ライフサイエンスコーパス: lysine residue

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

2 ther undergoes ubiquitylation on a conserved lysine residue.

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

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

5 macroH2A1/2 at the divergent N-terminal tail lysine residue.

6 pocket that normally accommodates the target lysine residue.

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

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

9 ostatic contacts involving several conserved lysine residues.

10 ranslation modification (PTM) that occurs on lysine residues.

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

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

13 lagens by mediating oxidative deamination of lysine residues.

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

15 evealed that podocin is ubiquitylated at two lysine residues.

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

17 ein interaction interfaces with little or no lysine residues.

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

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

20 nctions in the cell by deacetylating histone lysine residues.

21 e specific to particular protein domains and lysine residues.

22 lard reaction between the reducing sugar and lysine residues.

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

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

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

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

27 nucleotide-binding sites, but not at distant lysine residues.

28 reby instructs Rsp5 to ubiquitinate proximal lysine residues.

29 chment of inorganic polyphosphate (polyP) to lysine residues.

30 e S -> N-transfer of acyl groups to proximal lysine residues.

31 forms a stable, positively charged label at lysine residues.

32 and 2 can efficiently myristoylate specific lysine residues.

33 containing 235 glycated and 303 non-glycated lysine residues.

34 ctive amino acids within proteins, typically lysine residues.

35 at acts as the primary reader for acetylated lysine residues.

36 stone-methylation, and ethylation of histone lysine residues.

37 is on bromodomains, which bind to acetylated lysine residues.

38 eds via Schiff base chemistry facilitated by lysine residues.

39 bind a retinal chromophore with a conserved lysine residue [1, 2].

40 teract, whereupon SIRT1 deacetylates BRG1 at lysine residues 1029 and 1033, stimulating its ATPase ac

41 (+162.1 Da), partially processed heavy chain lysine residues (+128.1 Da), and loss of N-acetylglucosa

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

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

44 density is surrounded by the side chains of lysine residues 290 and 294 from R2 and lysine 370 from

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

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

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

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

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

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

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

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

53 Mutations of the transmembrane lysine residues ablate retrograde sorting and subject Sn

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

55 sult of increased acetylation of key histone lysine residues (acetylated histone 3 lysine 27 and hist

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

57 olactone then chemically reacts with protein lysine residues, affording KHcy-protein.

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

59 pha-lysine residues in melittin with epsilon-lysine residues and identified key residues that are imp

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

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

62 The lysine residues and the ubiquitination of BFRF1 regulate

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

64 Oxidized collagen, wherein lysine residues are converted to the aldehyde allysine,

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

66 In cells expressing Msh3 in which these lysine residues are mutated to arginine, the inhibitory

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

68 ubsites, and mutagenesis identified a mobile lysine residue as a key determinant of positional specif

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

70 We identified four lysine residues as the sites of ubiquitination and showe

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

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

73 as Lys-48-ubiquitin, which has only a single lysine residue at position 48.

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

75 Here, we show how acetylation of lysine residues at position 7 of characteristic heptad r

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

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

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

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

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

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

82 Here, we identify the lysine residues at which EZH1/EZH2 are automethylated wi

83 ate of Zta may be determined by the specific lysine residue being modified.

84 Our data add another key function to this lysine residue, besides its roles in viral DNA replicati

85 dermethylated at three contiguous N-terminal lysine residues but not at central or C-terminal regions

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

87 silon-amino groups of two internal conserved lysine residues by co-expressed toxin-activating acyltra

88 HATs) catalyze the acetylation of substrate lysine residues by employing the cofactor acetyl-coenzym

89 and FljB, are methylated at surface-exposed lysine residues by FliB.

90 The modification of protein lysine residues by the thioester homocysteine (Hcy)-thio

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

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

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

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

95 o direct fragmentation almost exclusively to lysine residues containing the charged label.

96 l peptides from ubiquitinated and unmodified lysine residues following trypsin digestion and secondar

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

98 odies containing a natural uniquely reactive lysine residue for site-specific conjugation to beta-lac

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

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

101 ity to modify the net charge of the modified lysine residue from + 1 to - 1 at physiological pH.

102 lity using a series of proteins with various lysine residues from multiple sample sources, with accum

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

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

105 re frataxin (79-207) in which the N-terminal lysine residue has been lost.

106 handful of proteins carrying Hcy on specific lysine residues have been identified and quantified in h

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

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

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

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

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

112 valent manner via conjugation to a catalytic lysine residue in the ATP-binding pocket of the enzymes,

113 Thus, substituting a single lysine residue in the context of a P301S disease-linked

114 ining receptors, and that a methionine and a lysine residue in the ligand binding pocket (GluN2D-Met7

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

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

117 ains used for modification of their acylated lysine residue in the second, more conserved acylation s

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

119 acute MGO toxicity or carboxymethylation of lysine residues in cells.

120 2-oxoglutarate 5-dioxygenase 2) hydroxylates lysine residues in collagen telopeptides and is essentia

121 (LH) isoform that specifically hydroxylates lysine residues in collagen telopeptides, a post-transla

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

123 We also noted a decrease in glycated lysine residues in collagen, indicating that the imine f

124 etyl group from the side chain of acetylated lysine residues in cytoplasmic proteins such as alpha-tu

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

126 cetylations at highly conserved cysteine and lysine residues in Gag and Gag-Pol polyproteins.

