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 ndicating that the covalent flavinylation is autocatalytic.

4 Polarity establishment involves autocatalytic accumulation of polarity regulators, inclu

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

6 eparate but interacting feedback mechanisms (autocatalytic activation and substrate depletion) are ca

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

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

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

10 The autocatalytic activation of an initiator caspase, exempl

11 Autocatalytic activation of epidermal growth factor rece

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

13 Whereas the autocatalytic activation of isoform gamma (AtLEGgamma) i

14 1 is approximately 3000-fold higher, and the autocatalytic activation of MASP-1 is about 140-fold fas

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

16 Autocatalytic activation of Parkin bolsters its accumula

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

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

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

20 regulate its multistep, compartment-specific autocatalytic activation.

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

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

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

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

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

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

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

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

29 PCSK9 has autocatalytic activity that releases the prodomain at th

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

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

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

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

34 ally and rationalized mechanistically for an autocatalytic alkylation reaction.

35 pand on our previous discovery of iterative, autocatalytic alpha- N-methylating precursor proteins in

36 This leads to autocatalytic amplification of aggregate mass and underl

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

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

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

40 mation, facilitating their own synthesis via autocatalytic and cross-catalytic pathways.

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

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

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

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

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

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

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

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

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

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

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

52 CGEP was shown to undergo autocatalytic C-terminal cleavage at E946, removing 15 r

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

54 Autocatalytic chemical reactions are widely studied as m

55 Autocatalytic chemical reactions, whereby a molecule is

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

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

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

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

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

61 Surprisingly, autocatalytic cleavage does not depend on proper localiz

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

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

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 Functional analysis reveals enhanced autocatalytic cleavage of the mutated protein and sponta

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

72 ues within close proximity to each other and autocatalytic cleavage sites.

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

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

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

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

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

78 The ribozymes rapidly undergo autocatalytic cleavage, leaving termini that are ligated

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

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

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

82 After initial autocatalytic cleavage, the prosegment remains tightly a

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

84 ficient release of the flanking proteins via autocatalytic cleavage.

85 concentrations and permanent inactivation by autocatalytic cleavage.

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

87 PRTN chromatin accessibility, and regulatory autocatalytic cleavage.

88 ition molecule in the immune system, driving autocatalytic complement cascade activation and acting a

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

90 ure of Pb matches previous models, including autocatalytic conversion of phycocyanobilin to phycoviol

91 The autocatalytic conversion of the cellular prion protein (

92 The autocatalytic cycle can be arrested by protein kinase G

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

94 The autocatalytic cycle of protein activation is initiated b

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

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

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

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

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

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

101 entral carbon metabolism are part of compact autocatalytic cycles.

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

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

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

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

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

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

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

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

110 drophobic azide results in a more pronounced autocatalytic effect.

111 The autocatalytic effects observed can be tuned by varying r

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

113 An autocatalytic enzyme reaction is used to stimulate refol

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

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

116 The autocatalytic feature of the MTH process implies that hy

117 such spatial patterns can form when a local autocatalytic feedback loop and a long-range inhibitory

118 such as the existence of self-sustaining (or autocatalytic) feedback cycles.

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

120 The system is driven by the autocatalytic formation of a metastable surfactant whose

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

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

123 We studied the vesicles' autocatalytic formation using UPLC to determine monomer

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

125 Autoxidation is an autocatalytic free-radical chain reaction responsible fo

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

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

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

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

130 The autocatalytic group II intron ai5gamma from Saccharomyce

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

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

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

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

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

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

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

138 termine the rate constants of nucleation and autocatalytic growth.

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

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

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

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

143 Their multidomain structure and autocatalytic incorporation of linear tetrapyrrole chrom

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

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

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

147 lation-dephosphorylation cycle kinetics with autocatalytic kinase.

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

149 or selective surfactant formation as well as autocatalytic kinetics; indeed, no selection is observed

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

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

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

153 rgy that is responsible for establishing the autocatalytic loop.

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

155 therwise maintain MELT phosphorylation in an autocatalytic manner.

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

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

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

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

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

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

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

163 ay be controlling kinase activity through an autocatalytic mechanism.

