ライフサイエンスコーパス: leucine zipper

1 nstituent domains: EF-hand, coiled coil, and leucine zipper.

2 e from experimental LOT measurements for the leucine zipper.

3 only when it is tethered to FtsN(TM) or to a leucine zipper.

4 at P6981 binds both the B-ZIP domain and the leucine zipper.

5 -binding domains are linked by a coiled-coil leucine zipper.

6 involved in interhelical salt bridges in the leucine zipper.

7 de sequence attached to N-terminal of bZIP53 leucine zipper.

8 and its C terminus is mediated by a putative leucine zipper.

9 i.e., the CA-SP1 junction region fused to a leucine zipper.

10 interactions, such as those between pairing leucine zippers.

11 osphotyrosine interacting with PH domain and leucine zipper 1 (APPL1) signaling endosomes and MYO6+ e

12 a regulatory pathway in which spermatogenic leucine zipper 1 (SPZ1) promotes EMT through its transac

13 has been shown previously to bind the basic leucine zipper 1 domain in the C3 promoter.

14 We temporally perturbed a master TF (Basic Leucine Zipper 1, bZIP1) and the nitrogen (N) signal it

15 he DNA binding activity of protagonist basic leucine zipper 53 (bZIP53) transcription factor and its

16 s-related host genes, including basic-region leucine zipper 60 (bZIP60), SKP1, ER luminal binding pro

17 sitol-requiring protein-1) and bZIP60 (basic leucine zipper 60), two RSRE containing unfolded protein

18 re, interdimer interactions between adjacent leucine zippers allow TbBILBO1 to form extended filament

19 We now report that C/EBPalpha or C/EBPalpha leucine zipper AML mutants bind in vivo to the nfkb1 (p5

20 Unexpectedly, the predicted leucine zipper and helix-loop-helix motifs do not form t

21 s of a coiled-coil protein based on the GCN4 leucine zipper and obtain a free-energy landscape that i

22 orm heterodimers and bind to DNA via a basic leucine zipper and regulate the cell cycle, apoptosis, d

23 switches to a helical state when fused to a leucine zipper and that these helical molecules further

24 ms an antiparallel dimer, and the C-terminal leucine zipper appears to contain targeting information.

25 Mutations in the GCN4 leucine zipper are known to change its preferred oligome

26 ent of a full-length myosin-X construct with leucine zipper at the C-terminal end of the tail (M10(Fu

27 The lower part of the leucine zipper, at the intracellular mouth of the channe

28 The basic leucine zipper ATF-like 3 (BATF3)-dependent CD103(+)CD11

29 After vaccination, both migratory basic leucine zipper ATF-like transcription factor 3 (BatF3)-d

30 rotein (VBP)] and two basic helix-loop-helix leucine zipper (B-HLH-ZIP) [USF (upstream stimulating fa

31 nd of the HTLV-1 genome encodes HTLV-1 basic leucine zipper (b-ZIP) protein (HBZ), a protein that inh

32 Several basic leucine zipper (B-ZIP) transcription factors have been i

33 through injury-induced stabilization of dual leucine zipper-bearing kinase (DLK/MAP3K12).

34 Leucine Zipper-bearing Kinase (LZK/MAP3K13) is a member

35 MAPKKK dual leucine zipper-bearing kinases (DLKs) are regulators of

36 I) and the C-terminal basic helix-loop-helix leucine zipper (bHLH-LZ) domains of the oncoprotein c-My

37 on factor (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein.