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

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

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

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

131 Methylation of lysine residues in histone proteins is catalyzed by S-ad

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

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

134 Acetylation of the lysine residues in histones and other DNA-binding protei

135 troducing thiol functional groups onto three lysine residues in IgGs using Fc affinity peptide reagen

136 by an E1 ligase inhibitor or by mutating two lysine residues in intracellular loop three causes Smo t

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

138 We systematically replaced three alpha-lysine residues in melittin with epsilon-lysine residues

139 Five key lysine residues in Msh3 are direct targets of HDAC3 deac

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

141 PAI-1 confirmed an essential requirement of lysine residues in PAI-1 for the interactions of both PA

142 -7) catalyze the removal of acyl groups from lysine residues in proteins in an NAD(+)-dependent manne

143 direct RNF168 orientation towards the target lysine residues in proximity to the H2A alpha1-extension

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

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

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

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

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

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

150 iated with an increase in the acetylation of lysine residues in the cysteine-rich domain of NPC1.

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

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

153 y oxPLs, forming stable pyrrole adducts with lysine residues in the helices 3-4 of another apoA-I or

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

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

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

157 Several lysine residues in the intrinsically disordered AL are a

158 Degradative sorting requires lysine residues in the juxtamembrane region of Snc1 and

159 his analysis revealed that mutation of three lysine residues in the lyase active site of pol beta, 35

160 eraction between tau and LRP1 is mediated by lysine residues in the microtubule-binding repeat region

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

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

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

164 are necessary for recognition of acetylated lysine residues in the N-terminal regions of histones.

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

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

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

168 Mutation of four out of a total of nine lysine residues in Zta largely abrogates its ubiquitinat

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

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

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

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

173 of the small ubiquitin-like protein NEDD8 to lysine residues, interrupts degradation of DNMT3A1.

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

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

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

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

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

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

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

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

182 l function of the acetylation of HBsu at key lysine residues is to regulate nucleoid compaction, anal

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

184 ough a mechanism dependent on its C-terminal lysine residue; its deletion led to modest reductions in

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

186 4 lysine residues (K(38)KKK) located in the N-terminal dom

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

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

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

190 tosis SETD6 binds and methylates PLK1 on two lysine residues: K209 and K413.

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

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

193 -1 by promoting K27-linked ubiquitination at lysine residues K32 and K263 on Beclin-1.

194 SIRT6 deacetylated DDB2 at two lysine residues, K35 and K77, upon UV stress and then pr

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

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

197 t human PRC2, we identified three methylated lysine residues (K510, K514, and K515) on a disordered b

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

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

200 p53, and that substitution of the conserved lysine residue K66 in the SMG7 14-3-3-like domain with t

201 We also identify that acetylation of two key lysine residues, K69 and K285, present on the DIX and PD

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

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

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

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

206 analysis in HEK293 cells, we identified six lysine residues (Lys-556, -1155, -1230, -1465, -1475, an

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

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

209 of PI3K signals depends on IFITM3 using two lysine residues (Lys83 and Lys104) in its conserved intr

210 Zta mutant carrying mutations at these four lysine residues (lysine 12, lysine 188, lysine 207, and

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

212 ated SM degradation and show that neither SM lysine residues nor the N terminus impart instability.

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

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

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

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

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

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

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

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

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

222 0) acetyltransferase mediates acetylation at lysine residues of SPZ1 at positions 369 and 374, and of

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

224 ts whether both or only one of two conserved lysine residues of the protoxin will be posttranslationa

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

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

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

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

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

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

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

232 iption by selectively recognizing acetylated lysine residues on chromatin.

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

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

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

236 er proteins that bind to specific acetylated lysine residues on histone tails where they facilitate t

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

238 a protein module that recognizes acetylated lysine residues on histones and other proteins, has rece

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

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

241 We uncovered four lysine residues on Ssa1, K86, K185, K354 and K562 that a

242 ompact chromatin, suggesting that acetylated lysine residues on the H3 tail domain play distinct role

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

244 We show that acetylation of two key lysine residues on TULP3 by p300 increases TULP3 protein

245 The ubiquitin modification targets 4 lysine residues on Zta, leading to both mono- and polyub

246 Mutation of a single SUMO-targeted lysine residue perturbs telomere dynamics.

247 Lysine residues play a role in templating the formation

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

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

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

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

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

253 S-acylate and N-acylate protein cysteine and lysine residues, respectively.

254 how that the inability to acetylate key HBsu lysine residues results in a more compacted nucleoid.

255 JD6 is reported to catalyze hydroxylation of lysine residue(s) of histones, the tumor-suppressor prot

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

257 that lactate-derived lactylation of histone lysine residues serves as an epigenetic modification tha

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

259 Acetylation or mutation of the lysine residue stabilizes FAAP20 by preventing its ubiqu

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

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

262 n ubiquitination and acetylation of a common lysine residue that controls FAAP20 stability and highli

263 ific toxin-channel interaction between a key lysine residue that serves as a "stinger" and penetrates

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

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

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

267 adjoining sequence motifs, and also internal lysine residues that function as polyubiquitylation site

268 46 treatment blocked acetylation of specific lysine residues that regulate p53 activity.

269 Herein, we report 12 DVL-1 lysine residues that show differential acetylation in re

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

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

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

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

274 Acylation at lysine residues through HlyC is known to activate proHly

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

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

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

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

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

280 mediated by three conserved, surface-exposed lysine residues (triK), which were previously shown to b

281 achine, to predict glycated and non-glycated lysine residues using structural properties of amino aci

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

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

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

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

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

287 53(KQ) mouse where all the C-terminal domain lysine residues were mutated to glutamines (K to Q mutat

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

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

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

291 through chemical modification of accessible lysine residues, which often results in heterogeneous po

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

293 L-lysine (EPL), a polypeptide formed by ~ 25 lysine residues with known antimicrobial activity agains

294 anages to classify glycated and non-glycated lysine residues with promising results consistently on v

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

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

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

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 Lysine residues within the transmembrane domain of Snc1