ライフサイエンスコーパス: amino acid identity

1 t similar to the human and mouse Sema3F (71% amino acid identity).

2 % identical at the nucleotide level (80%-83% amino acid identity).

3 s and are highly similar to each other (>48% amino acid identity).

4 h two other endo-beta-galactosidases (16-21% amino acid identity).

5 hat are related to IL-17 ( approximately 27% amino acid identity).

6 homologous to DegP of Escherichia coli (41% amino acid identity).

7 bserved in the VP1 gene (66.9%-100% pairwise amino acid identities).

8 are structurally similar and share about 20% amino acid identity.

9 of 157 genes encoding proteins with 15%-99% amino acid identity.

10 nes for Sfhex that encode proteins with >99% amino acid identity.

11 ch other and variants of RagB with 43 to 56% amino acid identity.

12 pressed primarily in the brain and share 53% amino acid identity.

13 ndary structure, sometimes at the expense of amino acid identity.

14 he nicotinic receptor, they only possess 33% amino acid identity.

15 dictated solely by solvent accessibility and amino acid identity.

16 The encoded proteins share 45-52% overall amino acid identity.

17 eminating nucleic acid triplets into correct amino acid identity.

18 desaturases, FAD2 and FADX, that shared 73% amino acid identity.

19 and 438 nm, respectively, while sharing 87% amino acid identity.

20 es, respectively, and share between them 94% amino acid identity.

21 es are absent or share a lower percentage of amino acid identity.

22 The two sequences showed 78% amino acid identity.

23 ity and their proteins share a high level of amino acid identity.

24 ins from enteric bacteria show more than 97% amino acid identity.

25 the two subfamilies share approximately 50% amino acid identity.

26 ven though these two SPOR domains share <20% amino acid identity.

27 le-chain I-OnuI family LHEs, spanning 40-70% amino acid identity.

28 s, LepB (PA0768) and PA1303, which share 43% amino acid identity.

29 in humans with the two proteins sharing 42% amino acid identity.

30 63 amino acids, respectively, and shared 78% amino acid identity.

31 ane proteins of unknown function sharing 61% amino acid identity.

32 d polytopic inner membrane proteins with 61% amino acid identity.

33 rogenase large subunits but at less than 35% amino acid identity.

34 r into two classes sharing approximately 30% amino acid identity.

35 and His) located in three of five blocks of amino acid identity.

36 allows an environment-dependent selection of amino acid identities.

37 ) were distantly related to known ARDs (mean amino acid identity 29.8%) and found little evidence sup

38 Bo/CV521-OH/02/US showed high nucleotide and amino acid identities (84 and 94%, respectively) with th

39 a robust measure of relatedness the average amino acid identity (AAI) of the shared genes.

40 erage nucleotide identity (ANI), and average amino acid identity (AAI), clearly differentiated B. ham

41 16 introns, and the extremely high degree of amino acid identity allows the evolution of its introns

42 sal of activase specificity, indicating that amino acid identity alone does not determine the specifi

43 ing from a codon insertion, and overall, the amino acid identity among paired microdomains ranged fro

44 ifferences correlate poorly with neighboring amino acid identities and instead indicate residual conf

45 Pairwise comparisons of amino acid identities and phylogenetic analyses of all d

46 a member of the B7 family that shares 10-18% amino acid identity and 23-33% similarity to other human

47 Mouse Liph shows 85% amino acid identity and 75% nucleotide identity to human

48 The mouse Bhmt2 gene shows 69% amino acid identity and 79% similarity to the mouse Bhmt

49 human and mouse protein sequences share 78% amino acid identity and 82% amino acid similarity.

