ライフサイエンスコーパス: bipartite

1 ow that SL1 is functionally and structurally bipartite.

2 and a less-characterized NLS2, thought to be bipartite.

3 nduced apoptosis or "anoikis." TMS1/ASC is a bipartite adaptor molecule that participates in inflamma

4 The bipartite adhesion G protein-coupled receptor CD97 shows

5 genomes of NW begomoviruses are exclusively bipartite and do not associate with satellites.

6 nal for promoter-proximal arrest at PrplN is bipartite and requires two elements: the extended -10 pr

7 The bipartite anthrax lethal toxin (LeTx) consisting of prot

8 ral feature in a pre-mRNA can be targeted by bipartite antisense molecules designed to hybridize with

9 RNase protection assays, we demonstrate that bipartite antisense molecules designed to simultaneously

10 This general bipartite antisense strategy could be employed to modula

11 The RNA-binding region has a bipartite architecture composed of ROQ and HEPN domains,

12 We also discovered that TprC has a bipartite architecture consisting of a soluble N-termina

13 The structure reveals a bipartite architecture of Core Factor and its recognitio

14 most other species, it was thought that the bipartite architecture of the heterocomplex was not like

15 This simplified, bipartite architecture offers a new framework to underst

16 provides insight into how a riboswitch with bipartite architecture uses dynamics to modulate express

17 Herein, we show that TprI also possesses bipartite architecture, trimeric structure, and porin fu

18 This configuration suggests that a bipartite arrangement is primitive and reinforces the vi

19 ms the generality of the previously observed bipartite arrangement.

20 TprI represent a new class of dual function, bipartite bacterial OMP.

21 Each bipartite bar is identified as being respectively equiva

22 ature is the branchial area with an array of bipartite bars.

23 st closely related to DNA-A components of NW bipartite begomoviruses.

24 The structures reveal that PEA-15 uses a bipartite binding mode, occupying two key docking sites

25 ively support an integrative structure and a bipartite binding model, wherein the TAR central loop en

26 cetylated tails of both histones 3 and 4 via bipartite binding pockets on the DPF2 surface.

27 binding affinity by a factor of 2,500 for a bipartite binding site on myosin-VI.

28 intracellular substrates are recruited to a bipartite binding site when the transporter rests in an

29 ese structures show that by forming a single bipartite binding site, MRP1 can recognize a spectrum of

30 o the receptor, Argos mimics EGFR by using a bipartite binding surface to entrap EGF.

31 h a H3.1 peptide shows that ATXR5 contains a bipartite catalytic domain that specifically "reads" ala

32 hanges accompany DNA deformation, creating a bipartite catalytic site that positions the DNA backbone

33 This bipartite character explains why the SP1 spacer is a cri

34 We discuss the rationale for a bipartite checkpoint mechanism in which a core Mad1(MDF-

35 ization of Ntg1 were identified, including a bipartite classical nuclear localization signal, a mitoc

36 n health systems performing CABG (SD for the bipartite clustering coefficient was 0.09).

37 To test whether teamwork (assessed with the bipartite clustering coefficient) among these physicians

38 hysician teamwork in these networks with the bipartite clustering coefficient.

39 tain two clusters of basic residues termed a bipartite cNLS.

40 ricted transcription factor TCF7L2/TCF4 as a bipartite co-effector of beta-catenin for regulating oli

41 Bipartite co-occurrence networks were constructed for ea

42 in E9 is ideal for its function as it allows bipartite complex affinity, whereby the stable colicin:i

43 By randomizing the relative phase between bipartite components of the W state, we observed the tra

44 omain (DBD) of progesterone receptor (PR) is bipartite containing a zinc module core that interacts w

45 We test the bipartite cooperation model on ten large pollination dat

46 Our stochastic model of bipartite cooperation uses simple specialization and int

47 Inactivation of the bipartite cyclinA2-CDK-binding site in the SAMHD1 C term

48 d displacing Cdc20 to disrupt formation of a bipartite D-box receptor with the APC/C subunit Apc10.

