ライフサイエンスコーパス: amino acid motif

1 rminal region termed REKLES (for a conserved amino acid motif).

2 eptides containing a SRRxFLK 'twin-arginine' amino acid motif.

3 80, bound to HLA-C allotypes carrying either amino acid motif.

4 gion of the protein has a novel repeating 90-amino acid motif.

5 plasmic proteins are glycosylated at a three amino acid motif.

6 s and glycosylate proteins at the same three amino acid motif.

7 oximately 100 amino acids) and conserved WXG amino acid motif.

8 sence of CDR3 fitting to an AGA(G(n))GG-like amino acid motif.

9 omain mapped the interaction to a minimal 12-amino-acid motif.

10 rchitecture of its coding sequence and novel amino acid motifs.

11 These domains are characterised by repeating amino acid motifs.

12 es bearing conserved SRRxFLK 'twin-arginine' amino acid motifs.

13 les, correlating in some cases with specific amino acid motifs.

14 ell nuclear antigen (PCNA) via a conserved 8-amino-acid motif [1].

15 cerevisiae-- E. coli HisRS possessing the 11 amino acid motif 2 loop of the yeast enzyme.

16 3F3A and a commercial anti-Gp78 mAb to an 8-amino acid motif (533-541) in mouse Gp78 isoform 2 that

17 letion/point mutants elucidated a specific 4-amino acid motif (535IVVY538) essential for osteoclastog

18 ed beta-turn ((58)GVWGG(62)) followed by two amino acid motifs ((72)KRRN(75) and (78)TKAR(81)) that a

19 al CAAX (C=cysteine, A=aliphatic, X=terminal amino acid) motif, a substrate for posttranslational mod

20 breast carcinoma cells is determined by a 12-amino-acid motif (amino acids 313 to 325) within the PKC

21 terized by a series of 10 repeats of a seven amino acid motif and an unusually high number of histidi

22 vage at Site 1 does not depend on a specific amino acid motif and differs from cleavage at Site 2 by

23 Trefoil factor (TFF) peptides, with a 40-amino acid motif and including six conserved cysteine re

24 The 12-amino acid motif and its adjacent regions contain highly

25 specifically to methylated DNA via a related amino acid motif and that can repress transcription.

26 ngth improved rapidly with the origin of GGX amino acid motifs and increased repetitiveness.

27 BV8S2 chains, with remarkably conserved CDR3 amino acid motifs and lengths in both chains.

28 The amino acid motifs and phylogenetic tree were predicted a

29 d highly conserved functional nucleotide and amino acid motifs and positions across all (sub)genotype

30 n machinery, we defined specific subregions, amino acid motifs and protein binding partners involved

31 Y113 and Y128) fall within an identical five amino-acid motif and are shown to be phosphorylated upon

32 ng AT hooks bind A/T-rich DNA through a nine-amino-acid motif and are thought to co-regulate transcri

33 mmunodeficiency virus SIVmac(239) p6 to a 10-amino-acid motif and introduced this sequence into an in

34 es based on the Arg-Gly-Asp (RGD) or related amino acid motifs, and RGD-based peptidomimetics.

35 ange of family members, related by conserved amino-acid motifs, and act as molecular binary switches

36 This activity is (a) mediated by the IGD amino acid motif; and (b) not expressed by (i.e., crypti

37 Proteins consisting of repeating amino acid motifs are abundant in all kingdoms of life,

38 , and LPEAT, we believe that these conserved amino acid motifs are diagnostic for the acyltransferase

39 Conserved amino acid motifs are found in numerous expressed genes.

40 -standing hypothesis that four conserved GXQ amino acid motifs are important in SIT function.

41 ytically activated by cleavage following the amino acid motif -Arg-Ser-Lys-Arg-.

42 least one of which, furin, cleaves after the amino acid motif -Arg-X-Arg/Lys-Arg-.

43 linked sites are associated with nonstandard amino acid motifs as a result of glycosylation by virus-

44 nserved cytoplasmic regions contain a common amino acid motif, Asn-Pro-Thr-Tyr, which has previously

45 hird, the S1 subunit possesses a distinctive amino acid motif at its carboxy terminus, including a te

46 esized that Lyn PTK associates with the YEEA amino acid motif at LMP2A tyrosine 112 (Y112).

