ライフサイエンスコーパス: carbonic anhydrase

1 determines enzyme activity of chloroplastic carbonic anhydrase.

2 ts reveal that the pH gradient is created by carbonic anhydrase.

3 ly converted to H2S by the ubiquitous enzyme carbonic anhydrase.

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

5 luding human serum albumin, beta-casein, and carbonic anhydrase.

6 e 1,5-bisphosphate carboxylase/oxygenase and carbonic anhydrase.

7 - by first converting it to CO2 via external carbonic anhydrase.

8 cy to be competitive with the native enzyme, carbonic anhydrase.

9 ed urea channel, UreI; and periplasmic alpha-carbonic anhydrase.

10 onstants for proton transfer in catalysis by carbonic anhydrase.

11 ription of the urease gene cluster and alpha-carbonic anhydrase.

12 porters ae1 and pendrin, and two isoforms of carbonic anhydrase.

13 art through the action of a shell-associated carbonic anhydrase.

14 on state similar to that at the zinc site in carbonic anhydrase.

15 ulfide, which is rapidly converted to H2S by carbonic anhydrase.

16 osphate carboxylase/oxygenase (RuBisCO) with carbonic anhydrase.

17 eature not previously observed in alpha-type carbonic anhydrases.

18 on of CO2-controlled stomatal development by carbonic anhydrases.

19 We characterized CARBONIC ANHYDRASE 1 (CAH1) as an essential component of

20 globin, Apolipoprotein E, Apolipoprotein A1, Carbonic anhydrase 1, and Hemoglobin subunit alpha upon

21 on of NP markers FoxF1, Pax-1, keratin-8/18, carbonic anhydrase-12, and NC markers brachyury, galecti

22 ubiquitin (8.6 kDa), myoglobin (17 kDa), and carbonic anhydrase (29 kDa) upon higher energy collision

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

24 s, anti-salivary gland protein 1 (SP1), anti-carbonic anhydrase 6 (CA6) and anti-parotid secretory pr

25 s, anti-salivary gland protein 1 (SP1), anti-carbonic anhydrase 6 (CA6) and parotid secretory protein

26 S-PLA2 (secreted phospholipase A2), and CA6 (carbonic anhydrase 6).

27 Another protein, carbonic anhydrase 6, is initially imported normally int

28 glycoprotein hormone luteinizing hormone and carbonic anhydrase-6 (CA6).

29 ion of hypoxia-regulated genes (for example, carbonic anhydrase 9 (CA9) and vascular endothelial grow

30 Immunostaining for carbonic anhydrase 9 (CAIX), reportedly an endogenous ma

31 rgen Art v 1 and a tumor-associated antigen, carbonic anhydrase 9.

32 Carbonic anhydrase activity emerges in the same region o

33 Exofacial carbonic anhydrase activity increases with exposure to h

34 ations, photosynthetic attributes along with carbonic anhydrase activity whereas its higher concentra

35 cable for rapid and simple quantification of carbonic anhydrase activity which is very important to p

36 half-saturation constants for CO2 fixation, carbonic anhydrase activity, CO2 /HCO3 (-) uptake, delta

37 in zinc deficiency, probably due to reduced carbonic anhydrase activity, validated by quantitative p

38 ganic carbon species preference and external carbonic anhydrase activity.

39 by the Ag NPs with no discernible effect on carbonic anhydrase activity.

40 well-defined system of protein and ligands--carbonic anhydrase and a series of structurally homologo

41 ng the rate constants of interaction between carbonic anhydrase and acetazolamide.

42 stem, using the well-defined model system of carbonic anhydrase and aryl sulfonamides.

43 is dependent on H(+) V-ATPase, together with carbonic anhydrase and five further transporters or chan

44 al hundred molecules of RuBisCO, and contain carbonic anhydrase and other accessory proteins.

45 Carbonic anhydrase and phosphoenolpyruvate carboxylase i

46 c carbon into the cell and colocalization of carbonic anhydrase and RuBisCO inside proteinaceous micr

47 CO2 better than any small molecule model of carbonic anhydrase and with an efficiency within 1400-fo

48 tified in key C4 metabolism genes, including carbonic anhydrases and a malate transporter.

