ライフサイエンスコーパス: amino acid sequence identity

1 identity) and N was the most conserved (95% amino acid sequence identity).

2 in domain organization they display just 31% amino acid sequence identity.

3 deficiency viruses (HIV), tend to share high amino acid sequence identity.

4 impressive than the previously reported 59% amino acid sequence identity.

5 55% nucleotide identity and a 39% predicted amino acid sequence identity.

6 and 1036 amino acids, respectively, with 76% amino acid sequence identity.

7 % nucleotide sequence identity and 81 to 95% amino acid sequence identity.

8 51 genes, CYP51A and CYP51B, which share 59% amino acid sequence identity.

9 The human and mouse genes have 88% amino acid sequence identity.

10 he basolateral membrane, despite 67% overall amino acid sequence identity.

11 ved two-domain tertiary fold despite minimal amino acid sequence identity.

12 last Mini-RNase III-like enzymes sharing 75% amino acid sequence identity.

13 ntain two closely-related paralogs with >75% amino acid sequence identity.

14 been identified and share approximately 35% amino acid sequence identity.

15 o which AMO exhibits a significant degree of amino acid sequence identity.

16 ghly homologous, displaying greater than 95% amino acid sequence identity.

17 a 57% nucleotide identity and 41% predicted amino acid sequence identity.

18 ino acid sequence similarity and 80% deduced amino acid sequence identity.

19 milies," members of which share at least 45% amino acid sequence identity.

20 length; mCBF1 and human CBF (hCBF) share>80% amino acid sequence identity.

21 and mouse IL-12R beta 2 proteins show a 68% amino acid sequence identity.

22 cted cytosolic localization and at least 70% amino acid sequence identity.

23 , even though they share between 90% and 99% amino acid sequence identity.

24 ntain the DCCL-conserved motif but share low amino acid sequence identity.

25 C-terminal region sequences sharing only 58% amino acid sequence identity.

26 12 transmembrane domains (TMs) and share 80% amino acid sequence identity.

27 The encoded proteins share ~85% amino acid sequence identity.

28 d into two subfamilies based on function and amino acid sequence identity.

29 backbone fold, despite very limited overall amino acid sequence identity.

30 hat have common tertiary structures and much amino acid sequence identity.

31 B/NS1 proteins) have only approximately 20% amino acid sequence identity.

32 Human and mouse link proteins share 81-96% amino acid sequence identity.

33 rent enzyme classes that share less than 60% amino-acid sequence identity.

34 on of main-chain atoms 0.66 A) given the low amino acid sequence identity (22 %).

35 n of the DopR99B receptor shows almost equal amino acid sequence identity (40-48%) with vertebrate se

36 shares functional motifs and a high level of amino acid sequence identity (56-75%) with geranylgerany

37 mino acid sequence of human CPA5 has highest amino acid sequence identity (60%) to CPA1.

38 Both AJH1 and AJH2 share high amino acid sequence identity (62 and 63%, respectively)

39 , but typically share only approximately 50% amino acid sequence identity among different donors.

40 The overall amino acid sequence identity among the four nematode cel

41 The shared amino acid sequence identity among the seven TBG clones

42 e mutations occur in regions that share 100% amino-acid sequence identity among the 3 isoforms.

43 Despite the high amino acid sequence identities and structural similariti

44 d NBU2 integrases shared any similarity (28% amino acid sequence identity and 49% sequence similarity

45 ve protein of 469 amino acids and shares 23% amino acid sequence identity and 64% similarity with the

46 Polycystin-L has 50% amino acid sequence identity and 71% homology to polycys

47 otein that exists as a monomer even with 58% amino acid sequence identity and a domain structure very

48 though the TEM-1 and SME-1 enzymes share 33% amino acid sequence identity and a similar fold, they di

49 These proteins have 45% deduced amino acid sequence identity and are highly conserved at

50 TRPC4 and TRPC5 proteins share 65% amino acid sequence identity and form Ca(2+)-permeable n

51 inidase (alpha-NAGAL, EC 3.2.1.49) share 46% amino acid sequence identity and have similar folds.