47 nal FAD synthetases, yet shorter and lacking amino acid motifs at the C terminus, were found by bioin

48 these H5N1 viruses possessed multiple basic amino acid motifs at the cleavage site, were HP for expe

49 We identified an approximately 30-amino-acid motif at the N terminus of p220 that has the

50 Ankyrin repeats are an amino-acid motif believed to function in protein recogni

51 The shared amino acid motif between HC3 and HC4 is composed of Asp(

52 e N-terminus of Dsh, we identify a short (21 amino acid) motif between the PDZ and DEP domains that i

53 mutagenesis demonstrated that a small basic amino acid motif (BIIa) in this region is essential for

54 o function by binding integrins through a 13 amino acid motif called the disintegrin loop.

55 interact with PCNA through a conserved eight-amino acid motif called the PIP-box.

56 ene proteins that share an approximately 250-amino-acid motif called a Dbl homology domain.

57 contain one to three modules of a common 70-amino-acid motif called the BIR domain.

58 PB1-F2-derived C-terminal peptide with this amino acid motif caused significantly greater weight los

59 ine, A is aliphatic amino acid, and X is any amino acid) motif (CCFV), suggesting that Wrch-1 may be

60 ither wild-type gB, mutant gB having the RGD amino acid motif changed to RAA, or K8.1 efficiently res

61 ion requires box B, a short highly conserved amino acid motif characteristic of BTG2/TOB family prote

62 g seven hydrophobic helical regions and a 17 amino acid motif characteristic of the R7G family of G-p

63 estriction-modification enzyme LlaGI reveals amino acid motifs characteristic of the Escherichia coli

64 The presence of amino acid motifs characteristic of the Rossmann dinucle

65 otein contains 50 contiguous Gly-X-X triplet amino acid motifs characteristic of the structure of hum

66 obic amino acid, Y is tyrosine, and X is any amino acid) motif characteristic of several proteasome a

67 erall sequence identity, but do contain a 12-amino acid motif common to all enzymes that activate the

68 ealed that the final beta-strand contains an amino acid motif common to other beta-barrel outer membr

69 target sequences coding for highly conserved amino acid motifs covering a region of approximately 800

70 different from that of animal beta subunits, amino acid motifs critical for this catalytic activity a

71 threonine residues within the specific three-amino acid motif D(S/T)(A/I/L/M/T/V).

72 of 29,038, and contains four copies of a 10-amino acid motif defining potential DNA-binding sites.

73 d using the BLAST2 algorithm and methods for amino acid motif detection.

74 An essential amino acid motif (DGXD) containing aspartate residues is

75 GF repeat/DHR domain, is an approximately 90-amino acid motif discovered in a recently identified fam

76 regulation, is the presence of a 130- to 140-amino acid motif dubbed the SET or Tromo domain.

77 Many ERK1/2-interacting proteins contain amino acid motifs, e.g., DEF or D-motifs, which regulate

78 nuclear localization sequences (NLSs), short amino acids motifs enriched in Lys and Arg residues.

79 HAMP domains, approximately 55 amino acid motifs first identified in histidine kinases,

80 Peptide library analyses defined a preferred amino acid motif for ATM that permits clear distinctions

81 ge, despite the presence of a suitable -3,-1 amino acid motif for signal peptidase recognition.

82 their binding sites are defined by conserved amino acid motifs, forming the structural basis for unde

83 enerate oligonucleotide based on a conserved amino acid motif found in all class A high-molecular-mas

84 domain of colicin E9 (the E9 DNase) is a 32 amino acid motif found in the H-N-H group of homing endo

85 ACBF shared sequence similarity to conserved amino acid motifs found in RNA-binding proteins.

86 In addition, several of the peptides contain amino acid motifs found in the G-H loop of the ephrin-B

87 domain, but rather is an uncharacterized 90 amino acid motif, found in both FCHo and SGIP proteins,

88 These lin-1 mutations all affect a four-amino-acid motif, FQFP, that is conserved in vertebrate

89 dicted size but are unified by the conserved amino acid motifs GGAI and FXXN repeated in the N-termin

90 n the RyRs has a predicted pore helix and an amino acid motif (GGGIG) similar to the selectivity filt

91 Thus, we show that one of the most common amino-acid motifs has spring properties that could be im

92 two related proteins that contain a repeated amino acid motif homologous to the anti-angiogenic type

93 M.CviPII possesses eight conserved amino acid motifs (I to VIII) typical of C5 MTases, but,

94 An N-terminal domain contains an amino acid motif identical with that forming the catalyt

95 identified a role for a conserved polybasic amino acid motif in an N-terminal domain previously impl

96 Asn-X-X-X-X-Gly-Tyr motif of loop C and a 14 amino acid motif in apoplastic loop E, Thr-Gly-Ile/Thr-A

97 ted the presence of a highly conserved novel amino acid motif in avirulence proteins from three diffe

98 mmunication, we report that the conserved 11-amino acid motif in dematin52 and protein 4.2 contains a

99 ipA which bind to a conserved, C-terminal 17 amino acid motif in FtsZ and to the membrane.

