ライフサイエンスコーパス: autocatalytic

1 luster edges, implying tetramer formation is autocatalytic.

2 ee energy barrier of 36.1 kcal/mol and to be autocatalytic.

3 and the specific ribosome synthesis rate is autocatalytic.

4 ndicating that the covalent flavinylation is autocatalytic.

5 nts of axon/dendrite formation involve local autocatalytic activation and long-range inhibition, as p

6 cells to generate metabolic oscillations via autocatalytic activation by its product fructose 1,6-bis

7 he PC7 precursor protein undergoes efficient autocatalytic activation in both oocytes and embryos.

8 To explore the model's assumption of an autocatalytic activation mechanism, we imaged cells expr

9 The autocatalytic activation of an initiator caspase, exempl

10 Autocatalytic activation of epidermal growth factor rece

11 was upregulated in SKOV3 cells, resulting in autocatalytic activation of HtrA1.

12 1 is approximately 3000-fold higher, and the autocatalytic activation of MASP-1 is about 140-fold fas

13 The obesity is associated with impaired autocatalytic activation of mature PC1 and reduced hypot

14 Autocatalytic activation of Parkin bolsters its accumula

15 signal of bioanalytical assays based on the autocatalytic activation of these mutated proenzymes.

16 Autocatalytic activation was retarded in glyco-pro-KLK2,

17 enzyme molecule of the same protease, and 2) autocatalytic activation, when the activated protease cl

18 regulate its multistep, compartment-specific autocatalytic activation.

19 as an excitable system in which a diffusive, autocatalytic activator causes actin polymerization; F-a

20 First, they showed that a 55-kDa autocatalytic active form of calpain is detected on immu

21 onstitutively active enzyme, with high basal autocatalytic activity and high basal activity toward pe

22 atalytic domain) display high basal Ser(916) autocatalytic activity and robust activity toward CREBti

23 tion requires ATG7 as the E1 enzyme and ATG3 autocatalytic activity as the E2, resulting in the coval

24 of ADAMTS17 requires O-fucosylation and its autocatalytic activity does not depend on propeptide pro

25 available for several classes of enzymes and autocatalytic activity encoded by nonenveloped viruses.

26 Furthermore, enhanced autocatalytic activity of pro-caspase-1 was observed fol

27 PCSK9 has autocatalytic activity that releases the prodomain at th

28 Neither LC/A3 nor LC/A4 possessed autocatalytic activity, a property of LC/A1 and LC/A2.

29 he inflammasome results in initiation of its autocatalytic activity, culminating in self-cleavage tha

30 s, identified 21 protein kinases that showed autocatalytic activity.

31 ty paradigm, which appears to be general for autocatalytic additions to heme prosthetic groups, sugge

32 lar particle agglomeration, B + B --> C, and autocatalytic agglomeration, B + C --> 1.5C, involved in

33 ally and rationalized mechanistically for an autocatalytic alkylation reaction.

34 Different autocatalytic and 'self-replicative' molecular species h

35 s likely to contain a subsystem that is both autocatalytic and able to survive on some ambient 'food'

36 self-assembles into nanostructures, coupling autocatalytic and assembly pathways to realize a reprodu

37 Chemical Mn(II) oxidation is autocatalytic and consists of a homogeneous and a hetero

38 However, those reactions with aniline were autocatalytic and had significant induction periods ( ap

39 Original feed forward, autocatalytic, and cross-catalytic systems have been des

40 ities of the two-segment compound enable the autocatalytic, and in general ROS-mediated, activation o

41 The process is treated as autocatalytic, and the kinetic profiles are fit using a

42 nd serve as mother filaments to initiate the autocatalytic assembly of the branched actin filament ne

43 e; however, it remains to be seen whether an autocatalytic-based drug delivery system has an advantag

44 ysts have been previously reported, coupling autocatalytic behavior to macromolecular self-assembly h

45 branches are generated by existing branches (autocatalytic behavior) or independently of existing bra

46 e case of upregulation gave rise to systemic autocatalytic behavior.

47 e molecular processes that give rise to this autocatalytic behavior.

48 sible chemical and physical stimuli, and the autocatalytic behaviours within DCLs which can result in

49 to build a network of organic reactions with autocatalytic, bistable and oscillatory behaviour, we id

50 ing/capping-protective zone (5.4 nm) and the autocatalytic branch rate (0.43/sec).