52 closely resembles the LH1 of many species in amino acid sequence identity and in some spectral proper

53 oded by the gene family has both significant amino acid sequence identity and other physical and biol

54 ibodies which share over 90% variable-region amino acid sequence identity and recognize identical str

55 approximately 83% DNA and approximately 90% amino acid sequence identity and show only limited conse

56 The integrases share only 59% amino acid sequence identity and the attP sites have few

57 These enzymes share 68% amino acid sequence identity and their atomic structures

58 similar recognition sequence and significant amino acid sequence identity and their nicking variants

59 n U.S. viruses, P was the most variable (81% amino acid sequence identity) and N was the most conserv

60 f two other OMPs, OmpU of V. cholerae (50.8% amino acid sequence identity) and OmpL of Photobacterium

61 line-derived neurotrophic factor (GDNF, 40% amino acid sequence identity) and, like GDNF, can promot

62 ia: (1) amino acid composition identity, (2) amino acid sequence identity, and (3) specific immunorea

63 The LHbeta and CGbeta subunits share 85% amino acid sequence identity, and functionally LH and CG

64 lthough kinesin and myosin have virtually no amino-acid sequence++ identity, and exhibit distinct enz

65 cal to the TA1/E16 protein, based on partial amino acid sequence identity, antibody cross-reactivity,

66 , the GTases from viruses and yeast have low amino acid sequence identity ( approximately 25%) with G

67 SV coat proteins, which share little primary amino acid sequence identity, are functionally interchan

68 are highly divergent, with 77% and 87% mean amino acid sequence identities between East Asian and no

69 l-acceptor substrates and the high degree of amino acid sequence identity between Coq3p and UbiG, the

70 Despite the high degree of amino acid sequence identity between family members, ASC

71 The overall degree of amino acid sequence identity between GlpE and the active

72 tein is evolutionarily conserved, with 98.5% amino acid sequence identity between human and mouse.

73 The overall amino acid sequence identity between KSbcl-2 and other B

74 Overall amino acid sequence identity between METH-1 and METH-2 i

75 Functional complementation correlates with amino acid sequence identity between orthologs, but vari

76 share only 43 and 47%, respectively, overall amino acid sequence identity between serotypes.

77 proteins also display extreme divergence in amino acid sequence identity between STs (i.e., 59%-61%

78 nds to both A3(OB) and A6, despite only ~40% amino acid sequence identity between the OB-folds of A3

79 ryptamine 3A (5-HT3A) receptors, despite 84% amino acid sequence identity between the receptors.

80 Amino acid sequence identity between the signal peptides

81 is of human 15-lipoxygenase, despite the low amino acid sequence identity between the soybean and mam

82 Amino acid sequence identity between the zSSIIa and zSSI

83 The alpha- and beta-tubulins share 40% amino-acid sequence identity, both exist in several isot

84 esignated alpha, beta, and gamma) share >95% amino acid sequence identity but differ at their N termi

85 tween the four FHFs show between 58% and 71% amino acid sequence identity, but each FHF shows less th

86 The amino-acid sequence identity compared to E. coli and Syn

87 Despite their high amino acid sequence identities, each enzyme produced a d

88 ass I alleles, L(d) and L(q), share complete amino acid sequence identity except in the alpha2 domain

89 Extremely high nucleotide and deduced amino acid sequence identity exists between the componen

90 ional human PDK isoform, as evidenced by its amino acid sequence identity (>65%) with other mammalian

91 Among caliciviruses, PEC has the highest amino acid sequence identities in the putative RNA polym

92 The protein has 46% amino acid sequence identity in its amino-terminal regio

93 e two regulatory systems is indicated by 54% amino acid sequence identity in the aligned primary stru

94 ed by two genes, RPL3A and RPL3B, with 80.2% amino acid sequence identity in tobacco.

95 Nevertheless, amino acid sequence identity is low, ranging from 60.7 t

96 These differences were seen despite amino acid sequence identities of 92% (Vibrio) and 98% (

97 Do the amino acid sequence identities of residues that make con

98 Despite an overall amino acid sequence identity of 33% between bovine and T

99 ium mortiferum, and the two proteins exhibit amino acid sequence identity of 73%.

100 have also been identified, with a predicted amino acid sequence identity of 86% between the human an

101 S1 is a SLAMF6 homolog with an amino acid sequence identity of 97% to SLAMF6 in its lig

102 oding the appendage-associated protein, with amino acid sequence identity of as low as 34% among stra

103 The amino acid sequence identity of human CA XIV relative to

104 ence between nacE and nacK, with a predicted amino acid sequence identity of only 79% and most of the

105 Despite the 78% amino acid sequence identity of the MDR1 and MDR2 transp

106 The amino acid sequence identity of the P28 proteins was 20-

107 ages, and with expectations based on the 66% amino acid sequence identity of the two isoforms, struct

108 f Escherichia coli TolA, despite the limited amino acid sequence identity of the two proteins (20%).