100 planation for the presence of this conserved amino acid motif in hundreds of functionally diverse mem

101 We recently identified an N-terminal di-amino acid motif in NS1 that modulates protein targeting

102 Mutational analysis of a cyclin F-specific amino acid motif in the C-terminal region of Vif indicat

103 that hsc70 binds directly to a specific five-amino acid motif in the cargo protein for its autophagic

104 In addition, we found that a QRD amino acid motif in the CD151 EC2 domain, which had been

105 he use of the BV17 family and the I/sRS(A)/S amino acid motif in the CDR3 region.

106 heir intron targets and that CRS2 binds a 22 amino acid motif in the COOH-terminal region of CAF2 tha

107 A three-amino acid motif in the core was also found to be critic

108 Here we show that a crucial Tyr-Ile-Asn-Met amino acid motif in the cytoplasmic tail of DAP10 couple

109 These isolates had a dibasic amino acid motif in the fusion protein cleavage site seq

110 ever, the biological significance of the FYF amino acid motif in the ITK-PH domain is unknown.

111 A ten-amino acid motif in the layilin cytoplasmic domain is su

112 Here, we identify a highly conserved 9 amino acid motif in the ligand binding domains (E domain

113 nding activity was finally localized to a 12-amino acid motif in the N-terminal CbpA by peptide mappi

114 2 domain combined with an exchange of a four amino acid motif in the R3 domain, could swap the pathwa

115 ell as in vitro binding assays revealed a 21-amino acid motif in the regulatory domain of SOS2 that i

116 We have identified a highly conserved 12-amino acid motif in the transcription factor Sall1 that

117 We also deleted a nine-amino acid motif in the Us9 protein of F strain (Us9-30)

118 re, we report the identification of a unique amino acid motif in the vesicular GABA transporter (VGAT

119 We leveraged the conserved amino acid motifs in Cys(2)His(2) zinc fingers to predic

120 rotein maturation and cleave at paired basic amino acid motifs in numerous cellular and viral glycopr

121 Alanine mutations to either of two dibasic amino acid motifs in the G2 cytoplasmic domain can also

122 Functional domains and amino acid motifs in the viral proteins that are conserv

123 some of which can be grouped based on common amino acid motifs in their E6-binding domains.

124 ll as intact Pro-Pro-AA-Tyr (where AA is any amino acid) motifs in Lats kinases.

125 ceptor-interacting LXXLL (L, leucine; X, any amino acid) motifs in PBP in a ligand-dependent manner.

126 ctors, the CAAX (where A indicates alipathic amino acid) motifs in the gamma1, gamma2, and gamma11 su

127 A distinct amino-acid motif in the viral polymerases, PB1/PA, suppr

128 rgo through the recognition of short, linear amino-acid motifs in their cytoplasmic portions by vesic

129 These data indicate that an amino acid motif including Y29, Y30, Y36, and Y196 is im

130 L-domains consist of core consensus amino acid motifs including PPxY, P(T/S)AP, and YPx(n)L/

131 The NS polyprotein revealed all typical CV amino acid motifs, including GXXGXGKT (NTPase), EYXEX (V

132 and confirmed the presence of four conserved amino acid motifs, including motif I, KXDG with lysine 1

133 sessing a single copy of the C1 domain, a 50-amino acid motif initially identified in protein kinase

134 In addition, this amino acid motif is also present in the Drosophila genom

135 The entire 70- amino acid motif is conserved in novel higher eukaryotic

136 The 22-amino acid motif is predicted to form an amphipathic hel

137 Interestingly, this 12-amino acid motif is sufficient to allow a Drosophila GSK

138 residue and that the Ser-X-X-X-Ser (X is any amino acid) motif is obligatory for beta-catenin phospho

139 P and that this interaction requires a basic amino acid motif (KKPAKK) within the cytosolic region of

140 terminal 142 amino acids, which contain a 53 amino acid motif known as the CBS domain.

