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1 ene segments (PB2, PB1, NA, MP, and NS; >98% sequence identity).
2 1-like enzyme from Arabidopsis thaliana (60% sequence identity).
3 e named species that share 99% 16S rRNA gene sequence identity.
4 rganization they display just 31% amino acid sequence identity.
5 YP51A and CYP51B, which share 59% amino acid sequence identity.
6 ompared with a polyhedrin with less than 10% sequence identity.
7 ies comparable to alignments based on actual sequence identity.
8 roteins of the two viruses sharing about 80% sequence identity.
9 d transposases annotated in GenBank with 80% sequence identity.
10 sequence identity, and northern bobwhite 97% sequence identity.
11 clustered in different families based on 90% sequence identity.
12 Nase III-like enzymes sharing 75% amino acid sequence identity.
13 losely-related paralogs with >75% amino acid sequence identity.
14 an 96% sequence coverage and more than 99.8% sequence identity.
15 tructure while tandem MS was used to confirm sequence identity.
16 hich often result in paralog genes with high sequence identity.
17 le is known about Kgp, which shares only 27% sequence identity.
18 ared structure despite low abundance and low sequence identity.
19 rties compared with gpASNase1, despite a 70% sequence identity.
20 e most divergent family members sharing <15% sequence identity.
21 nverting enzyme 2, sharing approximately 50% sequence identity.
22 ty and structural homology, they exhibit low sequence identity.
23 e fragments demonstrating very low levels of sequence identity.
24 iddle-domain across species, despite lack of sequence identity.
25 ic infection clusters, each having 99.8-100% sequence identity.
26 ipase-like proteins that share less than 20% sequence identity.
27 lic localization and at least 70% amino acid sequence identity.
28 gh they share between 90% and 99% amino acid sequence identity.
29 haC1, to which ChaC2 shows approximately 50% sequence identity.
30 miniviral genome and shares only 50% overall sequence identity.
31 pFI, although they lack significant pairwise sequence identity.
32 er despite the fact that they share only 21% sequence identity.
33 EpsL, with which it also shares virtually no sequence identity.
34 ing the same fold for two sequences with low sequence identity.
35 units of ~109 kb in size that have 97.7% DNA sequence identity.
36 her clinical EKC isolates showed nearly 100% sequence identity.
37 rthologs is more similar despite the lowered sequence identity.
38 for optimal function, despite possessing low sequence identity.
39 CCL-conserved motif but share low amino acid sequence identity.
40 es at the level of 90%, 50% and 30% pairwise sequence identity.
41 The encoded proteins share ~85% amino acid sequence identity.
42 ionally closely linked EF-Ts only shares 55% sequence identity.
43 -3CL(pro) and PEDV 3CL(pro) share only 45.4% sequence identity.
44 erent TrpB homologues with as little as 57 % sequence identity.
45 viruses (HIV), tend to share high amino acid sequence identity.
46 parate transcriptional programs despite high sequence identity.
47 ty to its T2S ortholog GspH, despite minimal sequence identity.
48 osome and the mRNA substrate given their low sequence identities.
49 l RNase architectures despite possessing low sequence identities.
54 ver dopamine D2 receptor (D2R), despite high sequence identity (78% in the transmembrane domain).
55 ce protein A (OspA, beta-sheet) to have high sequence identity (80 and 77%, respectively) with engine
57 These metrics include (i) average protein sequence identity across all orthologs shared by two gen
59 V-1 and HIV-2 proteases share just 38 to 49% sequence identity, all critical structural features of p
60 Us), which are clustered on the basis of DNA sequence identity alone, are the most commonly used micr
64 nt) but APRs are more conserved than average sequence identity among homologues that have at least 50
65 less than 10,000 y ago, have high levels of sequence identity among subgenomes that mask the effects
68 ork within the Drosophila genus, we analyzed sequence identities and similarities of clock protein ho
71 ette, which we call DC4, had a high level of sequence identity and cluster together phylogenetically.
