ライフサイエンスコーパス: anhydrase

1 es enzyme activity of chloroplastic carbonic anhydrase.

2 that the pH gradient is created by carbonic anhydrase.

3 ted to H2S by the ubiquitous enzyme carbonic anhydrase.

4 l function for Cd, an unusual Cd/Zn carbonic anhydrase.

5 man serum albumin, beta-casein, and carbonic anhydrase.

6 phosphate carboxylase/oxygenase and carbonic anhydrase.

7 t converting it to CO2 via external carbonic anhydrase.

8 competitive with the native enzyme, carbonic anhydrase.

9 hannel, UreI; and periplasmic alpha-carbonic anhydrase.

10 for proton transfer in catalysis by carbonic anhydrase.

11 f the urease gene cluster and alpha-carbonic anhydrase.

12 e1 and pendrin, and two isoforms of carbonic anhydrase.

13 gh the action of a shell-associated carbonic anhydrase.

14 hich is rapidly converted to H2S by carbonic anhydrase.

15 arboxylase/oxygenase (RuBisCO) with carbonic anhydrase.

16 t previously observed in alpha-type carbonic anhydrases.

17 -controlled stomatal development by carbonic anhydrases.

18 We characterized CARBONIC ANHYDRASE 1 (CAH1) as an essential component of the CCM

19 polipoprotein E, Apolipoprotein A1, Carbonic anhydrase 1, and Hemoglobin subunit alpha upon treatment

20 markers FoxF1, Pax-1, keratin-8/18, carbonic anhydrase-12, and NC markers brachyury, galectin-3 and C

21 (8.6 kDa), myoglobin (17 kDa), and carbonic anhydrase (29 kDa) upon higher energy collisional dissoc

22 a creatine kinase M-type (CK-M) and carbonic anhydrase 3 (CA-3) in the blood, more than 90% of which

23 alivary gland protein 1 (SP1), anti-carbonic anhydrase 6 (CA6) and anti-parotid secretory protein (PS

24 alivary gland protein 1 (SP1), anti-carbonic anhydrase 6 (CA6) and parotid secretory protein (PSP).

25 ecreted phospholipase A2), and CA6 (carbonic anhydrase 6).

26 Another protein, carbonic anhydrase 6, is initially imported normally into bbs4 ci

27 ein hormone luteinizing hormone and carbonic anhydrase-6 (CA6).

28 poxia-regulated genes (for example, carbonic anhydrase 9 (CA9) and vascular endothelial growth factor

29 Immunostaining for carbonic anhydrase 9 (CAIX), reportedly an endogenous marker of h

30 v 1 and a tumor-associated antigen, carbonic anhydrase 9.

31 Carbonic anhydrase activity emerges in the same region of the gla

32 hotosynthetic attributes along with carbonic anhydrase activity whereas its higher concentrations pro

33 rapid and simple quantification of carbonic anhydrase activity which is very important to prevent th

34 uration constants for CO2 fixation, carbonic anhydrase activity, CO2 /HCO3 (-) uptake, delta(13) Corg

35 deficiency, probably due to reduced carbonic anhydrase activity, validated by quantitative proteomics

36 bon species preference and external carbonic anhydrase activity.

37 g NPs with no discernible effect on carbonic anhydrase activity.

38 ined system of protein and ligands--carbonic anhydrase and a series of structurally homologous hetero

39 te constants of interaction between carbonic anhydrase and acetazolamide.

40 ng the well-defined model system of carbonic anhydrase and aryl sulfonamides.

41 ent on H(+) V-ATPase, together with carbonic anhydrase and five further transporters or channels that

42 d molecules of RuBisCO, and contain carbonic anhydrase and other accessory proteins.

43 Carbonic anhydrase and phosphoenolpyruvate carboxylase in vitro a

44 into the cell and colocalization of carbonic anhydrase and RuBisCO inside proteinaceous microcompartm

45 er than any small molecule model of carbonic anhydrase and with an efficiency within 1400-fold of the

46 key C4 metabolism genes, including carbonic anhydrases and a malate transporter.

