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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.
14                       Importantly, the Rad52 C-terminal portion alone can promote Rad51 presynaptic f
15          This interaction was refined to the C-terminal portion (amino acids 348-588) of ATDC and the
16                                          The C-terminal portion (amino acids 416 to 550) of the p65 s
17 kely corresponding to the cytoplasmic N- and C-terminal portions, and a more compact domain, correspo
18 , whereas none of the lysine residues in the C-terminal portion are protected.
19 motifs in the membrane-distal, nonstructural C-terminal portions are required for the exit from the E
20                                          Its C-terminal portion (CNK(C-term)) directly binds to RAF.
21 ilar fashion to GroEL, with the more compact C-terminal portion completely protected and the more fle
22      ORF57 interacts directly with the RBM15 C-terminal portion containing the SPOC domain to reduce
23                                          The C-terminal portion contributes further to hTAP's nuclear
24            The third antibody recognizes the C-terminal portion (deleted in NPM-ALK) and reacts only
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
33      We conclude that the intracellular Ctp1 C-terminal portion is essential for clipping, while the
34 hat the conserved T-box domain, with a small C-terminal portion, is required for recruiting histone m
35                                   Within the C-terminal portion, modification of four amino acids in
36 inuclear zinc center that is situated at the C-terminal portion of a "TIM" barrel motif.
37            The nucleotide is situated at the C-terminal portion of a five-stranded parallel beta-shee
38            UNC-96 and LIM-8 also bind to the C-terminal portion of a myosin heavy chain (MHC), MHC A,
39 e report that UNC-98 also interacts with the C-terminal portion of a myosin heavy chain.
40                                          The C-terminal portion of Aap contains a 135-aa-long, prolin
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
43                  Deletion mutants showed the C-terminal portion of apoptosis signal-regulating kinase
44                    Missense mutations in the C-terminal portion of ATP7A have also been shown to caus
45 iction algorithm suggest that the functional C-terminal portion of AvrRpt2 is a cysteine protease.
46                                          The C-terminal portion of Bcd(A57-61) is required to mediate
47 anslational modifications in the lysine-rich C-terminal portion of beta.
48 ibitors of the interaction between BRCT (the C-terminal portion of BRCA1, a key tumor suppressor prot
49                             Exclusion of the C-terminal portion of CALM from the fusion protein, whic
50     We also show that PBP interacts with the C-terminal portion of CAR, suggesting that PBP is involv
51 r HHV-6 receptor activity reside outside the C-terminal portion of CD46.
52 ing and primarily consist of residues in the C-terminal portion of CheY.
53                           One residue in the C-terminal portion of CNT2 was found to significantly co
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
56                 Second, we observed that the C-terminal portion of delta, which forms a jelly-roll be
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
60                                          The C-terminal portion of EiAPR, expressed separately, exhib
61  is located in an unstructured region of the C-terminal portion of eIF4G1 that coordinates assembly o
62                     Mutant mice in which the C-terminal portion of EphB2 is truncated had an intermed
63  is the autonomously expressed, noncatalytic C-terminal portion of FAK.
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
66                                          The C-terminal portion of FSA shares a striking sequence sim
67 ant in a priA mutant by mutating dif and the C-terminal portion of ftsK.
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
70                      Exposed residues in the C-terminal portion of GCAP1, including EF-hand 4 and the
71 ther, these data suggest that targets in the C-terminal portion of Gln3 required for the Gln3-Tor1 in
72 f in fork binding and the interaction of the C-terminal portion of gp59 with helicase and SSB.
73 he duplex DNA ahead of the fork, whereas the C-terminal portion of gp59 would provide the docking sit
74                             In addition, the C-terminal portion of gp7 shows conformational flexibili
75 dicate that the peptide corresponding to the C-terminal portion of GpIbalpha and the entire extracell
76               We further discovered that the C-terminal portion of hCCCAP is identical to the human c
77                                          The C-terminal portion of helix 3, which connects to the COR
78 in shows a close association of helix-1, the C-terminal portion of helix-2 and the N-terminal portion
79  the START domain present in the cytoplasmic C-terminal portion of human MLN64.
80 Here we present the crystal structure of the C-terminal portion of human POT1 (POT1C) complexed with
81                               We studied the C-terminal portion of human TSP2 from the third EGF-like
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
90                                          The C-terminal portion of maize CENPC shares similarity with
91 y and exhibit structural similarity with the C-terminal portion of major group 1 allergens.
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.
96              Finally, modeling the remaining C-terminal portion of Nup157 shows that it projects as a
97 stitutively turned on due to the loss of the C-terminal portion of p100.
98 ightly regulated by sequences located at the C-terminal portion of p100.
99                                 Although the C-terminal portion of P2X7 is thought to be essential fo
100 that the C-terminal part of Vpr binds to the C-terminal portion of p300/CBP within amino acids 2045 t
101 structure of the p55 domain extends into the C-terminal portion of p33.