49 We identified a novel bipartite degradation signal in the N-terminal domain of

50 The unusual assembly explains the basis of bipartite DNA recognition at hAT transposon ends, provid

51 ASC has a bipartite domain structure, consisting of an N-terminal

52 nant computational framework outlined only a bipartite, dorsal/ventral, division of striatum.

53 over a mechanistically important role of the bipartite Dvl DEP domain and C terminal region (DEP-C) i

54 IM domain protein Lmo2, and Ldb1 and binds a bipartite E-box-GATA DNA sequence motif.

55 2, TAL1, E47, GATA1 and LDB1 that recognizes bipartite E-box-GATA1 sites on target genes.

56 mRNA to the Ire1 focus requires a cis-acting bipartite element (3'BE) located at the 3' untranslated

57 FokI is a bipartite endonuclease with separate recognition and cle

58 at these HAMP/PAS pairs form a new family of bipartite energy taxis receptors.

59 sponsive expression of both genes requires a bipartite enhancer whose activity declines during L3.

60 ccumulation generated using a GAL4-dependent bipartite enhancer-trap system confirmed that PPhiB or p

61 standing open question of whether every pure bipartite entangled state is self-testable.

62 Bipartite entangled states of identical particles have b

63 catalytic domains of lambda-Int constitute a bipartite enzyme that mediates site-specific DNA cleavag

64 ts the mitochondrial-targeting signal into a bipartite ER-targeting signal, without destroying the mi

65 rk of an intronic splicing silencer (ISS), a bipartite exonic splicing silencer (ESS3a/b), and an exo

66 Our studies highlight how the bipartite function of Tolloid CUB domains, in substrate

67 ion, we characterize how ketamine impacts on bipartite functional interactions between neural subsyst

68 III viral fusion protein, having a predicted bipartite fusion domain comprising residues Trp-72, Tyr-

69 articles, we show a fundamental role for the bipartite fusion domain.

70 represent a functional analysis of predicted bipartite fusion loops of VSV G, a founder member of the

71 oligomeric state of gB with mutations in the bipartite fusion loops were similarly altered despite th

72 ture (YSS) in the 3' terminal regions of the bipartite genome of Lettuce chlorosis virus (LCV), a mem

73 Some appear to have had a bipartite genome organization, a unique characteristic a

74 is a positive-sense RNA insect virus with a bipartite genome.

75 ses) with origins in the New World (NW) have bipartite genomes composed of a DNA-A and DNA-B componen

76 viral infection, yet their importance in the bipartite genomes of the picorna-like, plant-infecting c

77 viruses are positive-sense RNA viruses with bipartite genomes that are most closely related to nodav

78 ase represents an unprecedented example of a bipartite glycosyltransferase that evolved by both fissi

79 pe is located in the internal segment of the bipartite GPC fusion peptide, which also contains four c

80 he genes with which they are associated as a bipartite graph and then uses the modular structure of t

81 m directly classifies the feature nodes in a bipartite graph as positive, negative or neutral with ne

82 chain protons to proximal main-chain HNs via bipartite graph matching.

83 hieved through an innovative exploitation of bipartite graph structure, and through computational red

84 f the similarities is provided by means of a bipartite graph, whose layout is heuristically optimized

85 We applied our bipartite graph-based functional module discovery algori

86 We use a bipartite graph-theoretic representation called a drug-e

87 bed that produces all maximal bicliques in a bipartite graph.

88 reads from different technologies through a bipartite-graph-based clustering algorithm, our approach

89 tionalization of a single sub-lattice of the bipartite graphene structure.

90 rticular, the embedding for general complete bipartite graphs and logical disjunctions may be of broa

91 nts disease-disease associations in terms of bipartite graphs and provides International Classificati

92 almost any applications environment in which bipartite graphs can be used to model relationships betw

93 Bipartite graphs can be useful for representing relation

94 mplete graphs with broken links and complete bipartite graphs, in particular, the star graph.

95 s in biological networks when represented by bipartite graphs.

96 iscriminative disease markers by learning on bipartite graphs.

97 inhibited during interphase by the essential bipartite GTPase-activating protein Byr4-Cdc16.