47 f inorganic carbon transporters and carbonic anhydrases (and other supporting components) that culmin

48 aper describes a synthetic dimer of carbonic anhydrase, and a series of bivalent sulfonamide ligands

49 Ion channels and transporters, carbonic anhydrase, and aquaporins were abundantly expressed.

50 ction, staying below saturation for carbonic anhydrase, and avoiding wasteful oxygenation reactions.

51 Assays for actin, AMP-kinase, carbonic anhydrase, and lysozyme are shown to demonstrate versati

52 luding: green fluorescent proteins, carbonic anhydrase, and oxidative stress proteins; and functional

53 rganic carbon transport components, carbonic anhydrases, and aggregation of Rubisco in the chloroplas

54 n a kappa(2)-fashion to the protein carbonic anhydrase as a ligand.

55 as the folding modulators and human carbonic anhydrase as a model protein, we demonstrate that PFAR i

56 We demonstrate this system using carbonic anhydrase as the target and a library of 144,000 proprie

57 ch is very important to prevent the carbonic-anhydrase-associated disorders in human.

58 tudy examined the effects of bovine carbonic anhydrase (BCA) and CO2-rich gas streams on the carbonat

59 ng the affinity of unlabeled bovine carbonic anhydrase (BCA) for a variety of ligands (most of which

60 clease (Rnase) A, myoglobin, bovine carbonic anhydrase (BCA) II, hemoglobin (Hb), and the hemoglobin-

61 Carbonic anhydrase buffers tissue pH by catalyzing the rapid inte

62 Carbonic anhydrase (CA) accelerates post combustion CO(2) capture

63 2) hydration, we first measured the carbonic anhydrase (CA) activity of the bladder epithelium.

64 The process employs the enzyme carbonic anhydrase (CA) as a catalyst to accelerate the rate of C

65 Monovalent carbonic anhydrase (CA) binds to benzenesulfonamide ligands prese

66 ctions of these inhibitors into the carbonic anhydrase (CA) catalytic site, thus highlighting the rel

67 Carbonic anhydrase (CA) catalyzes the first biochemical step of t

68 ar pressure (IOP) by inhibiting the carbonic anhydrase (CA) enzyme to reduce aqueous humor production

69 Carbonic anhydrase (CA) enzymes catalyze the chemical equilibrati

70 Carbonic anhydrase (CA) enzymes have gained considerable attentio

71 Carbonic anhydrase (CA) enzymes, expressed at various sites in ve

72 y inhibitors are reported for human carbonic anhydrase (CA) enzymes, few may be considered useful as

73 hibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA IX and XII, has

74 act as effective inhibitors of the carbonic anhydrase (CA) from Trypanosoma cruzi (TcCA).

75 estration based on a self-propelled carbonic anhydrase (CA) functionalized micromotor.

76 maltose binding protein (MBP), and carbonic anhydrase (CA) in the presence of hundreds of non-binder

77 t] Finally, we show that the enzyme carbonic anhydrase (CA) increases the dissolution rate across all

78 Prior studies with carbonic anhydrase (CA) inhibitors implicated mitochondrial CA in

79 possibility of developing selective carbonic anhydrase (CA) inhibitors, interactions between 17 benze

80 Carbonic anhydrase (CA) is one of nature's fastest enzymes and ca

81 gent targeting the tumor-associated carbonic anhydrase (CA) isoforms IX and XII.

82 ry DNAs encoding four distinct beta-carbonic anhydrase (CA) isoforms were characterized from leaf tis

83 le against therapeutically relevant carbonic anhydrase (CA) zinc metalloenzymes.

84 ns: (1) generation by extracellular carbonic anhydrase (CA), (2) release from acidic synaptic vesicle

85 carboxylase/oxygenase (RuBisCO) and carbonic anhydrase (CA), in an engineered protein cage based on l

86 However, carbonic anhydrase (CA), the enzyme that hydrolyses COS, is expec

87 ncement was completely abolished in carbonic anhydrase (CA)-deficient antisense lines of both C3 and

88 nolpyruvate carboxylase (PEPc), and carbonic anhydrase (CA).

89 ed to H2 S by the ubiquitous enzyme carbonic anhydrase (CA).