38 blastosis), SFH3 (SEC14-like 3), bZIP (basic-leucine zipper), bHLH (basic helix-loop-helix) and SBP (

39 ption partner Mlx are basic helix-loop-helix leucine zipper (bHLHZip) transcription factors that sens

40 nd the TIRs identified a heterodimeric basic leucine zipper (bZIP) complex between an uncharacterized

41 The protein consists of the basic region-leucine zipper (BZip) domain of the CCAAT/enhancer-bindi

42 esign peptides that bind to the basic region leucine zipper (bZIP) domain of the viral transcription

43 T-cell leukemia virus type 1 (HTLV-1) basic leucine zipper (bZIP) factor (HBZ) could be used for imm

44 The basic region and leucine zipper (bZIP) of C/EBPbeta, zinc finger (ZF) mot

45 The basic leucine zipper (bZIP) transcription factor AtfB, a membe

46 ich functions synergistically with the basic leucine zipper (bZIP) transcription factor bZIP10 to ind

47 ere, we use Hac1, a well-characterized basic leucine zipper (bZIP) transcription factor involved in t

48 ELONGATED HYPOCOTYL5 (HY5) is a basic domain/leucine zipper (bZIP) transcription factor, central for

49 components identified to date, HY5, a basic leucine zipper (bZIP) transcription factor, has been inv

50 s such as ABA-response element binding basic leucine zipper (bZIP) transcription factors (ABF/AREB/AB

51 We studied the basic region-leucine zipper (bZIP) transcription factors and quantifi

52 Basic leucine zipper (bZip) transcription factors regulate cel

53 Basic region leucine zipper (bZIP) transcription factors regulate gen

54 elong to the AP1 superfamily of basic region-leucine zipper (bZIP) transcription factors.

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

56 s to the G-group of Arabidopsis basic region leucine zipper (bZIP) type transcription factors.

57 Selective dimerization of the basic-region leucine-zipper (bZIP) transcription factors presents a v

58 Basic region leucine zippers (bZIPs) are modular transcription factor

59 nal domain of the protein: the coiled-coil 2-leucine zipper (CC2-LZ) domain and the zinc finger (ZF)

60 ranscription factors in hematopoiesis is the leucine zipper CCAAT-enhancer binding protein alpha (C/E

61 onse of two Arabidopsis thaliana homeodomain-leucine zipper class I genes; ATHB7 and ATHB12, both str

62 Leucine zipper coiled coils were combined with either gl

63 hydrophobic and hydrophilic residues of two leucine zipper coiled-coil (LZCC) structural proteins, c

64 In the presence of the ligand, the leucine zipper conformation is completely inhibited and

65 Phosphotyrosine Interaction, PH domain, and leucine zipper containing 1 (APPL1) that were identified

66 We recently identified that vimentin, a leucine zipper-containing intermediate filament protein,

67 The MAPKKK dual leucine zipper-containing kinase (DLK, Wallenda in Droso

68 ions, the MAP3K ZAK (Sterile alpha motif and leucine zipper-containing kinase) has also been proven t

69 ption factor 4 (ATF4), a member of the basic leucine zipper-containing protein subfamily.

70 action, pleckstrin homology (PH) domain, and leucine zipper-containing protein)) are localized to the

71 rotic fibrosarcoma oncogene homolog (MAF), a leucine zipper-containing transcription factor of the AP

72 Atf4 is a leucine zipper-containing transcription factor that acti

73 harboring mutations in residues critical for leucine zipper dimerization did not.

74 VCCs when the NC domain was replaced with a leucine zipper dimerization motif that promotes Gag mult

75 interaction between the LOV and basic region leucine zipper DNA-binding domain that together with LOV

76 n and one nuclear export signal (NES) in the leucine zipper domain (named LZ-NES).

77 A leucine zipper domain can replace NC in Gag and still le

78 ucleic acid-binding domain with a dimerizing leucine zipper domain leads to the assembly of RNA-free

79 ltransferase, interacts with the octapeptide/leucine zipper domain of AF10, and this region has been

80 The ATF3-AR interaction requires the leucine zipper domain of ATF3 that independently binds t

81 Deletion of the carboxy-terminal leucine zipper domain relaxed the constraint and permitt

82 e NF-kappaB members RelB and p52 through its leucine zipper domain.

83 1b splices the mRNA-encoding bZIP60, a basic leucine-zipper domain containing transcription factor as

84 he folding behavior of the well-studied GCN4 leucine-zipper domain is more complex than was previousl

85 inositol pyrophosphate kinase and the basic leucine zipper domains of KCS1 are required for INO1 exp

86 Both FLX and FLX4 contain leucine zipper domains that facilitate interaction with

87 ors is based on the shared capacity of their leucine zipper domains to interact with non-AP1 factors

88 rm, DLK-1S, that shares identical kinase and leucine zipper domains with the previously described lon

89 contains four coiled-coil and two N-terminal leucine zipper domains.

