ライフサイエンスコーパス: catalyse

1 ses the equilibrium for the reaction that it catalyses.

2 Transition-metal-catalysed [2+2+2] cycloadditions excell in this regard:

3 TET enzymes catalyse a key step in the removal of DNA methylation.

4 ics and genomics approaches that are helping catalyse a much-needed improved understanding of the bio

5 hly versatile electroactive molecules, which catalyse a multitude of redox reactions in biological sy

6 ed molecular mechanisms underlying how TPSTs catalyse a variety of substrate proteins with different

7 n scaffolds and unnatural metal cofactors to catalyse a wide range of abiological transformations.

8 e leader-side CRISPR repeat, and finally, it catalyses a nucleophilic attack that connects one strand

9 The resulting enzyme catalyses a reversible aldol reaction with high stereose

10 at steps can be taken in the next 5 years to catalyse action toward achieving the Sustainable Develop

11 PARP catalysed ADP-ribosylation is a post-translational modif

12 the literature is the cucurbit[6]uril (CB6) catalysed alkyne-azide cycloaddition (CB-AAC).

13 While copper(i)-catalysed alkyne-azide cycloaddition is the most widely

14 The palladium-catalysed allylic substitution reaction is one of the mo

15 ation of the substrates to achieve palladium-catalysed amine-directed conversion of C-H bonds to C-C

16 xidase-dependent generation of oxidants that catalyse an activating intermolecular-disulphide between

17 Here, we show that T. denticola FlgE self-catalyses an interpeptide crosslinking reaction between

18 Thermal, transition metal-catalysed, and also two different living anionic ROP met

19 within WSe2 monolayers, using a dislocation-catalysed approach.

20 ns confined in the nanopores of zeolite HBEA catalyse aqueous phase dehydration of cyclohexanol at a

21 Membrane transport proteins that catalyse arsenic uptake by roots, and translocation thro

22 eport a straightforward method for palladium-catalysed arylation of aryl(heteroaryl)methanes and diar

23 and practicality, via a chiral Bronsted base-catalysed asymmetric Mannich-type reaction of in situ ge

24 Here we report a rhodium-catalysed asymmetric Suzuki-Miyaura reaction with import

25 sesterifications-branching and exon ligation-catalysed at a single catalytic metal site in U6 small n

26 standing how YME1L recognizes substrates and catalyses ATP-dependent degradation has been hampered by

27 nto peptide oligomers via solid-phase copper-catalysed azide-alkyne cycloaddition (SP-CuAAC) click re

28 in muro labelling of RG-II through a copper-catalysed azide-alkyne cycloaddition reaction.

29 asizes the progress and potential in zeolite catalysed biomass conversions and relates these to conce

30 roRNA-expressing lines demonstrate that PPKs catalyse blue light-dependent CRY2 phosphorylation to bo

31 Diastase alpha-amylase extracted from malt, catalyses break down of starch into maltose.

32 It is catalysed by a cascade of three enzymes and results in t

33 results establish that ubiquitination can be catalysed by a single enzyme, the activity of which does

34 thyltransferase, suggesting this activity is catalysed by a unique heterodimer.

35 ks for repair by homologous recombination is catalysed by AddAB, AdnAB or RecBCD-type helicase-nuclea

36 ) the enzymatic hydrolysis of head cartilage catalysed by alcalase (55.7 degrees C/pH 8.2); (2) the c

37 ydroxy-tetrahydrofuran-3-one was found to be catalysed by amino acid metal salts.

38 molecule precorrin-2 in a chemical reaction catalysed by an S-adenosyl-L-methionine (SAM) dependent

39 hway, with one of the steps apparently being catalysed by an unlinked gene encoding a 6-methylsalicyl

40 lation of alpha, beta-unsaturated thioesters catalysed by crotonyl-CoA reductase/carboxylase (CCRC) h

41 Given the diversity of reactions catalysed by dirhodium complexes, we anticipate that dir

42 not both to probe the topological conversion catalysed by DNA topoisomerase and to study the DNA repl

43 used on development of a microbial fuel cell catalysed by E. coli, through triggering electroactive p

44 ad50-Xrs2 and Sae2; and long-range resection catalysed by either Exo1 or Sgs1-Dna2.