90 y ~100-fold less than that of human carbonic anhydrase (CA)II and at least 550-fold better than compa

91 A beta-carbonic anhydrase (CA, EC 4.2.1.1) from the fungal pathogen Mala

92 urified, and characterized an alpha-carbonic anhydrase (CA, EC 4.2.1.1) from the human pathogenic bac

93 An alpha-carbonic anhydrase (CA, EC 4.2.1.1) has been identified, cloned,

94 three established aminosulfonamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitor pharmacophores, cou

95 the underexposed sulfamate class of carbonic anhydrase (CA, EC 4.2.1.1) inhibitors was generated that

96 condary amines and COS as potential carbonic anhydrase (CA, EC 4.2.1.1) inhibitors, using the dithioc

97 ylphenyl-omega-aminoalkyl ethers as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

98 (DTCs) were recently discovered as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

99 te a novel class of mechanism-based carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

100 y were synthesized and evaluated as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

101 ide derivatives acting as effective carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

102 btained, which showed an increasing carbonic anhydrase (CA, EC 4.2.1.1) inhibitory action with the in

103 tivity against the tumor associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms hCA IX and XII are r

104 hagas disease, encodes for an alpha-carbonic anhydrase (CA, EC 4.2.1.1) possessing high catalytic act

105 A beta-carbonic anhydrase (CA, EC 4.2.1.1) was cloned and characterized

106 as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).

107 as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).

108 n (h) isoforms of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).

109 the immunohistochemical analysis of carbonic anhydrases (CA) IX and XII expression in thyroid cancer.

110 Carbonic anhydrases (CA), which catalyze the reversible hydration

111 man (h) isoforms of the zinc enzyme carbonic anhydrase, CA (EC 4.2.1.1), hCA I, II, IX, and XII, invo

112 ing 6- and 7-substituted coumarins (carbonic anhydrase, CA inhibitors) derivatized with clinically us

113 D8 features a carbonic anhydrase (CAH) fold that has evolved to bind to the gly

114 We find that the carbonic anhydrase CAH6 is in the flagella, not in the stroma tha

115 ggest that intra- and extracellular carbonic anhydrases can work in concert to ensure rapid shuttling

116 In this study, we show that carbonic anhydrase (Car) enzymes are up-regulated in type 2-assoc

117 In the hippocampus, extracellular carbonic anhydrase (Car) speeds the buffering of an activity-gene

118 Two putative carbonic anhydrases (CAs) are encoded in the genome of C. jejuni

119 n different Ci species catalyzed by carbonic anhydrases (CAs) are key components in the CCM, and an a

120 Soluble cytosolic carbonic anhydrases (CAs) are well known to participate in pH reg

121 s (CCMs) involving transporters and carbonic anhydrases (CAs) are well known, but the contribution of

122 Carbonic anhydrases (CAs) are zinc metalloenzymes that catalyze t

123 Carbonic anhydrases (CAs) are zinc metalloenzymes that interconve

124 Carbonic anhydrases (CAs) catalyze the hydration of CO(2) forming

125 Carbonic anhydrases (CAs) comprise a family of zinc-containing en

126 rter, suggesting that inhibition of carbonic anhydrases (CAs) confers the beneficial thiazide effect.

127 etween CO2 and HCO3(-) catalyzed by carbonic anhydrases (CAs), and active inorganic carbon (Ci) uptak

128 e discovered that CPOs also inhibit carbonic anhydrases (CAs), especially the IX and XII isoforms ide

129 availability that is determined by carbonic anhydrases (CAs).

130 Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous isozymes inv

131 phate carboxylase/oxygenase and the carbonic anhydrase CcaA, whereas the C-terminal peptide is essent

132 r a DMSO-free sample in the case of carbonic anhydrase-chlorothiazide binding.

133 icular for the tight binding system carbonic anhydrase-chlorothiazide.

134 tri-N-acetylchitotriose (NAG3), and carbonic anhydrase-chlorothiazide.