51 nmol/min for 2 min or more, which sets up an autocatalytic cascade triggered by activating type 2 nit

52 Autocatalytic chemical reactions are widely studied as m

53 Autocatalytic chemical reactions, whereby a molecule is

54 We show that an autocatalytic chemical transition between these forms ac

55 en involves large conformational changes and autocatalytic chemistry that can be hampered by small mo

56 ses with single-stranded RNA genomes undergo autocatalytic cleavage (autocleavage) as a maturation st

57 id substitution reduces the efficiency of Hh autocatalytic cleavage and its signaling function.

58 ondrial processing peptidase and Oct1 and an autocatalytic cleavage at a highly conserved LGST motif

59 ct whose existence supports the mechanism of autocatalytic cleavage at FlhB residue N269.

60 Surprisingly, autocatalytic cleavage does not depend on proper localiz

61 sitol-linked protein and undergoes a partial autocatalytic cleavage during its intracellular processi

62 in GPCR proteolytic site motifs that undergo autocatalytic cleavage during receptor processing to cre

63 We predict that regulated autocatalytic cleavage elements within pre-mRNAs may be

64 Thus the autocatalytic cleavage in Dronc induces its stable dimer

65 The present results show that while autocatalytic cleavage is necessary for proper substrate

66 s serine proteinase activity and can undergo autocatalytic cleavage liberating distinct fragments.

67 wn protein fold and a functionally important autocatalytic cleavage mechanism and provides a framewor

68 tivation of the AIM2 inflammasome results in autocatalytic cleavage of caspase-1, resulting in the pr

69 Here we demonstrate that the autocatalytic cleavage of Dronc, an important initiator

70 inositol hexakisphosphate (InsP6) induces an autocatalytic cleavage of the toxins, releasing an N-ter

71 lowered from 7.6 to 5, and this activates an autocatalytic cleavage of the viral subunit at residue 5

72 dimension between pH 5.5 and 5 requires the autocatalytic cleavage to achieve its final compact size

73 tide precursor that undergoes intramolecular autocatalytic cleavage to generate a fully active hetero

74 Hemojuvelin normally undergoes an autocatalytic cleavage, and as in vivo, recombinant hemo

75 Owing to its rapid autocatalytic cleavage, however, procaspase-9 per se con

76 e 226 on delta-secretase and accelerates its autocatalytic cleavage, leading to its cytoplasmic trans

77 ssion disrupts prohormone convertase 2 (PC2) autocatalytic cleavage, processing of secretogranin II t

78 The ADGRE2 receptor undergoes autocatalytic cleavage, producing an extracellular subun

79 dgehog (hh) encodes a protein that undergoes autocatalytic cleavage, releasing a signaling molecule i

80 After initial autocatalytic cleavage, the prosegment remains tightly a

81 ngle polypeptide (propeptide) that undergoes autocatalytic cleavage, which results in the formation o

82 concentrations and permanent inactivation by autocatalytic cleavage.

83 es a particle size reduction of 100 A and an autocatalytic cleavage.

84 PRTN chromatin accessibility, and regulatory autocatalytic cleavage.

85 ficient release of the flanking proteins via autocatalytic cleavage.

86 rification of the pyromellitate system under autocatalytic conditions; minor ester exchange with pre-

87 ally altered host protein that multiplies by autocatalytic conversion has gained wide acceptance.

88 Because autocatalytic conversion is considered a key element of

89 the role of the pro domain, we monitored the autocatalytic conversion of BACE1 by heteronuclear NMR s

90 The autocatalytic conversion of the cellular prion protein (

91 ain and the entire pro domain, and undergoes autocatalytic conversion to yield the well-folded mature

92 tudy the structural changes accompanying the autocatalytic conversion.

93 site conformations are conserved during the autocatalytic conversion.

94 We characterize the autocatalytic core of the CoTC ribozyme and show its fun

95 The rTCA reaction sequence is a network-autocatalytic cycle along the relaxation pathway for red

96 We have designed an autocatalytic cycle based on the highly efficient 10-23

97 The autocatalytic cycle can be arrested by protein kinase G

98 ovided by supramolecular ordering enables an autocatalytic cycle favouring the growth of DNA chains,

99 The autocatalytic cycle of protein activation is initiated b

100 tween three subcomponents of the network: an autocatalytic cycle that generates thiols and amides fro

101 hypercycle defines the simplest model of an autocatalytic cycle, providing major theoretical insight

102 to synthesize more of that metabolite is an autocatalytic cycle.

