ライフサイエンスコーパス: cysteine

1 ts are reversed by the anti-oxidant N-Acetyl Cysteine.

2 ) is significantly lower than a non-pi-clamp cysteine.

3 of sodium L-ascorbate, DL-Dithiothreitol or cysteine.

4 litate palmitoyl group transfer to substrate cysteine.

5 nces with four amino acids downstream of the cysteine.

6 e addition of diacylglycerol to an invariant cysteine.

7 us of aspartic acid and at the N-terminus of cysteine.

8 hur originates from intake of methionine and cysteine.

9 to retain the highly conserved undecapeptide cysteine.

10 the catalytically indispensable active-site cysteine.

11 oxidation and reduction of their active site cysteine.

12 ce assay for visual chiral discrimination of cysteine.

13 tion and thiol deprotonation of beta-subunit cysteines.

14 bonds in nested patterns and closely spaced cysteines.

15 rotein ligations with no influence on native cysteines.

16 the disulfide bond between the two conserved cysteines.

17 revealed a posttranslational modification on cysteine 328 (C328) by the oxidative adduct malondialdeh

18 We identified the conserved cysteine 97 (Cys-97) to be the only reactive thiol in hu

19 es (ROS) in podocytes and that NAC (N-acetyl-cysteine), a potent antioxidant, significantly eliminate

20 ective CysSSH synthesis from the substrate L-cysteine, a reaction catalyzed by prokaryotic and mammal

21 required site-specific labeling of nonnative cysteines, a labor-intensive process occasionally result

22 d that m4-1BBL formed a covalent dimer via 2 cysteines absent in h4-1BBL.

23 Using the substituted cysteine accessibility method (SCAM), we evaluated the r

24 with a combination of X-ray crystallography, cysteine accessibility, and solution spectroscopy.

25 thiols now allows determination of modified cysteines across the proteome and identification of thos

26 riking biases, such as the (near) absence of cysteine and aspartic peptidases and peptidase inhibitor

27 Similarly, combined N-acetyl-l-cysteine and catalase treatment also suppressed VDAC1-in

28 tes the turnover of SAM for the synthesis of cysteine and glutathione through transsulfuration.

29 presence of physiological concentrations of cysteine and glutathione, while those with longer sulfur

30 f lower than physiological concentrations of cysteine and glutathione.

31 s, some of which were previously ascribed to cysteine and GSH.

32 n was dependent on essential redox-sensitive cysteine and lysine residues within N-terminus of channe

33 GSH motif hosts a [2Fe-2S] cluster via three cysteine and one histidine residues.

34 id Mixture 1, Gelatin Peptone N3, N-Acetyl-L-Cysteine and Pluronic F-68) were assayed in order to imp

35 for serine and histidine tRNAs, while minor cysteine and selenocysteine tRNA species may have a modi

36 Cysteine and serine proteases function via protease-acti

37 gs, but have, so far, been mainly limited to cysteine and serine.

38 n which adds 16-carbon palmitate to specific cysteines and contributes to various biological function

39 er radical SAM proteins, HemW contains three cysteines and one SAM coordinating an [4Fe-4S] cluster,

40 the enzyme; then it oxidizes the peroxidatic cysteine, and finally, the rate-limiting disulfide bond

41 nd the major phosphatase PP2A, dependency on cysteine, and sensitivity to oxidative stress.

42 For example, the cardiac LIM protein, cysteine- and glycine-rich protein 3, is thought to medi

43 experiments demonstrated that the first two cysteines are necessary for McpM to inhibit susceptible

44 Greater than 5% of cysteines are reported to occupy these higher oxidation

45 All four cysteines are required for methylation of As(III) to MAs

46 The pi-clamp cysteine arylation reaction enthalpy of activation (Delt

47 In Turkey, usage of l-Cysteine as a food additive isn't allowed in wheat flour

48 ntaining a caspase recruitment domain (ASC), cysteine aspartase (caspase)-1, and interleukin (IL)-1be

49 Caspases are cysteine aspartate proteases that are major players in k

50 o cell destruction through activation of the cysteine-aspartic protease (caspase) cascade.