49 consist of inorganic carbon transporters and carbonic anhydrases (and other supporting components) th

50 This paper describes a synthetic dimer of carbonic anhydrase, and a series of bivalent sulfonamide

51 Ion channels and transporters, carbonic anhydrase, and aquaporins were abundantly expre

52 BisCO reaction, staying below saturation for carbonic anhydrase, and avoiding wasteful oxygenation re

53 Assays for actin, AMP-kinase, carbonic anhydrase, and lysozyme are shown to demonstrat

54 genes including: green fluorescent proteins, carbonic anhydrase, and oxidative stress proteins; and f

55 ctive inorganic carbon transport components, carbonic anhydrases, and aggregation of Rubisco in the c

56 fically in a kappa(2)-fashion to the protein carbonic anhydrase as a ligand.

57 revisiae as the folding modulators and human carbonic anhydrase as a model protein, we demonstrate th

58 We demonstrate this system using carbonic anhydrase as the target and a library of 144,00

59 ivity which is very important to prevent the carbonic-anhydrase-associated disorders in human.

60 This study examined the effects of bovine carbonic anhydrase (BCA) and CO2-rich gas streams on the

61 y measuring the affinity of unlabeled bovine carbonic anhydrase (BCA) for a variety of ligands (most

62 g: ribonuclease (Rnase) A, myoglobin, bovine carbonic anhydrase (BCA) II, hemoglobin (Hb), and the he

63 Carbonic anhydrase buffers tissue pH by catalyzing the r

64 Carbonic anhydrase (CA) accelerates post combustion CO(2

65 cs of CO(2) hydration, we first measured the carbonic anhydrase (CA) activity of the bladder epitheli

66 The process employs the enzyme carbonic anhydrase (CA) as a catalyst to accelerate the

67 Monovalent carbonic anhydrase (CA) binds to benzenesulfonamide liga

68 in interactions of these inhibitors into the carbonic anhydrase (CA) catalytic site, thus highlightin

69 Carbonic anhydrase (CA) catalyzes the first biochemical

70 intraocular pressure (IOP) by inhibiting the carbonic anhydrase (CA) enzyme to reduce aqueous humor p

71 Carbonic anhydrase (CA) enzymes catalyze the chemical eq

72 Carbonic anhydrase (CA) enzymes have gained considerable

73 Carbonic anhydrase (CA) enzymes, expressed at various si

74 hough many inhibitors are reported for human carbonic anhydrase (CA) enzymes, few may be considered u

75 ective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA IX and

76 es, which act as effective inhibitors of the carbonic anhydrase (CA) from Trypanosoma cruzi (TcCA).

77 etic sequestration based on a self-propelled carbonic anhydrase (CA) functionalized micromotor.

78 , pepsin, maltose binding protein (MBP), and carbonic anhydrase (CA) in the presence of hundreds of n

79 : see text] Finally, we show that the enzyme carbonic anhydrase (CA) increases the dissolution rate a

80 Prior studies with carbonic anhydrase (CA) inhibitors implicated mitochondr

81 g of the possibility of developing selective carbonic anhydrase (CA) inhibitors, interactions between

82 Carbonic anhydrase (CA) is one of nature's fastest enzym

83 itizing agent targeting the tumor-associated carbonic anhydrase (CA) isoforms IX and XII.

84 mplementary DNAs encoding four distinct beta-carbonic anhydrase (CA) isoforms were characterized from

85 ion profile against therapeutically relevant carbonic anhydrase (CA) zinc metalloenzymes.

86 eft protons: (1) generation by extracellular carbonic anhydrase (CA), (2) release from acidic synapti

87 hosphate carboxylase/oxygenase (RuBisCO) and carbonic anhydrase (CA), in an engineered protein cage b

88 However, carbonic anhydrase (CA), the enzyme that hydrolyses COS,

89 This enhancement was completely abolished in carbonic anhydrase (CA)-deficient antisense lines of bot

90 phosphoenolpyruvate carboxylase (PEPc), and carbonic anhydrase (CA).

91 hydrolyzed to H2 S by the ubiquitous enzyme carbonic anhydrase (CA).

92 iency only ~100-fold less than that of human carbonic anhydrase (CA)II and at least 550-fold better t

93 A beta-carbonic anhydrase (CA, EC 4.2.1.1) from the fungal path

94 cloned, purified, and characterized an alpha-carbonic anhydrase (CA, EC 4.2.1.1) from the human patho

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

96 ized from three established aminosulfonamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitor pharmacoph

97 nging to the underexposed sulfamate class of carbonic anhydrase (CA, EC 4.2.1.1) inhibitors was gener

98 rimary/secondary amines and COS as potential carbonic anhydrase (CA, EC 4.2.1.1) inhibitors, using th

99 4-sulfamoylphenyl-omega-aminoalkyl ethers as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

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

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

102 diversity were synthesized and evaluated as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

103 esulfonamide derivatives acting as effective carbonic anhydrase (CA, EC 4.2.1.1) inhibitors.