109 two isozymes of porcine aromatase share 93% amino-acid sequence identity, our results indicate that

110 te motif (H/V)C(X)5R(S/T) but display little amino acid sequence identity outside of the active site.

111 The GATA-6 and -4 proteins share high-level amino acid sequence identity over a proline-rich region

112 sitive regulators, sharing approximately 42% amino acid sequence identity over the length of SoxS and

113 ve been characterized to date exhibit 40-60% amino acid sequence identity overall, with the most cons

114 Despite sharing approximately 90% amino acid sequence identity, PP1beta and PP1gamma1 have

115 A and human angiogenin, which share only 35% amino acid sequence identity, provides a unique perspect

116 Thus, despite the low level of amino acid sequence identity, Ps-HppE is a close mimic o

117 , as well as hRSV revealed overall predicted amino acid sequence identities ranging from 4 to 16.5%,

118 a Thermus species are highly homologous with amino acid sequence identities ranging from 85 to 98%.

119 CBS-1 shares significant nucleotide and amino acid sequence identities (residues 51 to 182) with

120 es shared 31 to 49% nucleotide and 40 to 70% amino acid sequence identities, respectively, with other

121 These results suggest that, despite 95% amino acid sequence identity, similar intracellular dist

122 The predicted amino acid sequence identities/similarities are: for tek

123 homolog, termed dfmr1, has a high degree of amino acid sequence identity/similarity with the defined

124 osinophil-derived neurotoxin (EDN), with 47% amino acid sequence identity; slight cross-reactivity be

125 acterial terpenoid cyclases, despite minimal amino acid sequence identity, suggests divergence from a

126 and Pap2 are more similar to each other (84% amino acid sequence identity) than to Pap3 (46% and 44%,

127 ate-anion transporter (encoded by Sat-1; 29% amino acid sequence identity), the human diastrophic dys

128 V-1 topoisomerase II share approximately 67% amino acid sequence identity, the two enzymes displayed

129 Although these proteins share little amino acid sequence identity, their crystal structures c

130 Although these proteins lack amino acid sequence identity, their functional solution

131 Despite insignificant overall amino acid sequence identity, these enzymes share a stri

132 Even though both proteins share about 90% amino acid sequence identity, they exhibit different ope

133 otentially encodes a protein that shares 62% amino acid sequence identity through the catalytic domai

134 2], a gene encoding a protein with extensive amino acid sequence identity to a mammalian MAP kinase o

135 YmoA has a high amino acid sequence identity to and a similar overall fo

136 In addition, five genes were found with ~50% amino acid sequence identity to Arabidopsis tryptophan a

137 atode cellulases was from 71 to 83%, and the amino acid sequence identity to bacterial Family 5 cellu

138 at shares 99.7% nucleotide sequence and 100% amino acid sequence identity to bovine lens IRK1 (Kir2.1

139 size approximately 123-kDa proteins with 81% amino acid sequence identity to each other and 44-75% se

140 UBL proteins share little amino acid sequence identity to each other, yet they sha

141 redicted to encode a gene product with 31.5% amino acid sequence identity to Escherichia coli taurine

142 sophila ortholog was characterized, with 70% amino acid sequence identity to human HERC2 over the car

143 encodes a complete ORF with no less than 86% amino acid sequence identity to human RNase k6 with the

144 Both of them display approximately 50% amino acid sequence identity to human SULT1A1, rat SULT1

145 A protein, phogrin, that has 80% amino acid sequence identity to IA-2 in the cytoplasmic

146 in of 578 amino acid residues with up to 31% amino acid sequence identity to known cyclins in the C-t

147 Although M.BtsCI shows 62% amino acid sequence identity to M.FokI, BtsCI and FokI r

148 e a putative 74-kDa protein with significant amino acid sequence identity to methylmalonyl-CoA mutase

149 DBX has significant amino acid sequence identity to mouse PL10, an ATP-depen

150 ncodes a protein of 201 amino acids with 96% amino acid sequence identity to mouse Twist, and 100% se

151 Their amino acid sequence identity to other known cytosolic su

152 s cloned and sequenced to date reveal little amino acid sequence identity to other reported proteins.

153 Since the predicted MrpH has 30% amino acid sequence identity to PapG, the Galalpha(1-4)G

154 ains 16 cysteine residues and has 30% to 32% amino acid sequence identity to pathogenesis-related osm

155 oding capsid protein VP26) and shows partial amino acid sequence identity to positional homologs in h

156 plication functions of pADP-1 had 80 to 100% amino acid sequence identity to pR751, an IncPbeta plasm

157 edicted to encode an 83-kDa protein with 97% amino acid sequence identity to rat and human CLC5.