51 r major protease mechanistic classes-serine, cysteine, aspartyl, and metallo-proteases-and develop a

52 is facilitated by palmitoylation of a single cysteine at position 739 within the large intracellular

53 ine groups in its deprotonated form, NH2) of cysteine attached on the gold electrode surface.

54 Selenium incorporation was achieved using a cysteine auxotrophic Escherichia coli strain.

55 y of Cys-tRNA(Cys) synthesis (tRNA-dependent cysteine biosynthesis) to prevent challenge of translati

56 oxidation, and is a universal substrate for cysteine biosynthesis.

57 tRNase that is only active when bound to the cysteine biosynthetic enzyme CysK.

58 The cysteine-biotin conjugates remained fully intact, demons

59 each charge state, for both the lysine- and cysteine-biotin conjugates.

60 d by the conversion of tRNA-bounded Sep into cysteine by Sep-tRNA:Cys-tRNA synthase (SepCysS).

61 covalently modifies a critical stress-sensor cysteine (C151) of the E3 ligase substrate adaptor prote

62 troduced the HCM mutation E56G into a single-cysteine (C16) hVELC construct and substituted it for th

63 Cysteine can be synthesized by tRNA-dependent mechanism

64 composite material consisting of N-acetyl-L-cysteine capped CdAgTe quantum dots (NAC-CdAgTe QDs) and

65 sensor is developed to detect DA based on l-cysteine capped Mn doped ZnS quantum dots (l-cys ZnS:Mn

66 dies of payload release suggested that other cysteine cathepsins can cleave the VC(S) linker.

67 vestigate the relationship between exogenous cysteine, cellular metabolism, cellular localization, an

68 MAs(III) to DMAs(III) requires only the two cysteines closest to the C-terminus.

69 ysteine residue of 1Dx5 was substituted by a cysteine codon through site-directed mutagenesis.

70 the chemical reaction of [C2mim][OAc] with a cysteine-containing biomolecules can be tuned or even su

71 alysis of four small organic molecules and a cysteine-containing peptide we could postulate a general

72 ate to and are stabilized by a wide range of cysteine-containing peptides and the assembly of iron-su

73 xtensive persulfide formation is apparent in cysteine-containing proteins in Escherichia coli and mam

74 Both cobalt and cysteine coupling resulted in a high-density array of NF

75 Predictive cysteine cross-linking in E. coli membranes and PELDOR m

76 alytical system is based on the oxidation of cysteine (CSH) with hydrogen peroxide (H2O2) enzymatical

77 In this study, we used cysteine (Cys) mutants to test differential palmitoylati

78 lectrophiles through covalent binding at its cysteine (Cys) thiol group, followed by stepwise catalyz

79 Biothiols, such as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH

80 ein kinases changing in abundance, including cysteine (Cys)-rich receptor-like kinases (CRKs) that ar

81 inactivation through oxidation of a critical cysteine (Cys195) in the third transmembrane helix of Or

82 containing 3, interleukins 1beta and 6, and cysteine-cysteine chemokine ligand 5 [CCL5]) and profibr

83 ated with the artificial protease FeBABE and cysteine-cysteine cross-linking.

84 hydrogen bonding between an aspartate and a cysteine (D156-O...S-C128) that would define a direct-cu

85 We demonstrate that IpoC installs a cysteine-derived thiazoline, whereas PurCD alone is suff

86 unexplained processing of the mitochondrial cysteine desulfurase Nfs1 in yeast.

87 cture-function properties of a mitochondrial cysteine desulfurase.

