ライフサイエンスコーパス: zipper

1 tive inhibitor for miRNAs, termed 'small RNA zipper'.

2 rs self-assemble using electrostatic 'charge zippers'.

3 interface to allow the formation of a serine zipper.

4 C terminus is mediated by a putative leucine zipper.

5 he CA-SP1 junction region fused to a leucine zipper.

6 Ne/Epi) boundary just ahead of the advancing zipper.

7 -beta structure and assembly of a dry steric zipper.

8 nce attached to N-terminal of bZIP53 leucine zipper.

9 ckdown of miRNA levels by 30-50 nM small RNA zippers.

10 d disfavoring formation of pathogenic steric zippers.

11 tions, such as those between pairing leucine zippers.

12 h propensity to form fibers, known as steric zippers.

13 ition to the structural properties of steric zippers.

14 as a fusion clamp that restricts full SNARE zippering.

15 abilized the CTD, facilitating further SNARE zippering.

16 l contraction mechanism for robust efficient zippering.

17 ng, known to be faster than N-terminal SNARE zippering.

18 osine interacting with PH domain and leucine zipper 1 (APPL1) signaling endosomes and MYO6+ expressio

19 atory pathway in which spermatogenic leucine zipper 1 (SPZ1) promotes EMT through its transactivating

20 n shown previously to bind the basic leucine zipper 1 domain in the C3 promoter.

21 sociated transcription factor, BASIC LEUCINE ZIPPER 17 (bZIP17), and the membrane-associated RNA spli

22 egron-pathway(4,5) substrate known as LITTLE ZIPPER 2 (ZPR2)-which evolved to control the activity of

23 inding activity of protagonist basic leucine zipper 53 (bZIP53) transcription factor and its heterodi

24 quiring protein-1) and bZIP60 (basic leucine zipper 60), two RSRE containing unfolded protein-respons

25 yosin II along Ne/Epi junctions ahead of the zipper and inhibiting myosin II along newly formed Ne/Ne

26 pact pseudoknot, dock via an extended ribose zipper and jointly create a binding groove specific to t

27 n factors: ERF/AP2 class I, homeobox-leucine zipper and R2R3 MYB.

28 rodimers and bind to DNA via a basic leucine zipper and regulate the cell cycle, apoptosis, different

29 s to a helical state when fused to a leucine zipper and that these helical molecules further associat

30 AP-25 C terminus promote tight SNARE complex zippering and are required for high release frequency an

31 ishes the semi-rosette formation, preventing zippering and causing spina bifida.

32 ractility along tissue boundaries to control zippering and neural tube closure in the basal chordate,

33 each other through their shafts, leading to zippering and unzippering behavior that regulates their

34 pathogenic seeds of alpha-syn contain steric zippers and suggest a therapeutic approach targeted at t

35 s that promote tetramerization when fused to zippers and those that permit the proper assembly of ful

36 el homodimer linked by an N-terminal leucine zipper, and we show that the WT chain in WT-RQ heterodim

37 ant when the SNAREpins are nearly completely zippered, and from this state, each SNAREpin can deliver

38 Taken together, small RNA zippers are a miRNA inhibitor, which can be used to indu

39 We show that zippering arises from the competition of axon-axon adhes

40 in the opposite strands in a so-called (+1)-zipper arrangement.

41 ne and 2,6-diaminopurine, and +1 interstrand zipper arrangements of intercalator-functionalized nucle

42 te amnioserosa internalization and epidermal zippering, as well as cardia bifida.

43 full-length myosin-X construct with leucine zipper at the C-terminal end of the tail (M10(Full)LZ) a

44 er vaccination, both migratory basic leucine zipper ATF-like transcription factor 3 (BatF3)-dependent

45 In addition, we demonstrate that the miR-221 zipper attenuates doxorubicin resistance with higher eff

46 alleles of wallenda (wnd, encoding a leucine zipper bearing kinase similar to human DLK and LZK) were

47 Leucine Zipper-bearing Kinase (LZK/MAP3K13) is a member of the m

48 Zippering begins with slow N-terminal association follow

49 Pore nucleation requires zippering between vesicle-associated v-SNAREs and target

50 Thus, a specific primary sequence or zippering beyond the SNARE domains is not a prerequisite

51 r (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein.