90 These LZD (leucine zipper dual-binding) peptides were derived by fu

91 rter (MCU), uncoupling protein 2 (UCP2), and leucine zipper EF-hand-containing transmembrane protein

92 Leucine zipper-EF-hand containing transmembrane protein

93 : the novel uncoupling proteins 2 and 3, the leucine zipper-EF-hand containing transmembrane protein

94 tochondrial calcium uniporter-dependent, but leucine zipper-EF-hand containing transmembrane protein

95 ing transmembrane protein 1-independent to a leucine zipper-EF-hand containing transmembrane protein

96 X (mitochondrial Na/Ca exchanger) and LETM1 (leucine zipper-EF-hand-containing transmembrane protein

97 homology to the mitochondrial protein LETM1 (leucine zipper-EF-hand-containing transmembrane protein)

98 HTLV-1 basic leucine zipper factor (HBZ) is one of the viral proteins

99 V-1 regulatory proteins Tax and HTLV-1 basic leucine zipper factor (HBZ) play a major role in ATLL de

100 and of its proviral genome, the HTLV-1 basic leucine zipper factor (HBZ), which inhibits Tax-1-mediat

101 e receptor beta2 (TRbeta2) and neural retina leucine zipper factor (NRL) lack M cones and rods, respe

102 The neural retina leucine zipper factor (NRL) transcription factor critica

103 f the ATF/CREB subfamily of the basic region-leucine zipper family and has been known as a tumor supp

104 ription factor 2 (ATF2) belongs to the basic leucine zipper family of transcription factors.

105 eoblast-enriched transcription factor of the leucine zipper family.

106 cted protein product, compared to the intact leucine zipper found in two YAP1 (alpha) isoforms.

107 Purified c-Jun leucine zipper fragments could also form stable homodime

108 NC domain had been replaced by a dimerizing leucine zipper [Gag(LZ)].

109 (CD2), a member of the class IV homeodomain-leucine zipper gene family, previously only associated w

110 found that it encodes a class I homeodomain leucine zipper gene that promotes lateral bud dormancy a

111 oid responsive genes [glucocorticoid-induced leucine zipper (GILZ) and FK506 binding protein-51 (FKBP

112 Induction of glucocorticoid-induced leucine zipper (GILZ) by glucocorticoids plays a key rol

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

114 at expression of glucocorticoid (GC)-induced leucine zipper (GILZ) in bone marrow mesenchymal lineage

115 Glucocorticoid-induced leucine zipper (GILZ) is a rapidly, potently, and invari

116 Glucocorticoid-induced leucine zipper (GILZ) is an anti-inflammatory protein fi

117 he upregulated genes, glucocorticoid-induced leucine zipper (GILZ) responded to alcohol in a dose-dep

118 n at serine 211 and expression of GC-induced leucine zipper (GILZ) were significantly reduced in ASM

119 Glucocorticoid-induced leucine zipper (GILZ), a recently identified molecule ex

120 ranscription factor glucocorticoid-inducible leucine zipper (GILZ).

121 ated transcription of glucocorticoid-induced leucine zipper (GILZ).

122 Class III homeodomain-leucine zipper (HD ZIP) transcription factors have been

123 The gamma-clade of class I homeodomain-leucine zipper (HD-Zip I) transcription factors (TFs) co

124 uxin levels activating class III homeodomain leucine zipper (HD-ZIP III) transcription factors (TFs).