104 re thus obtained, which showed an increasing carbonic anhydrase (CA, EC 4.2.1.1) inhibitory action wi

105 ity/selectivity against the tumor associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms hCA IX and

106 gent of Chagas disease, encodes for an alpha-carbonic anhydrase (CA, EC 4.2.1.1) possessing high cata

107 A beta-carbonic anhydrase (CA, EC 4.2.1.1) was cloned and chara

108 d assayed as inhibitors of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).

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

110 vant human (h) isoforms of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1).

111 ged from the immunohistochemical analysis of carbonic anhydrases (CA) IX and XII expression in thyroi

112 Carbonic anhydrases (CA), which catalyze the reversible

113 f four human (h) isoforms of the zinc enzyme carbonic anhydrase, CA (EC 4.2.1.1), hCA I, II, IX, and

114 ncorporating 6- and 7-substituted coumarins (carbonic anhydrase, CA inhibitors) derivatized with clin

115 D8 features a carbonic anhydrase (CAH) fold that has evolved to bind t

116 We find that the carbonic anhydrase CAH6 is in the flagella, not in the s

117 esults suggest that intra- and extracellular carbonic anhydrases can work in concert to ensure rapid

118 In this study, we show that carbonic anhydrase (Car) enzymes are up-regulated in typ

119 In the hippocampus, extracellular carbonic anhydrase (Car) speeds the buffering of an acti

120 Two putative carbonic anhydrases (CAs) are encoded in the genome of C

121 on between different Ci species catalyzed by carbonic anhydrases (CAs) are key components in the CCM,

122 Soluble cytosolic carbonic anhydrases (CAs) are well known to participate

123 mechanisms (CCMs) involving transporters and carbonic anhydrases (CAs) are well known, but the contri

124 Carbonic anhydrases (CAs) are zinc metalloenzymes that c

125 Carbonic anhydrases (CAs) are zinc metalloenzymes that i

126 Carbonic anhydrases (CAs) catalyze the hydration of CO(2

127 Carbonic anhydrases (CAs) comprise a family of zinc-cont

128 cotransporter, suggesting that inhibition of carbonic anhydrases (CAs) confers the beneficial thiazid

129 version between CO2 and HCO3(-) catalyzed by carbonic anhydrases (CAs), and active inorganic carbon (

130 We discovered that CPOs also inhibit carbonic anhydrases (CAs), especially the IX and XII iso

131 HCO3 (-) availability that is determined by carbonic anhydrases (CAs).

132 Carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous iso

133 5-bisphosphate carboxylase/oxygenase and the carbonic anhydrase CcaA, whereas the C-terminal peptide

134 r than for a DMSO-free sample in the case of carbonic anhydrase-chlorothiazide binding.

135 , in particular for the tight binding system carbonic anhydrase-chlorothiazide.

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

137 Carbonic anhydrase converts COS into H2S, allowing NTAs

138 The carbonic anhydrase (Cpb) from Clostridium perfringens st

139 en alga Chlamydomonas reinhardtii, a luminal carbonic anhydrase, CrCAH3, was suggested to improve pro

140 For comparison we assayed recessive ca1ca4 carbonic anhydrase double mutant plants, based on their

141 recently isolated Arabidopsis thaliana beta-carbonic anhydrase double mutants (ca1 ca4) exhibit an i

142 Many microalgae induce an extracellular carbonic anhydrase (eCA), associated with the cell surfa

143 ndogenous metal affinity of Escherichia coli carbonic anhydrase (ECCA).

144 Clostridium perfringens strain 13, the only carbonic anhydrase encoded in the genome, was characteri

145 ing atmospheric CO2 elevation, including the carbonic-anhydrase-encoding genes CA1 and CA4 and the se

146 eties were investigated as inhibitors of the carbonic anhydrase enzyme (CA; EC 4.2.1.1).

