ライフサイエンスコーパス: decarboxylase

1 se, 2-oxoglutarate dehydrogenase and glycine decarboxylase).

2 d the GABA-synthesizing enzyme glutamic acid decarboxylase.

3 ehydrogenase and a subsequent glutaconyl-CoA decarboxylase.

4 synthesized putrescine via a SpeC ornithine decarboxylase.

5 synthase reaction involves a glycyl radical decarboxylase.

6 70 interacts with TH and aromatic amino acid decarboxylase.

7 lipoylation of the photorespiratory glycine decarboxylase.

8 pression level of Cmoxdc1 coding for oxalate decarboxylase.

9 ggering degradation of its target, aspartate decarboxylase.

10 ompetitive substrate, or inhibitors of human decarboxylase.

11 arboxylate levodopa to dopamine via tyrosine decarboxylases.

12 dependent regulation of S-adenosylmethionine decarboxylase 1 (AMD1) stability.

13 ed conditional null alleles of Glutamic acid decarboxylase 1 (Gad1) and Resistant to dieldrin (Rdl),

14 used by epigenetic upregulation of glutamate decarboxylase 1 (GAD1), a regulator of the GABA neurotra

15 a-aminobutyric acid (GABA) and glutamic acid decarboxylase 1 (GAD1), the enzyme that synthesizes GABA

16 show that this mechanism requires aconitate decarboxylase 1 (IRG1), which synthesizes itaconate, a m

17 ), which is a suicide inhibitor of ornithine decarboxylase 1 (ODC1), and diethylnorspermine (DENSpm),

18 nd polyamine metabolism, including Ornithine Decarboxylase 1 (ODC1), are affected by DNA methylation

19 hibits the expression of c-MYC and ornithine decarboxylase 1 (ODC1), the rate-limiting enzyme for pol

20 Interaction with ornithine decarboxylase 1 (ODC1), the rate-limiting enzyme of poly

21 Phosphatidylserine decarboxylase 1 (Psd1p), an ancient enzyme that converts

22 zyme that generates PE is phosphatidylserine decarboxylase 1 (Psd1p).

23 RNA-sequencing demonstrated Acod1 (Aconitate decarboxylase 1) as one of the top genes induced by PM i

24 deficits in the induction of GAD1 (glutamate decarboxylase 1) protein expression.

25 ynaptosomal-associated protein 29, glutamate decarboxylase 1, metabotropic glutamate receptor 1, and

26 n antizyme-mediated degradation of ornithine decarboxylase-1 and a resulting reduction in cellular po

27 -(THBS 1), interleukin 6 (IL6), and arginine decarboxylase 2 (ADC2)) were down-regulated.

28 ctivated a small population of glutamic acid decarboxylase 2 (GAD2)-expressing neurons in the lateral

29 ne released from neurons expressing tyrosine decarboxylase 2 (Tdc2) signal directly to astrocytes to

30 The glutamic acid decarboxylase 2 but not the parvalbumin subset of SNr ga

31 ed autoantigens [proinsulin or glutamic acid decarboxylase 65 (GAD)] delayed T1D onset, but published

32 l as thyroperoxidase (TPO) and glutamic acid decarboxylase 65 (GAD65) Abs.

33 Glutamic acid decarboxylase 65 (GAD65) and autoantibodies specific for

34 ed, including orexin cells and glutamic acid decarboxylase 65 (GAD65) cells, but their interplay in o

35 cond GABA-synthesizing enzyme, glutamic acid decarboxylase 65-kDa isoform (GAD65), remains unclear.

36 lsed with preproinsulin (PPI), glutamic acid decarboxylase (65-kDa isoform; GAD65), and insulinoma-as

37 ATP-alpha, but increased levels of glutamate decarboxylase-65 and glutamine synthetase in PFC; reduce

38 sion levels of parvalbumin and glutamic acid decarboxylase 67 (GAD67) in schizophrenia subjects but n

39 istently found lower levels of glutamic acid decarboxylase 67 (GAD67) messenger RNA (mRNA) in the pre

40 ychiatric candidate promoters (glutamic acid decarboxylase 67, Reelin, and brain-derived neurotrophic

41 f the GABA-synthesizing enzyme glutamic acid decarboxylase 67-kDa isoform (GAD67) in the PFC have bee

42 lpha-amino-beta-carboxymuconic--semialdehyde decarboxylase, a class III amidohydrolase, with a single