88 Unlike prokaryotic cysteine desulfurases, the SDA structure adopts an unexp

89 Gallic acid and l-cysteine did not exhibit browning inhibition effect at t

90 n is intimately tied to the function of both cysteine dioxygenases (CDOs) and nitrile hydratases (NHa

91 00 s(-1)) and quantify the energetics of the cysteine disulfide redox-reaction (reversible potentials

92 Under reducing conditions, the cysteines do not form disulfides, but under oxidizing co

93 analysis of sporozoite factors reveals the 6-cysteine domain protein P36 as a major parasite determin

94 s an adenylation domain but lacks a distinct cysteine domain.

95 showed that modification of a conserved BiP cysteine during stress beneficially alters BiP chaperone

96 st, miropin uniquely blocked many serine and cysteine endopeptidases of disparate architecture and su

97 tical role for the N glycosylation sites and cysteines for the structure and function of the amino te

98 Mutation of the cysteines forming the disulfide loop of the platelet GPI

99 -4-methylpentan-2-one-N-(l-gamma-glutamyl)-l-cysteine (gammaGluCys-4MMP) but at too low concentration

100 phosphatidylethanolamine to this N-terminal cysteine, generating a mature, triacylated lipoprotein.

101 e potential interference from ascorbic acid, cysteine, glutamic acid, and glucose was also studied, a

102 in which a nitroxide spin label attached to cysteine has been introduced at its N-terminus.

103 erately added to various flour types since l-Cysteine has enabled favorable baking conditions such as

104 Group F TabZIPs contain the group-defining cysteine-histidine-rich motifs, which are the predicted

105 g bioavailability in swordfish (glutathione, cysteine, homocysteine).

106 Cysteine, homocysteine, glutathione, quercetin, albumin

107 Acid ceramidase (AC) is a lysosomal cysteine hydrolase that catalyzes the conversion of cera

108 Cysteine hydropersulfide (CysSSH) occurs in abundant qua

109 Substitution of cysteine in AOX1A by glutamate mimicked its activation b

110 position 112, which is arginine in apoE4 and cysteine in apoE3.

111 a concomitant decrease of cystathionine and cysteine in blood and tissues.

112 ed to be energy-dependent and is enhanced by cysteine in diverse species of bacteria under aerobic an

113 res efficiently inserted serine, alanine and cysteine in response to stop and sense codons, depending

114 ) for regio- and chemoselective arylation of cysteine in ribosomally produced proteins.

115 However, no cysteine in the protein was modified; instead, we demons

116 determine the enantiomeric excess (ee) of D-cysteine in the whole range of ee values (from -100% to

117 tive method was developed for detection of l-Cysteine in wheat flour using Raman microscopy.

118 Detection of l-Cysteine in wheat flour was accomplished successfully us

119 t C91 has the highest redox potential of all cysteines in MAL.

120 onal reagents of multiple predicted pairs of cysteines in TMH 6 and 12 and 6 and 9.

121 l-Cysteine is deliberately added to various flour types si

122 How this cysteine is reduced to reestablish 'normal' BiP activity

123 vealing that a central core of palmitoylated cysteines is essential for aggregation of ANCL CSPalpha

124 ribed carbon-sulfur lyase SUR1 in processing cysteine-isothiocyanate conjugates, as well as the S-met

125 lent linkages between lectin molecules and a cysteine layer immobilized over gold-coated TiO2 butterf

126 wild-type hCNT1 and the corresponding TMs of cysteine-less NupC(C-) yielded results that validate the

127 Sulfide and cysteine ligand-exchange reactions with as-synthesized C

128 geting of the catalytic subunit of glutamate cysteine ligase (Gclc) blocked GSH production specifical

129 quinone 1, glutathione reductase, glutamate-cysteine ligase catalytic subunit, ABCC1, peroxiredoxin

130 Cysteine linkages are likely to enhance electron flow al

131 a reactive metabolite that forms adducts on cysteine, lysine and arginine residues of proteins, ther

132 r, or an extra amine group such as arginine, cysteine, lysine, methionine, and tryptophan had the str

133 n changes, part of which was attributable to cysteine-mediated dimer formation.

