ライフサイエンスコーパス: C2H2

1 C2H2 zinc finger bearing proteins are a large superfamil

2 C2H2 zinc finger protein genes encode nucleic acid-bindi

3 C2H2 zinc finger proteins that do not bind arsenic were

4 C2H2 zinc fingers are found in several key transcription

5 C2H2 zinc fingers define the largest transcription facto

6 C2H2 zinc-finger family members are key targets of DE mi

7 C2H2 zinc-finger proteins play important roles in plant

8 KS1 contains 10 C2H2 zinc fingers, a KRAB-A/B motif, and an ID sequence

9 st three protein isoforms that contain 12-18 C2H2 zinc fingers.

10 ula, a member of the Cysteine-2/Histidine-2 (C2H2) family of plant TFs that is required for normal sy

11 dt =1,3-propanedithiolate and dppv = cis-1,2-C2H2(PPh2)2), was generated by reduction of the differou

12 A domain and a SCAN domain, but lacks the 22 C2H2-type zinc fingers present in ZnF197.

13 brid screen, encoded a protein containing 29 C2H2 zinc fingers of the TFIIIA type.

14 transcription factors that share a common 3 C2H2 zinc finger DNA binding domain and have broad activ

15 ription factors and is found in more than 60 C2H2 zinc finger genes in the human genome, including th

16 OVOL2 encodes ovo-like zinc finger 2, a C2H2 zinc-finger transcription factor that regulates mes

17 Our previous studies showed that UNC-98, a C2H2 Zn finger protein, acts as a linkage between UNC-97

18 usly reported structures, Sgf73 ZnF adopts a C2H2 coordination with unusual tautomeric forms for the

19 We cloned grauzone and identified it as a C2H2-type zinc finger transcription factor.

20 gle DNA binding homeodomain but lacks both a C2H2 zinc finger DNA binding domain and an apparent Dig1

21 ee different protein isoforms that contain a C2H2 zinc-finger domain.

22 Peg3 encodes a C2H2 type zinc finger protein that is implicated in a no

23 The die-1 gene encodes a C2H2 zinc finger protein containing four fingers, which

24 RABBIT EARS (RBE) encodes a C2H2 zinc finger transcriptional repressor and is requir

25 tlp-1 encodes a C2H2 zinc-finger protein that is a member of the Sp fami

26 him-8 encodes a C2H2 zinc-finger protein that is expressed during meiosi

27 We show that lin-48 encodes a C2H2 zinc-finger protein that is similar to the product

28 Mutants of pita, which encodes a C2H2 zinc-finger protein, are homozygous lethal and show

29 We cloned ehn-3, and found that it encodes a C2H2 zinc-finger protein.

30 oned pag-3 and found that the gene encodes a C2H2-type zinc finger protein related to the mammalian G

31 UP, also called FLO10) gene, which encodes a C2H2-type zinc finger protein, is involved in maintenanc

32 The grauzone gene encodes a C2H2-type zinc-finger transcription factor that binds to

33 ene, No Transmitting Tract (NTT), encoding a C2H2/C2HC zinc finger transcription factor specifically

34 Here we provide evidence for a C2H2 zinc finger gene family with similarity to Ikaros a

35 identified SUF4 (SUPPRESSOR OF FRIGIDA4), a C2H2 transcription factor, as a direct regulator of the

36 e that was in turn ultimately derived from a C2H2 Zn-finger domain.

37 odes several functional domains, including a C2H2 zinc finger, a leucine zipper, and a winged-helix/f

38 nine aminopeptidases (MetAPs), and Rei1 is a C2H2 zinc finger protein whose function in ribosome biog

39 ction of two conserved DNA-binding motifs, a C2H2 zinc finger (ZF) and a Myb motif, located within th

40 eotide primer, for the facile isolation of a C2H2 zinc finger protein cDNA (Pszf1) from pea petals.

41 the identification of a natural allele of a C2H2-type transcription factor in rice that confers non-

42 Cocultures of Pelobacter SFB93, a C2H2-fermenting bacterium, with D. mccartyi strain 195 o

43 , changing a C2C2 type Zn-binding motif to a C2H2 motif.

44 nit in the C terminus of the HYB domain to a C2H2-like zinc finger in HYB(DeltaC).