141 ORT), and by examining queried sequences for amino acid motifs known to serve critical roles in endoc

142 Ran binding was mediated by a three-amino acid motif (Leu(13)/Val(14)/Asn(25)) located withi

143 2) To what extent are multi-amino acid motifs likely to represent genuine cooperativ

144 t amino acid residues, including a conserved amino acid motif located downstream of each of the NFATc

145 cture-function studies, we found that a YLGA amino-acid motif located near the extracellular N termin

146 It recognizes a C-terminal penta-amino acid motif, LPXTG, and cleaves the amide bond betw

147 ith TFIIB support the notion that this basic amino acid motif may influence the overall structure and

148 Sequence analyses indicate that the euAP1 amino acid motifs may have arisen via a translational fr

149 The POZ (or BTB) domain, a 120-amino-acid motif, mediates homomeric and, in some protei

150 itor of Ran1/Pat1 kinase and contains a nine-amino-acid motif, Mei3-RKDIII, that resembles two region

151 Furthermore, we have identified a 14-amino acid motif near the AP-2-binding domain of Eps15 t

152 the export of E. coli SecM is blocked, a 17 amino acid motif near the C terminus of the protein indu

153 stop codons on the mRNA via their conserved amino acid motifs (NIKS in eRF1 and SPF in RF2) and by t

154 ely charged aspartate residues within the 11 amino acid motif of FL trkB were mutated to examine the

155 o-valine change in the highly conserved YMDD amino acid motif of HIV-1 RT (M184V), which has been sho

156 nding sequence in PDZ-RhoGEF with a critical amino acid motif of IIxxFE.

157 lize the interaction to the C-terminal -TTPV amino acid motif of stargazin and the PDZ1, PDZ3, and PD

158 This identified a 55-amino acid motif of the potato small subunit that is cri

159 ns and cotransfected cells, through specific amino acid motifs of both proteins.

160 octadecadienoic acid recognizes the specific amino acid motifs of His75, Ala76, and Lys77 in bovine h

161 The unique conserved amino acid motifs of MIG proteins are proposed to distin

162 Amino acid motifs of the CDR3 region from Vbeta6+ cells

163 risingly, Piv contains none of the conserved amino acid motifs of the lambda Int or Hin/Res families

164 cooperative interactions arise from the YPWM amino-acid motif of Ultrabithorax-located amino-terminal

165 Specific amino acid motifs often contribute to such interactions

166 studies led to the identification of a four-amino-acid motif on the m2 receptor (Val385, Thr386, Ile

167 ter-binding PNA sequence embedded within two amino acid motifs: one leads to efficient cell/nuclear e

168 stic C-terminal domain, containing different amino acid motifs or repeated residues.

169 es all contain a SET domain, a conserved 130 amino acid motif originally identified in polycomb- and

170 olase superfamily recognizable by a specific amino acid motif outside of the Nudix box.

171 We demonstrate that a highly conserved 8-amino acid motif (P3) located in the linker between tran

172 sity, and, of note, all clones contained the amino acid motif PGGN (or minor variations) in the CDR3

173 a cellular phosphoprotein, CtBP, through a 5-amino acid motif, PLDLS, conserved among the E1A protein

174 (NLS-c), which consists of a bipartite basic amino acid motif plus the last 39 residues of ADAR1.

175 , ESXR1 contains 12 repeats of a unique nine amino acid motif, PPMAP(V/L)PPG, located C-terminal to t

176 be NMR resonances to the specific repetitive amino acid motifs prevalent in spider silk proteins.

177 additional amino acids downstream of the 12-amino acid motif provide necessary structural or conform

178 These results show that the 11-amino acid motif provides an ATP binding site in dematin

179 The amino acid motif provides opportunities for the controll

180 f 12 predicted transmembrane segments and an amino acid motif, R-X-G-R-R, present at equivalent posit

181 dsRNA do so by utilizing an approximately 70 amino acid motif referred to as the dsRNA-binding domain

182 data from mollusks, mammals and insects, and amino acid motifs reported to be associated with cleavag

183 on of mutant Eps15 protein, which lacks a 14-amino acid motif representing the AP-1 binding site of E

184 edicted polymerase domain containing the GDD amino acid motif required for viral RNA synthesis, was s

185 While not harbouring amino acid motifs resembling previously defined c-di-GMP

186 vian strains of HEV contain a conserved PXXP amino acid motif, resembling either Src homology 3 (SH3)

187 t direct its subcellular trafficking, but an amino acid motif responsible for the targeting of the tr

188 The identification of amino acid motifs responsible for increased virulence an

189 on of Cys102, found in the other radical SAM amino acid motif, resulted in the loss of C-7 methylatio