102  immature HRI, but not with Hsp90, while the C-terminal portion of p50(cdc37) interacted with Hsp90.
103           We now report that deletion of the C-terminal portion of p69, which encodes the highly basi
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
107                        mAb102.1F10 bound the C-terminal portion of Phl p 7 in a calcium-dependent man
108 also requires pXI, which is identical to the C-terminal portion of pI.
109                                          The C-terminal portion of pIII, termed the "C" domain, is re
110 milk a malaria vaccine candidate, the 42-kDa C-terminal portion of Plasmodium falciparum merozoite su
111   An apoptotic function was localized to the C-terminal portion of PR3.
112                                    Thus, the C-terminal portion of PSD-95 serves a dual function.
113 human T-cell lymphomas, and we show that the C-terminal portion of RAG2 is required for this.
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
121                             We show that the C-terminal portion of Sox10 is sufficient to mediate thi
122 P16-PRLBD and VP16-GRLBD interacted with the C-terminal portion of steroid receptor coactivator-1, th
123                            Expression of the C-terminal portion of STIM1 with Orai1 was sufficient to
124                  A sequence motif within the C-terminal portion of Streptococcus gordonii SspB (AgI/I
125 xpressing high levels of HSPGs mapped to the C-terminal portion of SU.
126  and peptides corresponding to the conserved C-terminal portion of T. maritima FliF.
127 ry module" and specific sequences within the C-terminal portion of the "regulatory module" of HSL (am
128 moves one residue from an alpha-helix in the C-terminal portion of the AAA+ domain.
129  of TraR contributing to TraM binding to the C-terminal portion of the activator protein.
130 zation of the TfR binding site on HFE to the C-terminal portion of the alpha1 domain helix and an adj
131 high-affinity binding to DR6 requires a more C-terminal portion of the APP ectodomain.
132  30-amino acid peptides corresponding to the C-terminal portion of the beta- and/or gamma-rat epithel
133  required for activity are positioned at the C-terminal portion of the beta-barrel.
134 n bacterial intimin-like proteins and on the C-terminal portion of the BsaB protein.
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
137 lmodulin and alpha-actinin bind to the short C-terminal portion of the C0 region of NR1.
138 DRBMs) of ADAR1 while the second maps to the C-terminal portion of the catalytic domain.
139                                          The C-terminal portion of the chain plays an important role
140 nt changes in structure were detected in the C-terminal portion of the channel upon activation of the
141                             In contrast, the C-terminal portion of the checkpoint protein RAD9p is es
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
145  region (residues 34 and 43), and one in the C-terminal portion of the ectodomain (residue 277).
146 coiled coils via interactions throughout the C-terminal portion of the ectodomain.
147 on, possibly by chemical modification of the C-terminal portion of the enzyme containing the TIMP-1 b
148              We further demonstrate that the C-terminal portion of the enzyme is disordered and not e
149 ers encodes an Arg to Cys replacement in the C-terminal portion of the extracellular domain of neurol
150        Expression of the region encoding the C-terminal portion of the FCV ORF1 (amino acids 942 to 1
151                                          The C-terminal portion of the fibrin alpha chain extends int
152 Site-directed mutagenesis indicated that the C-terminal portion of the first transmembrane domain was
153                     A peptide containing the C-terminal portion of the FtsA divisome protein is a sub
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
156                     Internal deletion of the C-terminal portion of the Gag p10 region resulted in the
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
162             Finally, we demonstrate that the C-terminal portion of the inv(16) fusion protein contain
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
165 asparagine for glutamine at codon 322 of the C-terminal portion of the LMP1 gene.
166 sus AvrRpm1 specificity is determined by the C-terminal portion of the LRR domain.
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
170                 Many mutations affecting the C-terminal portion of the molecule block the pre-B-trans
171            On A. fumigatus, PTX3 exposed the C-terminal portion of the molecule, probably resulting i
172 ding solid-supported synthesis to access the C-terminal portion of the molecule.
173                                          The C-terminal portion of the Mus308 polypeptide encodes a D
174                            Truncation of the C-terminal portion of the N protein by protease digestio
175 t the C terminus of CD2AP interacts with the C-terminal portion of the nephrin cytoplasmic domain.
176                                          The C-terminal portion of the NG2 cytoplasmic domain, theref
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
185                                          The C-terminal portion of the peptide forms a helix with zin
186                                The conserved C-terminal portion of the peptide is biochemically stabl
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
191                              The cytoplasmic C-terminal portion of the polycystin-1 polypeptide (PKD1
192                 Our results suggest that the C-terminal portion of the pore region within the alpha-s
193                             In contrast, the C-terminal portion of the predicted PerA protein that co
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
196                           In particular, the C-terminal portion of the protein (Met-135-Gly-248) is s
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
201                                          The C-terminal portion of the protein has homology to glutat
202  kinase A of the beta-subunit of eIF2 in the C-terminal portion of the protein increased the guanine
203                             In contrast, the C-terminal portion of the protein that harbors at least
204 ns of the illness, antibody responses to the C-terminal portion of the protein were more prominent.
