ライフサイエンスコーパス: monooxygenase

1 rsible ether lipid cleavage by alkylglycerol monooxygenase.

2 for the membrane-bound (particulate) methane monooxygenase.

3 l, and stores copper for particulate methane monooxygenase.

4 nase and peptidylglycine alpha-hydroxylating monooxygenase.

5 to create an efficient NADPH oxidase from a monooxygenase.

6 hane monooxygenase (pMMO) and polysaccharide monooxygenase.

7 dicopper site within the particulate methane monooxygenase.

8 me operates as an NADH oxidase rather than a monooxygenase.

9 etheneotrophs by inducing the enzyme alkene monooxygenase.

10 hich are currently misannotated as nitronate monooxygenase.

11 DPH-dependent cytochrome P450 membrane-bound monooxygenases.

12 lycoside hydrolases and lytic polysaccharide monooxygenases.

13 ain pathway for PCET in the dinuclear copper monooxygenases.

14 cluded copper-dependent lytic polysaccharide monooxygenases.

15 hydroperoxide acting as oxidizing agents in monooxygenases.

16 ohydrate esterases, and lytic polysaccharide monooxygenases.

17 ylamine N-oxide by hepatic flavin-containing monooxygenases.

18 y proteins of other bacterial multicomponent monooxygenases.

19 onsists of a large number of heme-containing monooxygenases.

20 ur understanding of the mononuclear dicopper monooxygenases.

21 t to the catalytic cycle of flavin-dependent monooxygenases.

22 ysiologically important mononuclear dicopper monooxygenases.

23 hydroxylation step is typically catalyzed by monooxygenases.

24 e biochemical repertoire of flavin-dependent monooxygenases.

25 thylglutaryl-CoA synthase 1 and methylsterol monooxygenase 1 in humans.

26 We focused on the Flavin-containing monooxygenase-2 (Fmo-2) gene, a likely direct dsx target

27 otic detoxification enzyme flavin-containing monooxygenase-2 (FMO-2).

28 ds, we identify the enzyme flavin-containing monooxygenase 3 (Fmo3) to be a target of insulin.

29 Human flavin-containing monooxygenase 3 (hFMO3), a membrane-bound hepatic protei

30 ent formation of TMA and host hepatic flavin monooxygenase 3-dependent (FMO3-dependent) formation of

31 including a multifunctional cytochrome P450 monooxygenase, a hydroxylating nonheme-iron-dependent di

32 factor beta1, suggesting that alkylglycerol monooxygenase activity affects IFN-gamma/lipopolysacchar

33 wo distinct [Cu-O-Cu](2+) sites with methane monooxygenase activity are identified in the zeolite Cu-

34 and reveal that alteration of alkylglycerol monooxygenase activity has a profound impact on the lipi

35 Monooxygenase activity levels were significantly higher

36 Alkylglycerol monooxygenase activity manipulation modulated the IFN-ga

37 It has the highest reported monooxygenase activity of the P450 enzymes, and this cat

38 ssociated with deltamethrin resistance, with monooxygenase activity playing a stronger role.

39 Here we found intracellular alkylglycerol monooxygenase activity to be an important regulator of a

40 oth knockdown resistance (kdr) mutations and monooxygenase activity were significantly associated wit

41 Possibly as a result of reduced kynurenine 3-monooxygenase activity, elevated central nervous system

42 Although mutation of this residue abolishes monooxygenase activity, recent work has shown that mutat

43 Purified PA1024 did not exhibit nitronate monooxygenase activity; however, it displayed NADH:quino

44 p.Lys234Arg) mutations of the alkylglycerol monooxygenase (AGMO) gene were associated with KA relaps

45 ic oxide synthases (NOSs), and alkylglycerol monooxygenase (AGMO).

46 thrin, ribonucleotide reductase, and methane monooxygenase, all of which can bind NO and O2.

47 w that a single enzyme, the flavin-dependent monooxygenase AlpJ, can generate these metabolites from

48 overy of the copper-dependent polysaccharide monooxygenases, also classified as auxiliary-activity en

49 is a highly divergent homolog of the ammonia monooxygenase (AMO).