50 9% similarity to the mouse Bhmt gene and 82% amino acid identity and 87% similarity to the human BHMT

51 between Gal1p and Gal3p ( approximately 70% amino acid identity and approximately 90% similarity) ha

52 The sequences share approximately 80% amino acid identity and are approximately 25% identical

53 Ankyrins contain significant amino acid identity and are co-expressed in many cell ty

54 The cognate proteins share only 25% amino acid identity and are highly expressed in petunia

55 and CMG2 VWA domains share approximately 60% amino acid identity and bind PA directly in a metal-depe

56 Mouse and human PAP7 share an 85% amino acid identity and contain a conserved acyl-CoA-bin

57 The CSN6A and CSN6B proteins share 87% amino acid identity and contain a MPR1p and PAD1p N-term

58 s as two isoforms, A and B, which have a 70% amino acid identity and different substrate and inhibito

59 and rGSTT2-2 (rat GSTTheta-2-2) share 54.3% amino acid identity and exhibit different substrate spec

60 ype 1 (HIV-1) proteases (PRs) share only 23% amino acid identity and exhibit distinct specificities y

61 oeologous gene (Bn-CLG1C), which shows 99.5% amino acid identity and is also constitutively and equal

62 activator Relish (GmmRel), which shows high amino acid identity and structural similarity to its Dro

63 olog of Dscam and showed that it shares high amino acid identity and structure with the mammalian hom

64 4 amino acids, respectively, which share 59% amino-acid identity and an atypical plant homeo-domain (

65 c subunits of IkappaB kinase (IKK) share 51% amino-acid identity and similar biochemical activities:

66 gments that produce inactivation show little amino-acid identity and tolerate appreciable mutational

67 red by PTAG1 and PTAG2 in both sequence (89% amino acid identity) and expression indicates that they

68 ighly conserved between human and mouse (98% amino acid identity) and is homologous to a nuclear regu

69 similar to snapdragon myrcene synthases (92% amino acid identity) and produces predominantly (E)-beta

70 > dS) but remain similar to one another (81% amino acid identity) and to the mammalian angiogenins.

71 the G(1) phase of the cell cycle, share 71% amino acid identity, and are expressed ubiquitously.

72 early equivalent variation in nucleotide and amino acid identity, and frequencies of synonymous and n

73 each fHbp variant group, there was 92%-100% amino acid identity, and the proteins expressed conserve

74 teins encoded by TUBG1 and TUBG2 share 97.3% amino acid identity, and the two genes are coexpressed i

75 ino-acid decarboxylases and shares extensive amino acid identity (approximately 65%) with plant L-tyr

76 potyviruses), sequence conservation is low (amino acid identity, approximately 16%), and a role for

77 Two related proteins (>60% amino acid identity) are encoded by genes on mouse chrom

78 Ras proteins share ~85% amino acid identity, are activated by and signal through

79 With the N-terminal amino acid identities as a threshold, the identification

80 genetic code allows nucleic acids to encode amino acid identity as well as noncoding information for

81 The amino acid identities, as well as their structures by su

82 t 73% of nonexposed positions and the native amino acid identities at 34% of positions in naturally o

83 ted of a 49.7-kDa homodimer that showed 100% amino acid identity at its N terminus to NADH peroxidase

84 in sequence revealed striking differences in amino acid identity at positions 24 and 25 compared to r

85 e 4 GSTs is in agreement with the low shared amino acid identity at the molecular surface.

86 d with slow cell growth, suggesting that the amino acid identity at this site may influence ribosomal

87 either absent or share a lower percentage of amino acid identity (average of 43%).

88 genes share a high degree of colinearity and amino acid identity (average of 65%) with genes of other

89 ation (PSSMSeq) outperform those that use an amino acid identity based representation (IDSeq) or a sm

90 f human BRI1, with the highest percentage of amino acid identity being concentrated on the C-terminal

91 genes in this Puerto Rican fireworm, finding amino acid identities between Japanese and Puerto Rican

92 Despite the high amino acid identity between ACSL3 and ACSL4, rosiglitazo

93 Despite the moderate level of amino acid identity between Arabidopsis and human NAP125

94 The degree of amino acid identity between B virus and HSV proteins ran

95 atai and Ilesha viruses revealed 95% deduced amino acid identity between Batai virus and Ngari virus.