135 Carbonic anhydrase converts COS into H2S, allowing NTAs to serve

136 The carbonic anhydrase (Cpb) from Clostridium perfringens strain 13,

137 hlamydomonas reinhardtii, a luminal carbonic anhydrase, CrCAH3, was suggested to improve proton remov

138 parison we assayed recessive ca1ca4 carbonic anhydrase double mutant plants, based on their slowed st

139 isolated Arabidopsis thaliana beta-carbonic anhydrase double mutants (ca1 ca4) exhibit an inversion

140 microalgae induce an extracellular carbonic anhydrase (eCA), associated with the cell surface, at lo

141 metal affinity of Escherichia coli carbonic anhydrase (ECCA).

142 ium perfringens strain 13, the only carbonic anhydrase encoded in the genome, was characterized both

143 pheric CO2 elevation, including the carbonic-anhydrase-encoding genes CA1 and CA4 and the secreted pr

144 e investigated as inhibitors of the carbonic anhydrase enzyme (CA; EC 4.2.1.1).

145 t are achieved by the activity of a carbonic anhydrase enzyme combined with the maintenance of a low

146 Carbonic anhydrase enzymes (CAs) catalyse the reversible hydratio

147 clinical benefits of inhibitors of carbonic anhydrase enzymes and the water channel Aquaporin-1 for

148 lex, containing the ancestral gamma-carbonic anhydrase (gamma-CA), gamma-carbonic anhydrase-like, and

149 drase gene (ca19) beyond the single carbonic anhydrase gene (ca18) that was known previously.

150 We have identified a novel carbonic anhydrase gene (ca19) beyond the single carbonic anhydra

151 1, CCP2 and LCIA) and mitochondrial carbonic anhydrase genes (CAH4 and CAH5) are up regulated in ligh

152 d synteny studies suggest that both carbonic anhydrase genes form one or two independent gene lineage

153 Benzenesulfonamide and carbonic anhydrase have been chosen as the ligand and protein, re

154 ystem of protein and ligands--human carbonic anhydrase (HCA) and a series of benzothiazole sulfonamid

155 was synthesized and bound to human carbonic anhydrase (HCA) using a nanomolar active site ligand.

156 ng reactions and evaluated as human carbonic anhydrase (hCA, EC 4.2.1.1) inhibitors against isoforms

157 harmacologically relevant human (h) carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, the cytosolic enzy

158 This study uses mutants of human carbonic anhydrase (HCAII) to examine how changes in the organiza

159 panel of metalloenzymes, including carbonic anhydrase (hCAII), several matrix metalloproteinases (MM

160 itors of the tumor-associated human carbonic anhydrases (hCAs) IX and XII.

161 four physiologically relevant human carbonic anhydrases (hCAs, EC 4.2.1.1), isoforms hCA I, II, IX, a

162 mutation of Haemophilus influenzae carbonic anhydrase (HICA), which mimics the endogenous metal affi

163 Carbonic anhydrase I (Car1) is a gene expressed uniquely in colon

164 lity and unfolding process of human carbonic anhydrase I (HCA-I).

165 digestion of differentially labeled carbonic anhydrase I and hemoglobin allowed the identification of

166 proteins, the strict association of carbonic anhydrase I and S100A8 with ECM was verified by western

167 erum albumin, hemoglobin, and human carbonic anhydrase I were successfully labeled.

168 was demonstrated by modification of carbonic anhydrase I with electrochemically generated reactive me

169 Expression of carbonic anhydrase I, glucosaminyl (N-acetyl) transferase 2, and

170 factor binding protein (IGFBP), and carbonic anhydrase-I and -II.

171 ual mobility in complexes of bovine carbonic anhydrase II (BCA) and para-substituted benzenesulfonami

172 We present a new approach to carbonic anhydrase II (CA II) inhibitor design that enables close

173 affinity to the zinc metalloenzyme carbonic anhydrase II (CA II).

174 nt screening campaign against human carbonic anhydrase II (CA II).

175 lyze the direct interaction between carbonic anhydrase II (CAII) and MCT1, MCT2, and MCT4, respective

176 o acidic motifs homologous to known carbonic anhydrase II (CAII) binding sequences.