50 substrate for the oxidative enzyme, ammonia monooxygenase, AMO) as well as the product, CH(3)OH, its

51 6S rRNA gene amplicon sequencing and ammonia monooxygenase (amoA) abundance quantification through qu

52 We showcase ROCker using ammonia monooxygenase (amoA) and nitrous oxide reductase (nosZ)

53 lse addition of AgNPs on AOB and AOA ammonia monooxygenase (amoA) gene abundances and benthic nitrifi

54 ammonia and nitrite-oxidizing taxa (ammonia monooxygenase-amoA, nitrite oxidoreductase-nxrB, respect

55 otent and selective inhibitors of kynurenine monooxygenase and competitive for kynurenine.

56 ydrocarbon oxidations by particulate methane monooxygenase and heterogeneous zeolite systems.

57 flavin adenine dinucleotide (FAD)-dependent monooxygenase and is located in the outer mitochondrial

58 e identifies RIFMO as a class A flavoprotein monooxygenase and is similar in fold and quaternary stru

59 olite data demonstrate that the kynurenine-3-monooxygenase and kynurenine aminotransferase branches o

60 raction reactions catalyzed by dopamine beta-monooxygenase and peptidylglycine alpha-hydroxylating mo

61 ic mechanism of the first known plant flavin monooxygenase and provides a foundation for further inve

62 described biosensor based on Baeyer-Villiger monooxygenase and the first reported application of bios

63 etoxification as measured by the activity of monooxygenases and glutathione S-transferases (GSTs) was

64 repertoire of genes encoding cytochrome P450 monooxygenases and glutathione S-transferases associated

65 While CYP81Fs encoding cytochrome P450 monooxygenases and IGMTs encoding indole glucosinolate O

66 ation by substrate free lytic polysaccharide monooxygenases and provide insights that can be extended

67 ssed genes (DEGs), including cytochrome P450 monooxygenases and UDP-glycosyltransferases, was shared

68 ygenase (peptidylglycine alpha-hydroxylating monooxygenase) and lyase (peptidyl-alpha-hydroxyglycine

69 e PA4202 (nmoA) gene, coding for a nitronate monooxygenase, and ddlA (PA4201), encoding a d-alanine a

70 Iron metabolism, monooxygenases, and secondary metabolism appeared to par

71 ction of L-lysine-alpha-oxidase and lysine-2-monooxygenase are analyzed.

72 All three cytochrome P450 1 (CYP1) monooxygenases are believed to participate in lipid medi

73 dG-like proteins and antibiotic biosynthesis monooxygenases are close sequence and structural relativ

74 ible implications of the results for toluene monooxygenases are considered as well.

75 TMTT The DMNT biosynthetic pathway and both monooxygenases are distinct from those previously charac

76 N-Hydroxylating monooxygenases are involved in the biosynthesis of iron-

77 Methane monooxygenases are nature's primary biological mechanism

78 -5 SDIMOs (i.e., tetrahydrofuran and propane monooxygenases), are of significant interest due to thei

79 Our findings have thus defined a novel monooxygenase-based oxygen sensing mechanism that has th

80 beta,beta-Carotene 15,15'-monooxygenase (BCMO1) converts beta-carotene to retinald

81 of hydrocarbons by bacterial multicomponent monooxygenases (BMMs) requires the interplay of three or

82 ther lipid species upstream of alkylglycerol monooxygenase but also other more complex lipids includi

83 to known oxidases, lysine demethylases, and monooxygenases, but its active site bears no resemblance

84 ilarity with well characterized flavoprotein monooxygenases, but the protein has not been isolated an

85 ysis using flavin-containing Baeyer-Villiger monooxygenases (BVMOs) is a well-established tool to add

86 istinguished from other class A flavoprotein monooxygenases by its unique middle domain, which is inv

87 ts host gene, MICAL3 (microtubule-associated monooxygenase, calponin, and LIM domain containing 3gene

88 detoxification gene families, including P450 monooxygenases, carboxyl/cholinesterases, glutathione-S-

89 The vast majority of flavin monooxygenases catalyze hydroxylation reactions on a sin

90 rmaldehyde as the end product of the dicamba monooxygenase-catalyzed O-demethylation of the herbicide