125 Class III homeodomain leucine zipper (HD-ZIP III) transcription factors regula

126 M fate is specified by class III HOMEODOMAIN-LEUCINE ZIPPER (HD-ZIP III) transcription factors, which

127 rotein 1 (HAT1), which encodes a homeodomain-leucine zipper (HD-Zip) class II transcription factor, w

128 Here we report that a homeodomain-leucine zipper (HD-ZIP) transcription factor, GhHOX3, co

129 analysis revealed that ATHB13, a homeodomain-leucine zipper (HD-Zip) transcription factor, was consti

130 The broadly conserved Class III homeodomain leucine zipper (HD-ZIPIII) and KANADI transcription fact

131 on in three paralogous class III homeodomain leucine zipper (HD-ZIPIII) genes leads to aberrations in

132 ontext, members of the class III homeodomain leucine zipper (HD-ZIPIII) transcription factor family s

133 PKGIalpha (residues 1-59), which includes a leucine zipper heptad repeat motif.

134 d to tune ZF-TF response by fusing ZF-TFs to leucine zipper homodimerization domains.

135 d also form stable homodimers, whereas c-Fos leucine zipper homodimers were found to be much less sta

136 Characterization of the homeodomain leucine zipper I transcription factor AtHB13, which is e

137 rylstibonic acid, NSC13778, bound to the VBP leucine zipper identified electrostatic interactions bet

138 lish SiMPull in plants using the HOMEODOMAIN LEUCINE ZIPPER III (HD-ZIPIII) and LITTLE ZIPPER (ZPR) i

139 a GFP reporter system, we defined a putative leucine zipper in the N terminus of human pro-EMAP II pr

140 We have identified a leucine zipper in the S5 segment of HCNs, regulating hyp

141 Residues of the leucine zipper interact with the adjacent S6 segment of

142 The leucine zipper interaction between MAX and c-MYC has bee

143 Thus, our data indicate that the leucine zipper is an important molecular determinant for

144 ation and functional characterization of the leucine zipper is an important step toward the understan

145 The leucine zipper is essential for HCN channel gating.

146 bZIP transcription factor NRL (neural retina leucine zipper) is critical for rod versus cone photorec

147 GILZ (glucocorticoid-induced leucine zipper) is inducible by glucocorticoids and play

148 identification of an Arabidopsis homeodomain-leucine zipper IV (HD-ZIP IV) protein, HOMEODOMAIN GLABR

149 ronal stress response controlled by the Dual Leucine Zipper Kinase (DLK) and contributes to DLK-media

150 Two convergent pathways, involving dual leucine zipper kinase (DLK) and fragile X mental retarda

151 NK activation in neurons is mediated by dual leucine zipper kinase (DLK) and JNK-interacting protein

152 The screen identified dual leucine zipper kinase (DLK) as a key neuroprotective tar

153 Dual leucine zipper kinase (DLK) has been implicated in cell

154 Here we show that the mixed-lineage dual leucine zipper kinase (DLK) is an essential upstream med

155 We show that dual leucine zipper kinase (DLK) is essential for excitotoxic

156 Dual leucine zipper kinase (DLK) is required for stress-induc

157 ue of Neuron, Shin et al. show that the dual leucine zipper kinase (DLK) is responsible for the retro

158 Dual leucine zipper kinase (DLK) promotes growth cone motilit

159 Here we demonstrate that the dual leucine zipper kinase (DLK) promotes robust regeneration

160 , we show that the mixed lineage kinase dual leucine zipper kinase (DLK) selectively regulates the JN

161 We find that the dual leucine zipper kinase (DLK) signaling pathway in Drosoph

162 The Wallenda (Wnd)/dual leucine zipper kinase (DLK)-Jnk pathway is an evolutiona

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

164 Dual leucine zipper kinase (DLK, MAP3K12) was recently identi

165 e family with high sequence identity to Dual Leucine Zipper Kinase (DLK/MAP3K12).