103 g thiol species that are produced during the autocatalytic cycle.

104 minimal stochastic model that is based on an autocatalytic cycle.

105 tworks are competed directly against selfish autocatalytic cycles, the former grow faster, indicating

106 entral carbon metabolism are part of compact autocatalytic cycles.

107 echanism whereby interphase cells can oppose autocatalytic cyclin E degradation and maintain cyclin E

108 of Cr intermediate species that promoted the autocatalytic decay of chlorine.

109 ocumented characteristics of autoactivation, autocatalytic degradation and Ca2+-dependence.

110 ncomplete glycosylation stimulates extensive autocatalytic degradation and self-inactivation of MT1-M

111 e results we propose that TIR1 is subject to autocatalytic degradation when assembled into an SCF.

112 cantly increased (10-20-fold) propensity for autocatalytic degradation, relative to cationic trypsino

113 bly of cullin complexes by counteracting the autocatalytic destruction of adaptor proteins.

114 RING ubiquitin ligases (CRL) by limiting the autocatalytic destruction of substrate adapters such as

115 Autocatalytic dissociation of water on the Cu(110) metal

116 : catalytic formation of branched junctions, autocatalytic duplex formation by a cross-catalytic circ

117 The important autocatalytic effect of the HCl reaction product was con

118 ycles or to molecular specificity, i.e., the autocatalytic emergence of a single species.

119 er mild conditions by using the output of an autocatalytic enzyme reaction to drive both the polymeri

120 We propose that the termination of autocatalytic ethylene biosynthesis of system 2 in ripe

121 itself out of a precursor polypeptide in an autocatalytic fashion with concomitant linkage of the tw

122 The autocatalytic feature of the MTH process implies that hy

123 activates the positive regulator Cdc25 in an autocatalytic feedback loop.

124 d RFP (cpRFP) scaffold, which maintained its autocatalytic fluorescence, from a red fluorescent Ca(2+

125 A mechanism for Met-Tyr-Trp autocatalytic formation by KatG compound I is proposed f

126 A mechanism for Tyr-Trp autocatalytic formation by KatG compound I is proposed f

127 d carboxyl group is the sole requirement for autocatalytic formation of a heme-protein link in P450 e

128 ormation and provide a working model for the autocatalytic formation of protocells from the coupling

129 NAzyme units, thus leading to the isothermal autocatalytic formation of the reporter elements.

130 ht chain of botulinum A neurotoxin undergoes autocatalytic fragmentation that is accelerated by the p

131 , when >95% of the light chain had undergone autocatalytic fragmentation, the preparation retained 35

132 (2)), and hydrogen peroxide (H(2)O(2)) in an autocatalytic free radical chain reaction, which could p

133 it is often claimed that self-sustaining or autocatalytic front propagation is well described by mea

134 As with methylation of H3 lysine 9, autocatalytic G9a methylation is necessary and sufficien

135 thiols to disulfides and the thiol-mediated autocatalytic generation of H2O2 from oxygen.

136 tRNA(Tyr) and act as splicing cofactors for autocatalytic group I introns.

137 The autocatalytic group II intron ai5gamma from Saccharomyce

138 eation (A --> B, rate constant k 1) and fast autocatalytic growth (A + B --> 2B, rate constant k 2),

139 r nucleation (A --> B, rate constant k1) and autocatalytic growth (A + B --> 2B, rate constant k2), w

140 meration (B + B --> C) and secondary surface autocatalytic growth (A + C --> 1.5C) involved in suppor

141 The use of the F-W 2-step nucleation and autocatalytic growth kinetic model to fit 3 literature e

142 een used to infer the presence or absence of autocatalytic growth processes such as fibril fragmentat

143 e crossover between nucleation-dominated and autocatalytic growth regimes.

144 termine the rate constants of nucleation and autocatalytic growth.

145 during the lag time: primary nucleation and autocatalytic growth.

146 dialkyl disulfides; a trigger that controls autocatalytic growth; and inhibitory processes that remo

147 tween the T7 RNA polymerase promoter and the autocatalytic hepatitis delta virus ribozyme of a transc

148 ns between phenomena generally attributed to autocatalytic hydrolysis and mass transfer limitation ef

149 om chains grow more informational and become autocatalytic (i.e., increasing their own concentrations

150 of amplification is performed by a reaction autocatalytic in Co(2+).