134 This mutation transformed cells via cysteine-mediated intermolecular disulfide bonds, leadin

135 e a model to explain the interplay between l-cysteine metabolism, H2S production, and oxidative stres

136 Large-scale characterisation of cysteine modification is enabling study of the physicoch

137 Overexpression of a PP1c cysteine mutant (C127S-PP1c) abrogated the H2S effect on

138 Comparison of N-linked glycosylation and cysteine mutant replication kinetics identified disparat

139 Spin-labeled double-cysteine mutants of VcSiaP were analyzed in the substrat

140 Cysteine mutants retain function and stability for doubl

141 nd the application of ROS scavenger N-acetyl cysteine (NAC) completely blocked these effects by S17 i

142 on with acetyl-L-carnitine (LAC) or acetyl-N-cysteine (NAC) rapidly increases xCT and activates a net

143 rocess, an isoprenoid group is attached to a cysteine near the C terminus of a substrate protein by p

144 when the PTL was conjugated to an engineered cysteine near the dopamine binding site.

145 inst 12 RGS proteins, as well as against the cysteine-null mutants for 10 of these proteins.

146 ing the polyhistidine tail to include a free cysteine on each protomer of model BG505 NFL trimers to

147 oxidation to a disulfide with a neighboring cysteine or dissociation upon reduction of Fe(3+)- to Fe

148 ino acids (4R)-hydroxyproline and proline by cysteine or homocysteine, which reduces the preorganizat

149 We discovered that the combination of cysteine or other small thiols with either isoniazid or

150 ered by depleting the cell of the amino acid cysteine, or by inhibiting the phospholipid hydroperoxid

151 od was shown to be highly chemoselective for cysteine over other potentially nucleophilic residues, a

152 by reviewing chemical principles underlying cysteine pairing and oxidation.

153 f protein characterization to ensure correct cysteine pairings.

154 tional importance of conserved extracellular cysteine pairs in CSF3R and suggest the necessity for br

155 e further showed that disruption of original cysteine pairs in the CSF3R extracellular domain resulte

156 Phytocystatins are reversible inhibitors of cysteine peptidases that are found naturally in plants.

157 sfer of the sulfane sulfur from an SQR-bound cysteine persulfide intermediate to a small-molecule acc

158 ts that these enzymes serve as the principal cysteine persulfide synthases in vivo.

159 Cysteine-persulfide (Cys-SSH) is a cysteine whose sulfhy

160 CARSs also catalyze co-translational cysteine polysulfidation and are involved in the regulat

161 In vivo, EspL cysteine protease activity contributes to persistent col

162 calpain with high selectivity versus related cysteine protease cathepsins, other proteases, and recep

163 ve mechanisms to fine-tune the activity of a cysteine protease dubbed RD21 (RESPONSIVE TO DESICCATION

164 he activity of EspL defines a family of T3SS cysteine protease effectors found in a range of bacteria

165 ity ligation (ADPL), to serine hydrolase and cysteine protease enzymes enables quantification of diff

166 The cysteine protease inhibitor cystatin C is internalized b

167 ile and ubiquitously-expressed member of the cysteine protease inhibitor family that is present at no

168 le abnormalities similar to that seen with a cysteine protease inhibitor, E-64 (I-1).

169 A secreted cysteine protease known as streptococcal pyrogenic exoto

170 Cathepsin L (Cat L) is a cysteine protease that can proteolytically activate CCAA

171 opeptidase (AEP) or legumain, is a lysosomal cysteine protease that cleaves both amyloid precursor pr

172 n of the gene encoding cathepsin S (Ctss), a cysteine protease that cleaves invariant chains and prod

173 al extension also encode a sequence-specific cysteine protease, Prp, which carries out this cleavage.