52 s), SFH3 (SEC14-like 3), bZIP (basic-leucine zipper), bHLH (basic helix-loop-helix) and SBP (SQUAMOSA

53 rtner Mlx are basic helix-loop-helix leucine zipper (bHLHZip) transcription factors that sense and ex

54 gnificantly reduced the energy of C-terminal zippering by 10 kBT, but did not affect N-terminal assem

55 IRs identified a heterodimeric basic leucine zipper (bZIP) complex between an uncharacterized protein

56 protein consists of the basic region-leucine zipper (BZip) domain of the CCAAT/enhancer-binding prote

57 leukemia virus type 1 (HTLV-1) basic leucine zipper (bZIP) factor (HBZ) could be used for immunothera

58 Here, a novel basic leucine zipper (bZIP) family transcription factor TubZIP28 was f

59 ED HYPOCOTYL 5 (HY5), a basic domain/leucine zipper (bZIP) transcription factor, acts as a master reg

60 nts identified to date, HY5, a basic leucine zipper (bZIP) transcription factor, has been investigate

61 act with TGACG-motif binding (TGA) basic Leu zipper (bZIP) transcription factors for recruitment to D

62 ive dimerization of the basic-region leucine-zipper (bZIP) transcription factors presents a vivid exa

63 Basic region leucine zipper (bZIP) transcription factors regulate gene expres

64 ng Locus T 1 (RFT1), OsFD-like basic leucine zipper (bZIP) transcription factors, and Gf14 proteins a

65 cytosolic domain containing a basic leucine zipper (bZIP) transcriptional activator.

66 d ICIRD spectroscopy on basic-region leucine zipper (bZIP)-LOV of aureochrome 1a from the diatom Phae

67 long newly formed Ne/Ne junctions behind the zipper, Cadherin2 promotes tissue-level contractile asym

68 periment, and show that 2 populations of DNA zippers can be distinguished using per-molecule statisti

69 tion factors in hematopoiesis is the leucine zipper CCAAT-enhancer binding protein alpha (C/EBPalpha)

70 conserved mechanism of general relevance for zippering closure of epithelial gaps whose disturbance c

71 tyrosine Interaction, PH domain, and leucine zipper containing 1 (APPL1) that were identified by mean

72 -DB to elucidate kinetics of regulated SNARE zippering containing degenerate states.

73 e MAP3K ZAK (Sterile alpha motif and leucine zipper-containing kinase) has also been proven to positi

74 brosarcoma oncogene homolog (MAF), a leucine zipper-containing transcription factor of the AP1 superf

75 en the NC domain was replaced with a leucine zipper dimerization motif that promotes Gag multimerizat

76 ion between the LOV and basic region leucine zipper DNA-binding domain that together with LOV dimeriz

77 ent to 5RK, believed to be crucial for final zippering, do not abolish this transition.

78 A leucine zipper domain can replace NC in Gag and still lead to th

79 cid-binding domain with a dimerizing leucine zipper domain leads to the assembly of RNA-free VLPs.

80 paB members RelB and p52 through its leucine zipper domain.

81 SNARE-domain zippering draws the bilayers into immediate apposition a

82 e uncover the molecular mechanism underlying zippering during mouse spinal neural tube closure.

83 ore, we introduce a biophysical model of the zippering dynamics, and we quantitatively relate the ind

84 key biophysical SNARE properties such as the zippering energy landscape and the surface charge distri

85 In simulations the approximately 65-kT zippering energy was almost entirely dissipated, with fu

86 the other tested IBV strains produced DMVs, zippered ER and spherules.

87 hese unprecedented findings show that steric zippers exhibit a characteristic nanomechanical signatur

88 ts proviral genome, the HTLV-1 basic leucine zipper factor (HBZ), which inhibits Tax-1-mediated viral

89 Ala-Ala in many members of the basic leucine-zipper family of transcription factors, important in gen

90 We have found that steric zippers form globular structures on route to making fibe

91 shortening of Ne/Epi junctions, driving the zipper forward and drawing the neural folds together.

