2) but significantly, not N
192 tions as a Cl(-) channel and consists of two membrane spanning domains (MSDs), two cytosolic nucleoti
194 These transporters are assembled from two membrane-spanning domains (MSDs) and two nucleotide-bind
195 o different extracellular loops of the three membrane-spanning domains (MSDs) of the transporter.
196 membrane-proximal external region (MPER) and membrane-spanning domains (MSDs) of viral glycoproteins
197 a chloride ion channel constructed from two membrane-spanning domains (MSDs), two nucleotide-binding
200 ns are at a conserved position in a presumed membrane-spanning domain not previously known to have a
201 lecule having the carboxyl-terminal tail and membrane spanning domain of CBATP and the amino-terminal
204 monstrated that replacing all or part of the membrane-spanning domain of a viral fusion protein with
208 orylation-induced binding of cdb3-PO4 to the membrane-spanning domain of band 3 in intact cells cause
210 quence similarity between a three contiguous membrane-spanning domain of cytochrome b, which contains
211 obic region immediately preceding the second membrane-spanning domain of each subunit contribute to t
212 (501), located in the hydrophobic C-terminal membrane-spanning domain of eNTPDase3, was found to be t
213 It is suggested here that the ectodomain and membrane-spanning domain of Env are directly responsible
214 served at three hydrophobic positions in the membrane-spanning domain of G2 (F427, W428, and F438).
215 eins by replacing either the first or second membrane-spanning domain of human CFTR with the equivale
219 We have examined the interaction of the membrane-spanning domain of one of the membrane glycopro
220 -restricted epitope, KSPWFTTL located in the membrane-spanning domain of p15TM of AKR/Gross murine le
222 rotational diffusion models suggest that the membrane-spanning domain of that population of band 3 th
223 ocalized two myotonic mutations in the sixth membrane-spanning domain of the first repeat (IS6) regio
224 imply a direct role for the residues in the membrane-spanning domain of the murine leukemia virus en
225 d leucine (to serine) in the putative second membrane-spanning domain of the rat alpha 1(alpha L263S)
226 us with VirD4, and, further, an NH2-terminal membrane-spanning domain of VirD4 is dispensable for com
227 sn-X-Arg is conserved in the first and third membrane-spanning domains of all light-harvesting chloro
228 lpharENaC and mutations preceding the second membrane-spanning domains of alpha-, beta-, and gammarEN
229 dies demonstrating that mutations within the membrane-spanning domains of alpharENaC and mutations pr
230 aken together, our results indicate that the membrane-spanning domains of both caveolins-1 and -2 pla
232 ta suggest that interactions between the two membrane-spanning domains of CFTR may mediate associatio
234 ind that both the extracellular and multiply membrane-spanning domains of IAP are necessary for syner
235 o acid protein encompassing the C-terminal 3 membrane-spanning domains of intestinal PepT1 protein, w
236 These findings together indicate that the membrane-spanning domains of LMP-1 contribute multiple f
238 of a triangular cleft lined by the M1 and M2 membrane-spanning domains of one subunit and the M2 doma
245 iral membrane, consistent with the predicted membrane-spanning domains of the unprocessed polyprotein
247 ed that the first intracellular loop between membrane-spanning domains one and two and the second ext
248 ol for the production of proteins containing membrane-spanning domains or otherwise unstable gene pro
251 hich an HR2-derived (located proximal to the membrane-spanning domain) peptide binds, thus protecting
253 , the remaining family member that has three membrane-spanning domains, possesses the cardinal bioche
255 PT1 and LePT2 genes belong to a family of 12 membrane-spanning domain proteins and show a high degree
257 ate that LMP-1 has specific sequences in its membrane-spanning domains required for these activities.
259 ent located near the cytoplasmic face of the membrane spanning domain (residues Lys-652 to Ala-674) t
261 teines in the hydrophobic core of the second membrane-spanning domain revealed that positions 48 and
262 Although GRASP does not harbor a predicted membrane spanning domain(s), the protein was observed to
265 otional freedom for all tryptophans in these membrane spanning domains that exceed the dynamics for t
266 ally interacts with CD9, a protein with four membrane spanning domains that is frequently coexpressed
267 th an extracellular Ig domain and a multiple membrane-spanning domain that can synergize with antigen
268 main, induces a conformational change in the membrane-spanning domain that is similar to a portion of
269 focused on a leucine heptad in LMP1's first membrane-spanning domain that was shown to be necessary
270 ch encodes a novel protein with no predicted membrane-spanning domains that is polymorphic among Arab
273 toplasmic mass by 20 degrees relative to the membrane-spanning domain; the second is a rearrangement
275 wo and the second extracellular loop between membrane-spanning domains three and four of NKCC1 are ne
277 revealed that four of these also function as membrane-spanning domains, thus supporting an 11 TM stru
278 RMA1 involves the inability of CFTR's second membrane-spanning domain to productively interact with a
279 can also be proteolytically cleaved from its membrane-spanning domain to release a freely diffusible
280 ays the effects of cation binding within the membrane-spanning domain to the nucleotide-binding site,
282 PepT1, is a member of the Slc15 family of 12 membrane-spanning domain transporters; PepT1 has proton/
285 omplex (which contains six to eight putative membrane-spanning domains) was rapidly degraded (t1/2 ap
286 mbrane-spanning domain, the second and third membrane-spanning domains were both required for Lcb1p s
287 constructs expressing the first two or more membrane-spanning domains were capable of co-assembling
288 3p reside in the cytoplasm, and six putative membrane-spanning domains were identified by insertion o
290 these conformational changes extend into the membrane-spanning domain where the channel gate is locat
291 he C-terminal cytoplasmic loop of the second membrane-spanning domain, which forms an interface with
292 kinase/phosphatase domain and the N-terminal membrane-spanning domain with six transmembrane helices
293 eplacement of the N-terminal cytoplasmic and membrane-spanning domains with a membrane-spanning domai
294 n is proposed in which the protein has eight membrane-spanning domains with both the N terminus and t
295 composed of three subunits, each having two membrane-spanning domains with intracellular amino and c
296 tes and encode proteins predicted to have 12 membrane-spanning domains with structural homology to kn
297 a hydropathy profile suggestive of a single membrane-spanning domain, with no apparent regions capab
298 l family members had at least four potential membrane-spanning domains, with N- and C-terminal cytopl
299 of an activity's being linked to individual membrane-spanning domains within LMP-1's polytopic trans
300 , whereas similar substitutions in its first membrane-spanning domain yielded a derivative which aggr
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