45 P gene encodes a transcription factor with a C2H2-type zinc finger motif, a serine/proline-rich domai

46 performed genome-wide ChIP-seq for ZNF263, a C2H2 ZNF that contains 9 finger domains, a KRAB repressi

47 ive to high-temperature hydrogen-abstraction-C2H2-addition (HACA) sequences to form polycyclic aromat

48 Acetylene (C2H2) can be generated in contaminated groundwater sites

49 rs or so), whereas methane (CH4), acetylene (C2H2), ethylene (C2H4), and ethane (C2H6) are abundant m

50 ith simple prototype hydrocarbons acetylene (C2H2) and ethylene (C2H4).

51 protocol we measured intrabreath acetylene (C2H2) and carbon monoxide (CO) transfer, pulmonary funct

52 tunneling spectra for an isolated acetylene (C2H2) molecule adsorbed on the copper (100) surface show

53 ing of the molecular structure of acetylene (C2H2) 9 femtoseconds after ionization.

54 acids form by one-pot reaction of acetylene (C2H2) and carbon monoxide (CO) in contact with nickel su

55 Here we report the detection of acetylene (C2H2) in the infrared spectrum of comet C/1996 B2 (Hyaku

56 to the selective hydrogenation of acetylene (C2H2) to ethylene (C2H4).

57 th the nonphysiological substrate acetylene (C2H2) to generate deuterated ethylenes (C2H3D and C2H2D2

58 pper sheet at 850 degrees C using acetylene (C2H2) as carbon source in an argon (Ar) and nitrogen (N2

59 AMO activity was inactivated with acetylene (C2H2) after mRNA depletion.

60 ron monosulfide radical (BS) with acetylene (C2H2) under single collision conditions in the gas phase

61 an extensive and largely unstudied adaptive C2H2-ZF regulatory network that targets a diverse range

62 analog 1-N6-ethenoadenosine diphosphate (ADP[C2H2]) from the active site of Cys707-modified (by N-eth

63 ked (by N,N'-p-phenylene dimaleimide) S1.ADP[C2H2].AlF4- and S1.ADP[C2H2].BeFx.

64 e dimaleimide) S1.ADP[C2H2].AlF4- and S1.ADP[C2H2].BeFx.

65 sts, and evidence is presented that C2H4 and C2H2 formation occur via C2H6 and C2H4 dehydrogenation,

66 h small hydrocarbons, namely C2H6, C2H4, and C2H2, are investigated by experiment and density functio

67 tion is inhibited noncompetitively by CO and C2H2 with Ki values of ca. 0.0008 and 0.006 atm, respect

68 on factor that contains a BTB/POZ domain and C2H2 zinc finger motifs.

69 enoLOGOS and C2H2-enoLOGOS are accessible over the web at http://biod

70 ichloroethene (TCE) by in situ minerals, and C2H2 is known to inhibit bacterial dechlorination.

71 nscription factors (AP2-EREBP, WRKY, NAC and C2H2), osmoprotectants, ion transporters and heat shock

72 of the structure of randomly oriented O2 and C2H2 molecules, with pig and piu symmetries, respectivel

73 motifs for the nuclear hormone receptor and C2H2 zinc finger families and reveal unexpected diversit

74 t contaminated sites containing both TCE and C2H2.

75 tobacco has a higher proportion of ERF/AP2, C2H2 zinc finger, homeodomain, GRF, TCP, zinc finger hom

76 ption of 5S rRNA genes and is the archetypal C2H2 zinc finger protein.

77 itated by repeats of sequence motifs such as C2H2 zinc fingers.

78 he temperature changes for molecules such as C2H2, O2, H2O, and NH3.

79 LA (SAP) genes and novel subfamilies of BES, C2H2 zinc finger, SAP, and NAC genes.

80 the potential energy surface (PES) between (C2H2)n(+) isomers and provide evaporative cooling to dis

81 ynthetic protein libraries to select binding C2H2-ZF domains for each possible three base pair target

82 In survivors of BPD C2H2 transfer with exercise did increase, but not as muc

83 rinciple of recognition of methylated CpG by C2H2 ZnF proteins, which involves a spatially conserved

84 tal biological processes: DNA recognition by C2H2 zinc-finger proteins and homology-directed repair o

85 Predictions for the CH4 = CH3 + H and C2H3 = C2H2 + H reaction systems are in excellent agreement wit

86 hat one of these zinc fingers is a canonical C2H2 DNA binding domain.

87 e contains binding sites for a non-canonical C2H2 zinc finger protein.

88 actor family containing three characteristic C2H2-type zinc finger motifs.

89 v)Ni(mu-pdt)Fe(CO)(dppv) ([1](0); dppv = cis-C2H2(PPh2)2) and its hydride derivatives have yielded to

90 he invariant 12 amino acids in the classical C2H2 motif.

