ライフサイエンスコーパス: acidic residue

1 motifs cannot be fully substituted by other acidic residue.

2 no group of the bound amino acid by using an acidic residue.

3 igh-affinity FXR modulator not comprising an acidic residue.

4 nine 51 (Met51) with upstream and downstream acidic residues.

5 omerases, with an active site clustered with acidic residues.

6 , with SpxA1 containing an unusual number of acidic residues.

7 basic residue interacts with only one of the acidic residues.

8 linical strains, and to mutagenize conserved acidic residues.

9 contains a disproportionately high number of acidic residues.

10 for short peptide substrates with N-terminal acidic residues.

11 tor is coordinated by three highly conserved acidic residues.

12 ty to sense H(+) signals by acquiring buried acidic residues.

13 t not N-terminal) EH-domains are followed by acidic residues.

14 nced ability to glycosylate sites flanked by acidic residues.

15 His90 orient their side chains toward these acidic residues.

16 n Ca(2+) is absent) as H(+) dissociates from acidic residues.

17 than a formal negative charge from proximal acidic residues.

18 ding requires neutralization of a cluster of acidic residues.

19 ssential for aldolase binding, and clustered acidic residues.

20 ide-chains from the zipper and two invariant acidic residues.

21 be linked to the staggered titration of key acidic residues.

22 light conditions and sensed by lumen-exposed acidic residues.

23 of the cytoplasmic domain, which is rich in acidic residues.

24 d in a molecular surface that is coated with acidic residues, a marked difference from beta-lactamase

25 8 UMI (UIM- and MIU-related UBD) hydrophilic acidic residues abolishes RNF168-mediated ubiquitination

26 Mutation of the acidic residue also abolishes auxin transport activity b

27 Q AceI mutant with a mutation in a conserved acidic residue, although unable to mediate chlorhexidine

28 multidomain extracellular region enriched in acidic residues and carboxyl-carboxylate pairs within 3

29 l residues at standard protonation), low pH (acidic residues and His protonated), and highly acidic e

30 sequence features indicated a preference for acidic residues and increased hydrophilicity in the regi

31 h water and participate in salt bridges with acidic residues and lipid phosphate groups.

32 Each monomer includes 34 acidic residues and only six basic residues.

33 in an inner chamber that contains a ring of acidic residues and that is near the channel entrance; t

34 Between the acidic residues and the transmembrane pore lies a disulp

35 YYEDSYED) within this region consist of five acidic residues and three sulfo-Tyr residues, thus repre

36 In an iterative process, we identified two acidic residues and two hydrophobic residues that form t

37 nts a hydrophobic residue, Phi is usually an acidic residue, and X is any residue) and able to inhibi

38 is change was due to a pK(a) shift of site I acidic residues, and to contributions of oxygen function

39 Mechanistically, the acidic residues are important in enhancing the efficienc

40 e form of gelsolin shows that the equivalent acidic residues are in close contact with G3, which may

41 mplex, while Arg(6), His(11), and C-terminal acidic residues are involved in stabilizing the final co

42 , enolase, and C-Raf) show that the relevant acidic residues are present in salt bridges with conserv

43 We found that acidic residues are required in LF(N) to utilize a proto

44 It is commonly believed that acidic residues are required near the orifice of such pr

45 tudies, we found that both N- and C-terminal acidic residues, as well as the C-terminal Cys residue o

46 The presence of acidic residues Asp and Glu near the peptide N-terminus

47 The carboxylate moieties of acidic residues Asp-109, Asp-207, Asp-298, and Asp-337 i

48 erminal site (amino acids 108-130) and by an acidic residue (Asp(641)) at the pore loop of TRPV3.

49 xternal site is under indirect control by an acidic residue (Asp-66), making it Ca(2+)-specific.

50 and S/T+1 positions, but strongly disfavors acidic residues (Asp or Glu) at the S/T-2 position and a

51 stabilizes the structure by coordinating two acidic residues (Asp(552) and Glu(648)), one from each o

52 We found that acidic residues (Asp-83 and Asp-84) in G1 of GSNL-1 are

53 ng group-accommodating groove, and a pivotal acidic residue, Asp-123, after the nucleophile Ser-122.