151 tions, that catalyst formation process being autocatalytic in H2O2.

152 edox cycle, unprecedented among LOX in being autocatalytic, in which the hydroperoxy substrate is iso

153 Their multidomain structure and autocatalytic incorporation of linear tetrapyrrole chrom

154 a glycosyltransferase that functions as the autocatalytic initiator for the synthesis of glycogen in

155 composed of a ligand ("hedge") domain and an autocatalytic intein ("hog") domain.

156 ht differentiates this protein splicing from autocatalytic inteins, and may allow the chloroplast to

157 We show that the bonds form through an autocatalytic intramolecular reaction catalyzed by an ad

158 s that the GPS proteolysis is mediated by an autocatalytic intramolecular reaction similar to that em

159 lation-dephosphorylation cycle kinetics with autocatalytic kinase.

160 unds act as acid amplifiers and decompose by autocatalytic kinetics to generate fluorinated sulfonic

161 honetria parasitica, encodes two papain-like autocatalytic leader proteases, p29 and p48, that also h

162 OH(cat.)/AcCl system was found to promote an autocatalytic-like condensation and facilitate the multi

163 h ordering and condensation would provide an autocatalytic link whereby complementarity promotes the

164 other molecule of the former to establish an autocatalytic loop.

165 rgy that is responsible for establishing the autocatalytic loop.

166 ectivity of flock house virus (FHV) requires autocatalytic maturation cleavage of the capsid protein

167 ion (TFR)-PR-FLAG, also undergoes N-terminal autocatalytic maturation when it is expressed in Escheri

168 at Dia2 protein turnover does not involve an autocatalytic mechanism and that Dia2 proteolysis is inh

169 mixed hydroxyl/water structures, through an autocatalytic mechanism promoted by H-bonding.

170 ivation of its E3 ligase activity through an autocatalytic mechanism that amplifies its E3 ligase act

171 stem reveals a new, enzyme-free, isothermal, autocatalytic mechanism that introduces means for effect

172 e the induction step, further implicating an autocatalytic mechanism.

173 ay be controlling kinase activity through an autocatalytic mechanism.

174 mobenzene to Pd(PtBu3)2 occurs by an unusual autocatalytic mechanism.

175 In autocatalytic models, the network growth velocity is rig

176 PR/Cas9 genome-editing system for generating autocatalytic mutations, to produce homozygous loss-of-f

177 oduces a molten silica shell that acts as an autocatalytic 'nanoreactor' by actively transporting oxy

178 ar, our results show that the characteristic autocatalytic nature of the growth process originates fr

179 d generalize to the robust efficiency of any autocatalytic network.

180 ed for the emergence of such self-sustaining autocatalytic networks.

181 Here, we combine autocatalytic nucleation and polymerization dynamics to

182 f short, unstable microtubules maintained by autocatalytic nucleation and provide a paradigm for the

183 e rate at the adjacent two amides, often the autocatalytic nucleophiles in deamidation, correlated wi

184 to a conserved acidic I-helix residue via an autocatalytic oxidation.

185 open reading frames (ORF), each encoding an autocatalytic papain-like leader protease.

186 d solvent effect and the determination of an autocatalytic pathway.

187 Here, we demonstrate an interaction between autocatalytic PCD and lytic viral infection in the cosmo

188 ecombinant protein allowed monitoring of the autocatalytic peroxide-driven formation of covalent heme

189 ormation of the enzyme and indicative of PKC autocatalytic phosphorylation and activation during bact

190 e targets for a protein kinase C-independent autocatalytic phosphorylation and that the PKD1-S744A/S7

191 Autocatalytic phosphorylation of tyrosine 845 on unligan

192 We designed an autocatalytic photochemical reaction based on the photoi

193 In addition, systems with autocatalytic positive feedback loop are shown to be mor

194 TPQ arises from the autocatalytic, post-translational oxidation of a tyrosin

195 TPQ arises from the autocatalytic, post-translational oxidation of a tyrosin

196 mbinant PrP displays specific features of an autocatalytic process and mimics the transmission barrie

197 We formulate phototrophic growth as an autocatalytic process and solve the resulting time-depen

198 Protein splicing is a precise autocatalytic process in which an intein excises itself

199 Protein splicing is a posttranslational autocatalytic process in which an intervening sequence,

200 uantitative understanding and control of the autocatalytic process involved in the synthesis of collo

201 Interestingly, the autocatalytic process is effective not only in eliminati

202 vo from purified native PrPC molecules in an autocatalytic process requiring accessory polyanions.