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

165 Autocatalytic models for the emergence of homochirality

166 This allows for a classification of minimal autocatalytic motifs called cores.

167 ility of such networks, which depends on the autocatalytic motifs they contain and is notably increas

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

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

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

171 stochastic model confirms the presence of an autocatalytic network involving molecular recognition an

172 able to catalyze their own formation via an autocatalytic network, which subsequently template the a

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

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

175 Here, we combine autocatalytic nucleation and polymerization dynamics to

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

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

178 (42 steps) and a representative part of the autocatalytic olefin cycle (63 steps).

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

180 e of suboptimal substrate binding leading to autocatalytic oxidative damage of these variants.

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

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

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

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

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

186 Autocatalytic phosphorylation of tyrosine 845 on unligan

187 We designed an autocatalytic photochemical reaction based on the photoi

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

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

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

191 taneous [Ca(2+)](i) peaks may result from an autocatalytic process and that [Ca(2+)](i) oscillation i

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

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

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

195 uorine bond scission has occurred during the autocatalytic process of cofactor biogenesis.

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

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

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

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

200 iency with a concomitant acceleration of the autocatalytic process.

201 ysiological and displayed key features of an autocatalytic process.

202 I), the oxidation of Pb(II) carbonate was an autocatalytic process.

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

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

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

206 Autocatalytic processing of active MT1-MMP generates an

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

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

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

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

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

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

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

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

215 60-kDa inactive precursor that must undergo autocatalytic processing to generate a 40-kDa/20-kDa het

216 SK9 small molecule inhibitors that block its autocatalytic processing.

217 ance of both CGEP peptidase activity and its autocatalytic processing.

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

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

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

221 a predominant contributor toward the rate of autocatalytic progression.

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

223 concentrations, the interaction inhibits the autocatalytic proliferation of amyloid fibrils by second

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

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

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

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

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

229 As a key prediction of a model integrating autocatalytic protein aggregation and a minimal Start ne

230 Inteins are autocatalytic protein cleavage and splicing elements.

231 This autocatalytic prototropic rearrangement in gas-phase pep

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

233 The autocatalytic reaction is explained as the result of the

234 e experimental example of such an amplifying autocatalytic reaction is the Soai reaction.

235 rk reveals how kinetics of a phase-separated autocatalytic reaction may be used to control the popula

236 we use experimental data from the model Soai autocatalytic reaction system to evaluate the energy req

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

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

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

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

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

242 ED process and the far-from-equilibrium Soai autocatalytic reaction.

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

244 The autocatalytic redox interaction between aqueous Fe(II) a

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

246 reduction of Ag(+) to form seeds followed by autocatalytic reduction of Ag(+) by ethylene glycol (and

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

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

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

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

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

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

253 A simple synthetic autocatalytic replicator is capable of establishing and

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

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

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

257 toichiometrically inhibited both primary and autocatalytic secondary nucleation processes, even in th

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

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

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

261 simple inorganic salt can spontaneously form autocatalytic sets of replicating inorganic molecules th

262 We also analyze autocatalytic signal transduction switches and show that

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

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

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

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

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

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

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

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

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

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

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

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

275 = 1.5(1.1) x 10(-3) h(-1)) followed by fast autocatalytic surface growth (A + B --> 2B, rate constan

276 2-step, slow continuous nucleation and then autocatalytic surface growth mechanism, A --> B (rate co

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

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

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

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

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

282 ation of cold-temperature exposure to induce autocatalytic system 2 ethylene biosynthesis and subsequ

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

284 ally plausible version of such an amplifying autocatalytic system is presented.

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

286 t tomatoes was due to an inability to induce autocatalytic system-2 ET synthesis, a characteristic fe

287 reaking and asymmetric amplification in this autocatalytic system.

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

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

290 inetic investigations revealed key traits of autocatalytic systems including molecular recognition an

291 While all known autocatalytic systems indeed contain minimal motifs, the

292 Selection in compartmentalized autocatalytic systems might provide a way for evolution

293 Novel synthetic autocatalytic systems provide a foundation for the desig

294 Comparison of three autocatalytic systems representing a continuum of nitrog

295 s framework extends the range of conceivable autocatalytic systems, by applying our stoichiometric an

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