54 -chain carboxylate groups from the conserved acidic residue, Asp-66 in NaK, conventionally thought to

55 Furthermore, mutation of two nearby acidic residues, Asp(367) and Glu(399), also reduced act

56 quence alignments identified three conserved acidic residues, Asp-166, Glu-167, and Glu-222, that are

57 dase whose activity depends on the conserved acidic residues, Asp-189 and Glu-247.

58 trescine binds in a buried pocket containing acidic residues Asp174, Glu178, and Glu256.

59 uires ribosome binding and is mediated by an acidic residue, Asp924, near the center of the putative

60 es are mostly driven by competing effects of acidic residues (aspartic acid and sialic acid) on ion-p

61 Two buried acidic residues assist in the reaction.

62 bc15 largely results from the presence of an acidic residue at its N-terminal region.

63 rophobic residue at the P-2 position plus an acidic residue at the P-3 position (class II) can also o

64 a conserved inner cavity position, although acidic residues at any pore-lining position in the inner

65 irect substitution or suppressor generation, acidic residues at one or both positions of the H168/H31

66 served arginine at position +1 and conserved acidic residues at positions -2 and/or -3 are required f

67 amers pack in crystal contacts, and that the acidic residues at the C-terminal tip of the protein int

68 domain and bind to C-terminal sequences with acidic residues at the P-2 position with low micromolar

69 In addition, the human MetAPs disfavor acidic residues at the P2'-P5' positions.

70 evealing a previously unknown preference for acidic residues at the substrate prime site position P1'

71 roteins, and it has been suggested that this acidic residue be removed prior to digestion, thus sacri

72 ot exhibit preferential cleavage adjacent to acidic residues but did show enhancement next to proline

73 AAV2 and AAV4 showed a higher propensity of acidic residues but similar volumes, consistent with com

74 Mutational analysis indicated that the acidic residues, but not the threonine, within the EDTEE

75 ein, we determined the role of the conserved acidic residues by using alanine point mutants to invest

76 the presequence is optimized in its natural acidic residue content for efficient DeltapH-driven unfo

77 h basic and acidic residues or predominantly acidic residues contribute to actin affinity.

78 Acidic residues critical to protein function were identi

79 which are characterized by multiple flanking acidic residues, CTRC shows substrate specificity that i

80 To that end, acidic residues, D and E, and their neutral amides, N an

81 In addition to the aromatic amino acids, two acidic residues, D111 and E113, form salt bridges with b

82 mutation that mimics protonation of the key acidic residue (D158N) was shown to trigger a global con

83 ve centre has a Mg ion co-ordinated by three acidic residues, D401, E458 and D542.

84 high-affinity interaction with the innermost acidic residue (D523) of the selectivity filter and subs

85 d that 2 of the 8 MiRP2 extracellular domain acidic residues (D54 and D55) are important for KCNQ1-Mi

86 egion to be critical in DNA binding, whereas acidic residues D88 and E89 (wing), D8 and E11 (metal-bi

87 ong with an arginine and a second cluster of acidic residues defining the other prong.

88 himera stabilized GFP, while deletion of the acidic residues destabilized GFP::SpxA1(tail) .

89 ree proteins where phosphosites evolved from acidic residues (DNA topoisomerase II, enolase, and C-Ra

90 otif (NDSM) carries an additional stretch of acidic residues downstream of the consensus Psi-K-x-E/D

91 moval of the CTD or mutations that eliminate acidic residues dramatically increase the protein/DNA in

92 opose a model in which Arg(6) and N-terminal acidic residues drive the encounter complex, while Arg(6

93 lectrophysiological data have shown that the acidic residues E106 in transmembrane helix 1 (TM1) and

94 G465D and K486N, and by single mutations in acidic residues E460 and D461.

95 (D641) in the extracellular pore loop or two acidic residues (E679, E682) in the inner pore region si

96 , whereas the combined neutralization of six acidic residues eliminated inactivation entirely.

97 demonstrates that the Glu(309) and Glu(771) acidic residues (empty Ca(2+)-binding sites I and II) ar

98 ages N-terminal to proline and C-terminal to acidic residues (especially for the lowest charge states

99 II substrates typically contain two or more acidic residues, especially at Tyr(P)-1 to Tyr(P)-3 posi

100 pendent on glutamate, thus establishing that acidic residues facilitate lysine modification and form

101 is, and NMR to demonstrate that the flanking acidic residues "fine tune" the binding affinity to EHD1

102 ns and identified main interaction sites for acidic residues flanking the SIM.