91 The flavoprotein tryptophan 2-monooxygenase catalyzes the oxidative decarboxylation of

92 The family 2a CBMs of two monooxygenases,CfLPMO10 andTbLPMO10 fromCellulomonas fim

93 , we describe the characterization of a P450 monooxygenase CnsC from Penicillium that catalyzes the h

94 The ubiquitous flavin-dependent monooxygenases commonly catalyze oxygenation reactions b

95 enzyme adopts a fold common to FAD-dependent monooxygenases, contains a tightly bound FAD prosthetic

96 Kynurenine 3-monooxygenase converts kynurenine to 3-hydroxykynurenine

97 We show here that the FAD-dependent monooxygenase Coq6, which is known to hydroxylate positi

98 Cytochrome P450 monooxygenases CYP101A1 and MycG catalyze regio- and ste

99 er stromal expression of the cytochrome P450 monooxygenase CYP26 modulates BTZ sensitivity in the BM

100 Specifically, overexpression of the monooxygenase CYP2C8 or genetic ablation or inhibition o

101 by the Brassicaceae-specific cytochrome P450 monooxygenase CYP705A1 and is transiently induced in a j

102 substrate production by the cytochrome P450 monooxygenase CYP81F2 is localized to the surface of the

103 We further identified cytochrome P450 monooxygenase CYP89A9 as being responsible for NDCC accu

104 on of (E)-nerolidol into DMNT maps to a P450 monooxygenase, CYP92C5, which is capable of converting n

105 g TMTT accumulation corresponds to a similar monooxygenase, CYP92C6, which is specific for the conver

106 f the important enzyme class cytochrome P450 monooxygenases (CYPs), thereby influencing the detoxific

107 he initial identification of cytochrome P450 monooxygenases (CYPs/P450s), great progress has been mad

108 lating monooxygenase (PHM) and dopamine beta-monooxygenase (DbetaM) are copper-dependent enzymes that

109 Kmo(-/-)) and characterized the kynurenine 3-monooxygenase-deficient mice using six behavioral assays

110 ique oxidative cleavage activity of the CTB3 monooxygenase domain in vitro.

111 This genomic region harbors monooxygenase dopamine beta-hydroxylase-like 1 gene (MOX

112 tion and down-regulation of both 1,4-dioxane monooxygenase (dxmB) and aldehyde dehydrogenase (aldH) g

113 ly a few bacteria can degrade it, using EDTA monooxygenase (EmoA) to initiate the degradation.

114 icroorganisms overexpressing Baeyer-Villiger monooxygenase enabling the production of enantiopure lac

115 Nitronate monooxygenases encoded by NMO genes catalyse the oxidati

116 emonstrated for both ammonia lyases and P450 monooxygenases expressed within live bacterial colonies

117 parallel way by modulation of alkylglycerol monooxygenase expression and of tetrahydrobiopterin bios

118 ctor was highly correlated with flavonoid 3'-monooxygenase (F3'H) and a DFR in spathes, suggesting th

119 Members of the antibiotic biosynthesis monooxygenase family catalyze O2-dependent oxidations an

120 ulated to be catalyzed by a flavin-dependent monooxygenase (FMO) activity internal to the last module

121 one to phenalenone requires an FAD-dependent monooxygenase (FMO) PhnB, which catalyzes the C2 aromati

122 ygenase (Tmm), a bacterial flavin-containing monooxygenase (FMO), is found widespread in marine bacte

123 Flavin-containing monooxygenases (FMOs) are primarily studied as xenobioti

124 onstrated that YUCCA (YUC) flavin-containing monooxygenases (FMOs) catalyze a rate-limiting step in a

125 al circulation, and hepatic flavin-dependent monooxygenases (FMOs) efficiently oxidize TMA to TMAO.

126 (YUC) proteins constitute a family of flavin monooxygenases (FMOs), with an important role in auxin (

127 ron-dependent dioxygenase, and an ABM family monooxygenase for oxidative cleavage of the polyketide m

128 nzymatic catalyst-based on a cytochrome P450 monooxygenase-for the highly enantioselective intermolec

129 osynthetic gene cluster, the cytochrome P450 monooxygenase Fr9R, was assigned as a 4-hydroxylase base

130 ignated CYP716Y1, encoding a cytochrome P450 monooxygenase from Bupleurum falcatum that catalyzes the

131 Physiologically, the monooxygenase from fungi protects the organism from the

132 soluble peptidylglycine alpha-hydroxylating monooxygenase from membrane-associated PAL.