96 eins encoded by these Fem1c genes share >99% amino acid identity between human and mouse, 79% amino a

97 nservation in mammals, as evidenced by 98.7% amino acid identity between mouse and human KLHL10.

98 o acid identity between human and mouse, 79% amino acid identity between mouse and zebrafish, and end

99 it has been described that despite the high amino acid identity between RAS family members, KRAS emp

100 ty is not a consequence of a higher level of amino acid identity between SARS-CoV and porcine CoV nuc

101 to 1 of 2 subfamilies (A or B), with 60%-75% amino acid identity between subfamilies and at least 83%

102 f DENV population genetics and revealed high amino acid identity between the E genes of vaccine strai

103 an open reading frame by 207 codons with 95% amino acid identity between the novel putative human and

104 The unusually low 78% amino acid identity between the orthologous human SLC26A

105 mbers are distinct, despite a high degree of amino acid identity between the proteins they encode.

106 rRNA gene sequence identity and 95% average amino acid identity between their orthologs.

107 of E. coli O128:B12 indicates a low level of amino acid identity between them; however, they share a

108 eins was not possible, despite the very high amino acid identity between these viruses.

109 esulted in the change of not only the tRNA's amino-acid identity but also the class of the amino-acyl

110 are structurally similar (approximately 32% amino acid identity) but differ in their substrate speci

111 TubZ-Ba and TubZ-Bt share only 21% amino acid identity, but they have remarkably similar bi

112 d 85 in the T. kodakaraensis sequence) whose amino acid identity changes according to the enzymes' tR

113 scheme based on the genome-aggregate average amino acid identity concept to determine the degree of n

114 don, it no longer encodes the fifth block of amino acid identity containing the predicted catalytic h

115 , showing 42.6%, 35.2%, and 44.6% of deduced amino acid identities corresponding to the P1, P2, and P

116 Despite MeCP2-e1 and MeCP2-e2 sharing, 96% amino acid identity, differences were identified.

117 herichia coli UvrD, with which it shares 39% amino acid identity, distributed throughout the protein.

118 lar in sequence to the Arabidopsis LCYe (77% amino acid identity), efficiently converted lycopene int

119 and snpn-1, despite relatively low levels of amino acid identity, encode Pallidin and Snapin BLOC-1 s

120 ar Typhimurium share high degrees of DNA and amino acid identity for 65% of the homologous genes shar

121 ylobacter isolates showed that the levels of amino acid identity for CfrA range from 89% to 98%.

122 of conservation (83.6, 69.4, 79.1, and 88.7% amino acid identity for MSA-2a(1), -2a(2), -2b, and -2c,

123 g to genotype II, and shares only 89 and 87% amino acid identity for the protective antigens F and HN

124 and 270 kDa, respectively), homologous (47% amino acid identity) glucosyltransferases that target sm

125 and 270 kDa, respectively), homologous (47% amino acid identity) glucosyltransferases that target sm

126 s from the same phylum, in which CYP51s (83% amino acid identity) have such profound differences in s

127 Excluding Moneuplotes crassus, amino acid identities in actin I range from 78 to 100%,

128 nt from all other bunyaviruses, showing <15% amino acid identity in the RdRp palm domain.

129 racheitis, as reflected by the high level of amino acid identity in their protein repertoires (averag

130 hat protein structure rather than individual amino acid identity in this region may be critical for M

131 logenetic analysis, genome organization, and amino acid identity indicate that SWPV is most closely r

132 ighest similarity to BHV-1 products (>or=95% amino acid identity) is found in proteins involved in vi

133 ed on VP1, VP6, VP7, and VP12 nucleotide and amino acid identities, KUNDV is proposed to be a new spe

134 peptidase 10 (DPP10) shares with DPP6 a high amino acid identity, lack of enzymatic activity, and exp

135 om Thermosipho africanus TCF52B has very low amino acid identities (less than 12%) to all known GH94

136 conserved in other tick species with >/= 60% amino acid identity levels.

