ライフサイエンスコーパス: lysine residue

1 RK clusters (clusters enriched for arginine-lysine residues).

2 pocket that normally accommodates the target lysine residue.

3 n ligase (CRL4(VprBP)) on a highly conserved lysine residue.

4 erring only a single ubiquitin to a specific lysine residue.

5 ther undergoes ubiquitylation on a conserved lysine residue.

6 psilon-amino group of a conserved, catalytic lysine residue.

7 post-translationally modified on a conserved lysine residue.

8 to a chelator that had been conjugated to a lysine residue.

9 V, stabilized by a hydrogen bond to a nearby lysine residue.

10 evealed that podocin is ubiquitylated at two lysine residues.

11 yze the NAD(+)-dependent deacylation of acyl-lysine residues.

12 ein interaction interfaces with little or no lysine residues.

13 tion is specific and involves a total of 4-5 lysine residues.

14 c modification of the mAb at solvent-exposed lysine residues.

15 e specific to particular protein domains and lysine residues.

16 lard reaction between the reducing sugar and lysine residues.

17 ors installed via imidation of site-specific lysine residues.

18 rt1-3 to deacetylate two adjacent acetylated lysine residues.

19 et proteins at the varepsilon-amino group of lysine residues.

20 of a polyubiquitin chain to -amino groups of lysine residues.

21 CPs, resulting in pyrrolone formation at the lysine residues.

22 over an extended surface containing multiple lysine residues.

23 ed to reactions at nucleophilic cysteine and lysine residues.

24 yubiquitin chains through multiple ubiquitin lysine residues.

25 n by driving ubiquitination of two conserved lysine residues.

26 e enzymes, which remove methyl moieties from lysine residues.

27 romotes the sumoylation of SnoN1 at distinct lysine residues.

28 peptide, which is conferred by arginine and lysine residues.

29 beta-subunit of the ETF by trimethylation of lysine residues.

30 tylation of NEIL1 within the same C-terminal lysine residues.

31 ribosyl)ated aspartate and glutamate but not lysine residues.

32 lagens by mediating oxidative deamination of lysine residues.

33 to the antibody was achieved by coupling to lysine residues.

34 t that ubiquitination of the DUB ataxin-3 at lysine residue 117, which markedly enhances its protease

35 t Imd is rapidly Lys-63-polyubiquitinated at lysine residues 137 and 153 by the sequential action of

36 Substitution of malonylated lysine residue 184 in glyceraldehyde 3-phosphate dehydro

37 Lysine residues 199 and 202 of mature ETFbeta are almost

38 F and promotes the trimethylation of ETFbeta lysine residues 199 and 202.

39 egulated by its K63-linked ubiquitination at lysine residue 274, which is mediated by the E3 ubiquiti

40 The acetylation of CREBH at lysine residue 294 controls CREBH-PPARalpha interaction

41 Our A3G mutagenesis study showed that lysine residues 297, 301, 303, and 334 were not sufficie

42 HDAC6) increased the acetylation of HSPA5 at lysine residues 353 (K353) and reduced GP78-mediated ubi

43 In this study, we identify that the specific lysine residue 447 (K447) of HSPA5 could be modified wit

44 quitination of CAV1 occurs at any of the six lysine residues, 5, 26, 30, 39, 47, and 57, that are clu

45 superoxide dismutase 2 (Sod2) acetylation of lysine residue 68, thereby enhancing reactive oxygen spe

46 Here, we report that the conserved lysine residue 714 in the ErbB4 ICD undergoes SUMO modif

47 42-mediated mechanical stiffening, histone 3 lysine residue 9 (H3K9) methylation, Sox2 expression and

48 also known as G9a, methylates histone H3 on lysine residue 9 to predominantly produce a dynamic hist

49 deacetylases (HDACs) modulate acetylation of lysine residues, a protein modification important for re

50 Substitution of these proline and lysine residues accelerated PrP conversion such that spo

51 None of the individual lysine residues account completely for LRP1 binding, sug

52 sts that PrP's centrally located proline and lysine residues act as conformational switches in the in

53 ylase 1 (LSD1) demethylates at both of these lysine residues and has been shown to disrupt neuronal m

54 We identified three ubiquitylated lysine residues and showed that DNA ligase I interacts w

55 In addition, interactions between abundant lysine residues and silica surface are identified, and p

56 we show that USP22 is acetylated on multiple lysine residues and that alteration of a single lysine (

57 The lysine residues and the ubiquitination of BFRF1 regulate

58 lectively with these modified and unmodified lysine residues and with adjacent polar amino acids and

59 e was achieved in live cells by caging a key lysine residue, and excellent OFF to ON light-switching

60 These lysine residues appear to interact with the lysine-bindi

61 Lysine residues are implicated in driving the ligand bin

62 Because lysine residues are involved in collagen cross-linking,

63 utation at their putative ubiquitin-acceptor lysine residues are resistant to degradation.

