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1 2 peptide, whereas Rcf1 is homologous to the C-terminal portion.
2 able" distal helix may be valid only for the C-terminal portion.
3 ation of wild-type gene 37 inserted into its C-terminal portion.
4 NA polymerases (RdRps) in its nonoverlapping C-terminal portion.
5 r domain, and a DNA polymerase domain in the C-terminal portion.
6 near the conserved CxxC or RHR motif in the C-terminal portion.
7 id sequence identity to known cyclins in the C-terminal portion.
8 the E3 ligase activity and integrity of the C-terminal portion.
9 rylation sites and a more ordered and folded C-terminal portion.
10 N terminus of the MC160 protein but not the C-terminal portion.
11 e-homeobox domain of DUX4 but splice-out the C-terminal portion.
12 ess a conserved cis-proline located in their C-terminal portions.
13 ndependent genes corresponding to the N- and C-terminal portions.
17 kely corresponding to the cytoplasmic N- and C-terminal portions, and a more compact domain, correspo
19 motifs in the membrane-distal, nonstructural C-terminal portions are required for the exit from the E
21 ilar fashion to GroEL, with the more compact C-terminal portion completely protected and the more fle
25 ombinant human Slit-2 protein and the N- and C-terminal portions generated by in vivo proteolytic pro
26 hobic amino acid residues in the core of the C-terminal portion generates a protein with enhanced sta
27 iffers mainly in the presence of an extended C-terminal portion incorporating four closely spaced O-l
28 st large areas of p101 including both N- and C-terminal portions interact with the N-terminal half of
29 sted antiparallel beta-barrel with the N and C-terminal portions interacting with adjacent subunits.
30 ef heart mitochondrial F(1)-ATPase where the C-terminal portion is arranged as a two-alpha-helix hair
31 of CD151 we established that the cytoplasmic C-terminal portion is critical for activity of CD151 tow
32 to the C-terminus during secretion, and the C-terminal portion is critical to the co-dependent secre
34 hat the conserved T-box domain, with a small C-terminal portion, is required for recruiting histone m
41 elength anomalous dispersion, shows that the C-terminal portion of AhpF (residues 210-521) is structu
42 pended substrate, first being reduced by the C-terminal portion of AhpF, and subsequently reducing Ah
45 iction algorithm suggest that the functional C-terminal portion of AvrRpt2 is a cysteine protease.
48 ibitors of the interaction between BRCT (the C-terminal portion of BRCA1, a key tumor suppressor prot
50 We also show that PBP interacts with the C-terminal portion of CAR, suggesting that PBP is involv
54 complement cascade, primarily recognize the C-terminal portion of DEK protein and exhibit higher aff
55 complement cascade, primarily recognize the C-terminal portion of DEK protein, and exhibit higher af
57 rly postnatal, but not adult induction, of a C-terminal portion of DISC1 in mice results in a cluster
58 3-prime fragments that encode the conserved C-terminal portion of DUX4 and (iii) capped and polyaden
59 CCR5 ECL2-derived peptides, we show that the C-terminal portion of ECL2 (2C, comprising amino acids C
61 is located in an unstructured region of the C-terminal portion of eIF4G1 that coordinates assembly o
64 shorter segments of FGF-1 sequences into the C-terminal portion of FGF-7 or FGF-10 revealed that subs
65 one hybrid experiments demonstrated that the C-terminal portion of FL functions in transcriptional ac
68 ine-binding domain of FRS2alpha fused to the C-terminal portion of Gab1, the region including the bin
69 DE5Delta1-465 contained the C domain and the C-terminal portion of GAF-B; and PDE5Delta1-534 containe
71 ther, these data suggest that targets in the C-terminal portion of Gln3 required for the Gln3-Tor1 in
73 he duplex DNA ahead of the fork, whereas the C-terminal portion of gp59 would provide the docking sit
75 dicate that the peptide corresponding to the C-terminal portion of GpIbalpha and the entire extracell
78 in shows a close association of helix-1, the C-terminal portion of helix-2 and the N-terminal portion
80 Here we present the crystal structure of the C-terminal portion of human POT1 (POT1C) complexed with
82 that two additional forms consisting of the C-terminal portion of ICP34.5 are generated in infected
83 involved in binding of IFN-alpha2b while the C-terminal portion of IFN is critical for antiproliferat
84 IKKgamma-binding domain (NBD/gammaBD) in the C-terminal portion of IKKbeta in MEFs deficient in IKKbe
85 l DNA initially binds nonspecifically to the C-terminal portion of IN but the catalytic central regio
86 Abs that recognized epitopes located in the C-terminal portion of LAGE-1, which is distinct from NY-