137 despite the similarity of Rac2 to Rac1 (92% amino acid identity), macrophages derived from Rac2-/- m

138 ozymes have little or no selectivity for the amino acid identities near the tyrosine, but they are hi

139 Among caliciviruses, NB virus shows amino acid identities of 14.1 to 22.6% over the entire O

140 Comparison of MAP1-2s revealed amino acid identities of 75 to 100% (mean of 86%), compa

141 called adiC) gene product shared an overall amino acid identity of 22% with GadC.

142 A is 56% identical to MBD-1 with a predicted amino acid identity of 33%.

143 e highly related proteins sharing an overall amino acid identity of 72%.

144 in substrate specificity despite an overall amino acid identity of 85% between them.

145 ity with any sequenced IV; the low levels of amino acid identity of predicted proteins to IV homologu

146 ase family on the basis of variations in the amino acid identity of several other residues in the vic

147 ," in the riboswitch that corresponds to the amino acid identity of the downstream genes.

148 ng substrate specificities and low levels of amino acid identity of their catalytic domains.

149 prevented the conflict between anticodon and amino-acid identities of recruited tRNAs.

150 cross a panel of HIV-1 strains is due to the amino acid identity or glycosylation state at a small nu

151 1 amino acids, and they share 12.0% to 82.4% amino acid identities over their entire lengths.

152 zfAHR1 and zfAHR2 share 40% amino acid identity overall and 58% in the N-terminal ha

153 th mammalian BRCA2 proteins, having only 37% amino acid identity overall with human BRCA2.

154 The DBL1 domains averaged 80% amino acid identity (range, 72 to 89%), and the DBL5 dom

155 2 to 89%), and the DBL5 domains averaged 86% amino acid identity (range, 83 to 99%), similar to a bro

156 distinct subfamily of autotransporters with amino acid identities ranging from 35 to 55%, providing

157 7-89% 16S rRNA gene identity, 52-54% average amino acid identity), representing a new family within t

158 ine alpha3 receptor, which shares 45 and 43% amino acid identity respectively.

159 The rat and mouse orthologs show 80% and 83% amino acid identity, respectively, to the human GPR105 p

160 The new GHR1 shares 42% and 43% amino acid identity, respectively, with GHR2a and GHR2b,

161 Average nucleotide and amino acid identities revealed that the four Ca.

162 similar Cr-AGO2 and Cr-AGO 3 sequences (90% amino acid identity) revealed a glycine-arginine rich N-

163 reveal that a conserved twin-arginine GluRS amino acid identity signature cannot be incorporated int

164 risons indicated that SARS-CoV N protein has amino acid identity similar to that of infectious bronch

165 ical to one another (and/or greater than 85% amino acid identity), suggesting that the true number of

166 degree of capsid sequence conservation (96% amino acid identity) suggests that CAV15 and CAV18 shoul

167 Even with this low level of amino acid identity the human sequence could be efficien

168 Despite ~90% amino acid identity, the natural host of alpha3 is Esche

169 Despite sharing 54% amino acid identity, these polymerases display distinct

170 Although they have 84% amino acid identity, they displayed different expression

171 EHD1 and EHD3 have 86% amino acid identity; they homo- and heterodimerize and p

172 s of the genus Parvovirus, with >70% and 65% amino acid identities to nonstructural and capsid protei

173 nded on a C-terminal segment of A26 with 45% amino acid identity to A27.