72 RPC4 and TRPC5 proteins share 65% amino acid sequence identity and form Ca(2+)-permeable nonselective
75 es, with one gene in the pair having greater sequence identity and higher alignment scores with respe
76 re we surveyed the frequency of variation in sequence identity and length at CSB 2 amongst human mito
77 ilizes fixed-backbone design to optimize the sequence identity and nucleobase conformations of an RNA
78 fication of Proteins) domains with up to 70% sequence identity and present all similarities among the
79 ne mammalian Nav channel isoforms share high sequence identity and remain recalcitrant to high-resolu
80 of 131 submissions (79%) had >99% nucleotide sequence identity and resistance mutation concordance, c
82 One BLV miRNA, BLV-miR-B4, shares partial sequence identity and shared common targets with the hos
84 The integrases share only 59% amino acid sequence identity and the attP sites have fewer than 50%
85 we demonstrate a global correlation between sequence identity and the binding of small molecules wit
87 ee families according to their percentage of sequence identity and their pharmacological properties.
92 study in humans due to the large size, high sequence identity, and mosaic nature of segmental duplic
93 chicken myoglobin, Japanese quail showed 98% sequence identity, and northern bobwhite 97% sequence id
94 used only with parents of sufficient overall sequence identity, and provides no control over the resu
95 ToxB homologs, or for any protein with >30% sequence identity, and therefore what underlies activity
98 models built on template structures over 50% sequence identity are within 2.9 A of the experimental s
99 milar to the yeast homolog Ipk2, despite 17% sequence identity, as well as the active site architectu
100 for the BRD4 bromodomains that have over 90% sequence identity at the acetyl-lysine binding site.
101 simple tandem duplication of defensin7 with sequence identity at the junction, suggesting nonallelic
103 bes the specific parameters for a nucleotide-sequence-identity-based method of organizing the viral s
104 divergent, with 77% and 87% mean amino acid sequence identities between East Asian and non-Asian gro
105 lytic infection by the phage is dependent on sequence identity between CRISPR spacers and the target
109 ough three simple mutations despite only 26% sequence identity between native human and E. coli DHFRs
110 eys, it has been suggested that lowering the sequence identity between neighboring domains is one of
111 l complementation correlates with amino acid sequence identity between orthologs, but varies consider
112 ss rate of MR however drops quickly when the sequence identity between query and templates is reduced
114 (HIV-1) capsid, although there is negligible sequence identity between RSV and HIV-1 CA in the region
115 cleotide polymorphisms, although the protein sequence identity between strains exceeds 90% on average
116 lso display extreme divergence in amino acid sequence identity between STs (i.e., 59%-61% median iden
117 or toxicity testing is often reliant on high sequence identity between the human proteins and their a
118 A3(OB) and A6, despite only ~40% amino acid sequence identity between the OB-folds of A3 and A6.
119 ed using the template structure, the percent sequence identity between the template and target, and t
120 results highlight several key differences in sequence identity between these two steps, complement kn
122 g and homology modeling, especially when the sequence identity between two proteins under considerati
124 pite their evolutionary distance and limited sequence identity, both ClpXP and the proteasome share a
127 cent design of proteins displaying very high sequence identities but different 3D structure allows th
128 forms in the same individual displaying high sequence identities but large functional differences.
129 eins, including proteins with high levels of sequence identity but different folds, are exceptions to
130 ir subunit proteins FlgG and FlgE having 39% sequence identity, but show distinct mechanical properti
132 ficity so that only molecules with very high sequence identity can form cross-beta-sheet structures o
133 metabolic pathway, the homologous SnoN (38% sequence identity) catalyzes an epimerization step at th
136 ntifies the relative contributions of parent sequence identity, crossover locations, and protein fold
138 These features include regions of perfect sequence identity encompassing 700 bp at the hotspot cor
139 tionally caution against interpreting genome sequence identity for this pathogen as proof of a direct
141 istance between NAHR substrate elements, DNA sequence identity (fraction matching), GC content, and c
142 2 TMHs), size (from 183 to 420 residues) and sequence identity (from 15% to 70%), the method improves
143 yltransferase, the closely related RdmB (52% sequence identity) from the rhodomycin pathways is an at
144 sting of 5,696 unique microbial OTUs (at 97% sequenced identity) from 47 bacterial and three archaeal
145 In vitro, these enzymes, which share 78% sequence identity, generate distinct products from their
146 their complex structure, large size and high sequence identity, genetic variation within LCR22s among
148 in paralogs having up to approximately 99.6% sequence identity, identify small gene-disruptive deleti
150 us, Acinetobacter, but instead shows limited sequence identity in its N-terminal half with fungal DSD
151 rent deficit might arise from the erosion of sequence identity in numts originating from rapidly evol
154 hly related RalA and RalB small GTPases (82% sequence identity) in pancreatic ductal adenocarcinoma (
157 and encode an integrase, and attachment site sequence identity is carefully noted; therefore, the dat
158 effect on fusion triggering, suggesting that sequence identity is not critical for this function.