43 chanisms, with reduced aromatic L-amino acid decarboxylase (AAAD) activity closely related to the app

44 sphate (PLP)-dependent aromatic l-amino acid decarboxylase (AAAD) family has yielded an array of para

45 , is biosynthesized by aromatic-L-amino acid decarboxylase (AADC) and indolethylamine-N-methyltransfe

46 The aromatic L-amino-acid decarboxylase (AADC) defect appears to be consistently s

47 Aromatic l-amino acid decarboxylase (AADC) deficiency is an inborn error of mo

48 Aromatic l-amino acid decarboxylase (AADC) deficiency is an inherited disease

49 Children with aromatic l-amino acid decarboxylase (AADC) deficiency suffer from severe motor

50 ne substitution in the L-aromatic amino acid decarboxylase (AADC) enzyme was replicated in a meta-ana

51 ygous mutations in the aromatic l-amino acid decarboxylase (AADC) gene result in a severe depletion o

52 o its decarboxylation by aromatic amino acid decarboxylase (AADC), an enzyme overexpressed in these m

53 sine hydroxylase (TH), aromatic l-amino acid decarboxylase (AADC), and GTP cyclohydrolase I (GCH1) tr

54 amine transporter (DAT), aromatic amino acid decarboxylase (AADC), or vesicular monoamine type 2 were

55 lly express the enzyme aromatic L-amino acid decarboxylase (AADC), which synthesizes trace amines dir

56 tionally characterized aromatic l-amino acid decarboxylases (AADCs) and aromatic aldehyde synthases (

57 We also show that pyruvate decarboxylase (AceE), the E1 component of pyruvate dehyd

58 ing reaction, ACMS is decarboxylated by ACMS decarboxylase (ACMSD) for further metabolism and energy

59 ha-Amino-beta-carboxymuconate-e-semialdehyde decarboxylase (ACMSD) plays an important role in l-trypt

60 The UbiD family of reversible decarboxylases act on aromatic, heteroaromatic, and unsa

61 te with enhanced aconitase and cis-aconitate decarboxylase activities by controlling the expression o

62 onal switching between aldehyde synthase and decarboxylase activities.

63 vin mononucleotide (FMN)-binding protein, no decarboxylase activity has been detected.

64 rement of the enzyme responsible for in vivo decarboxylase activity remained unclear.

65 Hydroxycinnamate decarboxylase activity was measured by the ability to tr

66 naptic dopamine synthesis capacity (ie, DOPA decarboxylase activity).

67 dc1 is solely responsible for the reversible decarboxylase activity, and that it requires a new type

68 ved to be initiated by a change in glutamate decarboxylase activity, but the underlying mechanisms ar

69 lus cadaverine (CF) indicated biofilm lysine decarboxylase activity.

70 me are critical for proenzyme processing and decarboxylase activity.

71 We identify arginine decarboxylase (ADC) genes as the host targets of Brg11,

72 reveal that A. thaliana meso-diaminopimelate decarboxylase adopts a homodimeric assembly.

73 proteins in mtacp mutants, particularly Gly decarboxylase, affects the recovery of photorespiratory

74 s of Trypanosoma brucei S-adenosylmethionine decarboxylase alone and in functional complex with its c

75 hey are both functional meso-diaminopimelate decarboxylases, although with lower activities than thos

76 pyruvoyl cofactor of S-adenosyl-L-methionine decarboxylase (AMD1) is dynamically controlled by intrac

77 remains unknown whether adenosyl methionine decarboxylase (AMD1), a rate-limiting enzyme in polyamin

78 elenoprotein genes, and S-adenosylmethionine decarboxylase (AMD1).

79 Bacterial arylmalonate decarboxylase (AMDase) and evolved variants have become

80 made possible by the evolution of a pyruvate decarboxylase, analogous to that in brewer's yeast and t

81 ethylglutaryl-CoA synthase, a dehydratase, a decarboxylase and a dedicated acyl carrier protein.

82 CAD is not homologous to any known decarboxylase and appears to have evolved from prokaryot

83 lso analyzed the expression of the Histidine decarboxylase and ECP by flow cytometry and fluorescence

84 patients express higher levels of histidine decarboxylase and ECP than those from healthy volunteers

85 e show that cholangiocytes express histidine decarboxylase and its inhibition reduces CCA growth.