91 eceptors and proteins with three consecutive C2H2 zinc fingers.

92 a DNA binding domain with three consecutive C2H2 zinc fingers.

93 was localized to an evolutionarily conserved C2H2 zinc finger and leucine zipper motif.

94 ferentiation via an evolutionarily conserved C2H2 zinc finger motif.

95 , that encode proteins with highly conserved C2H2 zinc fingers.

96 nd primarily functions through its conserved C2H2 Kruppel type zinc finger and BTB/POZ domains.

97 e identification of a SCAN domain-containing C2H2 zinc finger protein, ZNF24, that represses the tran

98 de direct evidence that most KRAB-containing C2H2-ZF proteins bind specific endogenous retroelements

99 and DAZ2, which encode EAR motif-containing C2H2-type zinc finger proteins.

100 predicting a PWM given a protein containing C2H2-ZF domains is available online at http://zf.princet

101 Proteins containing C2H2 type zinc finger motifs represent one of the larges

102 , a class of zinc finger proteins containing C2H2 zinc fingers in tandem arrays of two or three is pr

103 In contrast, C2H2-ZF DNA binding in fungi, plants, and other lineages

104 yeast fbp1 gene, binding of Rst2 (a critical C2H2 zinc-finger TF) is mediated by a local loop structu

105 ain from the Zif268 protein, using different C2H2 ZF domains as structural templates.

106 BTB/POZ-domain C2H2 zinc(Zn)-finger proteins are encoded by a subfamily

107 1 is a 55-kDa protein that contains a double C2H2-type zinc finger domain.

108 d Hym hydrogenase were down-regulated during C2H2 inhibition, consistent with the physiological obser

109 aa, each having a DNA-binding domain (eight C2H2 zinc fingers) and a proline-rich transcription acti

110 Sequence analysis reveals eight C2H2 zinc finger motifs at the C-terminus of ZNF210 and

111 nding profiles for a benchmark set of eleven C2H2 zinc finger transcription factors, five of known an

112 rescence organs, ZFP8 and GIS2, which encode C2H2 transcription factors related to GLABROUS INFLORESC

113 re, that combines two functionally essential C2H2 zinc-finger domains, which are probably involved in

114 cardiac output at rest and during exercise (C2H2 rebreathing) were measured at the same time periods

115 Both at rest and during exercise, C2H2 transfer corrected for body surface area was lower

116 enitor of placental mammals, but that extant C2H2-ZF domains typically bind different sequences from

117 The C2H2 zinc finger (C2H2-ZF) is the most numerous protein domain in many met

118 Cys2-His2 zinc finger (C2H2-ZF) proteins represent the largest class of putativ

119 Cys2His2 zinc fingers (C2H2-ZFs) comprise the largest class of metazoan DNA-bin

120 (TFs) with multiple Cys2-His2 zinc fingers (C2H2-ZFs) remain poorly studied.

121 ing specificities for Cys2His2 zinc fingers (C2H2-ZFs), the largest family of DNA-binding proteins in

122 This screen identified the Zinc fingers, C2H2 and BTB domain containing (ZBTB) family members ZBT

123 milar DNA binding structure of four and five C2H2 zinc finger motifs (ZF), respectively.

124 an 83.8 kDa nuclear protein containing five C2H2-type Kruppel-like zinc finger motifs that exhibit 9

125 the C-terminal 174 amino acids contains five C2H2 zinc finger domains, and the N terminus (residues 1

126 a per-finger basis and merge predictions for C2H2-ZF domains that are arrayed within sequences.

127 ) representing DNA-binding specificities for C2H2-ZF proteins.

128 ith UNC-98, a 37-kD protein, containing four C2H2 Zn fingers, that localizes to M-lines.

129 l 310-residue polypeptide consisting of four C2H2 Zn fingers and several possible nuclear localizatio

130 n of 1920 amino acids that contains fourteen C2H2-type zinc fingers, and glutamine-rich and proline-r

131 ypes of zinc fingers separated from a fourth C2H2 finger by a long spacer; ID1 is distinct from other

132 ted Rox7, is shown here to be Mot3, a global C2H2 zinc finger regulator.

133 d, isomerization of acetylene (nomega+C2H2-->C2H2(2+)-->CH2++C+) is controlled via a barrier-suppress

134 volatiles (H2O, C2H6, HCN, CO, CH3OH, H2CO, C2H2, and CH4) in the Jupiter-family comet Tempel 1 usin

135 abundance of simple organic molecules (HCN, C2H2, and CO2), water vapor, and OH.