45 hus, both substrate PARylation and PARdU are catalysed by enzymes within the same protein complex, an

46 ed by our knowledge of biogeochemical cycles catalysed by extant biota.

47 bacterial activity, but instead are largely catalysed by fungal denitrification and/or abiotic react

48 The reaction catalysed by GABA-T is inhibited by vigabatrin, whereas

49 oncentrations on the CL intensity of luminol catalysed by GNPs.

50 e show that increased transamination, mainly catalysed by GOT1, leads to increased levels of 2-hydrox

51 Although the S-nitrosylation catalysed by haem proteins is well known, no direct evid

52 amic and reversible acetylation of proteins, catalysed by histone acetyltransferases (HATs) and histo

53 mplexed with two substrate peptides that are catalysed by human TPST1 with significantly different ef

54 es are surfactants and their assembly can be catalysed by hydrophobic-hydrophilic interfaces (an air-

55 (SAM-dependent) retro-Claisen rearrangement catalysed by LepI.

56 Protein N-myristoylation is catalysed by N-myristoyltransferase (NMT), an essential

57 N-terminal acetylation (NTA) catalysed by N-terminal acetyltransferases (Nats) is amo

58 o create enzymes that catalyse reactions not catalysed by native Fe-enzymes or other metalloenzymes.

59 protein engineering, the scope of reactions catalysed by native metalloenzymes has been expanded rec

60 The production of oxygen free radicals catalysed by non-haem iron was investigated in an in vit

61 oly(ADP-ribosyl)ation (PARylation) is mainly catalysed by poly-ADP-ribose polymerase 1 (PARP1), whose

62 ins (NODD and CODD) of HIFalpha isoforms, as catalysed by prolyl hydroxylases (PHD 1-3).

63 protein increases the rate of ATP hydrolysis catalysed by RecN during the DNA pairing reaction.

64 tic pathway of TTR fibrillogenesis in vitro, catalysed by selective proteolytic cleavage, which produ

65 h1) and requires Chk1 activation known to be catalysed by ssDNA-RPA-ATR signalling at the ends design

66 nt attachment of ubiquitin to a substrate is catalysed by the E1, E2 and E3 three-enzyme cascade, whi

67 , luciferin, with molecular oxygen, which is catalysed by the enzyme luciferase.

68 is generated by the crosslinking of VEGF165, catalysed by the enzyme tissue transglutaminase, and ass

69 generate lipid X in lipid A biosynthesis is catalysed by the membrane-associated enzyme LpxH.

70 n in both coding and non-coding RNAs that is catalysed by the METTL3-METTL14 methyltransferase comple

71 e research of a generation of ecologists was catalysed by the recognition that the number and identit

72 Integration is catalysed by the retrovirus-encoded integrase (IN), whic

73 This reaction is catalysed by the virally encoded enzyme integrase (IN) a

74 The E1/E2-independent ubiquitination catalysed by these enzymes is energized by nicotinamide

75 to the efficiency and diversity of reactions catalysed by this class of enzymes.

76 of post-translational protein modifications catalysed by TPSTs.

77 the reactivity and selectivity of reactions catalysed by transition metals.

78 Lysine demethylation, as catalysed by two families of lysine demethylases (the fl

79 conclude that non-photochemical quenching is catalysed by two independent mechanisms, with the fastes

80 e-promoted alpha-hydroxyketone rearrangement catalysed by vanadium-dependent haloperoxidases to accou

81 plex activates H2 under mild conditions, and catalyses C-H hydride abstraction plus H2 generation fro

82 ct distribution and production rate for NGQD-catalysed carbon dioxide reduction is comparable to thos

83 ) necessary for the glove-box-free palladium-catalysed carbon-fluorine, carbon-nitrogen, and carbon-c

84 Several examples on Pd-catalysed carbonylation of methyl C(sp(3))-H bonds with

85 de (oligoTEA) macrocycles via a one-pot acid-catalysed cascade reaction.

86 ties generate hot charge carriers, which can catalyse chemical reactions or induce redox processes in

87 rge 'hook' structure of Scc2 responsible for catalysing cohesin loading.