64 tations at their putative ubiquitin-acceptor lysine residues are resistant to MG-induced degradation.

65 decarboxylation of propionate 4, but with a lysine residue as an essential proton shuttle.

66 Here we identified the unique lysine residue at position 124 of the NY-ESO-1 cancer/te

67 s an active DNA binding domain and an intact lysine residue at position 164.

68 Abs that reacted with a linear epitope at a lysine residue at position 169 (K169) in the HIV-1 envel

69 The lysine residue at position 395 in NuoN (NLys(395)) is co

70 Vaccine efficacy against viruses with a lysine residue at site 169, important to antibody bindin

71 iruses with a restored wild-type arginine or lysine residue at the NS3/4A site were obtained.

72 By replacing lysine residues at proposed phospholipid-binding sites w

73 transfer these fluorophores between proximal lysine residues at protein-protein interfaces, immunoglo

74 Here, we demonstrate that acetylation of lysine residues at the inner surface of PCNA is induced

75 bsequent interaction with positively charged lysine residues at the latch constriction of alphaHL.

76 chromatin assembly by reacting with histone lysine residues at the sites critical for chromatin asse

77 Two lysine residues at the tip of repeat 2-3 beta-hairpin (r

78 inhibitory activities are dependent on three lysine residues at the tip of the C-terminal zinc ribbon

79 additional hydroxylation of EF-P at the same lysine residue by the YfcM protein has also recently bee

80 er peptides are produced via modification of lysine residues by carbamylation of proteins.

81 t to acetylation of its four N-terminal tail lysine residues by the NuA4 and SAGA histone acetyltrans

82 prevents spurious discharge of Ub from E2 to lysine residues by: (1) harboring structural elements th

83 three well-characterized proteins labeled at lysine residues: calmodulin (CaM), maltose-binding prote

84 te cysteine residues, targeting nucleophilic lysine residues can also represent a viable approach to

85 odified by post-translational methylation of lysine residues, catalyzed by S-adenosylmethionine-depen

86 resonance (NMR) spectroscopy, suggests these lysine residues colocalize in a pocket near the C termin

87 charge-neutralizing mutations of four nearby lysine residues comprising the so-called central lysine

88 Histone methylation of lysine residues controls developmental processes in both

89 es elements of mRNA secondary structure with lysine residues encoded near the N-terminus of PRPS1.

90 tance of the positive charge of the arginine/lysine residue for dimer formation.

91 ine site-specific acetylation degrees of all lysine residues for all core histones of Trypanosoma bru

92 K5 targets two membrane-proximal VE-cadherin lysine residues for ubiquitination, driving endocytosis

93 esponsible for trimethylation of a conserved lysine residue found in several human Hsp70 (HSPA) prote

94 of an isopeptide bond between glutamine and lysine residues found on the surface of proteins, but it

95 Given that proximal lysine residues frequently reside at protein-protein int

96 t to the PIP2-binding site, generated by two lysine residues from neighbouring subunits.

97 he high-affinity GAG binding ligand and that lysine residues from the N-loop, 40s turn, beta3 strand,

98 introduced specifically at three individual lysine residues, generate distinct PRE profiles, indicat

99 Although amine-reactive reagents targeting lysine residues have been successful, it remains difficu

100 cholic Dopa (3,4-dihydroxyphenylalanine) and lysine residues hint at a synergistic interplay in adhes

101 es that catalyze deacetylation of acetylated lysine residues; however, the specificity and substrate

102 the N terminus of beta1, which contains two lysine residues (i.e., K3 and K4), which upon substituti

103 ansgene containing a mutation in a conserved lysine residue important for phosphorylation activity of

104 e demonstrate that a catalytically important lysine residue in a number of FadD (fatty acyl CoA synth

105 A conserved lysine residue in RGS1 (Lys(259) ) is directly involved

106 like protein Pup is covalently attached to a lysine residue in target proteins, thus resembling ubiqu