174 n system in rice by combining Brassica napus cysteine-protease gene (BnCysP1) with anther-specific P1

175 erility, the coding region of Brassica napus cysteine protease1 (BnCysP1) was isolated from developin

176 The caspase family of cysteine proteases are highly sought-after drug targets

177 article describes a novel role for Giardia's cysteine proteases in pathogenesis and how Giardia's dis

178 a family of intracellular, calcium-dependent cysteine proteases involved in a variety of regulatory p

179 c peptide sequence for the inhibition of the cysteine proteases rhodesain of Trypanosoma brucei rhode

180 to investigate the substrate specificity of cysteine proteases, serine proteases and metalloproteina

181 The 6-cysteine protein P47, known to be important for P. bergh

182 Cathepsin S is one of the most important cysteine proteinases and plays key roles in nematodes an

183 ntration range and drastically different d/l-cysteine ratios in simulated body fluids.

184 reactive oxygen species scavenger N-acetyl-l-cysteine reduced the levels of interleukin-6, interleuki

185 eficient T cells with metabolically active L-cysteine rescued mTOR activation and proliferation but n

186 The mutation of cysteine residue 107 in NDUFB10 impaired oxidation and e

187 ed by maleimide coupling of NOTA to a unique cysteine residue and chelation of (18)F-AlF.

188 itor, 3-bromopyruvate, also targets the same cysteine residue and that our electrophilic quinazolines

189 eat and contained an extra repetitive-domain cysteine residue in 1Dx5 that was important for understa

190 demonstrate the in situ labeling of a buried cysteine residue in BSA during extensional stress.

191 reductase, independently of H2O2 A conserved cysteine residue in OxyR2 is critical for this function.

192 of the 1Ax1 gene corresponding to the extra cysteine residue of 1Dx5 was substituted by a cysteine c

193 holipid to the amine group of the N-terminal cysteine residue of the apolipoprotein.

194 , the role of this highly conserved reactive cysteine residue remains largely unknown.

195 rc homology 2 (SH2) or SH3 domains or of the cysteine residue that undergoes LPS-induced palmitoylati

196 pically have severe effects, mutation of the cysteine residue to alanine has minor effects on overall

197 We show that one natural cysteine residue, Cys327, out of three, has an enhanced

198 or stabilized oxidation of SHP-1's catalytic cysteine residue, which inhibited the tyrosine-phosphata

199 minal undecapeptide, which contains a single cysteine residue.

200 R domain of FisR through the three conserved cysteine residues (C53, C64 and C71), FisR activates the

201 strategy, we identified 1,276 S-nitrosylated cysteine residues [S-nitrosothiol (SNO)] on 491 proteins

202 al infectivity by >100-fold and included two cysteine residues and neighboring residues.

203 Three cysteine residues and one disulfide bond conserved withi

204 Vicinal disulfides between sequence-adjacent cysteine residues are very rare and rather startling str

205 mic one another by substituting the variable cysteine residues at position III in the protein.

206 experiments produced similar results of many cysteine residues bound to N-acetylglucosamine (GlcNAc).

207 rmolecular disulfide bonds between conserved cysteine residues in neurexins and CA10.

208 functional analysis of the role of reactive cysteine residues in the protein.

209 d VKORL form disulfide-linked oligomers, the cysteine residues involved in the oligomerization appear

210 t in Cox4i2(-/-) PASMCs and was dependent on cysteine residues of Cox4i2.

211 lysis showed that ACR-adducts were formed on cysteine residues of some synaptic proteins.

212 ins through site-selective bis-alkylation of cysteine residues present as disulfides under mild and b

213 is regulated by palmitoylation of C-terminal cysteine residues that allows Golgi localization.

214 ding bulls and humans, also contain multiple cysteine residues that form intra- and interprotamine su

215 amino acid motif and including six conserved cysteine residues that form intramolecular disulfide bon

216 donating the sulfur atom of their exclusive cysteine residues to the substrate.