88 Lysyl oxidase-like 2 (LOXL2) catalyses collagen cross-linking and is implicated in th

89 anocrystals embedded in NbOx glass) via acid-catalysed condensation of polyniobate clusters.

90 electron reduction of CO2 for the photoredox-catalysed continuous flow synthesis of alpha-amino acids

91 -scale genetic data sets, as one paradigm to catalyse convergence of these efforts.

92 In recent times, transition-metal-catalysed coupling reactions have dominated in the devel

93 port the detailed investigation of a surface-catalysed cross-coupling and sequential cyclization casc

94 of regioselective halogenase enzymes with Pd-catalysed cross-coupling chemistry, in one-pot reactions

95 The field of Ni-catalysed cross-coupling has seen rapid recent growth be

96 Whereas advances in the related field of Pd-catalysed cross-coupling have been driven by ligand desi

97 To address this issue, nickel-catalysed cross-coupling processes can be used to form s

98 alternative to traditional transition-metal-catalysed cross-coupling reactions.

99 ally employed in sequential transition-metal-catalysed cross-coupling sequences to unite heterocyclic

100 hiation with (-)-sparteine followed by Pd(0) catalysed cross-coupling to prepare alpha-arylated amine

101 entify several new ligand classes for nickel-catalysed cross-electrophile coupling.

102 ose a class of phosphines that enable the Ni-catalysed Csp(3) Suzuki coupling of acetals with boronic

103 This ruthenium-catalysed decarboxylative alkyne hydroarylation eliminat

104 In all domains of life, the catalysed degradation of RNA facilitates rapid adaptatio

105 ara-phenylene) nanowires produced by surface-catalysed dehalogenative reaction.

106 will focus on the development of main group catalysed dehydrocoupling reactions as a route to hetero

107 polymeric polyphenols, before and after acid-catalysed depolymerisation in the presence of a nucleoph

108 ce of monster symmetry in number theory that catalysed developments in mathematics and physics.

109 demonstrate that cucurbit[7]uril (CB[7]) can catalyse Diels-Alder reactions for a number of substitut

110 TET enzymes catalyse DNA demethylation through 5-methylcytosine oxid

111 l voltage-gated Ca(2+) channels (VGCCs) that catalyse dopamine (DA) transmission are incompletely def

112 rug transporter LmrP from Lactococcus lactis catalyses drug efflux in a membrane potential and chemic

113 cognate RDFs to create single proteins that catalyse efficient attL x attR recombination in vivo and

114 Hydrogen evolution reaction is catalysed efficiently with precious metals, such as plat

115 able contribution to multidrug resistance by catalysing efflux of myriad structurally and chemically

116 Here we report a Pd(II)-catalysed enantioselective alpha-C-H coupling of a wide

117 Here, we report a copper-hydride-catalysed, enantioselective synthesis of gamma- or delta

118 endogenous let-7 miRNA-induced and Argonaute-catalysed endonucleolytic cleavage on target mRNAs at va

119 They iteratively catalyse epimerization, methylation and hydroxylation of

120 Here we report on the nature of nano-catalysed ethylene hydrogenation, investigated through e

121 creased levels of endogenous TNT-active GSTs catalyse excessive glutathionylation of endogenous subst

122 hed with PfVIT revealed that the transporter catalysed Fe(2+/)H(+) exchange driven by the proton elec

123 Here, we report a multicomponent, Ti-catalysed formal [2+2+1] reaction of alkynes and diazene

124 eductase (MDR) from Catharanthus roseus that catalyses formation of a heteroyohimbine isomer.

125 ce of carbazolyne cyclization followed by Rh-catalysed fragmentation to install the seven-membered ri

126 This study should catalyse further work to unite these two parallel and co

127 been shown to induce DNA repair and thereby catalyse genome editing.

128 involvement of both Vps75 and Asf1 in Rtt109 catalysed histone H3 K9 acetylation.

129 PRC1 and PRC2 modify chromatin by catalysing histone H2A lysine 119 ubiquitylation (H2AK11

130 In this study, copper-catalysed hydrogen peroxide induced oxidation of C-horde

131 nometre particle size may be used for tuning catalysed hydrogenation activity and selectivity.