107 a strictly conserved and fully trimethylated lysine residue in the lipid head-group region of the mem

108 w that asymmetric SUMOylation of a conserved lysine residue in the N domain of both yeast (K178) and

109 Here we report that the lysine residue in the PP1-binding motif of BRCA1 is high

110 portant role during PTI and that a conserved lysine residue in the putative kinase domain is importan

111 These ChRs do not contain a lysine residue in the second helix, conserved in higher

112 use the epsilon-amino group of an N-terminal lysine residue in transpeptidation reactions to create a

113 up from post-translationally modified acetyl-lysine residues in a wide variety of essential cellular

114 2-oxoglutarate 5-dioxygenase 2) hydroxylates lysine residues in collagen telopeptides and is essentia

115 riments showed that Hcy-thiolactone modifies lysine residues in collagen type I alpha-1 chain.

116 econd enzyme that removes acetyl groups from lysine residues in E. coli been discovered and represent

117 u-84, and Glu-87) form salt bridges with key lysine residues in ER-alpha (Lys-299, Lys-302, and Lys-3

118 3) caused homogenous acetylation at multiple lysine residues in high yield.

119 ses by catalyzing the hydrolysis of acetyl-l-lysine residues in histone and nonhistone proteins.

120 g N-varepsilon-acetyl-lysine in place of six lysine residues in histone H3 enables deposition of pre-

121 morphic missense mutations affecting crucial lysine residues in histone H3 genes significantly contri

122 hyl group from S-adenosylmethionine (SAM) to lysine residues in histone tails and core histones.

123 The acetylation status of lysine residues in histone tails is one of a number of e

124 ns, such as methylation and demethylation of lysine residues in histones, play important roles in chr

125 spectrometry, we identified SIRT3-regulated lysine residues in LRP130 that generated a lysine-to-arg

126 The acetylation of lysine residues in MDH could enhance its enzyme activity

127 for the global and quantitative analysis of lysine residues in native biological systems.

128 hosphoglycerate (1,3-BPG) reacts with select lysine residues in proteins to form 3-phosphoglyceryl-ly

129 Here, we acylated a fraction of lysine residues in SOD1 with groups of variable hydropho

130 the active site of E2 conjugating enzymes to lysine residues in substrates.

131 The acylation of lysine residues in superoxide dismutase-1 (SOD1) has bee

132 the conjugation of SUMOs to -amino groups of lysine residues in target proteins.

133 Interestingly, several different lysine residues in Tat can function as ubiquitin accepto

134 which is likely due to conjugation of DM1 on lysine residues in the C(H)2 domain.

135 xygenase Jmjd6 has been shown to hydroxylate lysine residues in the essential splice factor U2 auxili

136 Here we show that acetylation of lysine residues in the globular domain of histone H3 (ly

137 Of the many lysine residues in the H3 and H4 tails, only acetylation

138 so provide evidence that NuA4 acetylation of lysine residues in the histone H4 tail stimulates SAGA i

139 ion could be prevented by mutation of all 12 lysine residues in the I-II loop to arginines.

140 fication studies confirm the requirement for lysine residues in the interaction of fVIII with LRP1.

141 we now study the contribution of individual lysine residues in the interaction with the largest memb

142 Several lysine residues in the intrinsically disordered AL are a

143 Positive charges of acetylable lysine residues in the N-terminal domain of APE1 are ess

144 eutralization of the positive charges of the lysine residues in the N-terminal domain of APE1 induces

145 e attachment of additional SUMO molecules to lysine residues in the N-terminal extensions of SUMO.

146 ession by inhibiting acetylation of specific lysine residues in the p53 DNA binding domain.

147 from caveolae thus leads to exposure of key lysine residues in the PI-binding region, acting as a tr

148 ey had less surface accessibility than other lysine residues in the protein.

149 lase that adds fatty acid chains to internal lysine residues in the protoxin, which is then secreted

150 and ubiquitylation by competing for the same lysine residues in the regulation of fatty acid synthesi

151 ylase 2 (LH2) catalyzes the hydroxylation of lysine residues in the telopeptides of fibrillar collage

152 astin-like polypeptides, and the presence of lysine residues in these domains may serve to prevent in

153 Mutation of five lysine residues in this region significantly stabilizes

154 sttranslational acetylation/deacetylation of lysine residues, in which a protein encoded by a gene wi

155 ions marked by histones modified at specific lysine residues, including H3K27ac, H3K4me3, H3K79me2, H

156 Here, we report that acrolein reacts with lysine residues, including lysines 5 and 12, sites impor

157 wo residues are very close to the acetylated lysine residue, indicating that they may directly intera

158 An ATP analogue that reacts with lysine residues inhibited catalytic activity and labeled

159 if could induce ubiquitin chain formation on lysine residues interspersed throughout A3G.