87 structure at 1.5 A of the immunosuppressive C-terminal portion of Lassa virus NP and illustrate that
88 binding of LPL to GPIHBP1 requires only the C-terminal portion of LPL and does not depend on full-le
89 LPL binding to GPIHBP1, suggesting that the C-terminal portion of LPL is important for GPIHBP1 bindi
92 other autotransporter proteins, whereas the C-terminal portion of MapA resembled the translocation d
93 sites) in the first 294 residues, while the C-terminal portion of MeCP2 (residues 295 to 486) contai
94 ant vaccine, bvMSP1(42), based on the 42-kDa C-terminal portion of MSP1, was expressed as a secreted
95 olved single-amino-acid substitutions in the C-terminal portion of nsP2, the viral helicase-protease.
100 that the C-terminal part of Vpr binds to the C-terminal portion of p300/CBP within amino acids 2045 t
102 immature HRI, but not with Hsp90, while the C-terminal portion of p50(cdc37) interacted with Hsp90.
104 s H3 and H4 interact preferentially with the C-terminal portion of PARP1 protein and that the N-termi
105 nd C/H3 domains of CBP and p300 and with the C-terminal portion of PBP that encompasses amino acids 1
106 Moreover, the data indicate that the unique C-terminal portion of perilipin A is responsible for its
110 milk a malaria vaccine candidate, the 42-kDa C-terminal portion of Plasmodium falciparum merozoite su
114 The co-localization did not occur when the C-terminal portion of RetGC1, containing its regulatory
115 etention signal is likely present within the C-terminal portion of RyR, a region that contains four p
116 use of GPS-linker scanning mutagenesis, the C-terminal portion of SadB was shown to be dispensable f
117 eral regulators have been shown to contact a C-terminal portion of sigma(70) that harbors conserved r
118 ed by SIKE phosphorylation, clustered in the C-terminal portion of SIKE (Ser-133, -185, -187, -188, -
119 at least 4 LIM domains in FHL2, whereas the C-terminal portion of SK1 mediates the binding of FHL2 i
120 gest that glypican binding to the releasable C-terminal portion of Slit may serve as a mechanism for
122 P16-PRLBD and VP16-GRLBD interacted with the C-terminal portion of steroid receptor coactivator-1, th
127 ry module" and specific sequences within the C-terminal portion of the "regulatory module" of HSL (am
130 zation of the TfR binding site on HFE to the C-terminal portion of the alpha1 domain helix and an adj
132 30-amino acid peptides corresponding to the C-terminal portion of the beta- and/or gamma-rat epithel
135 f norepinephrine leads to an ordering of the C-terminal portion of the C-terminal domain into an alph
136 ch other and highlight the importance of the C-terminal portion of the C-terminal lobe in this intera
140 nt changes in structure were detected in the C-terminal portion of the channel upon activation of the
142 omain from Gly8 to Gly44 (domain 2), and the C-terminal portion of the collagen-like domain from Gly4
143 of a 111-amino acid peptide derived from the C-terminal portion of the cystic fibrosis transmembrane
144 functions of LIN-3 in all tissues, while the C-terminal portion of the cytoplasmic domain is involved
147 on, possibly by chemical modification of the C-terminal portion of the enzyme containing the TIMP-1 b
149 ers encodes an Arg to Cys replacement in the C-terminal portion of the extracellular domain of neurol
152 Site-directed mutagenesis indicated that the C-terminal portion of the first transmembrane domain was
154 ort that the SCAN domain is derived from the C-terminal portion of the gag capsid (CA) protein from t
155 acid residue extension corresponding to the C-terminal portion of the Gag p10 protein, has been dete
157 tide, Gly-Pro-Arg-Pro-Pro, that binds to the C-terminal portion of the gamma-chain of fibrin can dete
158 -chain, N-terminal peptide that binds to the C-terminal portion of the gamma-chain of fibrin has been
159 high level of endogenous proteolysis at the C-terminal portion of the GFP-Spf1 molecule that abolish
160 the minimal PY-NLS in yeast consists of the C-terminal portion of the human consensus, R/H/KX(2-5)PY
161 LR, viable M. genitalium and the recombinant C-terminal portion of the immunogenic protein MG309 (rMG
163 escribed by a "two-site" model, in which the C-terminal portion of the ligand interacts with the N-te
164 obes located on the C-terminal helix and the C-terminal portion of the linker increased further as a
167 (2+) is characterized by condensation of the C-terminal portion of the metal-binding loops with monod
168 ltiprotein-binding scaffold exhibited by the C-terminal portion of the MICALs represents a unique com
169 4 to bind peptide sequences derived from the C-terminal portion of the MIIA rod with submicromolar af
175 t the C terminus of CD2AP interacts with the C-terminal portion of the nephrin cytoplasmic domain.