132 The onset of catalysed hydrogenation occurs for Ptn (n >/= 10) cluste

133 ol products using sequential, copper-hydride-catalysed hydrosilylation and hydroamination of readily

134 troscopy showed that Ag NPs were not able to catalyse hydroxyl radical generation, but that they dire

135 dies establish that the enzyme is capable of catalysing imine formation as well as reduction.

136 rstanding of palaeoclimate dynamics, and has catalysed improvements in the accuracy and precision of

137 bacteria, lipid modification of proteins is catalysed in a three-step pathway.

138 terconversion of phosphoglycerate isomers is catalysed in numerous pathogenic microorganisms by a cof

139 Retrovirus integrase catalyses insertions of both ends of the linear viral DN

140 meric integrase components are sufficient to catalyse integration, the flanking integrase dimers were

141 h spatially organized alpha-helices that can catalyse its own formation.

142 rough the activity of S1P lyase (S1PL) which catalyses its irreversible degradation.

143 phiphilic imine dissolved in chloroform that catalyses its own formation by bringing together a hydro

144 Here, we show that Ufd2p catalyses K48-linked multi-monoubiquitination on K29-lin

145 The acid/base-catalysed Kemp elimination of 5-nitro-benzisoxazole form

146 Sortase A-catalysed ligation also obviously improved Tms and produ

147 mplex (LUBAC) is a multimeric E3 ligase that catalyses M1 or linear ubiquitination of activated immun

148 preserves the young surface of our planet by catalysing mantle convection, lubricating plate tectonic

149 However, enzymes likely catalysed many different reactions already in the last u

150 c carboxylates, we generated mutant proteins catalysing membrane potential-independent dye efflux by

151 ling mechanistic uncertainties in human P450-catalysed metabolism of the immunomodulatory drug leflun

152 Here we describe an iron-catalysed method for the direct (3)H labelling of pharma

153 of acetate release, it was shown that AnCDA catalyses mono-deacetylation of (GlcNAc)2 and full deace

154 TET2 is a dioxygenase that catalyses multiple steps of 5-methylcytosine oxidation.

155 stingly, we have identified two enzymes that catalyse NEIL1 polyubiquitylation, Mcl-1 ubiquitin ligas

156 Palladium-catalysed non-directed C-H activation could potentially

157 collagen protein, whose degradation by metal-catalysed oxidation has been intensively studied.

158 ectivity arises through a relayed photoredox-catalysed oxidation of a nitrogen-hydrogen bond.

159 No information exists on the metal catalysed oxidation of C-hordein, however.

160 ic cascades; herein illustrated by the Pd/Pt-catalysed oxidation of cinnamyl alcohol to cinnamic acid

161 e intermediacy of Co(IV)-O species in cobalt-catalysed oxidation of organic substrates as well as in

162 South American crude oils with ruthenium ion catalysed oxidation to characterize their n-alkyl append

163 low coordination numbers-are more active in catalysing oxidation and reduction of chemically active

164 ed bioanode with alcohol dehydrogenase (ADH) catalysing oxidation of glycerol and glyceraldehyde.

165 The two main strategies of gold-catalysed oxidative cyclisation are discussed in this tu

166 Semicarbazide-sensitive amine oxidase (SSAO) catalyses oxidative deamination of primary amines.

167 filament on single-stranded (ss) DNA, which catalyses pairing with homologous double-stranded (ds) D

168 ft the exchange behaviour towards the HLA-DM-catalysed pathway and further allow us to conceptualize

169 correlates with the propensity of the HLA-DM-catalysed pathway.

170 mcr-1 encodes a membrane-bound enzyme catalysing phosphoethanolamine transfer onto bacterial l

171 Fungal inositol polyphosphate (IP) kinases catalyse phosphorylation of IP3 to inositol pyrophosphat

172 ubixanthin and (all-E)-lycopene using iodine-catalysed photoisomerisation showed that the (5'Z)-isome

173 hypothesized to be the Na(+) /Pi symporters catalysing Pi uptake in chlorophytes, whereas PHOSPHATE

174 m transfer radical polymerization or rhodium-catalysed polymerization of phenylacetylene.