92 Purified c-Jun leucine zipper fragments could also form stable homodimers, wher

93 Induction of glucocorticoid-induced leucine zipper (GILZ) by glucocorticoids plays a key role in the

94 Glucocorticoid (GC)-induced leucine zipper (GILZ) has been shown to mediate or mimic several

95 ssion of glucocorticoid (GC)-induced leucine zipper (GILZ) in bone marrow mesenchymal lineage cells o

96 Glucocorticoid-induced leucine zipper (GILZ) is a rapidly, potently, and invariably GC-

97 ine 211 and expression of GC-induced leucine zipper (GILZ) were significantly reduced in ASM cells fr

98 nscription of glucocorticoid-induced leucine zipper (GILZ).

99 at GTPase activation and trans-SNARE complex zippering have opposing effects on fragment formation an

100 e gamma-clade of class I homeodomain-leucine zipper (HD-Zip I) transcription factors (TFs) constitute

101 els activating class III homeodomain leucine zipper (HD-ZIP III) transcription factors (TFs).

102 expression of CLASS III HOMEODOMAIN-LEUCINE ZIPPER (HD-ZIP III) transcription factors, promotes xyle

103 Members of the class III homeodomain-leucine zipper (HD-ZIPIII) gene family are critical players in t

104 ree paralogous class III homeodomain leucine zipper (HD-ZIPIII) genes leads to aberrations in ovule i

105 members of the class III homeodomain leucine zipper (HD-ZIPIII) transcription factor family specify t

106 orm stable homodimers, whereas c-Fos leucine zipper homodimers were found to be much less stable in e

107 Characterization of the homeodomain leucine zipper I transcription factor AtHB13, which is expressed

108 Pull in plants using the HOMEODOMAIN LEUCINE ZIPPER III (HD-ZIPIII) and LITTLE ZIPPER (ZPR) interacti

109 porter system, we defined a putative leucine zipper in the N terminus of human pro-EMAP II protein (a

110 nal approaches to identify the mechanism for zippering in a basal chordate, Ciona intestinalis.

111 that corresponds to the structure of steric zippers in peptide crystals.

112 cell-cell contacts, filopodia, and membrane zippers, indicative of involvement in cell-cell adhesion

113 A novel inhibitor of zipper-interacting protein kinase (ZIPK) was used to exa

114 eveal tightly packed beta-sheets with steric zipper interfaces characteristic of the amyloid state.

115 orm a dimer driven by formation of a glycine zipper involving alpha helix formed by amino acid residu

116 Unidirectional zippering is a key step in neural tube closure that rema

117 In contrast, when complete C-terminal SNARE zippering is prevented, fusion strictly requires Sec18 a

118 dent fusion which occurs upon complete SNARE zippering is stimulated by Sec17 and Sec18:ATP without r

119 GILZ (glucocorticoid-induced leucine zipper) is inducible by glucocorticoids and plays a key

120 and possibly cooperates with homeodomain Leu zipper IV transcription factors.

121 uch as the widely used GCN4-based isoleucine zipper (IZ) and the T4 bacteriophage fibritin foldon (Fd

122 ress response controlled by the Dual Leucine Zipper Kinase (DLK) and contributes to DLK-mediated neur

123 ation in neurons is mediated by dual leucine zipper kinase (DLK) and JNK-interacting protein 3 (JIP3)

124 After axonal insult and injury, Dual leucine-zipper kinase (DLK) conveys retrograde pro-degenerative

125 Dual leucine zipper kinase (DLK) has been implicated in cell death si

126 Dual leucine zipper kinase (DLK) has emerged as a key mediator of thi

127 Dual leucine-zipper kinase (DLK) is critical for axon-to-soma retrogr

128 Dual leucine zipper kinase (DLK) is required for stress-induced JNK s

129 Dual leucine zipper kinase (DLK) promotes growth cone motility and mu

130 ing to ApoE receptors activates dual leucine-zipper kinase (DLK), a MAP-kinase kinase kinase that the