86 ania donovani have shown that both ornithine decarboxylase and spermidine synthase, two enzymes of th

87 synthesis-responsive genes, namely ornithine decarboxylase and spermidine synthase, were induced by G

88 tudy, we describe the use of tyrosinases and decarboxylases and combine these with a transaminase enz

89 ikimate hydroxycinnamoyl transferase, lysine decarboxylase, and acyltransferase gene families.

90 e biosynthesis (spe1Delta, lacking ornithine decarboxylase, and spe2Delta, lacking SAM decarboxylase)

91 y, many patients with SPS have glutamic acid decarboxylase antibodies (GAD-ab), but these 2 disorders

92 Little is known of glutamic acid decarboxylase antibodies (GAD-abs) in the paraneoplastic

93 itions, retinopathy, and serum glutamic acid decarboxylase antibody (GADA) titers in relation to reti

94 ral interactive partners, of which ornithine decarboxylase antizyme-1, NEEP21 (NSG1), and ADAM10 were

95 ornithine and polyamine synthesis, ornithine decarboxylase appeared to be the rate-limiting enzyme fo

96 Arginase, arginine deiminase and arginine decarboxylase are potential enzymes that may be used for

97 Inducible amino acid decarboxylases are known to promote adaptation to acidic

98 techols, employing 3,4-dihydroxybenzoic acid decarboxylases (AroY) that belong to the UbiD enzyme fam

99 ses identify an operon encoding oxaloacetate decarboxylase as diagnostic for the tongue-abundant subg

100 rom incomplete catalysis by TpcK (a putative decarboxylase), as its deletion results in a nearly 10-f

101 her relative abundance of bacterial tyrosine decarboxylases at the site of levodopa absorption, proxi

102 ge, sex, disease duration, and glutamic acid decarboxylase autoantibody titers.

103 8)F]FMT; a substrate for aromatic amino acid decarboxylase), baseline D2/3 receptor-binding potential

104 athogens (FBPs) was investigated in tyrosine decarboxylase broth (TDB) using HPLC.

105 cis-Aconitate decarboxylase (CAD, also known as ACOD1 or Irg1) convert

106 res provide molecular insights into malonate decarboxylase catalysis.

107 of triarylmethanols, and (3) benzoylformate decarboxylase-catalyzed enantioselective benzoin condens

108 meso-Diaminopimelate decarboxylase catalyzes the decarboxylation of meso-diam

109 Ferulic acid decarboxylase catalyzes the decarboxylation of phenylacr

110 Coproheme decarboxylase catalyzes two sequential oxidative decarbo

111 A member of the PdxA family of oxidative decarboxylases catalyzes a novel decarboxylation that us

112 e 4-phosphate dehydrogenase (PdxA) oxidative decarboxylase, class II aldolase, or ribulose 1,5-bispho

113 lyase neofunctionalization and cysteic acid decarboxylase co-option.

114 ABCD) and syntrophic terephthalate-degrading decarboxylase complexes.

115 PSDs are unusual decarboxylase containing a pyruvoyl prosthetic group wit

116 Histidine decarboxylase-containing varicosities diffusely innervat

117 acterized clostridial p-hydroxyphenylacetate decarboxylase (CsdBC).

118 Diaminopimelate decarboxylase (DAPDC) catalyzes the final step in the di

119 genes in Drosophila encode the enzymes dopa decarboxylase (Ddc) and tyrosine hydroxylase (ple).

120 idase (MAO) and L-3,4-dihydroxyphenylalanine decarboxylase (DDC) for microbe-based production of tetr

121 In the kidney, the enzyme DOPA Decarboxylase (DDC) originating from the circulation.

122 l-carbidopa, which is known to inhibit DOPA decarboxylase (DDC), a key protein in Parkinson's diseas

123 identified one dopamine synthesis gene, DOPA decarboxylase (DDC), as a suppressor of tau toxicity in

124 uences of tyrosine hydroxylase (TH) and dopa decarboxylase (DDC), two key enzymes in the biosynthesis

125 ic neurons, some of which still express DOPA decarboxylase (DDC).