166 on of POSH, or two POSH-associated proteins, leucine zipper kinase (LZK) and Shroom3, with RNAi in co

167 on is only partially protective, we identify leucine zipper kinase (LZK) as cooperating with DLK to a

168 Maternal embryonic leucine zipper kinase (MELK) belongs to the subfamily of

169 The Maternal Embryonic Leucine Zipper Kinase (MELK) has been reported to be a g

170 ment of a novel selective maternal embryonic leucine zipper kinase (MELK) inhibitor HTH-01-091, CRISP

171 The protein kinase maternal and embryonic leucine zipper kinase (MELK) is critical for mitotic pro

172 on after injury is regulated in part by dual-leucine zipper kinase 1 (DLK-1), a conserved regulator o

173 se selectivity of type II maternal embryonic leucine zipper kinase inhibitors by applying these two c

174 conserved, retrograde DLK-1 MAPK (DLK-1/dual leucine zipper kinase) pathway, which triggered synaptic

175 K (zipper protein kinase, also known as dual leucine zipper kinase), a mitogen-activated protein kina

176 n the level of the MAPKKK Wallenda/DLK (dual leucine zipper kinase), a previously identified substrat

177 e) expression and loss of wallenda/DLK (dual leucine zipper kinase).

178 nase (MAPK) kinase kinase homologous to dual leucine zipper kinase, functions as an upstream mediator

179 This decrease was independent of the dual leucine zipper kinase-Wallenda pathway and required func

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

181 poE binding to ApoE receptors activates dual leucine-zipper kinase (DLK), a MAP-kinase kinase kinase

182 Here we identify the Dual Leucine-zipper Kinase (DLK, Wnd in Drosophila) as a crit

183 e show here that long glucocorticoid-induced leucine zipper (L-GILZ) is highly expressed in spermatog

184 cysteine substitution analysis of predicted leucine zipper-like amphipathic helices in both PspB and

185 on is driven by hydrophobic interactions via leucine zipper-like motifs.

186 ow that scaffold assembly requires conserved leucine zipper (LZ) and Cnn-motif 2 (CM2) domains that c

187 ted the domains of K-bZIP and found that the leucine zipper (LZ) domain is essential for the interact

188 -terminal coiled-coil domain (CC) and/or the leucine zipper (LZ) domain of the myosin light-chain pho

189 presence or absence of a central insert and leucine zipper (LZ).

190 ynthesized, along with the corresponding MAX leucine zipper (MAX-Zip residues 74-102).

191 uman retina, we used Nrl(-/-) (neural retina leucine zipper) mice, to generate Rpgr(ko)::Nrl(-/-) dou

192 n, phosphotyrosine-binding (PTB) domain, and leucine zipper motif (APPL)-positive endosomes and EEA1-

193 ain, a phosphotyrosine-binding domain, and a leucine zipper motif (APPL)1, an early endosomal protein

194 n, phosphotyrosine-binding (PTB) domain, and leucine zipper motif 1 (APPL1) in regulating cell migrat

195 23 skipped isoform coding for the C-terminal leucine zipper motif caused increased sensitivity of the

196 We have identified a highly conserved leucine zipper motif in the S5 segment of HCN family mem

197 that an evolutionarily conserved, truncated leucine zipper motif near the N terminus as well as a st

198 ntrast, substitution of the TRPC3 C-terminal leucine zipper motif or TRPC3 phosphorylation sites Ser-

199 y domain, phosphotyrosine binding domain and leucine zipper motif) mediates rab5 overactivation in Do

200 he first 936 amino acids, followed by a GCN4 leucine zipper motif, to force dimerization.

201 t only activated PKGIalpha binds RhoA, and a leucine zipper mutant PKGIalpha was unable to bind RhoA

202 Leucine zipper mutants traffic to the plasma membrane, b

203 Furthermore, the non-Leucine zipper N-terminal helical bundle contains severa

204 repeatedly occur at core positions a and d (leucine zipper nomenclature) in homologous and nonhomolo

205 The transcription factor neural retina leucine zipper (Nrl) is a critical determinant of rod ph

206 Neural retina leucine zipper (NRL) is an essential transcription facto

207 cantly higher in cone-dominant neural retina leucine zipper (Nrl) knock-out mouse retinas compared wi

208 tors-cone--rod homeobox (CRX), neural retina leucine zipper (NRL), and nuclear receptor subfamily 2,

209 ne zipper transcription factor neural retina leucine zipper (NRL).

210 We observed the expression of genes like leucine zipper, ntd, nced, geraniol synthase, raffinose

211 Thus, we conclude that the leucine zipper of HCN channels is a major determinant fo

212 he proline- and acidic amino acid-rich basic leucine zipper (PAR-bZip) clock-controlled genes.