136 In this study, we show that while high C2H2 (1.3 mM) concentrations reversibly inhibit reductiv

137 roteins that contain two atypical Cys2/His2 (C2H2) zinc finger-like domains that are evolutionarily w

138 ents Zfp335 as a model for understanding how C2H2-ZF TFs may use multiple recognition motifs to contr

139 ization in the series of simple hydrocarbons C2H2, C2H4, and C2H6, we show that double-slit interfere

140 Eu(II)DTPA, displaying a strong activity in C2H2 reduction while demonstrating an ability to reduce

141 Further, CN- did not induce cooperativity in C2H2 reduction and, therefore, CO and CN- are unlikely t

142 form holodinitrogenase 2, which functions in C2H2, H+, and N2 reduction.

143 Members of one group include C2H2 zinc finger motifs.

144 Examples explored in this study include C2H2 zinc finger, homeodomain and bHLH DNA-binding motif

145 N2 also inhibits C2H2 reduction catalyzed by the alpha-195(Gln) nitrogena

146 ated by products whose empirical formula is (C2H2) n(+), just like ionized acetylene clusters.

147 hrough sequence-specific DNA binding via its C2H2 zinc finger (ZF) tandem array, which is highly poly

148 ve been identified: lanthanacyclopropene [La(C2H2)], La(cyclobut-1-en-3-yne) [La(C4H2)], and La(benzy

149 criptomic profiling of three mutants lacking C2H2 zinc finger proteins, ypr013cDelta,ypr015cDelta and

150 We now find that the hunchback/Ikaros-like C2H2 zinc-finger factor ztf-16 is also required.

151 ent cultures containing D. mccartyi sp., low C2H2 (0.4 mM) concentrations do not inhibit growth or me

152 unsaturated substrates (e.g., CS2, Me3SiCCH, C2H2, and CH3CN).

153 However, for most C2H2-ZF proteins it is unknown whether they even bind DN

154 e transcripts were found to contain multiple C2H2-type zinc finger motifs in tandem arrays, indicatin

155 dsRNA binding domain consisting of multiple C2H2 zinc fingers.

156 ters (V(m)O(n)) with C2H2 molecules, V(m)O(n)C2H2 are assigned as the major products of the associati

157 mprise the majority of zinc fingers, namely, C2H2-like finger, treble clef finger and the zinc ribbon

158 ng DNA-binding data for thousands of natural C2H2-ZF domains.

159 est our approach on a diverse set of natural C2H2-ZF proteins with known binding specificities and de

160 precipitation analyses, we show that natural C2H2-ZFs encoded in the human genome bind DNA both in vi

161 ption factors characterized by seven to nine C2H2 zinc finger motifs.

162 form of apodinitrogenase 2 that exhibits no C2H2, H+, or N2 reduction activities in the in vitro FeV

163 ances the binding of H, C, N, O, O2, CO, NO, C2H2, and C2H4 on the Ag(111) surface.

164 Second, isomerization of acetylene (nomega+C2H2-->C2H2(2+)-->CH2++C+) is controlled via a barrier-s

165 A novel C2H2 zinc finger gene, ZNF277, has been localized to hum

166 Here, we describe lsy-2, a novel C2H2 zinc finger transcription factor that is required f

167 thought to occur only in eukaryotes, a novel C2H2 zinc finger transcription factor, Ros, which regula

168 Here, we report that ZFP3, a nuclear C2H2 zinc finger protein, acts as a negative regulator o

169 lso shows impressive selective adsorption of C2H2, C2H4, and C2H6 over CH4 at room temperature, indic

170 onal analyses uncovered important aspects of C2H2-ZF domain-DNA interactions, including the roles of

171 n the adsorption energy and configuration of C2H2, while the influence of the ensemble structure is w

172 Our results suggest that the evolution of C2H2-ZFs in metazoans was expedited by the interaction o

173 rotein 1) is one member of a small family of C2H2 zinc finger-encoding sequences previously character

174 is the founding member of a small family of C2H2 zinc-finger DNA-binding proteins that carry out cri

175 a nematode-specific, fast-evolving family of C2H2 zinc-finger transcription factors, lsy-27, is mutat

176 t integrates crystallographic information of C2H2 zinc finger-DNA complexes with binding data from 11

177 uce N2 and insensitivity to CO inhibition of C2H2 reduction.