126 in, and trace amines, relies in part on DOPA decarboxylase (DDC, AADC), an enzyme that is required fo

127 PS's classification as a carboxy-lyase (i.e. decarboxylase), decarboxylation is not a completely esse

128 Knockdown of MC histidine decarboxylase decreased cholangiocyte and HSC proliferat

129 congeners originates from the activity of a decarboxylase-dehydrogenase enzyme with high similarity

130 (a-FMHis), a suicide inhibitor of histidine decarboxylase, displayed impaired IA memory when tested

131 a drug that targets host aromatic amino acid decarboxylase does not prevent gut microbial l-dopa deca

132 Bacterial tyrosine decarboxylases efficiently convert levodopa to dopamine,

133 Certain host cells express the histidine decarboxylase enzyme (HDC), which is responsible for cat

134 d carbon nanotubes (MWCNT-COOH), and oxalate decarboxylase enzyme (OxDc) immobilized onto a carbon cl

135 esis, of the bacillaene synthase dehydratase/decarboxylase enzyme couple PksH/PksI, responsible for t

136 The activity of the reversible decarboxylase enzyme Fdc1 is dependent on prenylated FMN

137 GAD1 encodes the glutamate decarboxylase enzyme GAD67, a critical actor of the gamm

138 t through direct activation of glutamic acid decarboxylase enzyme isoforms that convert glutamate to

139 Fdc1 is a decarboxylase enzyme that requires the novel prenylated

140 atidylserine catalyzed by phosphatidylserine decarboxylase enzymes (PSD) as a suitable target for dev

141 POMC neurons, as these encode the glutamate decarboxylase enzymes GAD67 and GAD65, respectively.

142 meso-diaminopimelate decarboxylase enzymes whose structures provide clues to

143 ed here indicate that dedicated oxaloacetate decarboxylases exist in eukaryotes.

144 arousal states, is synthesized in histidine decarboxylase-expressing hypothalamic neurons of the tub

145 line expressing cre recombinase in histidine decarboxylase-expressing neurons (Hdc-Cre) followed by a

146 at members of the beta-hydroxyacid reductive decarboxylase family employ different active site featur

147 n NAD-ME, suggesting that NAD-ME was the key decarboxylase for CAM.

148 cterization studies of a novel phenylacetate decarboxylase from an anaerobic, sewage-derived enrichme

149 ctural studies on the mevalonate diphosphate decarboxylase from E. faecalis (MDDEF).

150 by a pyridoxal phosphate-dependent tyrosine decarboxylase from Enterococcus faecalis is followed by

151 ependent, irreversible inactivator of lysine decarboxylase from Hafnia alvei.

152 phosphorylation and activation of glutamate decarboxylase (GAD) 65.

153 tyric acid synthesizing enzyme glutamic acid decarboxylase (GAD) and choline acetyltransferase (ChAT)

154 th region-specific changes in glutamate acid decarboxylase (GAD) and vesicular GABA transporter expre

155 h levels of antibodies against glutamic acid decarboxylase (GAD) are observed in patients with differ

156 signaling becomes predominant when glutamate decarboxylase (GAD) function is compromised.

157 ed by enzymes derived from two glutamic acid decarboxylase (GAD) genes, GAD1 and GAD2, both of which

158 Antibodies to glutamic acid decarboxylase (GAD) have been associated with several ne

159 (Fos) of GABAergic neurons and glutamic acid decarboxylase (GAD) mRNA expression in the aBST.

160 ainst tyrosine hydroxylase (TH) or glutamate decarboxylase (GAD) to systematically compare the propor

161 s and activity measurements of glutamic acid decarboxylase (GAD), a PLP-dependent enzyme synthesizing

162 hosphate-diaphorase (NADPH-d), glutamic acid decarboxylase (GAD), cytochrome oxidase (CO), and calret

163 e parvalbumin-, calbindin-, or glutamic acid decarboxylase (GAD)-67-positive.

164 transmitter, is synthesized by glutamic acid decarboxylase (GAD).

165 Additionally, glutamic acid decarboxylase (GAD)65-loaded tolDCs from well-controlled

166 , we study the distribution of glutamic acid decarboxylase (GAD)67 and GLY transporter 2 (T2) in axon

167 ombinase in cells that contain glutamic acid decarboxylase (GAD; GAD2-cre).

168 factor, which we report to bind to glutamate decarboxylase (Gad1), which encodes GAD67, a rate-limiti

169 orters (vglut1, vglut2.1, vglut3), glutamate decarboxylases (gad1, gad2), and choline acetyltransfera

170 ntional GABA-synthesizing enzymes, glutamate decarboxylases GAD65 and GAD67.