177 In nature, the zinc metalloenzyme carbonic anhydrase II (CAII) efficiently catalyzes the conversion

178 d MCT4 is enhanced by the cytosolic carbonic anhydrase II (CAII) independent of its catalytic activit

179 Carbonic anhydrase II (CAII)(Cre);Pdx1(Fl) mice were euglycemic f

180 TFGs containing CB[6]- and carbonic anhydrase II (CAII)-binding domains were synthesized in

181 Human carbonic anhydrase II (HCA II) uses a Zn-bound OH(-)/H2O mechanis

182 Variants of human carbonic anhydrase II (HCA II) with amino acid replacements at re

183 In human carbonic anhydrase II (HCA II), the mutation of position 64 from

184 , TPMA) to the active site of human carbonic anhydrase II (hCAII) has been investigated.

185 -HOPTO) in the active site of human carbonic anhydrase II (hCAII) has been investigated.

186 onding inhibitor complexes of human carbonic anhydrase II (HCAII) indicated that HpalphaCA possesses

187 he binding of sulfonamides to human carbonic anhydrase II (hCAII) is a complex and long-debated examp

188 ion of the CD spectrum of the Human Carbonic Anhydrase II (HCAII), with main focus on the near-UV CD

189 er uses the binding pocket of human carbonic anhydrase II (HCAII, EC 4.2.1.1) as a tool to examine th

190 We have reported previously that carbonic anhydrase II augments transport activity of MCT1 and MCT

191 conversion between CO2 and HCO3(-) Carbonic anhydrase II facilitates this reversible reaction inside

192 ate-resistant acid phosphatase, and carbonic anhydrase II in bone marrow macrophages (BMMs), RANKL re

193 eprotonation of zinc-bound water in carbonic anhydrase II is the rate-limiting step in the catalysis

194 mainly from extrainsular PDX-1(+), carbonic anhydrase II(-) (mature ductal), elastase 3a (acinar)(-)

195 teins (ubiquitin, cytochrome c, and carbonic anhydrase II) were investigated.

196 lected scFvs was shown to recognize carbonic anhydrase II, an up-regulated enzyme involved in resorpt

197 rate-resistant acid phosphatase, or carbonic anhydrase II.

198 wn genes, whereas Srpx2, Cd200, and carbonic anhydrase III (CAIII) were identified as novel markers o

199 Carbonic anhydrase III protects osteocytes from oxidative stress.

200 nic anhydrase XII (CA12) is the key carbonic anhydrase in epithelial fluid and HCO3 (-) secretion and

201 phosphate carboxylase/oxygenase and carbonic anhydrase in the microcompartment shell.

202 of Rubisco and the thylakoid lumen carbonic anhydrase in the pyrenoid rose substantially, coincident

203 igate the repertoire of cytoplasmic carbonic anhydrases in the sea lamprey (Petromyzon marinus), that

204 MTZ is known to be a carbonic anhydrase inhibitor (CAI); however, CAIs acetazolamide,

205 ensitive to Na(+)withdrawal, to the carbonic anhydrase inhibitor acetazolamide and to H2DIDS inhibiti

206 B. pertussis-infected mice with the carbonic anhydrase inhibitor acetazolamide reduced lung inflammat

207 Given methazolamide, a potent carbonic anhydrase inhibitor, can penetrate the blood-brain barri

208 e co-transporter (P </= 0.0001) and carbonic anhydrase inhibitors (P = 0.0021).

209 edema (CME), and review the role of carbonic anhydrase inhibitors in management.

210 Carbonic anhydrase inhibitors may be effective in promoting resol

211 Carbonic anhydrase inhibitors may promote resolution of the cysts

212 Azide derivatives of 2 carbonic anhydrase inhibitors, 4-(2-aminoethyl)benzenesulfonamide

213 onnection, we report a new class of carbonic anhydrase inhibitors, based on the thiopyrano-fused pyra

214 e of topical beta blockers, topical carbonic anhydrase inhibitors, daily dose of BAK, and glaucoma fi

215 laucoma medications (beta blockers, carbonic anhydrase inhibitors, parasympathomimetics, and prostagl

216 were more potent agents with higher carbonic anhydrase inhibitory action than the parent dye.