131 The Wallenda (Wnd)/dual leucine zipper kinase (DLK)-Jnk pathway is an evolutionarily con

132 ule dynamics was independent of dual leucine zipper kinase (DLK)-mediated stress but was rescued by c

133 The dual leucine zipper kinase (DLK)/c-Jun-N-terminal kinase (JNK) pathwa

134 Dual leucine zipper kinase (DLK, MAP3K12) was recently identified as

135 Here we identify the Dual Leucine-zipper Kinase (DLK, Wnd in Drosophila) as a critical tar

136 with high sequence identity to Dual Leucine Zipper Kinase (DLK/MAP3K12).

137 ly partially protective, we identify leucine zipper kinase (LZK) as cooperating with DLK to activate

138 The maternal embryonic leucine zipper kinase (MELK) has been implicated in the regulati

139 The Maternal Embryonic Leucine Zipper Kinase (MELK) has been reported to be a genetic d

140 a novel selective maternal embryonic leucine zipper kinase (MELK) inhibitor HTH-01-091, CRISPR/Cas9-m

141 rotein kinase maternal and embryonic leucine zipper kinase (MELK) is critical for mitotic progression

142 injury is regulated in part by dual-leucine zipper kinase 1 (DLK-1), a conserved regulator of axon r

143 tivity of type II maternal embryonic leucine zipper kinase inhibitors by applying these two complemen

144 tein kinase MELK (maternal embryonic leucine zipper kinase) has been considered an attractive therape

145 lain the increased rate for C-terminal SNARE zippering, known to be faster than N-terminal SNARE zipp

146 ned targeting, we introduce here the "Killer Zipper" (KZip(+)), a suppressor that makes Split GAL4 ta

147 cing can interlock with multiple TLR9 like a zipper, leading to multivalent electrostatic interaction

148 an self-assemble to form supramolecular DNA "zipper" like structures through intermolecular hydrogen

149 The synaptonemal complex is a 'zipper'-like protein assembly that synapses homologue pa

150 e-specific figure-of-eight, dumbbell-shaped, zipper-like and multi-loop quaternary structures were fo

151 barbs, allowing them to interlock in a tight zipper-like fashion to form vanes.

152 w that the C-terminal helices, arranged in a zipper-like fashion, play a crucial role in guiding the

153 In the present work, a stimuli encoded zipper-like graphene oxide (GrO)/polymer interface was f

154 spacing of the trans-Golgi cisternae through zipper-like interactions, thereby forcing cargo to the t

155 The study further indicated that the zipper-like interfacial bioelectrochemical properties co

156 cadherin gammaB4 ectodomain, which reveals a zipper-like lattice that is formed by alternating cis an

157 Golgin45 and GM130, we found that a leucine zipper-like motif in the central coiled-coil region of G

158 iven by hydrophobic interactions via leucine zipper-like motifs.

159 We also discover a zipper-like nature of antiphase boundaries, which are th

160 om apposed cell surfaces, possibly forming a zipper-like protein assembly, and thus providing a size-

161 ility of the complex for shear-like than for zipper-like pulling configurations.

162 This zipper-like structure assembles in a continuous manner b

163 The proteinaceous zipper-like structure known as the synaptonemal complex

164 e revealed hitherto unrecognized actin-based zipper-like structures (ZLSs) that arise between MGCs fo

165 etry, we detected a RIT1 interactor, leucine zipper-like transcription regulator 1 (LZTR1), that acts

166 ed by biallelic mutations within the leucine zipper-like transcription regulator 1 (LZTR1).

167 ith NS harboring mutations of LZTR1 (leucine zipper-like transcription regulator 1), an adaptor for C

168 ases (PPIases) play an important role in the zipper-like triple-helix formation in collagen.

169 Furthermore, DUSP23 knockdown produced "zipper-like" cell-cell adhesions, caused defects in tran

170 KRASG12D or BRAFV600E induced "zipper-like" contiguous expression of junctional protein

171 dependent or oncogenic RTK activation via a "zipper-like" mechanism for receptor activation.