171 UT1) and the 65 kDa isoform of glutamic acid-decarboxylase (GAD65) as markers of, respectively, Ia af

172 st insulin, the 65-kDa form of glutamic acid decarboxylase (GAD65), insulinoma-associated protein 2 (

173 oded 67-kDa protein isoform of glutamic acid decarboxylase (GAD67) is a hallmark of schizophrenia.

174 evels of the 67 kDa isoform of glutamic acid decarboxylase (GAD67) protein, the enzyme responsible fo

175 vels of tyrosine hydroxylase (TH), glutamate decarboxylase (GAD67), and vesicular glutamate transport

176 contain the 67 kDa isoform of glutamic acid decarboxylase (GAD67-GFP), or Cre-recombinase in cells t

177 no acid glutamate by the action of glutamate decarboxylases (GADs).

178 rom high-to-low CO(2) without changes in Gly decarboxylase (GDC) gene or protein expression.

179 photosynthesizing tissue is used for glycine decarboxylase (GDC), necessary for the high-flux photore

180 partate semialdehyde dehydrogenase, arginine decarboxylase gene activator, GTP cyclohydrolase I and a

181 otype 2-mediated human aromatic L-amino acid decarboxylase gene therapy development programme.

182 omato plants over-expressing mouse ornithine decarboxylase gene under the control of fruit-specific p

183 es an upregulation of the insect's ornithine decarboxylase gene, which sequesters arginine for polyam

184 pression and activity of three tea glutamate decarboxylase genes (CsGAD1, 2, and 3), and their encode

185 Glycine decarboxylase (GLDC) acts in the glycine cleavage system

186 Loss of glycine decarboxylase (GLDC) can severely impact neurological de

187 associated with loss of function of glycine decarboxylase (Gldc) in mice and in humans suffering fro

188 re, we report that the gene encoding glycine decarboxylase (GLDC), which catalyzes the first and rate

189 a triplication of the gene encoding glycine decarboxylase, GLDC, presumably resulting in reduced ava

190 e, catalase, superoxide dismutase, ornithine decarboxylase, glutamate receptor, and ammonia transport

191 -malic enzyme (ME), the most widespread C(4) decarboxylase, has increased its catalytic efficiency an

192 Wild-type (WT) and l-histidine decarboxylase (Hdc(-/-)) mice were fed a control diet or

193 Histidine decarboxylase (HDC) and histamine receptor (HR) expressi

194 Histidine decarboxylase (HDC) deficiency has been shown to promote

195 s on dietary histidine and also on histidine decarboxylase (Hdc) depends upon their growth requiremen

196 in one integrated device to detect histidine decarboxylase (HDC) gene directly from human white blood

197 carboxypeptidase A3 (CPA3), and L-histidine decarboxylase (HDC) gene expression; and serum markers (

198 ure termination codon in the human histidine decarboxylase (Hdc) gene has been identified in a family

199 Histidine decarboxylase (HDC) is the main enzyme involved in hista

200 n anti-HA antibody and a probe for histidine decarboxylase (HDC), a synthetic enzyme for HA.

201 ematopoietic progenitors marked by histidine decarboxylase (Hdc).

202 crystal structure of a Pseudomonas malonate decarboxylase hetero-tetramer, as well as biochemical an

203 The malonate decarboxylase holoenzyme contains four subunits, having

204 a NIS synthetase FslA/FigA and an ornithine decarboxylase homolog FslC/FigC, required for rhizoferri

205 antigens are established (insulin, glutamate decarboxylase, IA2, and zinc transporter-8), but the mol

206 ctures of Escherichia coli methylmalonyl-CoA decarboxylase in complex with our analogs affords insigh

207 the GABA-synthesizing enzyme, glutamic acid decarboxylase in EC were confirmed by immunostaining and

208 by high abundance of gut bacterial tyrosine decarboxylase in patients with Parkinson's disease.

209 c protein-immunocytochemistry, glutamic acid decarboxylase in situ hybridization, and parvalbumin-imm

210 n addition, we identified TbPSD as type I PS decarboxylase in the mitochondrion and found that it is

211 ically, that abundance of bacterial tyrosine decarboxylase in the proximal small intestine can explai

212 bunit of the photorespiratory enzyme glycine decarboxylase, increased accumulation of glycine and gly

213 te after use of an oral levodopa plus a dopa-decarboxylase inhibitor combination.

214 amine analog and potent S-adenosylmethionine decarboxylase inhibitor, decreases HIV expression in mon

215 difluoromethylornithine (DFMO), an ornithine decarboxylase inhibitor, may further decrease immunosupp

216 ce treated with saline, histamine, histidine decarboxylase inhibitor, or cromolyn sodium.