190 We discovered that Saps 4-6 each contains amino acid motifs RGD/KGD to bind integrins on epithelia

191 primers were designed based on two conserved amino acid motifs, RITGLD, and DI/(F)Y/(F)PNGG, in the t

192 We conclude that exposure of a three amino acid motif (RKR) can explain how assembly of an io

193 We have mapped a six-amino acid motif (RKRVKR) that serves as a necessary and

194 d Saccharomyces cerevisiae contain the three amino acid motif RX( downward arrow)(F/L/I)XX(T/S/G)XXXX

195 Presently, little is known of the amino acid motif(s) participating in bradykinin B2 recep

196 to its activity, we identify a conserved 30-amino-acid motif, separable from Dsh-binding regions, th

197 ners are recognised through a conserved four amino acid motif, (serine-X-isoleucine-proline) which ex

198 The primary sequence of the unique amino acid motif shares features with surface proteins o

199 The N terminus of Arix contains an amino acid motif similar to a region in Brachyury and Pa

200 ce analysis revealed that SphK2 contains a 9-amino acid motif similar to that present in BH3-only pro

201 The interaction is mediated by a short amino acid motif similar to that used by the rab-5 effec

202 An amino acid motif similar to the phytaspase cleavage site

203 For instance, the amino acid motifs SNG, ENN, LNG, and LNN were found to b

204 WNK4, and CR2 contains a highly conserved 22 amino acid motif specific to chordate species.

205 A 12-amino-acid motif (SRVERAIRHAIE) that forms the putative

206 e showed that a majority of NDN-encoded CDR3 amino acid motifs start at CDR3 position four, well with

207 d trafficking; however, the presence of a 12-amino acid motif starting at this Tyr residue was suffic

208 d reading frame of DSP2, suggesting that the amino acid motif STMIT may contact insulin and contribut

209 d by structurally homologous CDR3 beta-chain amino acid motifs suggesting Ag drive.

210 encodes a protein with four copies of the WD amino acid motif, suggesting involvement in protein-prot

211 ted with their lack of a conserved CDR1alpha amino acid motif, suggesting that fine specificity for a

212 Nanomolar affinity for PI(3)P by these short amino acid motifs suggests that a newly identified mecha

213 tethered to DNA, tandem repeats of an eight amino acid motif taken from this region stimulate the tr

214 to have significant identity with 72- and 75-amino-acid motifs tandemly repeated in the 190-kDa surfa

215 amily contain a highly conserved 130- to 140-amino acid motif termed the SET domain.

216 The CTDs contain a conserved 7-amino acid motif that connects blades 1 and 6 of the bet

217 of these genes encode proteins with an LPXTG amino acid motif that covalently links many virulence fa

218 e identified and used to construct a 130-180 amino acid motif that delimits the bilin lyase domain, a

219 trate that ASP5 cleaves a highly constrained amino acid motif that has similarity to the PEXEL-motif

220 This loop contains an amino acid motif that is also found in a portion of reco

221 In addition, SEMA3A has an amino acid motif that is analogous to hanatoxin, an inhi

222 nkyrin consists of 24 tandem repeats of a 33-amino acid motif that is present on a wide variety of ot

223 Each helix contains an amino acid motif that is repeated twice in mArfN37, once

224 erminal region we previously identified a 14 amino acid motif that is required for the up-regulation

225 This study identifies an amino acid motif that is responsible for the membrane bi

226 Our earlier studies identified a three-amino acid motif that is shared by toxins, ribosome-inac

227 cturally highly conserved negatively charged amino acid motif that is strictly required for Mg(2+) ca

228 The amino acid motif that links the KRAB domain and zinc fin

229 repeat domain of ATG16L1 to interact with an amino acid motif that recognizes this region.

230 Neither region contains an amino acid motif that resembles those reported for other

231 a and -1beta, we have identified a conserved amino acid motif that serves as a docking site for host

232 lon was dependent on the integrity of a five-amino acid motif that was identical to the recognition s

233 oteins, all of which contain repeats of a 36-amino acid motif that we named "motif 36".