147 hloroplast are achieved by the activity of a carbonic anhydrase enzyme combined with the maintenance

148 Carbonic anhydrase enzymes (CAs) catalyse the reversible

149 possible clinical benefits of inhibitors of carbonic anhydrase enzymes and the water channel Aquapor

150 a subcomplex, containing the ancestral gamma-carbonic anhydrase (gamma-CA), gamma-carbonic anhydrase-

151 onic anhydrase gene (ca19) beyond the single carbonic anhydrase gene (ca18) that was known previously

152 We have identified a novel carbonic anhydrase gene (ca19) beyond the single carboni

153 LCI1, CCP1, CCP2 and LCIA) and mitochondrial carbonic anhydrase genes (CAH4 and CAH5) are up regulate

154 alysis and synteny studies suggest that both carbonic anhydrase genes form one or two independent gen

155 Benzenesulfonamide and carbonic anhydrase have been chosen as the ligand and pr

156 defined system of protein and ligands--human carbonic anhydrase (HCA) and a series of benzothiazole s

157 oldamer 2 was synthesized and bound to human carbonic anhydrase (HCA) using a nanomolar active site l

158 ss-coupling reactions and evaluated as human carbonic anhydrase (hCA, EC 4.2.1.1) inhibitors against

159 lly and pharmacologically relevant human (h) carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, the cytos

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

161 A panel of metalloenzymes, including carbonic anhydrase (hCAII), several matrix metalloprotei

162 ent inhibitors of the tumor-associated human carbonic anhydrases (hCAs) IX and XII.

163 against four physiologically relevant human carbonic anhydrases (hCAs, EC 4.2.1.1), isoforms hCA I,

164 Arg160His mutation of Haemophilus influenzae carbonic anhydrase (HICA), which mimics the endogenous m

165 Carbonic anhydrase I (Car1) is a gene expressed uniquely

166 ral stability and unfolding process of human carbonic anhydrase I (HCA-I).

167 Tryptic digestion of differentially labeled carbonic anhydrase I and hemoglobin allowed the identifi

168 ng these proteins, the strict association of carbonic anhydrase I and S100A8 with ECM was verified by

169 , human serum albumin, hemoglobin, and human carbonic anhydrase I were successfully labeled.

170 s, which was demonstrated by modification of carbonic anhydrase I with electrochemically generated re

171 Expression of carbonic anhydrase I, glucosaminyl (N-acetyl) transferas

172 e growth factor binding protein (IGFBP), and carbonic anhydrase-I and -II.

173 of residual mobility in complexes of bovine carbonic anhydrase II (BCA) and para-substituted benzene

174 We present a new approach to carbonic anhydrase II (CA II) inhibitor design that enab

175 r binding affinity to the zinc metalloenzyme carbonic anhydrase II (CA II).

176 a fragment screening campaign against human carbonic anhydrase II (CA II).

177 ts to analyze the direct interaction between carbonic anhydrase II (CAII) and MCT1, MCT2, and MCT4, r

178 P1 has two acidic motifs homologous to known carbonic anhydrase II (CAII) binding sequences.

179 In nature, the zinc metalloenzyme carbonic anhydrase II (CAII) efficiently catalyzes the c

180 f MCT1 and MCT4 is enhanced by the cytosolic carbonic anhydrase II (CAII) independent of its catalyti

181 Carbonic anhydrase II (CAII)(Cre);Pdx1(Fl) mice were eug

182 TFGs containing CB[6]- and carbonic anhydrase II (CAII)-binding domains were synthe

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

184 Variants of human carbonic anhydrase II (HCA II) with amino acid replaceme

185 In human carbonic anhydrase II (HCA II), the mutation of position

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

187 ione (1,2-HOPTO) in the active site of human carbonic anhydrase II (hCAII) has been investigated.

188 e corresponding inhibitor complexes of human carbonic anhydrase II (HCAII) indicated that HpalphaCA p

189 The binding of sulfonamides to human carbonic anhydrase II (hCAII) is a complex and long-deba

190 nvestigation of the CD spectrum of the Human Carbonic Anhydrase II (HCAII), with main focus on the ne

191 This paper uses the binding pocket of human carbonic anhydrase II (HCAII, EC 4.2.1.1) as a tool to e

192 We have reported previously that carbonic anhydrase II augments transport activity of MCT

193 res rapid conversion between CO2 and HCO3(-) Carbonic anhydrase II facilitates this reversible reacti

194 K, tartrate-resistant acid phosphatase, and carbonic anhydrase II in bone marrow macrophages (BMMs),

195 Deprotonation of zinc-bound water in carbonic anhydrase II is the rate-limiting step in the c

196 lls arise mainly from extrainsular PDX-1(+), carbonic anhydrase II(-) (mature ductal), elastase 3a (a

197 three proteins (ubiquitin, cytochrome c, and carbonic anhydrase II) were investigated.