158 .5) protein of 17.3 kDa and had close to 40% amino acid sequence identity to SmpA (small protein A) o

159 y(A) polymerase I, revealing an ORF with 36% amino acid sequence identity to that protein.

160 These regions exhibit substantial amino acid sequence identity to the A regions of other s

161 eacetylase/N-sulfotransferase, which has 95% amino acid sequence identity to the above enzyme postula

162 730.1 and shown to encode a protein with 90% amino acid sequence identity to the CCRs of Streptomyces

163 encode proteins exhibiting greater than 30% amino acid sequence identity to the confirmed oxaloaceta

164 e encoding a putative ArcA homolog with ~81% amino acid sequence identity to the E. coli ArcA protein

165 ,101-bp open reading frame that exhibits 61% amino acid sequence identity to the Escherichia coli D-x

166 kb mRNA transcript and shares 99, 96 and 97% amino acid sequence identity to the human, mouse and cow

167 of the purified isolated protein showing 77% amino acid sequence identity to the kinase domain of Apl

168 ng transporter from K. lactis but showed 53% amino acid sequence identity to the mammalian UDP-galact

169 367 amino acid residues, sharing 96 and 87% amino acid sequence identity to the murine and human CXC

170 f the puc2A-encoded polypeptide there is 58% amino acid sequence identity to the original puc1A-encod

171 The amino acid sequence identity to the phosphotriesterase (

172 , POR2, encoding a protein (YVDAC2) with 49% amino acid sequence identity to the previously identifie

173 transmembrane domains and approximately 25% amino acid sequence identity to the Streptococcus pyogen

174 DNMT3A and DNMT3B proteins with 98% and 94% amino acid sequence identity to their murine homologues.

175 Shp shows minimal amino acid sequence identity to these heme-binding prote

176 betaalphabetabetaalpha topology, despite low amino acid sequence identity to thioredoxin.

177 gag, pol, and env in PERV-MSL have over 99% amino acid sequence identity to those of Tsukuba-1 retro

178 ng frame encoding a protein with significant amino acid sequence identity to TipA, a helix-turn-helix

179 Complete copies of transposases with 99% amino acid sequence identity to TnpA from IS1071 and Tnp

180 AtzD showed 58% amino acid sequence identity to TrzD, a cyanuric acid am

181 The encoded protein (UBC1) shows very high amino acid sequence identity to ubiquitin-conjugating en

182 peptide (AbcC) has significant homology (56% amino acid sequence identity) to an E. coli ATP-binding

183 CaT1 shows homology (75% amino acid sequence identity) to the apical calcium chan

184 Despite 91% amino acid sequence identity, TraI36 domains from plasmi

185 arlier studies: two GAR transformylases (41% amino acid sequence identity), two very distantly relate

186 Based on the deduced amino acid sequence identity we designated GAPC1 and GAP

187 of a divergent strain (WSMV-El Batan 3; 86% amino acid sequence identity) were efficiently transmitt

188 s of the C-terminal domain III sequence (46% amino acid sequence identity) were well tolerated, with

189 mass of 51,789 Da, which exhibits 29 and 37% amino acid sequence identities with CDP-diacylglycerol s

190 ins, MC51L, MC53L, and MC54L, have 20 to 35% amino acid sequence identities with human interleukin-18

191 fied an Mtb protein (PPE15) that showed weak amino acid sequence identities with mammalian perilipin-

192 Though sharing several amino acid sequence identities with other hAT elements,

193 tein-Barr virus (EBV) BBLF1 shares 13 to 15% amino acid sequence identities with the herpes simplex v

194 mino acids in the N-terminus, and shares 95% amino acid sequence identity with AmNES/LIS-1, with only

195 cause of its substrate specificity and 28.5% amino acid sequence identity with an Aspergillus fumigat

196 This protein showed high amino acid sequence identity with basic and acidic PR1 p

197 The 39-kDa ARH3 shares amino acid sequence identity with both ARH1 and the cata

198 CML24, also known as TCH2, shares over 40% amino acid sequence identity with calmodulin, has four E

199 It shares 57% amino acid sequence identity with Cdc42, but possesses a

200 for transporter SQV-7, which shares a lower amino acid sequence identity with CO3H5.2 and SRF-3.