175 on in plant cell wall degradation, either by catalysing polysaccharide degradation itself, or by targ

176 To probe the nature of metal-catalysed processes and to design better metal-based cat

177 Palmitoyltransferase (PAT) catalyses protein S-palmitoylation which adds 16-carbon

178 Here, we report an efficient Palladium-catalysed protocol for reactions of beta-substituted ket

179 Enzyme catalysed PSRs with unactivated ketones are unprecedente

180 stem combining alkoxides with thioureas that catalyses rapid and selective ring-opening polymerizatio

181 Harnessing these cooperative interactions to catalyse reactions in synthetic systems, however, remain

182 logical, noble metals to create enzymes that catalyse reactions not catalysed by native Fe-enzymes or

183 trans-o-hydroxybenzylidene pyruvate aldolase-catalysed reactions between fluoropyruvate and many (het

184 his critical review the applications of gold catalysed reactions in total synthesis during the years

185 essential tool for the application of metal-catalysed reactions industrially, but these existing lib

186 ronsted acid, Lewis acid, or multifunctional catalysed reactions is discussed and generalised to prov

187 erization, wherein a series of enzymatically catalysed reactions is employed to generate secondary me

188 The sensitivity, or insensitivity, of catalysed reactions to catalyst structure is a commonly

189 ified ACFL550 and AC550 were applied in acid-catalysed reactions, the dehydration of methanol to dime

190 in contrast to traditional metal- or enzyme-catalysed reactions, with many impressive advances made

191 h makes ACFL550 a promising catalyst in acid-catalysed reactions.

192 ste and demonstrates its application in acid-catalysed reactions.

193 latory metabolic processes in which microbes catalyse reduction-oxidation reactions.

194 Thus, EGFR or HER2 can catalyse rigidity sensing after associating with nascent

195 rom a 2'-deoxyadenosine phosphate in an OxsB-catalysed ring contraction reaction initiated by hydroge

196 ing, accelerate RPR evolution, and allow RPR-catalysed RNA synthesis at near physiological (>/=1 mM)

197 teps, which follow a complex acid- and photo-catalysed route with oxygenation by both singlet and tri

198 ng involve both thermal and transition metal catalysed routes but recent developments have shown that

199 iew the rapidly expanding field of ruthenium catalysed sigma-activation as a tool in the selective me

200 rsally conserved Cas1-Cas2 integrase complex catalyses spacer acquisition using a direct nucleophilic

201 and define paracrystalline surfaces able to catalyse specific enantioselective chemical reactions.

202 onine (SAM)-dependent enzyme, LepI, that can catalyse stereoselective dehydration followed by three p

203 es two 3'-nucleotides from both LTR ends and catalyses strand transfer of the recessed 3'-hydroxyls i

204 We report the first nickel-catalysed Suzuki-Miyaura coupling of amides, which proce

205 irst step towards a general transition metal catalysed synthesis of tetraarylmethanes.

206 tant glycosynthases; enzymes which can still catalyse synthetic processes using oxazolines as donors,

207 cyl-tRNA synthetases (aaRSs), which not only catalyse the attachment of cognate amino acids to their

208 nsely packed with protein microcrystals that catalyse the bioluminescent reaction using ATP and the s

209 Here we identify the proteins that catalyse the biosynthesis of coenzyme F430 from sirohydr

210 2 and ME3) are oxidative decarboxylases that catalyse the conversion of malate to pyruvate and are es

211 oxide support suspended in aqueous solution, catalyse the direct conversion of methane to methanol an

212 e-size N-doped graphene quantum dots (NGQDs) catalyse the electrochemical reduction of carbon dioxide

213 ntiomer of the products of C-H insertion and catalyse the enantio- and diastereoselective cyclopropan

214 ect the binding sites of Cu(2+) available to catalyse the formation of VSCs such as H2S.

215 ed myoglobins containing an Ir(Me) site that catalyse the functionalization of C-H bonds to form C-C

216 pecial topological defects that consequently catalyse the growth of regular ice.

217 ocesses of silver-based nanoparticles, which catalyse the oxidation of multi-wall carbon nanotubes.