198 of the selected scFvs was shown to recognize carbonic anhydrase II, an up-regulated enzyme involved i

199 rker tartrate-resistant acid phosphatase, or carbonic anhydrase II.

200 lated known genes, whereas Srpx2, Cd200, and carbonic anhydrase III (CAIII) were identified as novel

201 Carbonic anhydrase III protects osteocytes from oxidativ

202 Carbonic anhydrase XII (CA12) is the key carbonic anhydrase in epithelial fluid and HCO3 (-) secr

203 resolved kinetics for dansylamide binding to carbonic anhydrase in solutions crowded with polyethylen

204 e-1,5-bisphosphate carboxylase/oxygenase and carbonic anhydrase in the microcompartment shell.

205 roportion of Rubisco and the thylakoid lumen carbonic anhydrase in the pyrenoid rose substantially, c

206 we investigate the repertoire of cytoplasmic carbonic anhydrases in the sea lamprey (Petromyzon marin

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

208 ich was sensitive to Na(+)withdrawal, to the carbonic anhydrase inhibitor acetazolamide and to H2DIDS

209 tment of B. pertussis-infected mice with the carbonic anhydrase inhibitor acetazolamide reduced lung

210 Given methazolamide, a potent carbonic anhydrase inhibitor, can penetrate the blood-br

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

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

213 Carbonic anhydrase inhibitors may be effective in promot

214 Carbonic anhydrase inhibitors may promote resolution of

215 Azide derivatives of 2 carbonic anhydrase inhibitors, 4-(2-aminoethyl)benzenesu

216 In this connection, we report a new class of carbonic anhydrase inhibitors, based on the thiopyrano-f

217 ation, use of topical beta blockers, topical carbonic anhydrase inhibitors, daily dose of BAK, and gl

218 Other glaucoma medications (beta blockers, carbonic anhydrase inhibitors, parasympathomimetics, and

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

220 ished nitrite bioactivation, but the role of carbonic anhydrase is abrogated when physiological conce

221 H(+)-extrusion mechanisms and extracellular carbonic anhydrase, is responsible for active transport-

222 was also observed, in line with patterns of carbonic anhydrase isoform expression in those tissues.

223 vatives have been developed as inhibitors of carbonic anhydrase isoform IX.

224 n efficiency within 1400-fold of the fastest carbonic anhydrase isoform, CAII, and 11-fold of CAIII.

225 While several carbonic anhydrase isoforms have been identified in nume

226 luated as inhibitors of the ubiquitous human carbonic anhydrase isoforms I, II, IX, XII, and XIV usin

227 t that the human genome encodes 15 different carbonic anhydrase isoforms that have a high degree of h

228 rs (encoded by Slc26a4, Slc4a8, and Slc4a9), carbonic anhydrase isoforms, and V-type H(+)-ATPase subu

229 ed for the inhibition of some selected human carbonic anhydrase isoforms.

230 -the-haystack" screen for inhibitors against carbonic anhydrase isozyme II is performed, in which kno

231 Carbonic anhydrase IV (Car4) was a top dysregulated gene

232 Carbonic anhydrase IX (CA IX) is a hypoxia-induced cell

233 Carbonic anhydrase IX (CA IX) is a target for hypoxic ca

234 Carbonic anhydrase IX (CA IX) is a transmembrane protein

235 Carbonic anhydrase IX (CA IX) is an extracellular transm

236 Human carbonic anhydrase IX (CA IX) is highly expressed in tum

237 Human carbonic anhydrase IX (CA IX) is overexpressed in a numb

238 n of hypoxic tumors is possible by targeting carbonic anhydrase IX (CA IX), an enzyme overexpressed i

239 Carbonic anhydrase IX (CA-IX) is upregulated in cancer i

240 Carbonic anhydrase IX (CA-IX), a transmembrane enzyme, m

241 Carbonic anhydrase IX (CA9) is a transmembrane glycoprot

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

243 chemical technique, using antibodies against carbonic anhydrase IX (CAIX) and copper pumps (Ctr1 and

244 body-mediated therapy with the chimeric anti-carbonic anhydrase IX (CAIX) antibody girentuximab (cG25

245 t vascularization and acid-extruding protein carbonic anhydrase IX (CAIX) expression.