160 arbamylation, as monitored by PTM of protein lysine residues into N()-carbamyllysine (homocitrulline)

161 cell nuclear antigen (PCNA), identified the lysine residue involved in ATP binding, and validated th

162 knock-in mutant mice by mutagenesis of a key lysine residue involved in Mg(2+)-ATP binding.

163 Notably, A3G degradation relied on the lysine residues involved in polyubiquitination.

164 We conclude that a transmembrane embedded lysine residue is essential for electrogenic transport i

165 previously described RpPat substrates, this lysine residue is located within a PX4GK motif that has

166 een methylation and demethylation of histone lysine residues is an essential component of gene expres

167 Acetylation of lysine residues is an important post-translational prote

168 odification of chromatin at selected histone lysine residues is interpreted by an acetyl-lysine speci

169 Acetylation of histone lysine residues is one of the most well-studied post-tra

170 ncoding K229R, mimicking a non-acetylated NP lysine residue, is severely impaired compared to wildtyp

171 lycine-glycine remnant bound to the modified lysine residue (K-epsilon-GG) that can be recognized by

172 n of the ubiquitin monomers, which has seven lysine residues (K(6), K(11), K(27), K(29), K(33), K(48)

173 me system, which is mainly determined by two lysine residues (K11 and K253).

174 identified that acetylation occurs at three lysine residues, K159, K185, and K404 (3K), and enhances

175 emonstrate that acetylation of C/EBPalpha at lysine residues K298 and K302, mediated at least in part

176 o electroneutral by the mutation of a single lysine residue (K305).

177 the C terminus of ZFP809, including a single lysine residue (K391), is required for the rapid turnove

178 cells (ESCs) carry methylation marks on two lysine residues, K4 and K27, in histone3 (H3).

179 According to our predicted P66 topology, a lysine residue (K487) known to be sensitive to trypsin c

180 Mutagenesis of two N-terminal lysine residues (K4R and K6R) inhibited ZnT2 ubiquitinat

181 With this treatment, all three lysine residues (K6, K9, and K15) in Nt(17) were signifi

182 Acetylation of single lysine residues, K6, K9 or K15, had no effect on Httex1

183 e we report that merlin can be sumoylated on Lysine residue (K76) in vitro and in vivo.

184 za A virus nucleoprotein (NP), including the lysine residues K77, K113 and K229.

185 Further, hydroxylation of the collagen lysine residue (K87) critical for crosslinking is reduce

186 lex II suggested that several SIRT5-targeted lysine residues lie at the protein-lipid interface of su

187 died by Western blotting, and acetylation of lysine residues Lys(237), Lys(380), Lys(611), and Lys(62

188 We identified lysine residues Lys-60, Lys-150, and Lys-440 as SUMOylat

189 A lysine residue (Lys(1112)) at the C-terminal tail of mGl

190 found to specifically methylate two adjacent lysine residues, Lys(200) and Lys(203), in ETFbeta both

191 esis identifies two evolutionarily conserved lysine residues, lys-270 and lys-277, in the Hsp90alpha

192 ion is greatly assisted by a highly flexible lysine residue Lys472 that swings its side chain to pull

193 Recent studies indicate that acetylated lysine residues mainly exhibit low acetylation occupancy

194 found to contain acetylation of a conserved lysine residue near the active site, while no evidence f

195 cetylates the Nepsilon amine of a C-terminal lysine residue of a peptide, suggesting it is a protein

196 lently attaches a beta-lysine to a conserved lysine residue of EF-P.

197 e in the hydroxylation of the beta-lysylated lysine residue of EF-P.

198 ptor 4, that primarily reacted with a single lysine residue of HSA.

199 rometric analysis indicates that most of the lysine residues of cingulins and the other insoluble org

200 reports claim that Naa10 may also acetylate lysine residues of diverse targets, including methionine

201 sembly factors, including Rtt106, CAF-1, and lysine residues of H3-H4.