133 responsible protein was identified as a P450 monooxygenase from the CYP82 family, a family not previo

134 transcript abundance of the archaeal ammonia monooxygenase gene (amoA) in nitrifying activated sludge

135 Previous analyses of the ammonia monooxygenase gene amoA suggest that pH is an important

136 cteria and archaea (AOB/AOA) via the ammonia monooxygenase gene amoA, less is known about their small

137 rchaeota 16S rRNA genes and archaeal ammonia-monooxygenase gene copy number (qPCR) were significantly

138 P450-BM3 and mutants of this monooxygenase generated by directed evolution are excell

139 me deletions of one hydroxylase and two P450 monooxygenase genes resulted in the production of novel

140 Cytochrome P450 monooxygenase, glycosyl transferase, and glutathione S-t

141 lysis of the dechlorinating flavin-dependent monooxygenase, HadA, from the aerobic organism Ralstonia

142 diiron(IV) intermediate Q of soluble methane monooxygenase have led to the synthesis of a diiron(IV)

143 Lytic polysaccharide monooxygenases have attracted vast attention owing to th

144 Crystal structures of polysaccharide monooxygenases have emerged, but experimental studies ar

145 Furthermore, methanotrophs and methane monooxygenases have enormous potential in bioremediation

146 sent high-resolution structures of toluene 4-monooxygenase hydroxylase complexed with its electron tr

147 ole of tetrahydrobiopterin and alkylglycerol monooxygenase in ether lipid metabolism of murine macrop

148 dioxygenase, the previous name for nitronate monooxygenase in the GenBank(TM) and PDB databases, but

149 tests further corroborated the vital role of monooxygenases in dioxane degradation.

150 t negatively regulate cytochrome P450 (P450) monooxygenases in response to physiological and pathophy

151 e (PAMO), a thermally robust Baeyer-Villiger monooxygenase, in the quest to access a mutant which dis

152 BCO1 has been thought to be a monooxygenase, incorporating oxygen from O2 and H2O into

153 s the first structural characterization of a monooxygenase involved in Q biosynthesis.

154 osynthases, which are flavin-dependent amine monooxygenases involved in the four-electron oxidation o

155 Nitronate monooxygenase is a flavin-dependent enzyme that catalyze

156 Peptidylglycine alpha-hydroxylating monooxygenase is a noninteracting bicopper enzyme that s

157 Most significantly, the P450 monooxygenase is shown to catalyze successive hydroxylat

158 PtmO5, a cytochrome P450 monooxygenase, is proposed to catalyze the formation of

159 smid-encoded soluble di-iron centre isoprene monooxygenase (IsoMO) is essential for isoprene metaboli

160 etabolism, including four-component isoprene monooxygenases (IsoMO), were identified and compared wit

161 ulatory enzymes in this pathway-kynurenine-3-monooxygenase (KMO) and tryptophan-2,3-dioxygenase (TDO)

162 mino transferase II (KATII) and kynurenine-3-monooxygenase (KMO) enzymes.

163 A number of inhibitors of kynurenine 3-monooxygenase (KMO) have previously been described as po

164 Here we report that the kynurenine 3-monooxygenase (KMO) inhibitor Ro 61-8048 increases brain

165 e enhanced by administering the kynurenine 3-monooxygenase (KMO) inhibitor, Ro 61-8048.

166 Kynurenine-3-monooxygenase (KMO) is a key FAD-dependent enzyme of try

167 Inhibition of kynurenine 3-monooxygenase (KMO) protects against multiple organ dysf

168 Here we show that kynurenine-3-monooxygenase (KMO), a key enzyme of tryptophan metaboli

169 Kynurenine 3-monooxygenase (KMO), a pivotal enzyme in the kynurenine

170 : indoleamine dioxygenase (IDO1), kynurenine monooxygenase (KMO), and kynurenine aminotransferase II

171 tion is critically dependent on kynurenine 3-monooxygenase (KMO).