217 rite bioactivation, but the role of carbonic anhydrase is abrogated when physiological concentrations

218 rusion mechanisms and extracellular carbonic anhydrase, is responsible for active transport-mediated

219 observed, in line with patterns of carbonic anhydrase isoform expression in those tissues.

220 ave been developed as inhibitors of carbonic anhydrase isoform IX.

221 ncy within 1400-fold of the fastest carbonic anhydrase isoform, CAII, and 11-fold of CAIII.

222 While several carbonic anhydrase isoforms have been identified in numerous vert

223 inhibitors of the ubiquitous human carbonic anhydrase isoforms I, II, IX, XII, and XIV using acetazo

224 e human genome encodes 15 different carbonic anhydrase isoforms that have a high degree of homology.

225 ed by Slc26a4, Slc4a8, and Slc4a9), carbonic anhydrase isoforms, and V-type H(+)-ATPase subunits in p

226 e inhibition of some selected human carbonic anhydrase isoforms.

227 tack" screen for inhibitors against carbonic anhydrase isozyme II is performed, in which known inhibi

228 Carbonic anhydrase IV (Car4) was a top dysregulated gene with 36-

229 Carbonic anhydrase IX (CA IX) is a hypoxia-induced cell surface e

230 Carbonic anhydrase IX (CA IX) is a target for hypoxic cancer ther

231 Carbonic anhydrase IX (CA IX) is a transmembrane protein that has

232 Carbonic anhydrase IX (CA IX) is an extracellular transmembrane h

233 Human carbonic anhydrase IX (CA IX) is highly expressed in tumor tissue

234 Human carbonic anhydrase IX (CA IX) is overexpressed in a number of sol

235 xic tumors is possible by targeting carbonic anhydrase IX (CA IX), an enzyme overexpressed in hypoxic

236 Carbonic anhydrase IX (CA-IX) is upregulated in cancer in respons

237 Carbonic anhydrase IX (CA-IX), a transmembrane enzyme, mediates c

238 Carbonic anhydrase IX (CA9) is a transmembrane glycoprotein relat

239 hypoxia is activated expression of carbonic anhydrase IX (CA9), a regulator of pH and tumor growth.

240 technique, using antibodies against carbonic anhydrase IX (CAIX) and copper pumps (Ctr1 and ATP7B).

241 ated therapy with the chimeric anti-carbonic anhydrase IX (CAIX) antibody girentuximab (cG250).

242 rization and acid-extruding protein carbonic anhydrase IX (CAIX) expression.

243 Carbonic anhydrase IX (CAIX) is a membrane-bound, tumor-related e

244 It was induced by carbonic anhydrase IX (CAIX) overexpression and inhibited by acet

245 ined unchanged, while expression of carbonic anhydrase IX (CAIX) was greatly enhanced.

246 , which also express high levels of carbonic anhydrase IX (CAIX), a HIF1-dependent protein.

247 ate the intraoperative detection of carbonic anhydrase IX (CAIX)-expressing tumor lesions with chimer

248 Carbonic anhydrase IX (CAIX, CA9) expression is highly upregulate

249 Inhibition of human carbonic anhydrase IX (hCA IX) has shown to be therapeutically ad

250 amics from tumor biomarkers such as carbonic anhydrase IX and topoisomerase I by immunohistochemistry

251 enin) and function (aquaporin 1 and carbonic anhydrase IX).

252 eric monoclonal antibody that binds carbonic anhydrase IX, a cell surface glycoprotein ubiquitously e

253 a novel acetazolamide derivative, a carbonic anhydrase ligand with high affinity for the tumor-associ

254 2), native extra- and intracellular carbonic anhydrase-like activities, the non-CO(2)/HCO(3)(-) (intr

255 arbonic anhydrase (gamma-CA), gamma-carbonic anhydrase-like, and 20.9-kDa subunits, had a significant

256 stem comprising synthetic dimers of carbonic anhydrase linked chemically through thiol groups of cyst

257 e find that expression of the Cd/Zn carbonic anhydrase makes no difference to the Cd isotope composit

258 Carbonic anhydrase members in this class of exofacial molecules f

259 The murine inhibitor of carbonic anhydrase (mICA), a member of the transferrin (TF) super

260 l molecules to proteins as large as carbonic anhydrase (molecular weight ca. 29,000).