201 The PPV capsid protein has 57 % and 49 % amino acid sequence identity with CPV and MVM, respectiv

202 Nevertheless, the maximum pairwise amino acid sequence identity with currently recognized f

203 its 60% nucleotide sequence identity and 53% amino acid sequence identity with cyclin G1, and like cy

204 elated molecule called DC-SIGNR exhibits 77% amino acid sequence identity with DC-SIGN.

205 ce analysis reveals that LS-DNase shares 46% amino acid sequence identity with DNase I.

206 The Spl proteins share 44 to 95% amino acid sequence identity with each other and 33 to 3

207 ber of the ERK family, ERK8, that shares 69% amino acid sequence identity with ERK7.

208 ncoding a protein (PhNikR) that shares 33.8% amino acid sequence identity with Escherichia coli nicke

209 de sequence identity and 52 to 78% predicted amino acid sequence identity with European subgroup A or

210 tromere protein A (CENP-A), shares about 50% amino acid sequence identity with H3.

211 onal homologues that share approximately 48% amino acid sequence identity with hbpA.

212 HCT2 shares only 34% amino acid sequence identity with HCT1 and has limited s

213 en-transmembrane-spanning GPCR sharing 40.8% amino acid sequence identity with HHV-8 ORF74 and 24.1%

214 The zPTH2R shared 63 and 60% amino acid sequence identity with human and rat PTH2Rs,

215 Feline CXCR4 displayed 94.9% amino acid sequence identity with human CXCR4 and was fo

216 e in Arabidopsis encodes an enolase with 72% amino acid sequence identity with human ENO1.

217 Pi. marina shared the highest percentage amino acid sequence identity with I. pallida but showed

218 type 2 (HSV-2) ICP47 (ICP47-2) has only 42% amino acid sequence identity with ICP47-1.

219 Although mMCP-9 exhibits a >50% overall amino acid sequence identity with its homologous chymase

220 full-length rat SLPI cDNA shares 81% and 63% amino acid sequence identity with its mouse and human ho

221 (COR) polypeptides, which have little or no amino acid sequence identity with known proteins, are sy

222 a new factor, termed LBP-9, that shares 83% amino acid sequence identity with LBP-1b.

223 This enzyme shares 50% amino acid sequence identity with Leishmania major PTR1

224 educed M(r) of 17,690 containing significant amino acid sequence identity with mammalian and prokaryo

225 encoding LP(A1) homologs (approximately 90% amino acid sequence identity with mammalian LP(A1)).

226 s cloned and sequenced and found to have 82% amino acid sequence identity with mammalian PrBP/delta.

227 olated from loblolly pine that showed 79-82% amino acid sequence identity with many angiosperm CCoAOM

228 lated receptor, despite sharing considerable amino acid sequence identity with melatonin receptors, d

229 s ten genes coding for proteins sharing high amino acid sequence identity with members of the Ros/Muc

230 ed peptide were identified, and they had 75% amino acid sequence identity with mouse epiregulin, an e

231 2 from Medicago truncatula, which shares 65% amino acid sequence identity with MsDef1, lacks antifung

232 predicted by molecular modeling based on 40% amino acid sequence identity with MTCP-1.

233 pen reading frame MMP1527 product shares 30% amino acid sequence identity with MTH52.

234 Na(V)PZ and Na(V)SP share approximately 40% amino acid sequence identity with NaChBac.

235 CE-1), a metalloprotease which displays high amino acid sequence identity with neutral endopeptidase

236 GFLOMT2 displayed the highest amino acid sequence identity with norlaudanosoline 6-OMT

237 of 118, 620 Da that shows approximately 40% amino acid sequence identity with occ and contains nine

238 ed outer membrane protease that exhibits 71% amino acid sequence identity with OmpT.

239 YST1 and YST2, encode proteins with over 95% amino acid sequence identity with one another and over 6

240 Despite considerable amino acid sequence identity with other human class alph

241 It shares less than 20% amino acid sequence identity with other lipases for whic

242 e domain protein of 385 amino acids with 33% amino acid sequence identity with PAR1, PAR2, and PAR3.

243 O2 shares 75.6% nucleotide and 89.5% deduced amino acid sequence identity with pENO1 and is encoded b

244 three Bla g 1 cDNA clones, which showed 70% amino acid sequence identity with Per a 1.