174 paralogs, CTRP9 shows the highest degree of amino acid identity to adiponectin in its globular C1q d

175 R1B15.1 is a 316-amino acid protein with 91% amino acid identity to AKR1B10; AKR1B15.2 has a prolonge

176 ond Arabidopsis BCCP (AtBCCP2) cDNA with 42% amino acid identity to AtBCCP1 and 75% identity to a cla

177 y morphogenesis gene 2 (CMG2), which has 60% amino acid identity to ATR/TEM8 within the VWA/I domain,

178 e), a novel gene of the DCoH family with 78% amino acid identity to DCoH, was identified as a Mirk-bi

179 QRFV and JAV PB1 and HA shared 80% and 70% amino acid identity to each other, respectively; the LKC

180 It exhibits appreciable amino acid identity to FRAT1 (77%) which was initially i

181 that encode proteins with significant (>40%) amino acid identity to GTP cyclohydrolase II (GCH II), w

182 ive HasB paralog, designated HasB2, with 45% amino acid identity to HasB at a distant location in the

183 ovine coronavirus (DB2 strain) showing 98.2% amino acid identity to HECV-4408 in the S protein.

184 bidopsis, members of which display extensive amino acid identity to human BI-1.

185 With only 38% amino acid identity to human IFITM3, duck IFITM3 possess

186 72 and 774 aa, respectively, each having 65% amino acid identity to human SART1.

187 aLeuRS sequence shows a significant level of amino acid identity to LeuRS from other organisms.

188 rom a human myoblast cDNA library show 94.3% amino acid identity to mouse Sox6 throughout the gene, a

189 mNudT5 has 81% amino acid identity to NUDT5 with catalytic activities s

190 , expresses hemoglobin (TremaHb) sharing 93% amino acid identity to ParaHb, but its phylogeny predict

191 pus paraxial protocadherin (PAPC) and 42-49% amino acid identity to Pcdh 8 in human, mouse, and zebra

192 eles encoded variants of RagA with 63 to 71% amino acid identity to RagA1 and each other and variants

193 CIN-4 has a high amino acid identity to the catalytic domain of topoisome

194 CysLT(2), a 346-amino acid protein with 38% amino acid identity to the CysLT(1) receptor.

195 The secreted mature protein demonstrates 34% amino acid identity to the extracellular domain of the I

196 s encodes a polypeptide of 339 aa with 87.3% amino acid identity to the human CysLT(1) receptor.

197 ene coded for a 659-residue protein with 70% amino acid identity to the human SGLT1.

198 The E2 protein exhibits approximately 30% amino acid identity to the LdMNPV E1 protein as well as

199 ull-length mouse EP24.15 cDNA revealed 96.7% amino acid identity to the rat sequence, and conservatio

200 sequences of the two subunits had about 30% amino acid identity to the respective subunits of the fo

201 RovA has 77% amino acid identity to the Salmonella typhimurium transc

202 ession of the E. coli FabH (bearing only 35% amino acid identity to the Streptomyces enzyme).

203 GIR shares 31-34% amino acid identity to the tachykinin receptors (substan

204 encodes a predicted protease with 54 to 68% amino acid identity to torovirus (ToV) papain-like prote

205 PCNS has 65% amino acid identity to Xenopus paraxial protocadherin (P

206 contain one or more mutations that revert an amino-acid identity to a residue found in one or more cl

207 hree potential transmembrane domains and 78% amino-acid identity to a S. cerevisiae gene, designated

208 enome exhibits little overall homology (<46% amino acid identity) to known polyomaviruses, and, due t

209 des a protein with significant homology (39% amino acid identity) to Pcs of S. meliloti.

210 A homologue of pglX with 76% amino acid identity was identified in S. coelicolor, and

211 Since RhCMV and HCMV gL share 53% amino acid identity, we determined whether the two prote

212 Despite considerable amino acid identity, we found that human SNAP-23 bound t

213 cturally similar and share approximately 60% amino acid identity, we postulated that differences with

214 human L-asparaginase 1 (hASNase1) share 70% amino-acid identity, we decided to humanize gpASNase1 by

215 Although amino acid identities were low, the presence of a charac

216 d regions of Pol show an average of only 23% amino acid identity when compared to other retroviruses.