246 Carbonic anhydrase IX (CAIX) is a membrane-bound, tumor-

247 It was induced by carbonic anhydrase IX (CAIX) overexpression and inhibite

248 MCT4 remained unchanged, while expression of carbonic anhydrase IX (CAIX) was greatly enhanced.

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

250 o facilitate the intraoperative detection of carbonic anhydrase IX (CAIX)-expressing tumor lesions wi

251 Carbonic anhydrase IX (CAIX, CA9) expression is highly u

252 Inhibition of human carbonic anhydrase IX (hCA IX) has shown to be therapeut

253 armacodynamics from tumor biomarkers such as carbonic anhydrase IX and topoisomerase I by immunohisto

254 beta-catenin) and function (aquaporin 1 and carbonic anhydrase IX).

255 is a chimeric monoclonal antibody that binds carbonic anhydrase IX, a cell surface glycoprotein ubiqu

256 escribed a novel acetazolamide derivative, a carbonic anhydrase ligand with high affinity for the tum

257 ty to CO(2), native extra- and intracellular carbonic anhydrase-like activities, the non-CO(2)/HCO(3)

258 l gamma-carbonic anhydrase (gamma-CA), gamma-carbonic anhydrase-like, and 20.9-kDa subunits, had a si

259 valent system comprising synthetic dimers of carbonic anhydrase linked chemically through thiol group

260 We find that expression of the Cd/Zn carbonic anhydrase makes no difference to the Cd isotope

261 Carbonic anhydrase members in this class of exofacial mo

262 The murine inhibitor of carbonic anhydrase (mICA), a member of the transferrin (

263 from small molecules to proteins as large as carbonic anhydrase (molecular weight ca. 29,000).

264 Contrastingly, transcripts of chloroplast carbonic anhydrases namely CAH6, CAH3 and LCIB are up re

265 alpha-Carbonic anhydrase of Helicobacter pylori (HpalphaCA) pl

266 Overexpression of carbonic anhydrases on cell surfaces further contributes

267 D-ME cycle via an aspartate-alanine shuttle, carbonic anhydrase, phosophoenolpyruvate carboxylase, al

268 Carbonic anhydrase plays a key role in CO2 transport, ac

269 of incubation at 750 microatm pCO2, reduced carbonic anhydrase protein activity and shell growth occ

270 ient CO2 We identified CAH1 as an alpha-type carbonic anhydrase, providing a biochemical role in CCM

271 rey metamorphosis resulting in distinct gill carbonic anhydrases reflecting the contrasting life mode

272 aria susceptibility in the murine model, and carbonic anhydrase, reflecting the blood's abnormal acid

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

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

275 ditions we find dorzolamide (an inhibitor of carbonic anhydrase) results in diminished nitrite bioact

276 showed reduced expression of colonic villin, carbonic anhydrase, secretory mucin muc2, and increased

277 beta-lactoglobulin (five peptides), 25% for carbonic anhydrase (six peptides), and 51% for bovine se

278 e, biotin, mannose) against matched targets (carbonic anhydrase, streptavidin, concanavalin A) to ide

279 Carbon acquisition enzymes, primarily carbonic anhydrase, stress, degradation and signaling pr

280 ely conserved proteins containing domains of carbonic anhydrase, Sushi, Von Willebrand factor type A,

281 Plants respond to elevated CO(2) via carbonic anhydrases that mediate stomatal closing, but l

282 Because spirochetes lack carbonic anhydrase, the corresponding reduction in bicar

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

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

285 1,5-bisphosphate carboxylase/ oxygenase and carbonic anhydrase to facilitate carbon fixation in cyan

286 Intracellular carbonic anhydrase transcript abundance increased with t

287 68 and mannose receptor-positive, expressing carbonic anhydrase type II, but relatively low levels of

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

289 lective inhibitors of five isoforms of human carbonic anhydrase was also explored.

290 cyclen, a small molecule mimic of the enzyme carbonic anhydrase, was evaluated under rigorous conditi

291 died: ribonuclease A, trypsin inhibitor, and carbonic anhydrase, where the latter had impurities of s

292 larly sodium bicarbonate co-transporters and carbonic anhydrases, which were also expressed in LAM lu

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

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

295 ed when buffering was augmented by exogenous carbonic anhydrase (XCAR).

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

297 Carbonic anhydrase XII (CA12) is the key carbonic anhydr

298 n of one specific gene in the FLC signature, carbonic anhydrase XII (CA12), at the protein level by w

299 Here we describe variants in CA12 encoding carbonic anhydrase XII in two pedigrees exhibiting CF-li

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