178 rise the most comprehensive investigation of C2H2-ZF DNA-binding interactions to date.

179 p elucidate the complex binding landscape of C2H2-ZF domains and provide a foundation for efforts to

180 The majority of C2H2-ZF proteins, including KRAB proteins, also show wid

181 Characteristic motifs of C2H2 zinc fingers and leucine heptad repeats are present

182 omain, SANT domains and a variable number of C2H2 type zinc fingers (3-14).

183 alternative splicing to one of four pairs of C2H2 zinc-finger domains (Z1, Z2, Z3, and Z4).

184 d to the successful design and prediction of C2H2-ZF DNA-binding specificities.

185 a-277His MoFe-protein-catalyzed reduction of C2H2 showed sigmoidal kinetics, which is consistent with

186 , KRIP-1 interacts with the KRAB-A region of C2H2 zinc finger proteins and may mediate or modulate KR

187 demonstrates highly selective separation of C2H2/CO2 at ambient temperature and pressure.

188 ans conformational change in the S1 state of C2H2 and the bond-breaking HCN-HNC isomerization.

189 found near the N-terminus of a subfamily of C2H2 zinc finger proteins.

190 ion factors (KLFs) constitute a subfamily of C2H2-type zinc finger proteins with distinct cell-type e

191 ino acid sequence identified a novel type of C2H2 zinc finger.

192 rogram, and the results of PCOAT analysis on C2H2 alignment and ACT domain alignment.

193 y DNA triplet was recognized by at least one C2H2-ZF domain in the common progenitor of placental mam

194 hydrocarbon ice such as CH4, C2H6, C2H4, or C2H2 on 1993SC.

195 No substrate reduction (H+ or C2H2) was detected when wild-type MoFe protein was compl

196 at of the catalyzed reduction of H+, HCN, or C2H2, the extent of azide reduction to either N2 or N2H4

197 h stroke volume derived from cardiac output (C2H2 rebreathing) and heart rate.

198 t of the isolation of a three-fingered plant C2H2 ZFP gene and we discuss its possible evolutionary o

199 JAGGED (JAG), a gene that encodes a putative C2H2 zinc-finger transcription factor, as a key regulato

200 Roaz, a rat C2H2 zinc finger protein, plays a role in the regulation

201 reductase component of nitrogenase to reduce C2H2 in an ATP-dependent reaction.

202 BCL11 proteins are related C2H2 zinc-finger transcription factors that act as trans

203 Here, we show that a family of four related C2H2 zinc-finger proteins plays a central role in these

204 c-binding motifs in the form of two separate C2H2 zinc finger sequences.

205 t splice isoforms, which contain up to seven C2H2 Zn-finger domains, and is localized to the nucleus,

206 ists of a basic N-terminal region with seven C2H2 zinc finger motifs and an acidic C-terminal region

207 These data show that single C2H2 zinc fingers can bind RNA specifically and suggest

208 ogene encodes a zinc finger protein with six C2H2-type, C-terminal zinc finger motifs and is activate

209 Another web interface for our software, C2H2-enoLOGOS, generates logos for the DNA-binding prefe

210 xidase protein, AtSWP1, and a plant-specific C2H2 zinc finger-SET domain protein, AtCZS, interact wit

211 ferase bi-domain module with a RET1-specific C2H2 zinc finger and RNA recognition (RRM) domains.

212 1C protein has a zinc finger-like structure (C2H2 motif) at its N terminus, which is conserved from y

213 the reduction of the alternative substrates, C2H2, HCN, HN3, and protons.

214 large and highly variable numbers of tandem C2H2 zinc finger (tandem ZF) transcription factor protei

215 We show that the conserved N-terminal C2H2 zinc finger domain is essential for direct DNA bind

216 ar domain structure, including an N-terminal C2H2 zinc finger domain, a central putative core transpo

217 with our recognition code and indicate that C2H2-ZF proteins recognize more motifs than all other hu

218 The C2H2 TFIIIA/Kruppel class of zinc finger proteins are an

219 The C2H2 zinc finger (C2H2-ZF) is the most numerous protein

220 The C2H2 zinc finger is one of the most abundant protein dom

221 The C2H2 zinc finger is the most commonly utilized framework

222 The C2H2 zinc finger is the most prevalent protein motif in

223 The C2H2 zinc-finger protein Pita binds to several BX-C boun

224 The C2H2 zinc-finger-containing transcription factors encode

225 The C2H2-type zinc finger protein ZNF764 acts as an enhancer

226 which regulate neuronal development, and the C2H2 superfamily of zinc-finger transcription factors.