172 usly identified member of YUCCA (YUC) flavin monooxygenase-like proteins (YUC8).

173 Lytic polysaccharide monooxygenase (LPMO) represents a unique principle of ox

174 tion: lpmo10B encodes a lytic polysaccharide monooxygenase (LPMO), while cbp2D and cbp2E encode prote

175 Bacterial lytic polysaccharide monooxygenases (LPMO10s) use redox chemistry to cleave g

176 Lytic polysaccharide monooxygenases (LPMOs) are a class of copper-containing

177 Lytic polysaccharide monooxygenases (LPMOs) are copper-dependent enzymes that

178 Copper-dependent lytic polysaccharide monooxygenases (LPMOs) are enzymes that oxidatively deco

179 ent work has shown that lytic polysaccharide monooxygenases (LPMOs) are important contributors to thi

180 Lytic polysaccharide monooxygenases (LPMOs) are industrially important copper

181 The recently discovered lytic polysaccharide monooxygenases (LPMOs) are known to carry out oxidative

182 Lytic polysaccharide monooxygenases (LPMOs) are recently discovered enzymes t

183 The recently discovered lytic polysaccharide monooxygenases (LPMOs) carry out oxidative cleavage of p

184 Lytic polysaccharide monooxygenases (LPMOs) catalyze the oxidative cleavage o

185 Copper-dependent lytic polysaccharide monooxygenases (LPMOs) contribute to the degradation of

186 it has been shown that lytic polysaccharide monooxygenases (LPMOs) contribute to this process by cat

187 Lytic polysaccharide monooxygenases (LPMOs) exhibit a mononuclear copper-cont

188 Lytic polysaccharide monooxygenases (LPMOs) offer tremendous promise for furt

189 t enzymes classified as lytic polysaccharide monooxygenases (LPMOs) were able to strongly enhance the

190 nases, chitobiases, and lytic polysaccharide monooxygenases (LPMOs).

191 ng to the AA9 family of lytic polysaccharide monooxygenases (LPMOs).

192 ose hydrolysis, such as lytic polysaccharide monooxygenase (LPO).

193 es is provided, with implications for copper monooxygenase mechanisms.

194 the sterol-dependent degradation of squalene monooxygenase mediated by the yeast Doa10 or mammalian T

195 e, we identified a role for the flavoprotein monooxygenase MICAL3, an actin disassembly factor, in or

196 to selectively oxidize methane using methane monooxygenase (MMO) and methyl coenzyme M reductase (MCR

197 Methane monooxygenase (MMO) catalyses the O2-dependent conversio

198 o methanol under mild conditions are methane monooxygenases (MMOs) found in methanotrophic bacteria;

199 Methane monooxygenases (MMOs) mediate the facile conversion of m

200 ogy (CH) domain always follows an N-terminal monooxygenase (MO) domain.

201 l characterization of Nocardia farcinica Lys monooxygenase (NbtG), which has similar biochemical prop

202 With our identification of UbiI, the three monooxygenases necessary for aerobic Q biosynthesis in E

203 to known detoxification families (like P450 monooxygenases), new gene families not previously associ

204 f dithranol, a substrate for the nogalamycin monooxygenase (NMO) from Streptomyces nogalater As with

205 Nitronate monooxygenase (NMO) oxidizes the mitochondrial toxin pro

206 E. coli overexpressing either cyclopentanone monooxygenase or cyclohexanone monooxygenase was immobil

207 Cytochrome P450 monooxygenases (P450) in the honey bee, Apis mellifera,

208 onformational state in solution for the heme monooxygenase P450cam when bound to its natural redox pa

209 Cytochrome P450 monooxygenases (P450s) are heme-thiolate proteins whose

210 Cytochrome P450 monooxygenases (P450s) are involved in metabolic resista

211 Cytochrome P450 monooxygenases (P450s) have enormous potential in the pr

212 than half (51.2%) of the CBP cytochrome P450 monooxygenases (P450s) that are up-regulated in the R st