202 In conclusion, four highly conserved lysine residues of hFXR, K122, K210, K339, and K460, hav

203 changes in the methylation level at specific lysine residues of histone H3 (H3K27 and H3K4) in the ch

204 HBO1 acetylates lysine residues of histones and is involved in DNA repli

205 he latter binds to acetylated and methylated lysine residues of histones.

206 individually replaced eight highly conserved lysine residues of human FXR (hFXR) with arginine.

207 zed piperacillin hapten was detected on four lysine residues of human serum albumin (HSA) isolated fr

208 ed linear polyubiquitination of two specific lysine residues of IRF-3 by LUBAC, the linear polyubiqui

209 ly modify active site catalytic cysteine and lysine residues of other enzyme classes, and was found t

210 ubiquitin (Ub)-like isopeptide bonds on the lysine residues of proteins by at least two distinct pat

211 (SUMO) proteins (SUMO1, SUMO2, and SUMO3) to lysine residues of proteins.

212 atalyzes the removal of an acetyl group from lysine residues of several non-histone proteins.

213 is capable of post-translationally modifying lysine residues of the ICDH protein leading to a reducti

214 ids, via an amide bond, to specific internal lysine residues of the protoxin.

215 s major ionic interactions between conserved lysine residues of their collagen stalks and surface exp

216 iquitin molecules to either one of the seven lysine residues of ubiquitin, or via its N-terminal alph

217 ometry, we identified two ubiquitin acceptor lysine residues of which only mutation of Lys-380 in the

218 nation is dependent on a critical C terminal lysine residue on C/EBPalpha.

219 n homocitrullination (hcit), including a key lysine residue on histone H1 (H1K34hcit).

220 Nepsilon-fructosyl-lysine residue on plasminogen was increased in diabetes

221 How this single lysine residue on the nucleosome core particle (NCP) is

222 Flucloxacillin bound covalently to selective lysine residues on albumin in a time-dependent manner an

223 referentially ubiquitinates juxtahydrophobic lysine residues on Bag6-associated clients.

224 BET) family of chromatin adaptors and acetyl-lysine residues on chromatin has emerged as a promising

225 iption by selectively recognizing acetylated lysine residues on chromatin.

226 ase 2 (LH2), which hydroxylates telopeptidyl lysine residues on collagen, shifted the tumor stroma to

227 methyltransferase reported to monomethylate lysine residues on histone and nonhistone proteins.

228 oped recombinant antibodies to trimethylated lysine residues on histone H3, important epigenetic mark

229 d2, Brd3, Brd4, and BrdT, bind to acetylated lysine residues on histone or nonhistone proteins recrui

230 The dynamic reversible methylation of lysine residues on histone proteins is central to chroma

231 r proteins specifically recognize methylated lysine residues on histone proteins.

232 hylases (KDMs) catalyze the demethylation of lysine residues on histone tails and are associated with

233 Bromodomains bind to acetylated lysine residues on histone tails and thereby facilitate

234 acetylases (HDACs) remove acetyl groups from lysine residues on histone tails, promoting transcriptio

235 uclear PDC decreased acetylation of specific lysine residues on histones important for G1-S phase pro

236 or S-adenosylmethionine to specific acceptor lysine residues on histones, leading to changes in chrom

237 in polyubiquitin chains through one of seven lysine residues on its surface and the C terminus of adj

238 of the Snf2 bromodomain with the acetylated lysine residues on Snf2 negatively regulates binding and

239 -mediated histone PTM changes at 15 critical lysine residues on the core histones H3 and H4.

240 lentiviral vector infectivity of HSPCs, the lysine residues on the N-terminal extremity of Vectofusi

241 er from an E2-ubiquitin conjugate (E2-Ub) to lysine residues on the protein substrate.

242 Such chains can be connected through seven lysine residues or the amino terminus of ubiquitin, ther

243 Lysine residues play a role in templating the formation

244 Previous data indicated that the domain 2 lysine residue plays a role in activating an adjacent se

245 Methylation of histone lysine residues plays important roles in gene expression

246 Further, mutating a single conserved lysine residue potently disrupted WAVE1's inhibitory eff

247 with CD133 to acetylate the protein on three lysine residues predicted to reside on the first extrace

248 eterodimers becomes acetylated on N-terminal lysine residues prior to its incorporation into chromati

249 oliferation and replacement of ubiquitylated lysine residues reduced the in vitro ubiquitylation of D