98 PKA)-dependent phosphorylation of Dock180, a bipartite guanine nucleotide exchange factor (GEF) for R

99 ator of cytokinesis 180 (Elmo1/Dock180) is a bipartite guanine nucleotide exchange factor for the mon

100 ts of a Cupin domain, a helical hairpin, and bipartite helix-turn-helix motif.

101 sing a dual complementation system involving bipartite HIV-1 gRNA, we observed that gRNA packaging is

102 to such relationships, here we constructed a bipartite human disease association network in which nod

103 ns at least 8 imprinted genes regulated by a bipartite imprinting center (IC) associated with the SNR

104 sequences common to these deletions define a bipartite imprinting center for the AS-PWS locus.

105 (PWS/AS) imprinted domain is regulated by a bipartite imprinting control center (IC) composed of a s

106 s ability to block replicative complexes via bipartite, independent, and additive N-terminal domains.

107 lent linkage of GE to a rifamycin provides a bipartite inhibitor having very high potency and very lo

108 we describe the rational design of a potent bipartite inhibitor of NFAT-calcineurin interaction, MCV

109 This occurs through a bipartite interaction in which the UBA domain of UBXN1 b

110 This novel F-box-protein-substrate bipartite interaction is susceptible to disruption by bo

111 We propose a bipartite interaction model in which the previously iden

112 n intrinsically disordered domain containing bipartite interaction motifs and provide valuable insigh

113 rs (KIR) and MHC class I is dominated by the bipartite interactions of inhibitory lineage III KIR wit

114 Bipartite interactions that affect agriculture as well a

115 Through mutational analysis, we identified a bipartite IP(6)-binding site in Ku and generated IP(6)-b

116 High-affinity hormone binding requires a bipartite JAZ degron sequence consisting of a conserved

117 ndicating that TPR3 and the C-helix define a bipartite localization determinant that is both necessar

118 The UL37x1 NH(2)-terminal bipartite localization signal, which remains uncleaved,

119 Snurportin 1 binds CRM1 in a bipartite manner by means of an amino-terminal LR-NES an

120 led Coverage Sensitive many-to-many min-cost bipartite Matching (CSM).

121 neralizes the standard (one-to-one) weighted bipartite matching problem, and can be solved using netw

122 identify an extensive FHA-BRCT interface, a bipartite MDC1-binding scaffold, an extended conformatio

123 We therefore propose a bipartite mechanism controlling leaf movement: ethylene

124 Our findings define a bipartite mechanism for stretch-induced actin remodeling

125 eplication initiation and elongation using a bipartite mechanism involving N-terminal exons lost in c

126 EcRppH interacts with RNA by a bipartite mechanism involving specific recognition of th

127 Thus, our results unveil a bipartite mechanism of Hop2-Mnd1 in homologous DNA pairi

128 DNA recognition by fly TCF occurs through a bipartite mechanism, involving both the HMG domain and t

129 at ADP-binding activates DNA binding using a bipartite mechanism.

130 Interestingly, on a bipartite microtubule consisting of tyrosinated and dety

131 This unique bipartite microtubule-binding structure may mediate the

132 light of our results, a universal eukaryotic bipartite mode of binding to eIF4E is proposed.

133 Recent studies have uncovered a bipartite mode of cytosolic DNA recognition, in which th

134 this phosphorylation is enabled by a unique bipartite mode of ERK2 engagement by Ets-1 and involves

135 NA and Zn2-DNA structures establish a novel, bipartite mode of sequence-independent DNA interaction t

136 HAT-C convex surface binds USP15 in a novel bipartite mode.

137 Our results support a bipartite model in which core first requires DGAT1 to ga

138 Given that miR-SPs rely on a bipartite modular expression system, they could be used

139 Phylloquinone (vitamin K(1)) is a bipartite molecule that consists of a naphthoquinone rin

140 ) of the scaffolding protein Sin3A through a bipartite motif comprising a helix and an adjacent exten

141 This bipartite motif in A36 is required for kinesin-1-depende

142 hnRNP A1 can bind simultaneously to a single bipartite motif of the human intronic splicing silencer

143 icate that a mechanism involving a conserved bipartite motif that is predicted to bind a homeodomain

144 engages the scaffolding protein Sin3A, via a bipartite motif within the Sin3 interaction domain (SID)

145 lity is negatively affected by nestedness in bipartite mutualistic networks.