103 The acidic residues flanking this basic cluster in PLC-zeta

104 A long loop (L3) carrying multiple acidic residues folds into the beta-barrel pore to form

105 rence for either a hydrophobic residue or an acidic residue following the aromatic residue in the LIR

106 The results indicate that the targeting of acidic residues for cross-linking provides distance rest

107 ronegative potential of B-NRP2 by exchanging acidic residues for uncharged alanine (B-NRP2 E284A,E291

108 Three conserved acidic residues form a pyramidal-shaped cation-binding s

109 ultiple ion-binding sites, and the conserved acidic residues form the luminal Ca(2+)-blocking site th

110 in and is adjacent to a cluster of conserved acidic residues found in diflavin oxidoreductases.

111 ily enzymes, and the catalytically important acidic residues found in family 43 enzymes were conserve

112 lution in which codons for the corresponding acidic residues found in Ocr were specifically re-introd

113 's endonuclease domain where at least three acidic residues from a ~185 residue segment (D401 to E58

114 tical: three conserved, calcium-coordinating acidic residues from each LDLR module encircle a lysine

115 oprotease that cleaves aspartic and glutamic acidic residues from the N-terminus of a number of prote

116 ine in JKJ05, which appears to interact with acidic residue Glu(767) in our model of the seven-transm

117 The acidic residue Glu-395 located at the active site of PPO

118 These elements consist of the acidic residues Glu(341), Asp(348), and Asp(355) located

119 Further, key acidic residues Glu(6), Asp(8), and Glu(16), believed cr

120 n of the Tyr(11) residue of NT[8-13] with an acidic residue (Glu(179)) located in the ECL2 of hNTS2 o

121 Substitution of the three acidic residues (Glu(571), Glu(235), and Glu(237)) and A

122 Furthermore, altering a single acidic residue, Glu-478, on the C-terminal domain to glu

123 Two acidic residues, Glu-48 and Glu-49, of cytochrome b5 (b5

124 Two acidic residues, Glu153 and Asp156, that lie in a conser

125 LeuT are chloride-independent but contain an acidic residue (Glu290 in LeuT) at a site where eukaryot

126 ce between two adjacent subunits where three acidic residues, Glu362 and Asp383 on one subunit, and A

127 which bridges His143 of cytochrome f and the acidic residue, Glu75, of cyt b(6); in addition, Cd1 is

128 owever, mutations at two conserved nonligand acidic residues, Glu95 and Glu100, result in low metal c

129 function was confirmed by substitution of an acidic residue (glutamate, BRCA2(Deltaex11/S3291E)) for

130 nhibition can be ascribed to the lack of two acidic residues--highly conserved in other ACA isoforms-

131 to an apolar residue or converting V96 to an acidic residue impedes the allosteric response to induce

132 Using Xenopus egg extracts, we identify an acidic residue in PCNA that is essential to support dest

133 stance are mutations of a specific serine or acidic residue in the A subunit of gyrase or topoisomera

134 nsin II receptors and export ability of each acidic residue in the di-acidic motifs cannot be fully s

135 ructural analysis reveals that the conserved acidic residue in the filter is essential for Ca(2+) bin

136 the present study, we identified a conserved acidic residue in the motor domain (Asp-136) and two con

137 two (or more) protons requires an additional acidic residue in the multidrug recognition pocket of Md

138 The final acidic residue in the N-arm that was tested, E15, is sho

139 Successive replacement of acidic residues in Ac-GPSLNPFDEED-NH(2) with neutral res

140 proteins, pK(a) values were measured for the acidic residues in both proteins using (13)C NMR chemica

141 Additionally, acidic residues in Csm5 are required for efficient matur

142 e neutralization mutations of two N-terminal acidic residues in DPP6-S eliminated the increase in gam

143 Interestingly, the acidic residues in helix alpha9a of CeFIGL-1-AAA are not

144 There are three, six, and six acidic residues in macrolittin70, pHD15, and MelP5_Delta

145 hospho-acceptor, and preference for basic or acidic residues in other positions.

146 Neutralizing the acidic residues in p6 improves the annealing and aggrega

147 In particular, DR0801 strongly preferred acidic residues in pocket 9.

148 monstrate the variation in importance of the acidic residues in regions of Ocr corresponding to diffe

149 bridge between a residue in the S4 helix and acidic residues in S2.