217 d histidine and intact histidine, lysine, or cysteine residues were discovered and characterized from

218 is approach utilizes sequential unmasking of cysteine residues with orthogonal protection to enable s

219 nteractions through covalent modification of cysteine residues within the RGS domain that are located

220 of a pair of hydrogen atoms from juxtaposed cysteine residues, contrasts with the substantial change

221 ing chemical reagents specific for lysine or cysteine residues, identification of gas-phase fragmenta

222 oach utilizes conjugation to native antibody cysteine residues, it is widely applicable and enables h

223 y, our data support that the seven conserved cysteine residues, present within the SPASM domain, are

224 y depends on one or two catalytically active cysteine residues, the peroxidatic Cys (CP) and, if pres

225 oxic moiety covalently linked, via lysine or cysteine residues, to a monoclonal antibody (mAb) scaffo

226 conjugated with biotin via native lysine and cysteine residues, under native-MS and solution conditio

227 d, activity was dependent on the presence of cysteine residues.

228 lmon nuclei despite salmon protamine lacking cysteine residues.

229 xidative post-translational modifications of cysteine residues.

230 ested disulfide bonds and motifs of adjacent cysteine residues.

231 thyltransferase requiring only two conserved cysteine residues.

232 ave ArsM orthologs with only three conserved cysteine residues.

233 the cell membrane through palmitoylation of cysteine residues.

234 5-aminoacid peptide guanylin containing four cysteine residues; the net simulation time using Amber f

235 e Herpesviridae; mutation of the active site cysteine results in a loss of enzymatic activity.

236 c crystals, whereas DNA functionalization of cysteines results in AB2 packing.

237 We show that NFS1 encodes a nodule-specific cysteine-rich (NCR) peptide.

238 ber of antimicrobial peptides, called nodule cysteine-rich (NCR) peptides, to control the outcome of

239 isingly, Loxl3 N-terminal scavenger receptor cysteine-rich (SRCR) repeats, rather than the C-terminal

240 Defensins are cysteine-rich cationic antimicrobial peptides contributi

241 inge domain (HD) and an intact extracellular cysteine-rich domain (CRD).

242 Stac3 protein (SH3 and cysteine-rich domain 3) is an essential component of the

243 Binding of a modulatory antibody to the cysteine-rich domain liberates the catalytic domain from

244 cipated architecture in which the C-terminal cysteine-rich domain partially occludes the enzyme activ

245 Wnts bind FZD cysteine-rich domains (CRDs) with high affinity through

246 at similar to other TNFRSFs, m4-1BB has four cysteine-rich domains (CRDs).

247 s process is orchestrated by nodule-specific cysteine-rich peptides (NCRs) delivered into developing

248 ibes chemistry that is broadly applicable to cysteine-rich peptides and the influence of a fourth dis

249 Among them, the Plasmodium falciparum Cysteine-Rich Protective Antigen (PfCyRPA) is a crucial

250 wth factor-like (EGF) repeats are also small cysteine-rich protein motifs that can be O-glycosylated

251 nd Western blot analysis, reversion-inducing cysteine-rich protein with kazal motifs (Reck) was ident

252 Highly diverse small cysteine-rich proteins (CRPs) have been found to play mu

253 well known that RET mutations affecting the cysteine-rich region of the protein (MEN2A-like mutation

254 opsis thaliana) that has similarities to the cysteine-rich zinc-binding domain of DnaJ chaperones.

255 5, Ala846, Leu847, and Gly848-located in the cysteine-serine-rich domain (CSRD).

256 ptide macrocyclization through perfluoroaryl-cysteine SNAr chemistry to improve the ability of peptid

257 protein secreted protein acidic and rich in cysteine (SPARC) is up-regulated and expressed intracell

258 We therefore conclude that germline ENPP1 cysteine-specific mutations, primarily affecting the mel

259 k, water-dispersible N-acetylcysteine- and l-cysteine-stabilized palladium nanoparticles are introduc

260 products with high sensitivity, we developed cysteine-stable isotope labeling using amino acids in ce

261 aptosomal-associated protein 25 (SNAP25) and cysteine string protein alpha (CSPalpha).