160 s (LCRs) >10 kb in size and sharing >97% DNA sequence identity, is responsible for the majority of re
161 2,890 operational taxonomic units (OTUs; 97% sequence identity level) including members of all eukary
164 BH3 binding grooves showed that, despite low sequence identity, M11 has structural similarities to Bc
165 deomycetes, and despite their modest primary sequence identity, many are perceived by the cognate tom
166 refolding of tandem repeats, independent of sequence identity, more than half of all molecules trans
167 omorphic pairs, displaying increasingly high-sequence identity (namely, 30%, 77%, and 88%), but diffe
171 ion between the MMP substrate preference and sequence identity of 50-57 discontinuous residues surrou
172 S1 is a SLAMF6 homolog with an amino acid sequence identity of 97% to SLAMF6 in its ligand-binding
173 from 45% to 81% and primarily depend on the sequence identity of aligned target sequences and templa
175 lates of the epidemic period had a very high sequence identity of at least 99.9% and formed a monophy
179 same surface patch on Blo t 1, as well as of sequence identity of surface-exposed residues, suggests
183 t efficient algorithms to optimize the local sequence identity or the nearest-neighbor approximation
185 Both clusters contain palindromes with high sequence identity, presumably maintained by gene convers
187 ve a puzzling drop in accuracy in the 40-60% sequence identity range, the so-called 'BRaliBase Dent'.
188 ss results in a 16 kb cluster that shares no sequence identity, regulation or organizational principl
189 1 to 49% nucleotide and 40 to 70% amino acid sequence identities, respectively, with other grapevine
190 ent could be reliably predicted based on the sequence identity seen in the original BLOSUM62 alignmen
191 and, despite these proteins sharing very low sequence identity, structure-based phylogenetic analysis
192 AE1.1 and Bn-FAE1.2 promoters possess strong sequence identity suggesting that transcriptional contro
193 teins due to difficulties in recognizing low-sequence identity templates with a similar fold to the t
200 spite their different functions and only 23% sequence identity, the two proteins have very similar ov
202 te the high structural similarity with 64.3% sequence identity, their responses to Gd@C82(OH)22 were
203 for naturally occurring neighbours with low sequence identity, these transient misfolds disappear mu
204 ugh both proteins share about 90% amino acid sequence identity, they exhibit different open probabili
206 such depositions, identifying them by a 95% sequence identity threshold, performs analysis of their
207 nate (CHM) hydratase (GalB), which has a 12% sequence identity to a previously identified CHM hydrata
208 al inner spore membrane protein and exhibits sequence identity to A subunits of the spore's nutrient
211 ltiple calmodulin (CaM) isoforms of variable sequence identity to animal CaM suggested an additional
213 , five genes were found with ~50% amino acid sequence identity to Arabidopsis tryptophan aminotransfe
216 e hemagglutinin cleavage site which had 100% sequence identity to chicken 28S rRNA, suggesting that t
217 of the mixed lineage kinase family with high sequence identity to Dual Leucine Zipper Kinase (DLK/MAP
220 s SegB is an archaea-specific factor lacking sequence identity to either eukaryotic or bacterial prot
221 ll protein chains in VIPERdb filtered at 40% sequence identity to identify distinct capsid folds, and
223 nated strain IS2.3), with 100% 16S rRNA gene sequence identity to Mycobacterium aurum, which degraded
224 three-finger toxin (3FTx) family, with high sequence identity to neurotoxins and low identity to the
225 a to membrane compartments and (ii) the high sequence identity to the preferentially cytoplasmic AKAP
226 s in crystal structures but lack significant sequence identity to the respective TGR5 sequence, we co
227 ally built from template structures with low sequence identity to the target sequence, using a sequen
229 rtificially evolved sequences, whose average sequence identity to the wild-type sequences is as low a
231 Their genomes show up to 68% nucleotide sequence identity to Thogoto virus (segment 2; approxima
232 cluding (1) novel strains with <98% 16S rRNA sequence identity to validly described species, (2) clos
235 d these two chemokines that only share a 37% sequence identity, we mapped their epitopes on human CXC
237 Protein-coding genes share 93% nucleotide sequence identity, whereas pseudogenes are only 82% iden
238 .1-p21 and is most homologous to CAPN13 (36% sequence identity), which is located 365 kb downstream o
239 protein (PPE15) that showed weak amino acid sequence identities with mammalian perilipin-1 and was u
240 irus (EBV) BBLF1 shares 13 to 15% amino acid sequence identities with the herpes simplex virus 1 UL11
242 ity among closely related homologues (>/=80% sequence identity with a parent) but APRs are more conse
246 nce of the alpha2 nAChR subunit and the high sequence identity with alpha4 (78%) and other neuronal n
247 s substrate specificity and 28.5% amino acid sequence identity with an Aspergillus fumigatus entity.