150 the formation of salt bridges with specific acidic residues in SH3 domains.

151 Basic residues in site 1 and acidic residues in site 2 were essential for positive re

152 ly 33 %) due to the protonation of a few key acidic residues in the A and B strands.

153 Acidic residues in the activation domain of protein C ar

154 Charge neutralization of the acidic residues in the activation peptide through Ala mu

155 We have identified four conserved acidic residues in the active site that are necessary fo

156 and OtCE15A possesses two putative catalytic acidic residues in the active site.

157 rimetry and NMR spectroscopy, we report that acidic residues in the BAZ2B PHD domain are essential fo

158 Acidic residues in the C-terminal linker of the E2b lipo

159 acidic cluster sorting protein-2 (PACS-2) to acidic residues in the carboxyterminal tail of K5.

160 f EmrE subsequent to protonation of critical acidic residues in the context of a global description o

161 Acidic residues in the core of the E1b heterotetramer, w

162 functional effects are caused by mutation of acidic residues in the cytoplasmic segment of Orai1/CRAC

163 estigated the contribution of the cluster of acidic residues in the distal C terminus of TRPA1 in the

164 analysis and revealed a pattern of basic and acidic residues in the first halves of the periodic repe

165 Replacement of the acidic residues in the flexible linker with alanine elev

166 nditions, implying that the highly conserved acidic residues in the gamma subunit influence thiol red

167 Of 11 acidic residues in the I-domain, seven participate in st

168 round the canonical cleft, especially to the acidic residues in the loops, as revealed by NMR titrati

169 esidues 316-326) interacts with a cluster of acidic residues in the middle of helix 4.

170 the interaction of scaffolding protein with acidic residues in the N-arm of coat protein, since this

171 tutions in betaS, we localized the switch to acidic residues in the N-terminal and non-amyloid compon

172 We show that mutation of acidic residues in the N-terminal helix impair the abili

173 tions map the key binding interface to a few acidic residues in the N-terminal region of MAD1, and po

174 thermore, protonation-mimicking mutations of acidic residues in the palm induce a dramatic accelerati

175 ntaining the peptide length but substituting acidic residues in the peptide with neutral or basic res

176 gated the role of electrostatic repulsion of acidic residues in the pH-dependent large conformational

177 asured at pH 5.2, suggesting the presence of acidic residues in the pore.

178 of the Wor1 TF revealed that substitution of acidic residues in the PrLD blocked its ability to phase

179 gating charge in the S4 segment (R4) and two acidic residues in the S2 segment during activation.

180 oposed to involve interactions with Bronsted acidic residues in the secondary coordination sphere.

181 Estimation of pKa values of the acidic residues in the transport sites indicates that at

182 ows us to estimate the pK(a) values of seven acidic residues in the unfolded state of HEWL.

183 of a conserved basic residue and presence of acidic residues in the vestibule regions, conserved only

184 ts assemble through contacts among basic and acidic residues in their transmembrane domains to form t

185 Acidic residues in this linker are required for its full

186 The acidic residues in this region are highly conserved in H

187 Acidic residues in v3 complement basic residue 110 of th

188 Acidic residues, in contrast, allowed the seal to form a

189 Mutagenesis shows that there are several acidic residues, including E99 and E107 as well as D29 (

190 des with phosphorylated residues proximal to acidic residues, including glutamic acid, aspartic acid,

191 demonstrate that the peculiar clustering of acidic residues increases the intrinsic disorder propens

192 T was observed at disulfide bonds but not at acidic residues, increasing and then apparently reversin

193 la enhanced enzyme CPT sensitivity, with the acidic residues inducing the greatest increase in drug s

194 Dyads of acidic residues inside the tail-tube present regularly-s

195 s further demonstrated that a mutation of an acidic residue involved in Ca(2+) binding, E454K, preven

196 -89 and 132-167) with the negatively charged acidic residues involved in Ca(2+) binding are critical

197 on-conventional FFAT motif where a conserved acidic residue is replaced by a serine/threonine.