213 ng high levels of the glucocorticoid-induced leucine zipper protein (GILZ) generate antigen-specific

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

215 IL-10, or TGF-beta upregulate the GC-Induced Leucine Zipper protein (GILZ).

216 e transcription of three related Homeodomain leucine zipper protein (HD-ZIP)-encoding genes: HOMEOBOX

217 Small heterodimer partner interacting leucine zipper protein (SMILE) has been identified as a

218 Arabodopsis thaliana homeodomain-leucine zipper protein 1 (HAT1), which encodes a homeodo

219 nal activation potential of the basic region leucine zipper protein ATF2.

220 dominant-negative mutant of the basic region leucine zipper protein c-Jun, a major constituent of the

221 The deadenylase and leucine zipper protein Nocturnin is now shown to play a

222 on factor (MITF) is a basic helix-loop-helix leucine zipper protein that plays major roles in the dev

223 ion, resulting in binding, with basic-region leucine zipper protein(s), to the antioxidant response e

224 JLP (JNK-associated leucine zipper protein) is a scaffolding protein that in

225 rl gene, encoding for Neural retina-specific leucine zipper protein, a rod fate determinant during ph

226 In these studies, the basic leucine zipper protein, NFIL3, is identified as a regula

227 mulated expression of glucocorticoid-induced leucine-zipper protein and the alpha-subunit of the epit

228 which compose a large group of basic region leucine zipper proteins whose members mediate diverse tr

229 Members of the leucine zipper putative tumor suppressor (LZTS) family p

230 3, we observed that the previously described leucine zipper region at the C terminus of MSP3 may not

231 5 extension, exon 6 or both would have their leucine zipper region disrupted in the predicted protein

232 x coiled-coil domain of the carboxy-terminal leucine zipper region of CNGA1 subunits, constraining th

233 We have demonstrated previously that the leucine zipper region of UL6 is important for intersubun

234 To determine the importance of the leucine zipper sequence of melittin in its neutralizatio

235 a indicated a probable important role of the leucine zipper sequence of melittin in neutralizing LPS-

236 ion of LPS aggregates with alteration in the leucine zipper sequence of melittin was observed.

237 Furthermore, with alteration in the leucine zipper sequence of melittin, these analogues fai

238 Peptides comprising the leucine zipper sequence with (c-MYC-Zip residues 402-434

239 of melittin with minor rearrangement in its leucine zipper sequence.

240 The helical leucine zipper structure previously determined from NMR

241 in which NC was replaced with a heterologous leucine zipper that promotes protein dimerization but no

242 entral to this platform is the addition of a leucine zipper to the C terminus of the C(H)3 domain of

243 ion domain of NPM1, ATF5 binds via its basic leucine zipper to the C-terminal region of NPM1 where it

244 imeric partner BTB and CNC homology 1, basic leucine zipper transcription factor 1 (BACH1), the chrom

245 Recently, basic leucine zipper transcription factor 2 (BACH2) has been a

246 inding that the BTB and CNC homology 1 basic leucine zipper transcription factor 2 (BACH2) induces ne

247 d differential BTB and CNC homology 1, basic leucine zipper transcription factor 2 expression.

248 ociated transcription factors, such as basic leucine zipper transcription factor 28 (bZIP28).

249 n large part by the ABA-induced basic domain/leucine zipper transcription factor ABA INSENSITIVE5 (AB

250 The basic Leucine zipper transcription factor ABSCISIC ACID INSENS

251 inding protein alpha (C/EBPalpha) is a basic leucine zipper transcription factor and is expressed in

252 poneurotic fibrosarcoma (c-Maf), Bcl6, basic leucine zipper transcription factor ATF-like (Batf), and

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

254 The basic leucine zipper transcription factor ATF6alpha functions

255 MENT-BINDING FACTOR2 (VvABF2), a grape basic leucine zipper transcription factor belonging to a phylo

256 Until recently, the basic leucine zipper transcription factor E4BP4 (also known as

257 We previously reported that the basic leucine zipper transcription factor E4BP4 (E4 binding pr

258 poplar ortholog of the class III homeodomain-leucine zipper transcription factor gene REVOLUTA (PtREV