213 Peptidylglycine alpha-amidating monooxygenase (PAM) (EC 1.14.17.3) catalyzes peptide ami

214 Peptidylglycine alpha-amidating monooxygenase (PAM) catalyzes a two-step reaction result

215 ATPase, and peptidylglycine alpha-amidating monooxygenase (PAM), a copper-dependent membrane enzyme.

216 c domains of peptidylglycine alpha-amidating monooxygenase (PAM), a type I integral membrane protein,

217 y identified peptidylglycine alpha-amidating monooxygenase (PAM), an enzyme required for generating a

218 sis (ISM) has been applied to phenyl acetone monooxygenase (PAMO), a thermally robust Baeyer-Villiger

219 acids derived from the cytochrome P450 (CYP) monooxygenase pathway serve as vital second messengers t

220 ation, through the sequential actions of its monooxygenase (peptidylglycine alpha-hydroxylating monoo

221 Cu(II)(O2(*-)) active species of the copper monooxygenase PHM and exhibits enhanced reactivity towar

222 perties closely matching those of the copper monooxygenase PHM.

223 Peptidylglycine alpha-hydroxylating monooxygenase (PHM) and dopamine beta-monooxygenase (Dbe

224 enter in peptidylglycine alpha-hydroxylating monooxygenase (PHM) or a catalytic center in copper nitr

225 that encode a novel particulate hydrocarbon monooxygenase (pHMO), degradation pathways for correspon

226 Particulate membrane-associated hydrocarbon monooxygenases (pHMOs) are critical components of the ae

227 Here, we report how the reactivity of a monooxygenase (PikC) from the pikromycin pathway is modi

228 anchoring mechanism of the biosynthetic P450 monooxygenase PikCD50N-RhFRED.

229 Cytochrome P450 monooxygenases play a critical role in insecticide resis

230 Flavin-dependent monooxygenases play a variety of key physiological roles

231 putative active site of particulate methane monooxygenase (pMMO) and polysaccharide monooxygenase.

232 methane C-H oxidation in particulate methane monooxygenase (pMMO) are currently unknown.

233 Particulate methane monooxygenase (pMMO) catalyzes the oxidation of methane

234 MALDI-MS analysis of the particulate methane monooxygenase (pMMO) complex, a three-subunit transmembr

235 Particulate methane monooxygenase (pMMO) is a membrane-bound metalloenzyme t

236 Particulate methane monooxygenase (pMMO) is one of the few enzymes that can

237 reaction is catalyzed by particulate methane monooxygenase (pMMO), a copper-dependent integral membra

238 Using particulate methane monooxygenase (pMMO), we create a biocatalytic polymer m

239 monooxygenase (sMMO) and particulate methane monooxygenase (pMMO).

240 h as tyrosinase (Ty) and particulate methane monooxygenase (pMMO).

241 nd the membrane-bound or particulate methane monooxygenase (pMMO).

242 asing copy numbers of the functional methane monooxygenase pmoA gene.

243 etection of 16S rRNA and particulate methane monooxygenase (pmoA) genes for two putative aerobic meth

244 ainst the highly-related particulate methane monooxygenase (pmoA).

245 The ubiquitous fungal polysaccharide monooxygenases (PMOs) (also known as GH61 proteins, LPMO

246 scovered fungal and bacterial polysaccharide monooxygenases (PMOs) are capable of oxidatively cleavin

247 Polysaccharide monooxygenases (PMOs), also known as lytic PMOs (LPMOs),

248 genes (encoding the alpha subunit of ammonia monooxygenases) preserved in a 5.8-m sediment core (span

249 n to be produced by cluster-independent P450 monooxygenases, probably to protect the fungus from the

250 3-NPA), confirming the role of the nitronate monooxygenase protein in the detoxification of nitronate

251 Bacterial multicomponent monooxygenases provide a fascinating example, where a di

252 Differently from the ornithine monooxygenases PvdA, SidA, and KtzI, NbtG can use both N

253 Cytochromes P450 catalyze a variety of monooxygenase reactions that require electron transfer f

254 ochrome b561 associated with a dopamine beta-monooxygenase redox domain (CYBDOM), which localizes to