249 d TPR-repeat protein, but shows only limited sequence identity with any protein of known structure.
252 We identified a novel gene based on its sequence identity with ccm2, which we have named ccm2-li
253 ne/threonine protein kinases that exhibit no sequence identity with conventional eukaryotic protein k
254 is 509 amino-acid enzyme, having 67% and 26% sequence identity with CotA from Bacillus subtilis and B
255 evertheless, the maximum pairwise amino acid sequence identity with currently recognized flaviviruses
256 ough this protein only has approximately 20% sequence identity with eukaryotic actin, phylogenetic an
260 milar transmembrane topology and significant sequence identity with human HASs and likely synthesizes
262 e-dominant chicken RPE65 (cRPE65) shares 90% sequence identity with human RPE65 (hRPE65) but exhibits
264 son revealed that the Bph32 gene shares 100% sequence identity with its allele in Oryza latifolia.
265 ing only 61.1% (whole genome) and 63.1% (L1) sequence identity with its closest relative in the Papil
266 ith prokaryotic UGM reveals that despite low sequence identity with known prokaryotic UGMs the overal
267 coding for proteins sharing high amino acid sequence identity with members of the Ros/MucR transcrip
270 GFLOMT2 displayed the highest amino acid sequence identity with norlaudanosoline 6-OMT, showed a
271 ntatively named BoNT/X, which has the lowest sequence identity with other BoNTs and is not recognized
274 hei ENT1 (PbENT1) shares only 60% amino acid sequence identity with PfENT1, we sought to characterize
275 SIGLEC1 Ig domain shares approximately 22% sequence identity with PILRalpha, an identity that inclu
276 trains 11a and 11a5 share 100% 16S rRNA gene sequence identity with previously sequenced Dhc strains
277 ic characterization of the ISPs is a lack of sequence identity with proteins of known structure or fu
278 enzyme: firstly by mutating RadA to increase sequence identity with RAD51 in the BRC repeat binding s
280 l despite retaining as low as 30% nucleotide sequence identity with rpoA genes from outgroups in the
281 Genome segment 5 of IND1988/02 shows >99% sequence identity with some other BTV isolates from Indi
282 be essential for viability and to have high sequence identity with SPases from other pseudomonads (>
283 COI gene of the Japanese specimen shared 99% sequence identity with the Bemisia 'JpL' genetic group.
284 hogen Pseudomonas aeruginosa shares over 84% sequence identity with the corresponding elongation fact
285 Hxs2) in Cryptococcus that share the highest sequence identity with the glucose sensors Snf3 and Rgt2
286 terminal transactivation (C-TAD) shared high sequence identity with the human HIF-1alpha and HIF-2alp
289 toxin was found to share only 87% amino acid sequence identity with the nearest Stx1 subtype referenc
291 treptomyces scabies Scabin shares nearly 40% sequence identity with the Pierisin family of mono-ADP-r
292 in particular shares virtually no amino acid sequence identity with the residues that have been repor
294 e c-type cytochrome domain of cN shares high sequence identity with those localized c-terminally in c
295 (PB2, PB1, PA, HA, NA, and NS) sharing >99% sequence identity with those of H7N8 turkey isolates was
297 actored" gene cluster that shares little DNA sequence identity with WT and for which the function of
298 of evolutionary conservation extending from sequence identity within the genome to the underpinnings
299 demonstrated that despite the high level of sequence identity, yapK is distinct from yapJ in its con
300 paramyxoviruses, these domains share little sequence identity yet are similar in length and structur
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