250 T-arm of the tRNA for alanine with conserved lysine residues required for binding.

251 Mutation of each lysine residue revealed that Lys-35 is the major SUMOyla

252 ased on the proposed LRP1 binding motif of 2 lysine residues separated by about 21 A and mutated the

253 s N termini of proteins rather than internal lysine residues, showing a preference for substrates wit

254 r acetylation and ubiquitination of the same lysine residues; some sites were also targeted by lysine

255 etry, flexibility, and energetics of channel lysine residues suggested that this arrangement of resid

256 the catalytic trajectory demonstrated that a lysine residue swings from the distinct P2 site to the P

257 acids 388 and 389 causes a shift in a single lysine residue that mimics the Old World monkey sequence

258 ty effects and by providing steric access to lysine residues that are otherwise not prioritized for p

259 her a polyQ AR or a polyQ AR lacking the two lysine residues that are SUMOylated.

260 of receptors, which is initiated by pairs of lysine residues that dock into acidic pockets on the rec

261 46 treatment blocked acetylation of specific lysine residues that regulate p53 activity.

262 ith LRP1 via an extended surface of multiple lysine residues that starts at the bottom of the C1 doma

263 We identified three SpGAPDH lysine residues that were instrumental in defining the k

264 rt, two conserved patches of surface-located lysine residues that were recognized by kringle 4 of the

265 ing a new method to site-specifically modify lysine residues that will be a valuable addition to the

266 e is required for ubiquitination at multiple lysine residues through a "non-canonical" ubiquitin link

267 diverse functional consequences of liganding lysine residues throughout the human proteome.

268 sferases is autoacetylated at an active site lysine residue to facilitate cognate substrate lysine bi

269 We needed to mutate two lysine residues to abolish trypsin inhibition, suggestin

270 ated by about 21 A and mutated the candidate lysine residues to alanine individually and in pairs.

271 Mutation of lysine residues to hydrophobic amino acids, tyrosine or

272 eophilic addition by histidine, cysteine, or lysine residues to the carbonyl-containing histidine oxi

273 en-printed carbon electrode via a C-terminal lysine residue using glutaraldehyde as a cross-linking a

274 ersible functionalization of the conjugate's lysine residues via an azobenzene self-immolative linkag

275 ant (CLRDelta9KR), lacking all intracellular lysine residues was functional and trafficked similar to

276 Critically, the positive charge of the lysine residues was necessary for fusion regulation, as

277 ydrolysed forms of the hapten bound to eight lysine residues was used to detect hapten-specific IgG 1

278 covalently between acetone and the catalytic lysine residue, was found to be the slowest step for the

279 Lysine residues were essential for both receptor-depende

280 Several potential lysine residues were identified as viable caging sites t

281 ulent strains contain multiple trimethylated lysine residues, whereas the avirulent strain contains m

282 stal ubiquitin to produce a glycinylglycinyl-lysine residue which is bound by trypsin.

283 activated Sde2-C fragment with an N-terminal lysine residue, which subsequently gets incorporated int

284 proteins that are phosphorylated at specific lysine residues, which are incompatible with solid-phase

285 bility to form isopeptide bonds with protein lysine residues, which generates N-homocysteinylated pro

286 rivatization of proteins to label unmodified lysine residues with a single glycine tag.

287 rically that substitution of these clustered lysine residues with alanines or asparagines results in

288 Substitution of these lysine residues with arginines (4KR-RasG) diminished Ras

289 his new strategy by labeling solvent-exposed lysine residues with commercially available tandem mass

290 the comparison of the labeling behaviors of lysine residues with the use of low and high concentrati

291 Surprisingly, a single lysine residue within the intracellular domain rescues s

292 at RNF145 triggers ubiquitination of SCAP on lysine residues within a cytoplasmic loop essential for

293 flow cytometry analysis with mutagenesis of lysine residues within CH1, we find that arginine substi

294 for unambiguous assignment of phosphorylated-lysine residues within histone peptides and that these p

295 nt on essential redox-sensitive cysteine and lysine residues within N-terminus of channel protein.

296 ses (HDACs) catalyze deacetylation of acetyl-lysine residues within proteins.

297 ce and in serum from healthy volunteers, the lysine residues within the peptides containing nuclear l

298 nonstructural protein of the virus and that lysine residues within the RPS17 insertion are important

299 o the ORF1 protein of Kernow P6 HEV and that lysine residues within the RPS17 insertion, but not nucl

300 that neutralization of the charges on these lysine residues would allow more stable parallel in-regi