172 with target membrane-associated t-SNAREs, a zippering-like process releasing approximately 65 kT per

173 circle transcription acts as both the "smart zipper lock" and the delivery carrier to alternately loc

174 be sealed into the RNA sequence-programmed "zipper lock" by controlled loading, avoiding mutual nons

175 nd rapid intracellular release based on the "zipper lock-and-key" strategy.

176 Ne/Epi --> Ne/Ne + Epi/Epi) just behind the zipper lower tissue resistance to zipper progression by

177 scaffold assembly requires conserved leucine zipper (LZ) and Cnn-motif 2 (CM2) domains that co-assemb

178 l coiled-coil domain (CC) and/or the leucine zipper (LZ) domain of the myosin light-chain phosphatase

179 o the LTCC C-terminus via a modified leucine-zipper (LZ) interaction.

180 a C(2) H(2) -zinc finger (ZF), and a leucine zipper (LZ), whose roles in FOXP2 remain largely unknown

181 arting from the experimentally observed half-zippered metastable state, the SNAREpins have to mechani

182 ina, we used Nrl(-/-) (neural retina leucine zipper) mice, to generate Rpgr(ko)::Nrl(-/-) double-knoc

183 Our results do not support the charge zipper model.

184 rA8; another proposed a so-called 'staggered zipper' model in which oligo(rA) strands overlap in mult

185 hosphotyrosine-binding domain, and a leucine zipper motif (APPL)1, an early endosomal protein, is req

186 ional orientation places an extended glycine zipper motif (G(40)xxxS(44)xxxG(48)) together with a pat

187 revealed a heptad repeat leucine-isoleucine zipper motif (LIZ).

188 l trend supports the hypothesis that the Phe zipper motif has functional significance.

189 evolutionarily conserved, truncated leucine zipper motif near the N terminus as well as a strictly c

190 ted diameter of 2 nm, as long as the glycine zipper motif remains intact.

191 pans the crystal lattice, featuring a steric-zipper motif that is common in structures of amyloid-for

192 A number of BASIC LEUCINE-ZIPPER MOTIF transcription factors involved in the endop

193 , phosphotyrosine binding domain and leucine zipper motif) mediates rab5 overactivation in Down syndr

194 n-like proteins CdzC and CdzD harbor glycine-zipper motifs, often found in amyloids, and CdzC forms l

195 dimer association featuring a "phenylalanine zipper" notable for the dual roles of phenylalanines in

196 bp) of Frmpd1 binds to neural retina leucine zipper (NRL) and cone-rod homeobox protein (CRX), two ro

197 rried out a detailed biophysical analysis of zippering, occurring either spontaneously or induced by

198 ons assemble into beta-hairpins via top down zippering of backbone hydrogen bonds to form the membran

199 The expanding integrin wave facilitates the zippering of Fcgamma receptors onto the target and integ

200 ted microtubule transport and oMAP4-mediated zippering of microtubules drives formation of a paraxial

201 tant hemocytes coupled with impaired midline zippering of mutant epithelium creates a situation in so

202 Zippering of SNARE complexes spanning docked membranes i

203 O goes beyond its participation in the final zippering of the complex, because mutations of residues

204 1 molecules unlocks the complex, allows full zippering of the SNARE complex, and triggers membrane fu

205 NARE serves as a spring to prevent premature zippering of the SNARE complex, thereby reducing the lik

206 SNARE assembly occurs by stepwise zippering of the vesicle-associated SNARE (v-SNARE) onto

207 st that the SM protein Munc18-1 promotes the zippering of trans-SNARE complexes and accelerates the k

208 ivated for DNA recognition by +1 interstrand zippers of pyrene-functionalized nucleotides.

209 l aspects of KYE28, constituting an aromatic zipper, of potential importance for the development of n

210 ly binds microtubules, mediating microtubule zippering or end-on microtubule interactions, depending

211 ins unclear how these mutations affect SNARE zippering, partly due to difficulties to quantify the en

212 Dimerization of the zipper places SP1 at a high local concentration, even at

213 nalysis revealed tissue expansion around the zippering point after ablation, but predominant tissue c

214 and simultaneously, a new caudal-to-rostral zippering point arises.