203 endogenous ROS production in a regenerative, autocatalytic process that ultimately results in global

204 dal metal nanocrystals typically involves an autocatalytic process, in which the salt precursor adsor

205 ysiological and displayed key features of an autocatalytic process.

206 results, we propose that FlhB cleavage is an autocatalytic process.

207 mal isoform displays specific features of an autocatalytic process.

208 cluding (1)O2 itself, in what constitutes an autocatalytic process.

209 iency with a concomitant acceleration of the autocatalytic process.

210 Theoretical models have long suggested that autocatalytic processes can result in kinetically contro

211 This autocatalytic processing generated six main forms of MT1

212 the 44-kDa form of MT1-MMP generated during autocatalytic processing in maintaining the pool of acti

213 It undergoes rapid autocatalytic processing in trans after its secretion fr

214 Autocatalytic processing of active MT1-MMP generates an

215 required for both N-terminal and C-terminal autocatalytic processing of CspA.

216 activation of SKI-1/S1P involves sequential autocatalytic processing of its N-terminal prodomain at

217 arked retardation of the in vitro N-terminal autocatalytic processing of TFR-PR(H69E) and suggesting

218 e dispensable for hypovirus replication, the autocatalytic processing of the leader proteases p29 and

219 ble from fully glycosylated TPP1 in terms of autocatalytic processing of the proform and enzymatic pr

220 icated that the p.G178R mutation impairs the autocatalytic processing of this enzyme resulting in the

221 Human separase also appears to undergo an autocatalytic processing on anaphase entry.

222 ivity is revealed by maturation following an autocatalytic processing resulting in the cleavage of bo

223 ome catalytically active, Psd1p undergoes an autocatalytic processing step involving a conserved LGST

224 n the cell surface, active MT1-MMP undergoes autocatalytic processing to a major membrane-tethered 44

225 60-kDa inactive precursor that must undergo autocatalytic processing to generate a 40-kDa/20-kDa het

226 SK9 small molecule inhibitors that block its autocatalytic processing.

227 of the coupling between the enzyme-catalyzed autocatalytic production and diffusion of hydrogen ions.

228 pagation saturates, leading to a switch from autocatalytic production of infectivity (phase 1) to a t

229 all, similarly sized segments-speed up their autocatalytic production.

230 whereas monomeric alpha-synuclein blocks the autocatalytic proliferation of Abeta42 (the 42-residue f

231 Disease is transmitted by the autocatalytic propagation of PrP(Sc) misfolding at the e

232 ollowed by Ca(2+)-driven, positive feedback, autocatalytic propagation.

233 r species, and NO(2) only plays a role as an autocatalytic propagatory species.

234 inducible signals that might accelerate its autocatalytic properties and dictate where inflammasome

235 rulence of TSE prions relative to many other autocatalytic protein aggregates.

236 Inteins are autocatalytic protein cleavage and splicing elements.

237 This autocatalytic prototropic rearrangement in gas-phase pep

238 Autocatalytic reaction displayed sensitivity to mixing;

239 ith oxyhemoglobin, and although this complex autocatalytic reaction has been studied for a century, t

240 An autocatalytic reaction in which the reaction product ser

241 The autocatalytic reaction is explained as the result of the

242 outcome of both biological and nonbiological autocatalytic reaction systems that display a threshold

243 of apoMSOX has been shown to proceed via an autocatalytic reaction that requires only FAD and is blo

244 Protein splicing is an autocatalytic reaction where an intervening element (int

245 mutants by active alpha-thrombin triggers an autocatalytic reaction which leads to more active thromb

246 erates the release of more sensitizer via an autocatalytic reaction.

247 pective offers a rationalization of the Soai autocatalytic reaction; accounting for enantiomeric exce

248 induced mass uptake typical for second-order autocatalytic reactions.

249 r restricted the diffusion of copper and the autocatalytic reduction limited the probability for seco

250 Seeding and autocatalytic reduction of platinum salts in aqueous sur

251 y a nucleation-and-growth scenario involving autocatalytic reduction of the copper phyllosilicate fol

252 uniform size of precursor particles and the autocatalytic reduction thus offers means to synthesize

253 and thus suggest a mechanism similar to the autocatalytic refolding and aggregation of prions.