234 and lacks any nonsynonymous substitutions in amino acid motifs that are well conserved among retrovir

235 The functions of conserved amino acid motifs that define this novel family of both

236 from basal spider lineages reveal mosaics of amino acid motifs that differ radically from previously

237 The cytoplasmic domain of megalin contains amino acid motifs that have the potential to bind to oth

238 FleQ does not have amino acid motifs that resemble previously defined c-di-

239 tact CAAX (C, cysteine; A, aliphatic; X, any amino acid) motif that is also known to mediate membrane

240 The F- box is a approximately 40-amino-acid motif that allows the F-box protein to bind S

241 Class I RFs possess a conserved GGQ amino-acid motif that is thought to be involved directly

242 ins contain an evolutionarily conserved five-amino acid motif (the regulatory domain motif (RDM)) tha

243 characterized by eight tandem copies of a 36 amino acid motif, the PUM repeat.

244 ction with eight conserved, approximately 35 amino acid motifs, the BRC repeats.

245 histidine residues as well as two conserved amino acid motifs, the FRAP and NPNL boxes.

246 gnalling proteins PatS and HetN use the same amino acid motif to regulate different stages of heteroc

247 e Francisella FTT0831c/FTL_0325 gene encodes amino acid motifs to suggest it is a lipoprotein and tha

248 s with altered CAAX (where A is an aliphatic amino acid) motifs to direct alternate or no prenylation

249 he vacuolar H(+)ATPase has a C-terminal DTAL amino acid motif typical of PDZ-binding proteins that as

250 ubunit (NFH) tail is composed of a repeating amino acid motif, usually X-lysine-serine-proline-Y-lysi

251 on of this activity identifies a conserved 9-amino acid motif ((V/A)P(I/L)AXXE(S/D)D) required for an

252 been shown to bind to a highly conserved six-amino acid motif very close to the C terminus of adenovi

253 o HhH motifs in conjunction with a conserved amino acid motif, VNINTA.

254 Three common amino acid motifs (W-SYP, TYVS, and VRH) were shared amo

255 In addition, a unique PPF/.GDS amino acid motif was located between these two sites tha

256 A dibasic amino acid motif was present at the predicted F protein

257 tant revealed that a conserved C-terminal 13-amino-acid motif was missing in Gap1.

258 We have identified a highly conserved amino acid motif, WDXNWD, located within the unique N-te

259 fine the properties of this approximately 20-amino acid motif, we designed a GPR consensus peptide an

260 Amino acid motifs were identified in both Hopie Gag and

261 Two candidate amino acid motifs were identified in the tail that could

262 Several different and repetitive amino acid motifs were present in both UspA1 and UspA2 f

263 M-CLL-derived peptides exhibited better amino acid motifs, were more similar to each other, alig

264 The predicted protein has amino acid motifs which share significant homologies wit

265 cterized by tandem arrays of a degenerate 35-amino-acid motif which form an alpha-solenoid structure.

266 We identify in this study a 27-amino-acid motif which is conserved between the Drosophi

267 We focused on the conserved WVPHEL amino acid motif, which forms part of the mariner transp

268 ne acetyltransferase complex through a novel amino acid motif, which is functionally conserved in E2F

269 The RXLR amino acid motif, which is present in these AVR proteins

270 nt of associated proteins containing an ETGE amino acid motif, which matches the KEAP1 interaction mo

271 a analyses, we demonstrate selection of CDR3 amino acid motifs, which strongly suggests Ag-driven oli

272 RFs have a conserved GGQ amino-acid motif, which is crucial for peptide release a

273 This point mutation resides within an eight-amino acid motif with homology to sequences important fo

274 alysis of this domain reveals a composite 10-amino acid motif with interdigitating residues that regu

275 52 kDa subunit of dematin shares a novel 11-amino acid motif with protein 4.2.

276 athy profile as well as transporter-specific amino acid motifs with a variety of bacterial and mammal

277 The protein contains several amino acid motifs with high similarity to those of other

278 Here we describe an evolutionarily conserved amino acid motif within APLF that is required for mediat

279 We have identified a 14 amino acid motif within the C-terminal region of the pro

280 In addition, we identify a nine amino acid motif within the highly conserved sequences o

281 eletion of domain VI or of a conserved eight amino acid motif within VI causes loss of all UNC-6 guid

282 MIT contains two duplicated 6- or 7-amino acid motifs within cytoplasmic loops, which are hi

283 s shuffling of a relatively conserved set of amino acid motifs within each of the four HVRs.

284 ces by targeting sites that encode conserved amino acid motifs within the major capsid protein, VP1.

285 ur analyses revealed a strictly conserved 14-amino-acid motif within the predicted alpha-helical link

286 Two short amino acid motifs, WXGDXNXR and PXWCDRXL, define a large

287 shares with all sequenced mammalian DSPs an amino acid motif, XILPXLXL, located approximately 80 ami