218 NAD(P)H oxidase 4 (NOX4), an enzyme known to catalyse the oxidation of NAD(P)H, is upregulated when p

219 IDH1/2 normally catalyse the oxidative decarboxylation of isocitrate int

220 itronate monooxygenases encoded by NMO genes catalyse the oxidative denitrification of nitroalkanes.

221 Understanding how materials that catalyse the oxygen evolution reaction (OER) function is

222 synthase from Thalictrum flavum (TfNCS) can catalyse the PSR between dopamine and unactivated ketone

223 zae (AspRedAm, Uniprot code Q2TW47) that can catalyse the reductive coupling of a broad set of carbon

224 hetic applications of these enzymes, i.e. to catalyse the reverse of their natural hydrolytic mode of

225 Eukaryotic box C/D small nucleolar (sno)RNPs catalyse the site-specific 2-O-methylation of ribosomal

226 Transition metals can catalyse the stereoselective synthesis of cyclic organic

227 roid 2-related factor 2 (Nrf2) to the liver, catalyse the transcription of Nrf2 downstream genes, and

228 A number of proteins catalyse the transfer and hydrolysis of ADPr, and also s

229 Histone methyltransferases EZH1 and EZH2 catalyse the trimethylation of histone H3 at lysine 27 (

230 The composite material catalysed the degradation of Rhodamine B at over double

231 invasions endured by organisms for eons have catalysed the evolution of gene-regulatory networks.

232 This electrode catalysed the oxidation of both glycerol and glyceraldeh

233 enase is the largest known metal cluster and catalyses the 6-electron reduction of dinitrogen to ammo

234 Ubiquitous tyrosinase catalyses the aerobic oxidation of phenols to catechols

235 Cyclooxygenase-2 catalyses the biosynthesis of prostaglandins from arachi

236 .1.1.7), encoded by two ace in most insects, catalyses the breakdown of acetylcholine, thereby termin

237 of VcINDY, a DASS from Vibrio cholerae that catalyses the co-transport of Na(+) and succinate.

238 se-1 (PFK1), the 'gatekeeper' of glycolysis, catalyses the committed step of the glycolytic pathway b

239 It catalyses the conversion of 2-hydroxyacetophenone to (S)

240 nsists of a self-labelling enzyme tag, which catalyses the covalent linking of exogenously supplement

241 mall and monomeric dehydratase, Pac13, which catalyses the dehydration of uridine-5'-aldehyde.

242 H3) (PNP=N[2-P(CHMe2)2-4-methylphenyl]2(-)), catalyses the dehydrogenation of cycloalkanes to cyclic

243 able and inexpensive potassium tert-butoxide catalyses the direct silylation of aromatic heterocycles

244 The enzyme leukotriene A4 hydrolase (LTA4H) catalyses the distal step in LTB4 synthesis and hence in

245 CCS) forms a transient complex with SOD1 and catalyses the final stages of its maturation.

246 cy of glucose-6-phosphatase, an enzyme which catalyses the final step of gluconeogenesis and glycogen

247 aY (phospho-MurNAc-pentapeptide translocase) catalyses the first and an essential membrane step of pe

248 -carboxylate synthase (P5CS), an enzyme that catalyses the first and common step of proline and ornit

249 ), which encodes a mitochondrial enzyme that catalyses the first committed reaction and rate-limiting

250 ritical yet severely inefficient enzyme that catalyses the fixation of virtually all of the carbon fo

251 te-limiting enzyme in BH4 biosynthesis which catalyses the formation of dihydroneopterin 3'triphosfat

252 is the only known E3 ubiquitin ligase which catalyses the generation of linear ubiquitin linkages de

253 nvolved in the recycling of ascorbate, which catalyses the glutathione (GSH)-dependent reduction of o

254 of Abeta) fibrils, fibrillar alpha-synuclein catalyses the heterogeneous nucleation of Abeta42 aggreg

255 in part, a cellular ceramidase activity that catalyses the hydrolysis of ceramide to produce sphingos

256 um (V)-nitrogenase of Azotobacter vinelandii catalyses the in vitro conversion of carbon monoxide (CO

257 Retroviral integrase catalyses the integration of viral DNA into host target

258 ctate dehydrogenase A (LDHA), an enzyme that catalyses the interconversion of pyruvate and lactate, p