177 hat CheZ localization requires the truncated C-terminal portion of the P1 domain present in CheA(S).
178 resides within a 70-amino acid domain in the C-terminal portion of the p10 region of Gag, and in vitr
179 ow mapped the nuclear export activity to the C-terminal portion of the p10 sequence and identified th
180 ripts expressed a p8 minicore containing the C-terminal portion of the p21 core protein and lacking t
181 o-acid truncated protein containing only the C-terminal portion of the passenger domain and the entir
182 the present study, we demonstrated that the C-terminal portion of the PB1-F2 protein binds to MAVS i
183 g synthetic peptides derived from the active C-terminal portion of the PB1-F2 protein from those two
184 subunit is homologous to the I subunit, the C-terminal portion of the pea D was used for antigen pro
187 I20 are in agreement with a location of the C-terminal portion of the peptide near the lipid/water i
188 l-l-phenylalanine (Bpa) in position 8 of the C-terminal portion of the peptide was identified previou
189 Ca(2+) is to increase the interaction of the C-terminal portion of the peptide with the N-terminal lo
190 a transmembrane fusion protein encoding the C-terminal portion of the PKD1 cytoplasmic tail, PKD1(11
194 onserved domains have been identified in the C-terminal portion of the preToc75 transit peptide from
195 ot appear to require its PH domain since the C-terminal portion of the protein (CRAC-DeltaPH) can sub
197 fied an insertion (hap2-1) that disrupts the C-terminal portion of the protein and tags mutant pollen
198 il of LDLR, and that conserved motifs in the C-terminal portion of the protein bind to clathrin and t
199 ndicate that fragments of Hrs containing the C-terminal portion of the protein can potently inhibit H
200 s, but work by others had suggested that the C-terminal portion of the protein contains a single surf
202 kinase A of the beta-subunit of eIF2 in the C-terminal portion of the protein increased the guanine
204 ns of the illness, antibody responses to the C-terminal portion of the protein were more prominent.