217 ns within each cluster have greater than 95% amino acid identity, whereas the conserved regions diffe

218 sequences were AAV2-like (approximately 98% amino acid identity), while the single spleen isolate wa

219 These HA genes shared high amino acid identities with genes of other H5N1 viruses i

220 Based on pairwise genome-wide and amino acid identities with reference smacovirus species,

221 shared 88 to 92% nucleotide and 94 to 99.5% amino acid identities with the NB BECV in the capsid gen

222 Derived protein sequences showed highest amino acid identities with those derived from the CiCHS1

223 The ACD shares 59% amino acid identity with a hypothetical protein from V.

224 The predicted SPIKE1 protein shares amino acid identity with a large family of adapter prote

225 HCT1 shares more than 75% amino acid identity with a number of well-characterized

226 NT ARREST9 [EDA9]) with a high percentage of amino acid identity with a previously identified PGDH.

227 of 27.1-31.6 kDa, share approximately 30-44% amino acid identity with beta1, and exhibit distinct but

228 tely 32,200) that exhibits approximately 58% amino acid identity with BglK.

229 TC 11168 Cj0444, shares approximately 34% of amino acid identity with CfrA.

230 e N-terminal third of the protein shares 65% amino acid identity with core histone H2A, while the rem

231 the subfamily partner CYP158A1, sharing 61% amino acid identity with CYP158A2, can also catalyze the

232 A encoded a 493-aa protein that has only 34% amino acid identity with CYP4C7, a terpenoid omega-hydro

233 Anopheles stephensi gene showed 72% inferred amino acid identity with Drosophila melanogaster Dox-A2

234 nd found to encode a protein that shares 67% amino acid identity with Drosophila synaptotagmin and 56

235 ins sharing approximately 99% nucleotide and amino acid identity with each other and with NIH-CQV, th

236 coded proteins, HisCl1 and HisCl2, share 60% amino acid identity with each other.

237 D4ST-1 has significant amino acid identity with HNK-1 sulfotransferase (21.4%),

238 It has 75 and 79% amino acid identity with human and rat VGLUT1, respectiv

239 RRV vCD200 shares 30% and 28% amino acid identity with human CD200 (huCD200) and HHV-8

240 esvirus 8 interleukin-6 (vIL-6) displays 25% amino acid identity with human IL-6 (hIL-6) and shares a

241 entity with Drosophila synaptotagmin and 56% amino acid identity with human synaptotagmin I.

242 ns that are similar in size and share 62-70% amino acid identity with human ZP1, ZP2, ZP3, and ZP4/ZP

243 It shares 63% to 65% amino acid identity with human, mouse and bovine RP2.

244 y 14 of infection, and was found to have 91% amino acid identity with intelectin (within our study te

245 s13 encodes a 157-aa protein that shares 82% amino acid identity with its 159-aa human counterpart.

246 givirus genus, although it shares only 35.3% amino acid identity with its closest relative, GB virus

247 e putative Brucella abortus Lon shares > 60% amino acid identity with its Escherichia coli counterpar

248 Murine CXCR1 shares 68 and 88% amino acid identity with its human and rat counterparts,

249 PIROGI shares only 30% amino acid identity with its human homolog.

250 essed 195-amino acid protein that shares 87% amino acid identity with its human orthologue and locali

251 man AP endonuclease (Ape1), which shares 94% amino acid identity with its murine homolog Apex.

252 l-length spearmint dehydrogenase shares >99% amino acid identity with its peppermint homolog and both

253 and its mouse homolog have approximately 35% amino acid identity with LPA4/GPR23.

254 2A gene, encoding macroH2A2 which shares 80% amino acid identity with macroH2A1.

255 ceptor termed MCH-2R, which shares about 38% amino acid identity with MCH-1R.

256 Ph5) predict isoforms that share 49% to 92% amino acid identity with members of glycoside hydrolase

257 The inhibitor has 46% amino acid identity with moubatin, a platelet aggregatio

258 had approximately 91% and approximately 97% amino acid identity with mouse protein.