227 a physical interaction between UNC-3 and the C2H2 zinc finger transcription factor PAG-3, the mammali

228 g protein HYPONASTIC LEAVES1 (HYL1), and the C2H2 Zn-finger protein SERRATE (SE), are required for th

229 es (e.g., tceA) were not affected during the C2H2-inhibition, while genes encoding for ATP synthase,

230 that the ASE motif is a binding site for the C2H2 zinc finger TF CHE-1, which is essential for the co

231 logenetically conserved binding site for the C2H2 zinc-finger transcription factor CHE-1, a previousl

232 ntrotus purpuratus genome, we identified the C2H2 zinc finger genes indicated in the sequence, and ex

233 We find that mutations in the C2H2 motif have no perceptible effect on UV sensitivity

234 Ub-PCNA was not affected by mutations in the C2H2 motif or the D570 residue.

235 ave examined the effects of mutations in the C2H2 zinc binding motif and in the conserved D570 residu

236 eviously reported a mutation (R1092W) in the C2H2-ZF TF Zfp335 that led to selective loss of binding

237 n containing seven zinc finger motifs of the C2H2 class, four of which are arranged in two pairs wide

238 n factor with four zinc-finger motifs of the C2H2 class.

239 d three carboxy-terminal zinc fingers of the C2H2 DNA-binding type.

240 s a global mechanism for inactivation of the C2H2 family.

241 621) contain seven zinc finger motifs of the C2H2 type as well as proline and glutamine rich areas.

242 ame contains seven zinc-finger motifs of the C2H2 type, as well as proline-, glutamine-, and glutamic

243 ar protein with 11 zinc-finger motifs of the C2H2 type.

244 ers indicates that ZBP-89 is a member of the C2H2 zinc finger family subclass typified by the Drosoph

245 We demonstrate that mutations of the C2H2 zinc fingers encoded by the him-8 (high incidence o

246 logos for the DNA-binding preferences of the C2H2 zinc-finger transcription factor family members.

247 In animal systems the C2H2 zinc finger protein (ZFP) gene family is the larges

248 These results demonstrate that the C2H2 motif provides a versatile platform for both sequen

249 Here, we show that the C2H2 zinc finger transcriptional repressor encoded by RA

250 Here, we show that the C2H2-ZF expansion in metazoans is facilitated by contrib

251 obtained snapshots as a proton departs the [C2H2](2+) ion.

252 strains generally correlated well with their C2H2- and proton-reduction activities, which range from

253 ied transcription factor that contains three C2H2 Kruppel-type zinc fingers.

254 The predicted Tef protein contains three C2H2 zinc-finger motifs, one at the amino terminus and t

255 Two C2H2 fingers in Ikaros are dedicated to homotypic intera

256 e observed upon postembryonic removal of two C2H2 zinc finger transcription factors, die-1 and che-1,

257 AD2 is located within two C2H2 ZFs, ZF1 and ZF2.

258 We have isolated Kruppel-type (C2H2) zinc-finger genes, ZIM3 (zinc-finger gene 3 from i

259 ists of 11 exons and encodes a Kruppel-type (C2H2) zinc-finger protein with a conserved Kruppel-assoc

260 er gene 1), encoding a typical Kruppel-type (C2H2) zinc-finger protein, located within 30 kb of a kno

261 Half of all human transcription factors use C2H2 zinc finger domains to specify site-specific DNA bi

262 ditionally, a dehydration reaction for VO3 + C2H2 to produce VO2C2 is also identified.

263 reactions VO3+C2H4 --> VO2CH2 + H2CO and VO3+C2H2 --> VO2C2 + H2O are thermodynamically favorable and

264 lations of the pathways for VO3+C2H4 and VO3+C2H2 reaction systems indicate that the reactions VO3+C2

265 des a large protein containing 12 widespread C2H2 zinc fingers and 3 motifs containing periodic proli

266 om exercise, but this did not correlate with C2H2 transfer or DL(CO)/VA.

267 hannel leading to the production of H2S with C2H2 also has been observed.

268 s of vanadium oxide clusters (V(m)O(n)) with C2H2 molecules, V(m)O(n)C2H2 are assigned as the major p

269 differentiation, her encodes a protein with C2H2-type zinc fingers.

270 unlikely to share common binding sites with C2H2.

271 , we performed detailed comparisons of yeast C2H2 ZF proteins with identical canonical recognition re