254 commitment requires efficient activation and autocatalytic release of caspase-8 into the cytoplasm to

255 C terminus is followed by an intramolecular autocatalytic removal of a 12-amino acid propeptide at t

256 ms of ADAM19 was first demonstrated by their autocatalytic removal of a purification tag (Myc-His) an

257 oteasome and a mutant form that prevents the autocatalytic removal of its pro-peptides.

258 plification (PMCA) technology to sustain the autocatalytic replication of infectious prions in vitro.

259 A simple synthetic autocatalytic replicator is capable of establishing and

260 quence NPTH and substitution of the proposed autocatalytic residue abolishes cleavage.

261 Group II introns are large, autocatalytic ribozymes that catalyze RNA splicing and r

262 trons remove themselves by protein-assisted, autocatalytic RNA splicing, thereby minimizing host dama

263 The CoTC sequence is an autocatalytic RNA structure that undergoes rapid self-cl

264 2) is a modifier in catalysis and acts in an autocatalytic role; there is a parallel, neutral catalys

265 nner mitochondrial membrane, must undergo an autocatalytic self-processing event to gain activity.

266 vities operating orthogonal from each other: autocatalytic self-replication of oligomers from native

267 ther a catalytic reaction system contains an autocatalytic, self-sustaining subsystem is unlikely to

268 An autocatalytic serine protease, cortical granule serine p

269 Such foldamer catalysts are shown to form an autocatalytic set, through which short chains grow into

270 We also analyze autocatalytic signal transduction switches and show that

271 ral conformation of the glycosylasparaginase autocatalytic site without influence from any inhibitor

272 inding of glucosamine-6-phosphate stimulates autocatalytic site-specific cleavage near the 5' of the

273 chemical reaction of a light-sensitive acid autocatalytic solution in which the actuator is immersed

274 and the H2 OHO2 radical complex represent an autocatalytic source of atmospheric HO2 .

275 ulator of auxin signalling, and modulate the autocatalytic stabilization of auxin signalling output.

276 ing misfolded Psd1(ts) vary depending on its autocatalytic status.

277 The presence of two autocatalytic steps in the same reaction scheme--double

278 formation of red fluorescence requires three autocatalytic steps, whereas only two are needed for gre

279 the prebiotic plausibility of each of these autocatalytic subsystems and combinations thereof: self-

280 of superenantiospecificity resulting from an autocatalytic surface explosion reaction of a chiral mol

281 be amplified by reaction mechanisms such as autocatalytic surface explosions which have nonlinear ki

282 on (A --> B, rate constant k(1)) followed by autocatalytic surface growth (A + B --> 2B, rate constan

283 = 1.5(1.1) x 10(-3) h(-1)) followed by fast autocatalytic surface growth (A + B --> 2B, rate constan

284 -> B, rate constant k(1obs)), then (ii) fast autocatalytic surface growth (A + B --> 2B, rate constan

285 2-step, slow continuous nucleation and then autocatalytic surface growth mechanism, A --> B (rate co

286 te constant k1), followed by typically fast, autocatalytic surface growth, A + B --> 2B (rate constan

287 uous nucleation, A --> B (rate constant k1), autocatalytic surface growth, A + B --> 2B (rate constan

288 + B --> C (rate constant k3), and secondary autocatalytic surface growth, A + C --> 1.5C (rate const

289 re we quantitatively analyze the kinetics of autocatalytic surface reduction in an effort to control

290 strate that the activation energy barrier to autocatalytic surface reduction is highly dependent on b

291 to visualize the spontaneous emergence of an autocatalytic system from an aqueous mixture of two chem

292 Here, we describe an autocatalytic system where two relatively simple compone

293 ues into a cage allowed for the design of an autocatalytic system: oxidation of the methylthio groups

294 tanding the spatiotemporal dynamics of other autocatalytic systems and emphasize the relevance of clu

295 Novel synthetic autocatalytic systems provide a foundation for the desig

296 , and it has no known function but undergoes autocatalytic truncations during purification and storag

297 Furthermore, degradation is regulated by the autocatalytic turnover of PUB22, which is stabilized upo

298 re stressed, Pyk2 and Pyk3 undergo increased autocatalytic tyrosine phosphorylation.

299 bonding picture is presented which predicts autocatalytic water dissociation to be a general phenome

300 f Cwp84, this cleavage does not appear to be autocatalytic, whereas in Cwp13 autocatalysis was demons