217 dual function enzyme, mevalonate 5-phosphate decarboxylase is unable to carry out the first phosphory

218 romoter regulatory elements of glutamic acid decarboxylase isoforms (Gad1 and Gad2), which regulate G

219 two putative eukaryotic meso-diaminopimelate decarboxylase isoforms from the plant species Arabidopsi

220 also improved by overexpression of keto-acid decarboxylases (KDC) and alcohol dehydrogenase (ADH).

221 strate nitrogen flow, such as 2-oxoglutarate decarboxylase (KGD).

222 5-Carboxyvanillate decarboxylase (LigW) catalyzes the conversion of 5-carbo

223 identified the pyridoxal phosphate-dependent decarboxylase-like proteins in the translated proteome o

224 Mice deficient for malonyl CoA decarboxylase (MCD(-/-)), a mouse model of reduced fat o

225 cteria contain a biotin-independent malonate decarboxylase (MDC), which allows them to use malonate a

226 with a distinct prosthetic group, as well as decarboxylase (MdcD-MdcE) and acyl-carrier protein trans

227 zyme in this pathway, mevalonate diphosphate decarboxylase (MDD), acts on mevalonate diphosphate (MVA

228 Mevalonate diphosphate decarboxylases (MDDs) catalyze the ATP-dependent-Mg(2+)-

229 The alternative malate decarboxylase, NADP-ME, did not appear to compensate for

230 RS1-Reg binds to ornithine decarboxylase (ODC) and inhibits ODC in a glucose-depend

231 ls (RWPE-1) with overexpression of ornithine decarboxylase (ODC) and used it for in vitro and in vivo

232 descendants, we observed increased ornithine decarboxylase (ODC) enzymatic activity and concentration

233 ornithine uptake and metabolism by ornithine decarboxylase (ODC) for survival.

234 alpha-difluoromethylornithine, an ornithine decarboxylase (ODC) inhibitor, and entered into DU145 ce

235 of Ptch1 haploinsufficiency on an ornithine decarboxylase (ODC) transgenic background (Ptch1(+/-)/OD

236 Inhibition of ornithine decarboxylase (ODC) using low-dose eflornithine (DFMO, C

237 erated by the rate-limiting enzyme ornithine decarboxylase (ODC), in gastric carcinogenesis.

238 Ornithine decarboxylase (ODC), the rate-limiting enzyme in polyami

239 The plasma levels of arginase I, ornithine decarboxylase (ODC), transforming growth factor beta (TG

240 axis leading to the translation of ornithine decarboxylase (ODC).

241 ing polyamine biosynthetic enzyme, ornithine decarboxylase (ODC).

242 e deletion of the orotidine 5'-monophosphate decarboxylase (OMPDC) and uridine phosphorylase (UP) gen

243 Orotidine 5'-monophosphate decarboxylase (OMPDC) catalyzes the decarboxylation of 5

244 to insulin, autoantibodies to glutamic acid decarboxylase or insulinoma-associated antigen 2, or dia

245 cterium tuberculosis by binding to aspartate decarboxylase PanD.

246 d, in microorganisms, the action of pyruvate decarboxylase (PDC) and pyruvate formate lyase (PFL)-enz

247 Plant pyruvate decarboxylases (PDC) catalyze the decarboxylation of pyr

248 iosynthesis, and identified a melon pyruvate decarboxylase, PDC1, that is highly expressed in ripe fr

249 Microorganisms - CCDM 824 and CCDM 946) with decarboxylase positive activity in a model system of Dut

250 in the ganglion cell layer is glutamic acid decarboxylase-positive and shows the morphology of widef

251 e formation of an unusual heterotrimeric PPC decarboxylase (PPCDC) complex crucial for CoA biosynthes

252 Ornithine decarboxylase produces putrescine from ornithine, but we

253 A specific cysteic acid decarboxylase produces taurine, while hydrogen sulfide i

254 e describe here, mevalonate 3,5-bisphosphate decarboxylase, produces isopentenyl phosphate.