215 Ablation of the zippering point at the embryonic dorsal midline causes f

216 This zone is biomechanically coupled to the zippering point by a supracellular F-actin network, whic

217 ransitory semi-rosette-like structure at the zippering point that promotes juxtaposition of cells acr

218 n vivo to generate a sufficient pause in the zippering process for the regulators to set in place.

219 icient to explain the speed and direction of zipper progression and highlight key advantages of a seq

220 behind the zipper lower tissue resistance to zipper progression by allowing transiently stretched cel

221 , where RhoA and myosin are activated during zipper progression.

222 tissue-level contractile asymmetry to drive zipper progression.

223 tions designed to disrupt v- and t-SNARE TMD zippering prolonged pore lifetimes dramatically.

224 and we quantitatively relate the individual zipper properties to global characteristics of the devel

225 show that the glucocorticoid-induced leucine zipper protein (GILZ), already known to regulate effecto

226 ription of three related Homeodomain leucine zipper protein (HD-ZIP)-encoding genes: HOMEOBOX PROTEIN

227 vation potential of the basic region leucine zipper protein ATF2.

228 -negative mutant of the basic region leucine zipper protein c-Jun, a major constituent of the AP-1 tr

229 human fibroblasts, we uncovered the leucine-zipper protein LUZP1 as an interactor of truncated SALL1

230 JLP (JNK-associated leucine zipper protein) is a scaffolding protein that interacts

231 encoding for Neural retina-specific leucine zipper protein, a rod fate determinant during photorecep

232 c transcription factors: bZIP (basic leucine-zipper) proteins, exemplified by the AP-1 and CEBPbeta r

233 a-Kocienski olefination, Wittig olefination, Zipper reaction, and Sonogashira reaction.

234 a switch to enable fast and controlled SNARE zippering required for synaptic vesicle fusion and neuro

235 ion conversion, four of which were in steric zipper segments where side chains from amino acids tight

236 inding) is shown to be dominated by a simple zipper sequence, only occasionally accelerated by loop f

237 The miR-221 zipper shows capability in rescuing the expression of ta

238 eous transitions between a loose and tightly zippered state at the SNARE complex C terminus.

239 arrier transiently traps SNAREpins in a half-zippered state similar to the partial assembly that enga

240 place while SNAREpins are trapped in a half-zippered state.

241 reduced probability to engage in the tightly zippered state.

242 ore how SNARE regulators operate on discrete zippering states.

243 ells as highly active recombinant isoleucine-zipper-tagged TRAIL (iz-TRAIL).

244 remains disordered, the H1 tail serves as a zipper that closes and stabilizes the structure through

245 eceptor, vimentin, fibrin, and phenylalanine zippers that vary in size and topology of their alpha-he

246 of the mammalian embryo involves a wave of "zippering" that passes down the elongating spinal axis,

247 The NTD zippering then dramatically stabilized the CTD, facilita

248 n via a trimerized membrane-bound isoleucine zipper (TMZ) CD40L.

249 SNARE proteins zipper to form complexes (SNAREpins) that power vesicle

250 the receptor extracellular domains with Jun zippers to control the position of its transmembrane (TM

251 of adjacent PrP molecules, known as "steric zippers," to explain these results.

252 and vesicle-attached (v-SNARE) proteins that zipper together to form a coiled-coil SNARE bundle that

253 The tail is critical for motors to zipper together two microtubules by generating substanti

254 virus (IBV), induces regions of ER that are zippered together and tethered open-necked double membra

255 ATF4 is a member of the basic leucine zipper transcription factor (bZIP) superfamily.

256 artner BTB and CNC homology 1, basic leucine zipper transcription factor 1 (BACH1), the chromatin rem

257 ential BTB and CNC homology 1, basic leucine zipper transcription factor 2 expression.