259 MtPT5 shares 84% amino acid identity with MtPT1, MtPT2, and MtPT3 but sho

260 ng START proteins, sharing approximately 30% amino acid identity with one another, approximately 20%

261 ted B7 homolog 3 (B7-H3), that shares 20-27% amino acid identity with other B7 family members.

262 ribed by Sato et al. that shares significant amino acid identity with other bacterial response regula

263 acids (mass, 24 kDa) and exhibited up to 65% amino acid identity with other nematode GSTs.

264 Pellino3 shares 84 and 85% amino acid identity with Pellino1 and Pellino2, respecti

265 Lk73.5 and Sph-like 2 share 95.1 and 97.7% amino acid identity with putative sphingomyelinases Sph2

266 Mouse PLM shares 93, 83 and 80% amino acid identity with rat, dog, and human PLMs, respe

267 us with approximately 76% nucleotide and 90% amino acid identity with representative members of linea

268 ) motif at its N terminus and an overall 40% amino acid identity with RSV M2-1.

269 ns, with sequences sharing between 60 to 81% amino acid identity with SepZ of EPEC.

270 The protein shares 85% amino acid identity with TANK1 in the ankyrin repeat, st

271 SpyA, MW 24.9, has amino acid identity with the ADP-riboslytransferases (AD

272 The protein it encodes has 70% amino acid identity with the amino acid sequences of Arl

273 -coupled receptors, and Ostbeta exhibits 22% amino acid identity with the C-terminal TM and intracell

274 spectively; the LKCV PB1 fragment shared 83% amino acid identity with the corresponding region of QRF

275 1080-base pair open reading frame shows 48% amino acid identity with the cyclic AMP-dependent kinase

276 VCaB45 contains significant amino acid identity with the dehydrin family signature m

277 th a predicted protein sequence that has 28% amino acid identity with the E. coli Hsp70 co-chaperone

278 -3B, and -3C homologues have 37, 40, and 36% amino acid identity with the EBV genes, respectively.

279 han nuclear receptors that share significant amino acid identity with the estrogen receptors, but for

280 Cl- dependent transporter shares 53% and 74% amino acid identity with the human and fruit fly seroton

281 ugh the latter exhibit only 25-41% predicted amino acid identity with the mammalian proteins.

282 ix-helix DNA binding protein that shares 30% amino acid identity with the Mnt repressor of Salmonella

283 eodomain and the WOX domain, PFS2 shared 95% amino acid identity with the PRESSED FLOWER and WUSCHEL

284 Human SPCA2 shares 64% amino acid identity with the protein defective in Hailey

285 TRAM2 shares 53% amino acid identity with the protein TRAM, which is a co

286 Strain EuroPRRSV shared 90.1 to 100% amino acid identity with the prototype European strain,

287 rotein sequence from fish ASIC1 revealed 76% amino acid identity with the rat orthologue.

288 ontains an open reading frame exhibiting 38% amino acid identity with the Salmonella MgtC protein.

289 of the NADPH oxidase complex and shares 92% amino acid identity with the ubiquitously expressed Rac1

290 It shares 82% amino acid identity with the well-studied protein barnas

291 Despite 62% amino acid identity with THIK1, THIK2 is not active upon

292 c-specific Rho family GTPase Rac2 shares 92% amino acid identity with ubiquitously expressed Rac1.

293 XPLAC has 37% and XTES has 31% amino acid identity with XK protein and they are predict

294 mino acids and has approximately 30% overall amino-acid identity with other members of the UGT family

295 ypic family as 4-4-20 and shares substantial amino acid identities within the VL and VH domains.

296 the meprin alpha and beta subunits share 55% amino acid identity within the protease domain and are n

297 r to mouse Sema4D and human Sema4G, with 38% amino acid identity within the Sema domain.

298 revotella disiens (PdCas12a) shared over 95% amino-acid identity yet recognized distinct PAM profiles

299 These receptors share 98% amino acid identity, yet their functional properties dif

300 ns and chimpanzees share some 99% of DNA and amino acid identity, yet they exhibit important biomedic