259 PIN1 also catalyses the isomerization of proline 205 of BRD4 and i

260 L-Galactono-1,4-lactone dehydrogenase (GLDH) catalyses the last enzymatic step of the ascorbate biosy

261 garia x ananassa Enone Oxidoreductase (FaEO) catalyses the last reductive step in the biosynthesis of

262 Importantly, dPARP16 catalyses the modification of Sec16, a key Sec body comp

263 ahydrofolic acid cofactors, and specifically catalyses the NADPH-dependent oxidation of dimethylamine

264 Haem-copper oxidase (HCO) catalyses the natural reduction of oxygen to water using

265 putative precursors, indicating that PNPLA1 catalyses the omega-O-esterification with linoleic acid

266 thylmalonic encephalopathy protein 1 (ETHE1) catalyses the oxygen-dependent oxidation of glutathione

267 t in the crystal one or more of the proteins catalyses the production of light using coelenterazine d

268 The enzyme catalyses the reversible conversion of fumaric to L-mali

269 ional, transmembrane glycoprotein human CD38 catalyses the synthesis of three key Ca(2+)-mobilising m

270 s and recruits the release factor RF2, which catalyses the termination of protein synthesis.

271 Apolipoprotein N-acyl transferase (Lnt) catalyses the third step in this pathway, whereby it tra

272 The NirE enzyme catalyses the transfer of a methyl group from the SAM to

273 BCAT2 catalyses the transfer of the amino group from branched-

274 WcaJ is an Escherichia coli membrane enzyme catalysing the biosynthesis of undecaprenyl-diphosphate-

275 mononuclear non-haem iron enzyme capable of catalysing the C-S bond formation and sulfoxidation, her

276 ve cross-disciplinary scientific approach is catalysing the creation of technologies and intervention

277 -1-carboxylic acid oxidase (ACO), the enzyme catalysing the final step of ethylene formation.

278 membrane domain restores barrier function by catalysing the formation of a receptor complex in the pl

279 re possessing Bi surface droplets capable of catalysing the formation of nanostructures during Bi-ric

280 ase from recognizing cyclin B and securin by catalysing the incorporation of the APC/C co-activator,

281 ies of the glf gene, which encodes an enzyme catalysing the last step in the synthesis of galactofura

282 blish that the PPKs are directly involved in catalysing the photoactivated-phy-induced phosphorylatio

283 Catalysing the reduction of oxygen in acidic media is a

284 oride salts are significantly more active in catalysing the SuFEx reaction compared to organosuperbas

285 otransferases are a diverse group of enzymes catalysing the transfer of a sulfuryl group from 3'-phos

286 riptional modifications and the enzymes that catalyse them modulate stem cell differentiation pathway

287 lated following DNA damage and the ARTs that catalyse these events are unknown.

288 A site-specific recombination system catalyses this dimer-resolution reaction at the chromoso

289 The enzyme that catalyses this reaction is carbon monoxide dehydrogenase

290 hyltransferases (PRMT1-9), whose members can catalyse three distinct types of methylation on arginine

291 the SUMO Targeted ubiquitin Ligase Rnf4 that catalyses transfer of ubiquitin from a ubiquitin loaded

292 This laccase-catalysed trifluoromethylation proceeds under mild condi

293 histidinol dehydrogenase (HDH, EC 1.1.1.23), catalyses two oxidation reactions: from L-histidinol (HO

294 scher indole synthesis, we report an iridium-catalysed tyrosinase-like approach to catechols, employi

295 , we show that these proteins are capable of catalysing ubiquitination without the need for the E1 an

296 ubiquitylating NEIL1 in vitro, and that both catalyse ubiquitylation of NEIL1 within the same C-termi

297 ted annulative cross-coupling and a new acid-catalysed vinylcyclopropane rearrangement cascade.

298 y formation of viral ribonucleoproteins that catalyse viral RNA synthesis is inhibited, causing decre

299 rgeted for OEC deposition, and whether sites catalysing water oxidation also contribute to competing

300 hanisms, with the fastest activated response catalysed within monomeric LHC proteins depending on bot