258 The basic leucine zipper transcription factor ATF-like 3 (BATF3) is requir

259 Here, we show that the basic leucine zipper transcription factor ATF-like, Batf is important

260 A complex between FT and the basic leucine-zipper transcription factor FD is proposed to form in th

261 ual specificity T-box/basic-helix-loop-helix-zipper transcription factor Mga is expressed in the plur

262 The Maf-family leucine zipper transcription factor NRL is essential for rod pho

263 The basic leucine zipper transcription factor nuclear factor (erythroid-de

264 photomorphogenesis promoting a basic leucine zipper transcription factor that is degraded by COP1 ubi

265 s (Arabidopsis thaliana) homeodomain-leucine zipper transcription factor that participates in hypocot

266 its is MLX, a basic helix-loop-helix leucine-zipper transcription factor that regulates metabolic pro

267 ugh the interaction with FD, a basic leucine zipper transcription factor which plays a critical role

268 essential and conserved plant basic leucine zipper transcription factor whose level controls seed ge

269 The AP-1 factor basic leucine zipper transcription factor, ATF-like (BATF) is importan

270 his correlated inversely BATF (basic leucine zipper transcription factor, ATF-like) and IRF4 (interfe

271 zinc deficiency B. distachyon basic leucine zipper transcription factor, BdbZIP10, and its role in o

272 n depth the NLSs of a P. sojae basic leucine zipper transcription factor, PsbZIP1.

273 Leucine Zipper Transcription Factor-like 1 (LZTFL1) is located i

274 Leucine zipper transcription factor-like 1 (LZTFL1) was upregula

275 g a newly developed BBS mouse model [Leucine zipper transcription factor-like 1 (Lztfl1)/Bbs17 mutant

276 lies in the supernode network, BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTOR1-TGA and HYPERSENSITIVITY TO

277 Here we show that basic LEUCINE ZIPPER TRANSCRIPTION FACTOR67 (bZIP67) acts downstream o

278 6 and BBF2H7 are transmembrane basic leucine zipper transcription factors and are subjected to RIP by

279 ich revealed that the group S1 basic leucine zipper transcription factors bZIP1 and bZIP53 reprogram

280 ctivity of the class-III homeodomain-leucine zipper transcription factors(6-8)-and thereby regulates

281 n-dependent CpA recognition by basic leucine-zipper transcription factors.

282 sequence-specific approach by basic leucine-zipper transcriptional factors.

283 The basic leucine zipper transcriptional regulator Cnc is necessary and su

284 SM subunit Vps33, is followed by subsequent zippering transitions that increase the probability of f

285 lical bundles such as those found in glycine zipper transmembrane oligomers.

286 d) di-ubiquitin to its coiled-coil 2-leucine zipper ubiquitin binding domain.

287 SNAREs zipper up from the N to C terminus bringing the two memb

288 eukaryotic life, requiring SNARE proteins to zipper up in an alpha-helical bundle to pull two membran

289 ease of an inserted tryptophan, facilitating zippering up of 20-bp guide RNA:target DNA heteroduplex

290 uently forming successive evaginations that "zipper" up proximally, but at their leading edges are fr

291 ally unwound and unpaired DNA duplex forms a zipper via alternating interstrand base stacking, rather

292 e ability of Munc18-1 to promote trans-SNARE zippering, whereas other known Munc18-1/SNARE-binding mo

293 oorly understood feature of this process is "zippering," whereby a fusion point moves directionally a

294 nal association followed by rapid C-terminal zippering, which serves as a power stroke to drive membr

295 y is the formation of a three-protein charge zipper with interdigitated complementary charged residue

296 ctivated the t-SNARE complex to initiate NTD zippering with the v-SNARE, a mechanism likely shared by

297 ex on the target plasma membrane, which then zippers with the vesicle (v)-SNARE on the vesicle to dri

298 ucture provides direct evidence for a steric zipper within a fibril formed by full-length Abeta pepti

299 mining sheet-to-sheet arrangements in steric zippers within amyloids.

300 IN LEUCINE ZIPPER III (HD-ZIPIII) and LITTLE ZIPPER (ZPR) interaction as proof-of-principle.