206 generated against an epitope in the deleted, C-terminal portion of the protein, these antibodies did
207 ominant negative form of PYK2 containing the C-terminal portion of the protein, which binds paxillin
208 334 and 504 that is apparently masked by the C-terminal portion of the protein, which includes six re
216 re and sequence optimization to redesign the C-terminal portion of the RGS14 GoLoco motif peptide so
217 ain (residues 198-227)] and C-terminal [RS2: C-terminal portion of the RS domain (residues 228-248)]
218 y N-terminal domains, phosphorylation of the C-terminal portion of the RS domain (RS2) by the nuclear
219 novel ETS-interacting subdomain (EID) in the C-terminal portion of the Runt homology domain (RHD) in
220 in two distinct cytoplasmic M3R regions, the C-terminal portion of the second intracellular loop (i2)
221 n of small varphi-values for residues in the C-terminal portion of the sequence (residues 35-76), cou
225 the surprising finding that swapping a small C-terminal portion of the tail between IIA and IIB inver
226 teract with amino acids contained within the C-terminal portion of the third extracellular domain (ED
227 tracellular loop and a second Cys within the C-terminal portion of the third intracellular loop, at p
228 erol-binding region is located partly at the C-terminal portion of the TMD and partly in the first am
229 fied by site-directed mutagenesis within the C-terminal portion of the tNOX protein corresponding to
232 ons complement biochemical evidence that the C-terminal portion of this PH domain participates in pro
233 ion mutants revealed that the 141-amino-acid C-terminal portion of this protein was capable of target
234 l features indicative of active kinases, the C-terminal portion of this segment sterically restricts
235 n induces a major rotational movement of the C-terminal portion of TM VII and increases the proximity
237 and mutations in residues 160 and 163 in the C-terminal portion of TNT1 adjacent to the cTnT H1-H2 li
238 ch contained one Cys substitution within the C-terminal portion of transmembrane domain (TM) VII (Val
239 nsmembrane domain 1 (M1) and domain 2 in the C-terminal portion of transmembrane domain 2 (M2) and th
241 a virus (MLV), whereas overexpression of the C-terminal portion of TSG101 (TSG-3') potently disrupts
246 S-transferase (GST) fused to the cytoplasmic C-terminal portion of UhpB, results in complete blockage
247 ssing the RCC1 homology domain followed by a C-terminal portion of variable lengths and sequences.
248 In contrast, high deuteration levels in the C-terminal portion of Vif indicated that this region was
252 NF reacts with antibodies to both the N- and C-terminal portions of actin on Western blots and migrat
254 quence analysis predicts that regions in the C-terminal portions of both MPs and MPt have high probab
256 phorylated fragments representing the N- and C-terminal portions of DMP1 have been identified, appare
258 sion of FH, miniFH, contains only the N- and C-terminal portions of FH linked by an optimized peptide
259 ts of SNV and ANDV NPcore exclude the N- and C-terminal portions of full polypeptide to obtain stable
262 Mutants with alterations in both the N- and C-terminal portions of p12 exhibited a distinct phenotyp
264 conclude that domains located in the N- and C-terminal portions of the Ac45 protein direct its traff
265 demarcation of the roles between the N- and C-terminal portions of the antibiotic was determined as
270 stabilize the monomer through contacts with C-terminal portions of the motor or recruit other compon
271 amined, only peptides representing the N-and C-terminal portions of the protein had the ability to so
272 of an interaction between the N-terminal and C-terminal portions of the protein that is required for
274 Here we demonstrate that the SIX domains and C-terminal portions of the SO and OPTIX proteins are req
276 Alanine substitutions in the N-terminal and C-terminal portions of the tail had no effect on either
277 there exist important functional domains in C-terminal portions of the Tbx3 protein that affect its
278 s suggested that sequences in both the N and C-terminal portions of the VP5 sequence contribute to th
280 that a direct interaction between the N- and C-terminal portions of UL9 might exist and serve to modu
283 A binding domains (stau-RBD) but lacking the C-terminal portion potentially involved in dendritic tar
286 n elongation results as a consequence of the C-terminal portion separating from the rest of the molec
287 t the site of interaction may lie within the C-terminal portion that is common to all NfeD homologues
288 g of two C2 domains and a core domain in the C-terminal portion that is homologous to the A domain fo
289 inding to the full-length protein and to the C-terminal portion that is released from the cell membra
290 MotA interact with region 4 of sigma70, the C-terminal portion that normally contacts -35 DNA and th
291 s necessary for RNA editing events include a C-terminal portion that shares structural characteristic
292 ion activity, which can be suppressed by its C-terminal portion via an intramolecular interaction.
294 bunits associate with alpha primarily in its C-terminal portion, which has a unique structure and the
295 targeting of the long isoform of TSLP at the C-terminal portion, which is common to both isoforms, mi
296 ntromere localization of SYCP2L requires its C-terminal portion, which is missing in truncated varian
297 erminal RING domain and the integrity of its C-terminal portion, while the restriction of HCoV-OC43 r
298 ns, and a > or =200 amino acid intracellular C-terminal portion with several phosphorylation signalin
300 TUSP are localized in the cytoplasm but the C-terminal portion with the two NLSs produced distinct d
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