245 use P. berghei ENT1 (PbENT1) shares only 60% amino acid sequence identity with PfENT1, we sought to c

246 PLDgamma shares a 66% amino acid sequence identity with PLDbeta, but only a 41

247 tease found in prostate tissues that has 78% amino acid sequence identity with prostate-specific anti

248 ein of 576 amino acids showed 81, 82 and 93% amino acid sequence identity with rabbit, human and rat

249 BbdA shows low amino acid sequence identity with reported amidases and

250 sequence identity with HHV-8 ORF74 and 24.1% amino acid sequence identity with rhesus macaque CXCR2.

251 he SEC animal variants have greater than 98% amino acid sequence identity with SEC1, a human-associat

252 On the basis of its approximately 43% amino acid sequence identity with SoxS, MarA and Rob, Te

253 F5H shows 34% amino acid sequence identity with the avocado ripening-i

254 The human RDH10 shares 100% and 98.6% amino acid sequence identity with the bovine and mouse p

255 (Caa) is a 42.7 kDa protein, which shows 60% amino acid sequence identity with the Clostridium perfri

256 er putative transporter has a high degree of amino acid sequence identity with the CMP-sialic acid tr

257 and shown to share a high level of predicted amino acid sequence identity with the corresponding dice

258 lobase mRNA, like mastocytoma cells, has 70% amino acid sequence identity with the corresponding enzy

259 spanning protein of 326 aa that had only 22% amino acid sequence identity with the corresponding tran

260 Murine ClpX shares 38% amino acid sequence identity with the E. coli homolog an

261 nine decarboxylase (cvADC), shares about 40% amino acid sequence identity with the eukaryotic ornithi

262 GPR38 and GPR39 share significant amino acid sequence identity with the GHS-R and NT-Rs 1

263 The feline cDNA shares approximately 93% amino acid sequence identity with the human thiamine tra

264 al coiled coil formation, and exhibits a 28% amino acid sequence identity with the intermediate filam

265 These transporters share 50-65% amino acid sequence identity with the kidney betaine tra

266 CspE has 69% amino acid sequence identity with the major cold shock p

267 yeast VDAC-like gene that retains about 20% amino acid sequence identity with the mouse VDAC genes a

268 f the mouse GATA-5 protein shares high level amino acid sequence identity with the murine GATA-4 and

269 nd the holotoxin was found to share only 87% amino acid sequence identity with the nearest Stx1 subty

270 function of the protein sharing the highest amino acid sequence identity with the OAH (An07g08390, S

271 er of this toxin family, sharing only 30-40% amino acid sequence identity with the others.

272 nd the encoded polypeptide showed 78 to 100% amino acid sequence identity with the partial sequence o

273 DNA encoding p150Glued from rat revealed 31% amino acid sequence identity with the product of the Dro

274 y DNA hybridization techniques, showed 98.7% amino acid sequence identity with the rabbit protein.

275 Ly49s and in particular shares virtually no amino acid sequence identity with the residues that have

276 rTP shares extensive amino acid sequence identity with the two proteins that

277 hat was microsequenced, and shows 42 and 53% amino acid sequence identity with the yeast and human RP

278 interestingly, they share approximately 31% amino acid sequence identity with those of glycogen-bran

279 t is a 538-amino acid protein and shares 65% amino acid sequence identity with TREK-1.

280 opology as, and shares the highest degree of amino acid sequence identity with two human proteins, ad

281 AtfA demonstrates significant amino acid sequence identity with type 1 major fimbrial

282 a novel gene that encodes a protein with 30% amino acid sequence identity with uteroglobin, the found

283 -amino-acid (62-kDa) protein that showed 35% amino acid sequence identity with vaccinia virus ATP-dep

284 e gene encodes a 17-kDa protein that has 56% amino acid sequence identity with yeast ubiquitin-conjug

285 a similar phospholipase motif as, but little amino acid sequence identity with, F13L, induced post-Go

286 uppressor p53-related p73 shares significant amino-acid sequence identity with p53.

287 rb2 consist of 217 amino acids and share 59% amino acid sequence identity, with highest homology in t

288 0s are classified according to the degree of amino acid sequence identity, with P450s of the same fam

289 i, and the deduced proteins shared 81 to 91% amino acid sequence identity within the ligand-binding d

290 ne products of which share approximately 80% amino acid sequence identity within their N termini and

291 zymes in the human liver, share >85% primary amino acid sequence identity yet exhibit different regio

292 ldo-keto reductase superfamily and share 67% amino acid sequence identity yet show positional and ste

293 RhoA and RhoB share 86% amino acid sequence identity, yet RhoA promotes whereas