198 Chemical cross-linking of acidic residues is achieved using homobifunctional dihyd

199 In the presence of calcium, the binding of acidic residues is enhanced as they ligate the cation, w

200 tion of the hinge histidine with neighboring acidic residues is proposed to be responsible for its ro

201 One feature of this stretch of acidic residues is that it lies adjacent to a functional

202 oop (named for its four invariably conserved acidic residues) is critical for Cdc34 function both in

203 In contrast, mutation of an acidic residue known to be at or near the quinol-binding

204 of their collagen stalks and surface exposed acidic residues located in CR1 CCP24 and/or CCP25.

205 upplied in part by surface-exposed conserved acidic residues located on helix 1 and strand 1 in the s

206 changes from 4.0 to 3.5 and identify the key acidic residue-lysine interactions responsible for the o

207 Acidic residues markedly increase the rate of DeltapH-dr

208 or proteins with regions containing multiple acidic residues may also be affected similarly.

209 Acidic residues may also be specifically accommodated in

210 iently assembled at pH <5.0, suggesting that acidic residues might be involved in the initial membran

211 allows binding of PEP-19 to CaM, whereas the acidic residues modify the nature of this interaction, a

212 Mutation of these acidic residues modulates the effects of putrescine.

213 More specifically, we show that acidic residues N-terminal to the substrate pTyr in EGFR

214 trostatics that would result from placing an acidic residue near the scissile phosphate of the bound

215 prisingly neither this residue nor any other acidic residues near the enzymes active site were essent

216 Acidic residues near the first residue decrease substrat

217 ins, preferentially at phosphothreonine near acidic residues, near the protein termini, and within me

218 These results suggest that acidic residues normally modulate access of RNAs to the

219 ace of human CTRC that interact with the P4' acidic residue of the inhibitor.

220 Mutations in key acidic residues of GreA and DksA suggest that properties

221 Arg82 and Arg132) on one side, and multiple acidic residues of L3 (Asp107, Asp113, Glu117, Asp121, A

222 e interfacial region modulate protonation of acidic residues of pHLIP responsible for transbilayer in

223 A mutant in which acidic residues of SP were replaced with alanine failed

224 401, E408, D465, E563, and E586, as critical acidic residues of TerL(lambda) 's endonuclease.

225 bridges between basic residues of IL-13 and acidic residues of the antibody.

226 h the structure of the complex, in which the acidic residues of the C-terminal extension cannot inter

227 ely interacts with both of the transmembrane acidic residues of the CD3 dimer.

228 c residues on either side, which bond to the acidic residues of the finger.

229 When the serine and acidic residues of the SRT were replaced with Ala, Leu,

230 Mutations of conserved basic or acidic residues on either face suppressed PsIAA4 PB1 hom

231 In this study, we have identified two acidic residues on helix-162 (Glu-167 and Glu-170) on th

232 e discrete interactions of myosin loop 4 and acidic residues on successive 39-42 residue-long tropomy

233 sidues form electrostatic complexes with two acidic residues on the channel.

234 actin subdomains 1 and 3 juxtaposed against acidic residues on the successive quasi-repeating units

235 jacent immunoglobulin-like domain (Ig5), and acidic residues on the surface of FN1 play a role in pol

236 In addition, specific acidic residues on the surface of the MAM domain are cri

237 ods P2, P3, P5, and P7, where both basic and acidic residues or predominantly acidic residues contrib

238 rprisingly, MD2 does not interact with three acidic residues or the Mg(2+) cofactor required for cata

239 tide charge was changed by mutating basic to acidic residues or vice versa, but the amino acid sequen

240 ing to the TiO2 surface, with both basic and acidic residues overwhelmingly preferred over the non-ch

241 ic residues in the N-terminal alpha-helix to acidic residues partially or completely restored normal

242 s of phage and viral TerL nucleases indicate acidic residues participate in metal ion-binding, part o

243 al peptide activity and membrane disruption, acidic residues positioned at the distal (Asp(20), Asp(2

244 just a measuring stick ensuring placement of acidic residues precisely at the catalytic centre but al

245 Interestingly, we found that LigY lacks the acidic residue proposed to activate water for hydrolysis

246 nteraction between a lysine and a cluster of acidic residues provides one prong with an arginine and

247 Alanine-scanning mutagenesis identified an acidic-residue putative ER export motif responsible for

248 receptor (SPRY) domain binds to a cluster of acidic residues, referred to as the D/E box, in RbBP5.

249 identical positioning of key hydrophobic and acidic residues relative to NSP3.

250 IKKbeta/NF-kappaB, whereas replacement with acidic residues rendered MEKK3 constitutively active.

251 otics in terms of both overall structure and acidic residue rich peptide core.