262 f the neighbouring leucine-116 (L116) in the cysteine-string domain cause CSPalpha to form high molec

263 The importance of specific residues in the cysteine-string domain was investigated, revealing that

264 ggregates is linked to palmitoylation of the cysteine-string domain, however the regions of the mutan

265 ical probe that specifically labels reactive cysteine sulfhydryls.

266 They are assembled from iron and cysteine sulfur on protein scaffolds.

267 PYK2 downregulation, l-cysteine supplementation, or CSE overexpression alleviat

268 blocking (or oxidation) of GAPDH active site cysteines suppressed GAPDH/Ape1 interaction and potentia

269 11 nM) is comparable to that of the E. coli cysteine synthase complex (K d 6 nM), and both complex

270 an effectively displace CysE from pre-formed cysteine synthase complexes, enabling toxin activation e

271 ng arsenate reductase (HAC1), gamma-glutamyl-cysteine synthetase (gamma-ECS), phytochelatin synthase

272 hypothesized this could be overcome using a cysteine-targeted irreversible inhibitor.

273 cids and biothiols do not interfere with the cysteine-targeted sensing.

274 Cysteine targets for S-palmitoylation, S-glutathionylati

275 e repressor by introduction of an additional cysteine that allows for three-coordinate As(III) bindin

276 alpha-Conotoxins have four cysteines that can have three possible disulfide connect

277 sents the first characterization of unpaired cysteines that mediate both gain- and loss-of-function p

278 etreatment with the ROS scavenger N-acetyl-L-cysteine, the ERK1/2 inhibitor UO126, or ERK1/2 siRNA kn

279 N-acetyl-L-cysteine therapy has been used in clinical studies; howe

280 we explore the effect of low dose N-acetyl-L-cysteine therapy, delivered using a targeted, systemic,

281 Cysteine thiols are among the most reactive functional g

282 osation (SNO), a redox-based modification of cysteine thiols.

283 eact with intact histidine, lysine, and free cysteine to form cross-links.

284 A cysteine-to-alanine mutation in LLO rendered the protein

285 n through the analysis of knock-in mice with cysteine-to-alanine substitution at the palmitoylated re

286 nt strain of L. monocytogenes expressing the cysteine-to-alanine variant of LLO was able to infect an

287 ession of NFS1 cooperates with inhibition of cysteine transport to trigger ferroptosis in vitro and s

288 In delta-proteobacteria, an additional cysteine tRNA with an 8/4 structure mimics selenocystein

289 enocysteine residues were replaced mainly by cysteine, tryptophan and arginine in a codon-specific ma

290 ficant effect on several compounds (proline, cysteine, tryptophan, phenylalanine, alpha-terpineol and

291 roups, such as the side chains of serine and cysteine, using electrophilic probes.

292 tects E. coli against oxidative stress via l-cysteine utilization and H2S-mediated sequestration of f

293 102 was bound directly to nanocapsid surface cysteines via direct ligand exchange.

294 fidelity, and may reflect the mechanism that cysteine was originally added into genetic code.

295 tion mass spectrometry (HRMS) revealing that cysteine was the preferred nucleophile for acrylamide el

296 Besides the sulfhydryl group of a cysteine, we make use of an azido group of a p-azido-l-p

297 Cysteine-persulfide (Cys-SSH) is a cysteine whose sulfhydryl group is covalently bound to s

298 inetics of the interactions between L- and D-cysteine with CdTe QDs led to chiral recognition of thes

299 Substitution of the thiol proton in cysteine with m-carborane furnished 2-amino-3-(1,7-dicar

300 McpM has four cysteines within the mature peptide and site-directed mu