261 A nitrite anhydrase (NA) reaction in which N2O3, a potent S-nitros

262 stingly, transcripts of chloroplast carbonic anhydrases namely CAH6, CAH3 and LCIB are up regulated i

263 alpha-Carbonic anhydrase of Helicobacter pylori (HpalphaCA) plays an im

264 Overexpression of carbonic anhydrases on cell surfaces further contributes to acidi

265 e via an aspartate-alanine shuttle, carbonic anhydrase, phosophoenolpyruvate carboxylase, alanine, an

266 Carbonic anhydrase plays a key role in CO2 transport, acid-base a

267 ation at 750 microatm pCO2, reduced carbonic anhydrase protein activity and shell growth occurs in M.

268 We identified CAH1 as an alpha-type carbonic anhydrase, providing a biochemical role in CCM function.

269 ble intermediate associated with the nitrite anhydrase reaction in both LtHb and HbA is supported bas

270 trosylation, and still controversial nitrite anhydrase reactions.

271 orphosis resulting in distinct gill carbonic anhydrases reflecting the contrasting life modes and hab

272 eptibility in the murine model, and carbonic anhydrase, reflecting the blood's abnormal acid base env

273 Moreover, kinetic analysis of human carbonic anhydrase refolding showed that 6AP decreased the yield

274 ted from mouse brain, we identified carbonic anhydrase-related proteins CA10 and CA11, two homologous

275 e find dorzolamide (an inhibitor of carbonic anhydrase) results in diminished nitrite bioactivation,

276 duced expression of colonic villin, carbonic anhydrase, secretory mucin muc2, and increased basal col

277 toglobulin (five peptides), 25% for carbonic anhydrase (six peptides), and 51% for bovine serum album

278 , mannose) against matched targets (carbonic anhydrase, streptavidin, concanavalin A) to identify des

279 rbon acquisition enzymes, primarily carbonic anhydrase, stress, degradation and signaling proteins we

280 rved proteins containing domains of carbonic anhydrase, Sushi, Von Willebrand factor type A, and chit

281 lants respond to elevated CO(2) via carbonic anhydrases that mediate stomatal closing, but little is

282 Because spirochetes lack carbonic anhydrase, the corresponding reduction in bicarbonate de

283 imately 10(5)-10(8) M(-1) s(-1) for carbonic anhydrase, the most efficient catalyst of CO(2) fixation

284 The presence of cytosolic carbonic anhydrases, the basolateral Na(+) bicarbonate cotranspor

285 hosphate carboxylase/ oxygenase and carbonic anhydrase to facilitate carbon fixation in cyanobacteria

286 Intracellular carbonic anhydrase transcript abundance increased with temperatur

287 nnose receptor-positive, expressing carbonic anhydrase type II, but relatively low levels of cathepsi

288 Carbonic anhydrase VA (CA-VA) was absent in liver in the child wi

289 nhibitors of five isoforms of human carbonic anhydrase was also explored.

290 small molecule mimic of the enzyme carbonic anhydrase, was evaluated under rigorous conditions resem

291 onuclease A, trypsin inhibitor, and carbonic anhydrase, where the latter had impurities of superoxide

292 ium bicarbonate co-transporters and carbonic anhydrases, which were also expressed in LAM lung tissue

293 The reactions of apo human carbonic anhydrase with [Rh(nbd)2]BF4 or [M(CO)2(acac)] (M=Rh, Ir

294 ylsulfonamide ligands bind to human carbonic anhydrase with a conserved binding geometry, an enthalpy

295 uffering was augmented by exogenous carbonic anhydrase (XCAR).

296 Carbonic anhydrase XII (CA XII) is a membrane-tethered cell surfa

297 Carbonic anhydrase XII (CA12) is the key carbonic anhydrase in ep

298 specific gene in the FLC signature, carbonic anhydrase XII (CA12), at the protein level by western bl

299 describe variants in CA12 encoding carbonic anhydrase XII in two pedigrees exhibiting CF-like phenot

300 Panning on carbonic anhydrase yielded a potent ligand, sulfonamide-WIVP, wit