252 lues may reflect binding interactions to the acidic residue-rich a1 and a3 segments adjacent to A1 do

253 We further demonstrate that an acidic residue-rich region in SRC-3 is an important dete

254 The structure reveals an acidic-residue-rich subdomain that is present in bocavir

255 A continuous axis of basic and acidic residues running centrally through the membrane a

256 orm pHinder, we identified a triad of buried acidic residues shared by all three receptors, a feature

257 Our comprehensive protein-wide acidic residue substitution screen shows that only mutat

258 found the interactions to depend strongly on acidic residues surrounding the central core LIR motifs.

259 ns, we present here the development of a new acidic residue-targeting sulfoxide-containing MS-cleavab

260 On the other hand, acidic residues tend to form "water bridges" between the

261 ficity helix." Additionally, in CANSDC a key acidic residue that interacts with the distal amino grou

262 rongly targeted, and mutagenesis revealed an acidic residue that is important for toxin binding.

263 dherins consisting of three highly conserved acidic residues that alternately serve as a p120-binding

264 ith an active site lined by highly conserved acidic residues that bind metal ions.

265 We have mutated all of the acidic residues that coordinate the Ca(2+) ions and have

266 he adaptable platform surface, and a trio of acidic residues that enables cation selectivity without

267 on in repression, the positions of basic and acidic residues that form inter-molecular salt bridges i

268 GNE-6640 and GNE-6776 interact with acidic residues that mediate hydrogen-bond interactions

269 The surface of Ocr is replete with acidic residues that mimic the phosphate backbone of DNA

270 handshake" interaction between two conserved acidic residues that our data suggest adds an additional

271 or is due to a network of interactions among acidic residues that would destabilize the alpha-helical

272 of two regions of the ectodomain enriched in acidic residues: the acidic pocket, which faces the outs

273 ting systematic mutagenesis of all conserved acidic residues thought to be exposed to the cytoplasm,

274 This adds an acidic residue to the CcO interior.

275 VIII were assessed following mutagenesis of acidic residues to Ala or Tyr residues to Phe and expres

276 ctivators that target sigma(70) directly use acidic residues to engage a basic surface of region 4.

277 Replacement of these serine residues with acidic residues, to mimic phosphorylation, reduced prote

278 gion, which houses three histidines and four acidic residues, to Mn(II) coordination at site 2.

279 embrane MCPs where reversible methylation of acidic residues tunes receptor activity.

280 However, mutation of a single acidic residue upstream of the dileucine-like motif lead

281 le, most eukaryotic genomes, with respect to acidic residue usages, select Glu over Asp, but the oppo

282 Furthermore, the FTIR signal of protonated acidic residues was perturbed in the presence of Zn(2+),

283 d by the carboxylate of two highly conserved acidic residues, water molecules, and the 3'-hydroxyl gr

284 Because only this first NPF is followed by acidic residues, we have utilized glutathione S-transfer

285 ovel electrostatic palmitoyl switch in which acidic residues weaken the membrane-binding strength of

286 Conserved acidic residues were confirmed through kinetic analysis

287 us) partitioned into membranes only when its acidic residues were neutralized by protonation.

288 Some acidic residues were observed to orient and move signifi

289 of Ocr, termed pocr, in which all of the 34 acidic residues were substituted for a neutral amino aci

290 se organization of conserved hydrophobic and acidic residues when compared with canonical BH3 sequenc

291 tatic requirements: one surprisingly prefers acidic residues when driven by either a Deltapsi or a De

292 addition, it is also proposed that a pair of acidic residues, which are totally conserved among the C

293 alization; mutational replacement of several acidic residues with neutral or basic residues rescues P

294 proteins is due to independent titration of acidic residues with pK(a) values perturbed primarily by

295 ystokinin receptor interacts with a specific acidic residue within the amino terminus of this recepto

296 rization of these mutants, we also define an acidic residue within the C-terminus of cyclin D1 that i

297 s studies on this enzyme, revealing that two acidic residues within the double E loop, Asp-147 and Gl

298 Mutation of basic amino acids to acidic residues within the polybasic domain results in i

299 The acidic residues within this region (Glu72, Asp74, Glu89,

300 al mutagenesis of each of the five conserved acidic residues within this region of the receptor in th