259 The class IV homeodomain leucine zipper transcription factor GLABRA2 (GL2) acts i

260 homeostasis are dependent on the basic motif leucine zipper transcription factor neural retina leucin

261 The basic leucine zipper transcription factor Nfil3 (E4bp4) is ess

262 Here, we report that the basic leucine zipper transcription factor NFIL3/E4BP4 is essen

263 The Maf-family leucine zipper transcription factor NRL is essential for

264 The basic leucine zipper transcription factor nuclear factor (eryt

265 on is enhanced expression of the homeodomain-leucine zipper transcription factor REVOLUTA/INTERFASCIC

266 riptional target of NRL, the key basic motif leucine zipper transcription factor that dictates rod ve

267 5) is a photomorphogenesis promoting a basic leucine zipper transcription factor that is degraded by

268 abidopsis (Arabidopsis thaliana) homeodomain-leucine zipper transcription factor that participates in

269 ing transcription factor 3 (ATF3) is a basic leucine zipper transcription factor that plays a regulat

270 factor E2-related factor 1 (Nrf1) is a basic leucine zipper transcription factor that plays important

271 ating transcription factor 4 (ATF4), a basic leucine zipper transcription factor that regulates the e

272 ors through the interaction with FD, a basic leucine zipper transcription factor which plays a critic

273 doplasmic reticulum (ER) transmembrane basic leucine zipper transcription factor whose mRNA and prote

274 Mice without the basic leucine zipper transcription factor, ATF-like (BATF) gen

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

276 ression of the Bcl6 target genes Batf (basic leucine zipper transcription factor, ATF-like) and Bcl6,

277 This correlated inversely BATF (basic leucine zipper transcription factor, ATF-like) and IRF4

278 We report here that BATF (basic leucine zipper transcription factor, ATF-like), an AP-1

279 cus on a zinc deficiency B. distachyon basic leucine zipper transcription factor, BdbZIP10, and its r

280 erized in depth the NLSs of a P. sojae basic leucine zipper transcription factor, PsbZIP1.

281 revealed that the SOR1 gene encodes a basic leucine zipper transcription factor, which controls its

282 The neural retina leucine zipper transcription factor-knockout (Nrl(-/-))

283 Leucine Zipper Transcription Factor-like 1 (LZTFL1) is l

284 Leucine zipper transcription factor-like 1 (LZTFL1) was

285 Using a newly developed BBS mouse model [Leucine zipper transcription factor-like 1 (Lztfl1)/Bbs1

286 is thaliana gene encoding for a basic region-leucine zipper transcription factor.

287 TF families in the supernode network, BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTOR1-TGA and HYPERSENSIT

288 ng sterol/lipid-binding class IV homeodomain leucine zipper transcription factors as potential regula

289 oots, which revealed that the group S1 basic leucine zipper transcription factors bZIP1 and bZIP53 re

290 NF1-related kinases and ABA-responsive basic leucine zipper transcription factors implicated in ABA s

291 dancy between GL2 and HDG11, two homeodomain leucine zipper transcription factors previously thought

292 the activator protein 1 superfamily of basic leucine zipper transcription factors that includes Fos,

293 y connected to two MtAP2/EREBP and two basic leucine zipper transcription factors.

294 lies on Rtg1 and Rtg3 basic helix-loop-helix leucine Zipper transcription factors.

295 A complex between FT and the basic leucine-zipper transcription factor FD is proposed to fo

296 The basic leucine zipper transcriptional regulator Cnc is necessar

297 tial and sequence-specific approach by basic leucine-zipper transcriptional factors.

298 M1-linked) di-ubiquitin to its coiled-coil 2-leucine zipper ubiquitin binding domain.

299 ible phosphorylation by RSK on Ser273 in the leucine zipper was required for DNA binding.

300 We now show that introduction of a leucine zipper (zip) dimerization motif in an IN truncat