205         Six highly conserved residues in the C-terminal portion of the protein were mutated to alanin
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
209 N-terminal portion and the LIM domain in the C-terminal portion of the protein.
210 ange from valine to glutamic acid within the C-terminal portion of the protein.
211 o-acceptor sites in HDAC2 are located in the C-terminal portion of the protein.
212 s identified a transactivation domain in the C-terminal portion of the protein.
213 poA-I cysteine substitution mutations in the C-terminal portion of the protein.
214 ted that the cleavage site is located in the C-terminal portion of the protein.
215  domain for ligand at a site adjacent to the C-terminal portion of the RGD triad.
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
222                              Remarkably, the C-terminal portion of the sequence in the protease domai
223                AsiA binds tightly within the C-terminal portion of the sigma70 subunit of RNA polymer
224 binding domain and the more highly conserved C-terminal portion of the surface (SU) subunit.
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
230 nce of a dileucine recognition signal in the C-terminal portion of the tyrosinase molecule.
231 ur isoforms that differ in the length of the C-terminal portion of their extracellular domains.
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
236                         E6 requires the same C-terminal portion of TNF R1 for binding as does TNF R1-
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
240                              Deletion of the C-terminal portion of TRIM56 abrogated the TRIM56-TRIF i
241 a virus (MLV), whereas overexpression of the C-terminal portion of TSG101 (TSG-3') potently disrupts
242           Furthermore, overexpression of the C-terminal portion of TSG101 (TSG-3') potently inhibits
243                The crystal structure for the C-terminal portion of Tup1 has been solved and, when seq
244                                          The C-terminal portion of Ty3 RT encodes a functional RNase
245             Internal deletions of either the C-terminal portion of UCR1 or the N-terminal portion of
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
249          Mutational analysis showed that the C-terminal portion of Vpr, known to harbor its cell cycl
250           In contrast, MT binding masked the C-terminal portion of WHAMM and prevented it from promot
251                                          The C-terminal portion of XPC (residues 492-940; XPC-C) has
252 NF reacts with antibodies to both the N- and C-terminal portions of actin on Western blots and migrat
253                                   Mainly the C-terminal portions of both CcmI and apocytochrome c(2)
254 quence analysis predicts that regions in the C-terminal portions of both MPs and MPt have high probab
255                                          The C-terminal portions of both toxins are composed of 20 an
256 phorylated fragments representing the N- and C-terminal portions of DMP1 have been identified, appare
257 half of dynamin-2 PRD but to both the N- and C-terminal portions of dynamin-1 PRD.
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
260                                       N- and C-terminal portions of mammalian G(i2) and G(16) were su
261 QSTM1 (sequestosome)-Nup214, both containing C-terminal portions of Nup214.
262  Mutants with alterations in both the N- and C-terminal portions of p12 exhibited a distinct phenotyp
263 ding frames that are predicted to encode the C-terminal portions of sensor kinases.
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
266          The structure shows that the N- and C-terminal portions of the GAP homologous regions togeth
267  Env function when inserted in the center or C-terminal portions of the hypervariable domain.
268 ins encompassing the N-terminal, middle, and C-terminal portions of the keratin 14 protein.
269 ins homologous with either the N-terminal or C-terminal portions of the M. bovis FbiC.
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
273                           Significant N- and C-terminal portions of the protein were found to be disp
274 Here we demonstrate that the SIX domains and C-terminal portions of the SO and OPTIX proteins are req
275 r procedure contained the N-terminal and the C-terminal portions of the tagged luciferase.
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
279                           Interestingly, the C-terminal portions of these H-N-H phage endonucleases c
280 that a direct interaction between the N- and C-terminal portions of UL9 might exist and serve to modu
281                                          The C-terminal portion (p55 domain) of wild-type p88 VacA co
282 lar growth in macrophages, where the Mh3881c C-terminal portion plays a critical role.
283 A binding domains (stau-RBD) but lacking the C-terminal portion potentially involved in dendritic tar
284 nstitute the prion domain, and the remaining C-terminal portion regulates nitrogen catabolism.
285 nal region (residues 1-71) and a well-folded C-terminal portion (residues 72-159).
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.
293    Six CHFI mutants lacking different N- and C-terminal portions were generated.
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
299 ges that alter the interaction of the mobile C-terminal portion with the active site.
300  TUSP are localized in the cytoplasm but the C-terminal portion with the two NLSs produced distinct d

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