255 The monooxygenase responsible for co-metabolic transformatio

256 Rifampicin monooxygenase (RIFMO) catalyzes the N-hydroxylation of t

257 Two soluble di-iron centre monooxygenase (SDIMO) gene clusters were identified and

258 Soluble di-iron monooxygenases (SDIMOs), especially group-5 SDIMOs (i.e.

259 Squalene monooxygenase (SM) is an important control point in chol

260 Squalene monooxygenase (SM) is the second rate-limiting enzyme in

261 Squalene monooxygenase (SM), which synthesizes a cholesterol prec

262 catalytic sites in two MMOs: soluble methane monooxygenase (sMMO) and particulate methane monooxygena

263 enzymes, the cytoplasmic or soluble methane monooxygenase (sMMO) and the membrane-bound or particula

264 to the diiron active site of soluble methane monooxygenase (sMMO) and to a series of high-valent diir

265 hydroxylase of a BMM enzyme, soluble methane monooxygenase (sMMO) from Methylococcus capsulatus (Bath

266 gulatory component (MMOB) of soluble methane monooxygenase (sMMO) has a unique N-terminal tail not fo

267 The expression of squalene monooxygenase (SQLE) was associated with lethal cancer i

268 esentation of members of the luciferase-like monooxygenase superfamily points toward an important rol

269 h of photoreceptors and suggest that the CYP monooxygenase system is a risk factor for retinal photod

270 Tyramine beta-monooxygenase (TbetaM) belongs to a family of physiologi

271 The enzyme tyramine beta-monooxygenase (TbetaM) belongs to a small eukaryotic fam

272 echanism of a two-component flavin-dependent monooxygenase that can catalyze oxidative dechlorination

273 jostii RHA1 is an NADH-specific flavoprotein monooxygenase that catalyzes the para-hydroxylation of 3

274 ver, knocking down shade (shd), encoding the monooxygenase that converts ecdysone (E) to the more act

275 hitin was enhanced by a lytic polysaccharide monooxygenase that increases substrate accessibility by

276 Coq6 is thus a rare example of a flavin monooxygenase that is able to act on two different carbo

277 ore A) is a flavin-dependent N-hydroxylating monooxygenase that is essential for virulence in Aspergi

278 EmoA is an FMNH2 -dependent monooxygenase that requires an NADH:FMN oxidoreductase (

279 IsdGs are heme monooxygenases that break open the tetrapyrrole, releasi

280 l, including the discovery of polysaccharide monooxygenases that enhance the activity of cellulases.

281 f physiologically important dinuclear copper monooxygenases that function with a solvent-exposed acti

282 As monooxygenases, they are universally thought to control

283 TMA monooxygenase (Tmm), a bacterial flavin-containing monoo

284 can oxidize DMS to DMSO using trimethylamine monooxygenase (Tmm).

285 to using the iron-containing soluble methane monooxygenase to catalyse methane oxidation, with this s

286 dopsis gene families such as cytochrome P450 monooxygenases to group the members functionally and sho

287 single amino acid was sufficient for such a monooxygenase-to-oxidase switch-a complete transition in

288 Toluene/o-xylene monooxygenase (ToMO) is a non-heme diiron protein that a

289 Cytochrome P450 monooxygenases typically catalyze the insertion of one a

290 aving CCO, NOV2, previously reported to be a monooxygenase, using a purified enzyme sample revealed t

291 Alkylglycerol monooxygenase was expressed and active also in primary m

292 yclopentanone monooxygenase or cyclohexanone monooxygenase was immobilised in the form of solid polye

293 Cytochrome P450 monooxygenase was involved in the production of the two

294 (SidA), a member of class B flavin-dependent monooxygenases, was selected as a model system to invest

295 nctional characterization of cytochrome P450 monooxygenases, we established that trans-sabin-3-ol but

296 ive-site component of the conserved isoprene monooxygenase, which are capable of retrieving isoA sequ

297 ivity of active sites in particulate methane monooxygenase, which are enzymes able to selectively oxi

298 unction of the encoded enzyme as a nitronate monooxygenase, which is needed to prevent the buildup of

299 n cytochrome P450 (P450) is a membrane-bound monooxygenase whose catalytic activities require two ele

300 is initiated by a remarkable decarboxylating monooxygenase with high specificity for arginine.