255 e first report in a virus of a phenolic acid decarboxylase, proteasomal subunit, or cysteine knot (de

256 ay by an inhibitor of arginase and ornithine decarboxylase protected the mice from AD-like pathology

257 ine hydroxylase (TH) and aromatic amino acid decarboxylase, providing a novel mechanism for dopamine

258 , we demonstrate that the phosphatidylserine decarboxylase Psd1, located in the inner mitochondrial m

259 of a key pathway enzyme, phosphatidylserine decarboxylase Psd1, which generates phosphatidylethanola

260 e (IM) and is executed by phosphatidylserine decarboxylase (Psd1).

261 Phosphatidylserine decarboxylase (PSDs) play a central role in the synthesi

262 Phosphatidylserine decarboxylases (PSDs) are central enzymes in phospholipi

263 Phosphatidylserine decarboxylases (PSDs) catalyze the conversion of phospha

264 Phosphatidylserine decarboxylases (PSDs) catalyze the decarboxylation of ph

265 This first-time study of the phenylacetate decarboxylase reaction constitutes an important step in

266 DFMO), known to inhibit the enzyme ornithine decarboxylase, reduces H. pylori-mediated gastric cancer

267 ne decarboxylase, and spe2Delta, lacking SAM decarboxylase) require externally supplied polyamines, b

268 In addition, higher expression of lysine decarboxylase resulted in a prolonged survival among ear

269 stal structure of the FigC N-citrylornithine decarboxylase reveals how the larger substrate is accomm

270 eat adaptation that uses rose phenylpyruvate decarboxylase (RyPPDC) as a novel enzyme.

271 variants of yeast orotidine 5'-monophosphate decarboxylase (ScOMPDC) at pD 8.1, and by the Q215A vari

272 erase (ScTIM), yeast orotidine monophosphate decarboxylase (ScOMPDC), and human liver glycerol 3-phos

273 cultured MCs were transfected with histidine decarboxylase short hairpin RNA to decrease histamine se

274 85% are present in the malonate semialdehyde decarboxylase subgroup.

275 trastructure, and tissue localization of Gly decarboxylase subunit P (GLDP) in nine Neurachninae spec

276 by inserting Shigella glutaminase-glutamate decarboxylase systems coexpressed with S. sonnei form I

277 ucei PS synthase 2 (TbPSS2) and T. brucei PS decarboxylase (TbPSD), two key enzymes involved in amino

278 oplast-localized enzyme uroporphyrinogen III decarboxylase (TgUroD).

279 e only known pyridoxal-5-phosphate-dependent decarboxylase that catalyzes the removal of a carboxyl g

280 bacteria have a biotin-independent malonate decarboxylase that is crucial for their utilization of m

281 lornithine, and FigC is an N-citrylornithine decarboxylase that together synthesize rhizoferrin witho

282 amily of alanine racemase-fold PLP-dependent decarboxylases that are not involved in polyamine biosyn

283 al malic enzymes (ME2 and ME3) are oxidative decarboxylases that catalyse the conversion of malate to

284 It belongs to a family of reversible decarboxylases that interconvert propenoic or aromatic a

285 revealed colocalization of DA, l-amino acid decarboxylase, the DA transporter, and vesicular monoami

286 ntibodies directed against the glutamic acid decarboxylase, the rate-limiting enzyme for the producti

287 Degradation of ornithine decarboxylase, the rate-limiting enzyme of polyamine bio

288 g pathway regulates translation of ornithine decarboxylase, thereby enhancing polyamine biosynthesis

289 the first characterized example of a diiron decarboxylase, thus expanding the repertoire of reaction

290 used immunohistochemistry for glutamic acid decarboxylase to distinguish GABAergic from glutamatergi

291 rreversibly catalyzed by UDP-glucuronic acid decarboxylase (UXS).

292 C supernatant fluids increased CCA histidine decarboxylase, vascular endothelial growth factor, and M

293 e mutant larvae, and expression of glutamate decarboxylase was reduced throughout the brain.

294 nerate mevalonate 3,5-bisphosphate and a new decarboxylase we describe here, mevalonate 3,5-bisphosph

295 pressing different isoforms of glutamic acid decarboxylase were found to have differential subregiona

296 e levels of mitochondrial phosphatidylserine decarboxylase, which is involved in the synthesis of mit

297 racterization of a branched-chain amino acid decarboxylase, which would appear to be responsible for

298 me complex that have evolved into a pyruvate decarboxylase, while other copies retained the essential

299 we also determine the structure of malonate decarboxylase with CoA in the active site of MdcD-MdcE.

300 he reaction of the UbiD-related ferulic acid decarboxylase with substituted propenoic and propiolic a