146 Furthermore, the bipartite nature of the ribosome is presumed to be essen

147 Because of its bipartite nature, FokI has received considerable interes

148 y, we demonstrate that the sIBB domain has a bipartite nature, which contains two distinct binding de

149 ry's economy by interpreting trade data as a bipartite network in which countries are connected to th

150 We constructed a bipartite network of archaeal viruses that includes two

151 Here we trace domain history onto a bipartite network of elementary functional loop sequence

152 d hierarchical analysis is the creation of a bipartite network of gene-phenotype relations, a unique

153 Starting with a bipartite network of known OD and OD-causing mutant gene

154 We analyze the temporal bipartite network of the leading Irish companies and the

155 ys regulatory interactions in the model as a bipartite network, and (iii) a tunable compression pipel

156 ethod, a genomic dataset is represented as a bipartite network, to which Markov chain updates (switch

157 o the end of 2013, but can be applied to any bipartite network.

158 or negative) between users from the original bipartite network.

159 rformance is better for tripartite than with bipartite networks and (iii) the measure of similarity u

160 trait locus (eQTL) analyses, we constructed bipartite networks in which edges represent significant

161 he simple rules of cooperation that generate bipartite networks may be generic, and could prove relev

162 In particular, by using bipartite networks methodology from Complex Network Theo

163 With six bipartite networks, we investigate the stabilities of fi

164 Building on our previous work about rewiring bipartite networks, we propose a method for rewiring any

165 can be applied to undirected, directed, and bipartite networks, yielding valuable insights into the

166 asets, and other data that can be modeled as bipartite networks.

167 duces to the problem of rewiring two induced bipartite networks.

168 method that follows from a basic property of bipartite networks: large dominant eigenvalues are assoc

169 Relish is a bipartite NF-kappaB precursor protein, with an N-termina

170 We designed a bipartite NFAT inhibitor that is more potent than VIVIT

171 : an N-terminal monopartite NLS and a unique bipartite NLS closer to the C terminus.

172 localization elements defined a new form of bipartite NLS consisting of a triplet of basic residues

173 EBP, identifying it as an extended classical bipartite NLS encompassing minimally residues 158-190.

174 is regulated by Ran via the association of a bipartite NLS in the tail of XCTK2 with importin alpha/b

175 dant import receptor, KPNA2, which binds the bipartite NLS in Tpr with nanomolar affinity.

176 We propose NLS1 and NLS2 form a bipartite NLS in trans, which ensures high avidity for i

177 bearing mutation in a previously identified bipartite NLS that maps at residues 494-511.

178 s in vitro, we show that the MRTF-A extended bipartite NLS uses the importin (Imp)alpha/beta-dependen

179 t import of FlbB into the nucleus requires a bipartite NLS, that FlbB localization at the tip require

180 jacent basic section defining the motif as a bipartite NLS.

181 positively charged amino acids and creates a bipartite NLS.

182 p8 location in the nucleolus is linked to a bipartite NoLS.

183 We show that, for a bipartite non zero-sum game, input local quantum correla

184 Computational analysis revealed many bipartite NRSE variants conserved between mouse and huma

185 nd potassium channel H6, another gene with a bipartite NRSE, were up-regulated by dominant-negative R

186 show that MRTF-A contains an unusually long bipartite nuclear localisation signal (NLS), comprising

187 d that the WH2 cluster overlaps an atypical, bipartite nuclear localization sequence (NLS) and contro

188 the APC/C binding of Cdh1 but inactivated a bipartite nuclear localization sequence (NLS) and thereb

189 ion sites included three Lys residues on the bipartite nuclear localization sequence (NLS) and two Ly

190 A) in the cytoplasm and that RSK1 contains a bipartite nuclear localization sequence that is necessar

191 ng bromodomains, an extra-terminal domain, a bipartite nuclear localization sequence, and almost the

192 e apoptosis and is mediated via a C-terminal bipartite nuclear localization sequence.

193 ct in which a kinase substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear

194 using a gain-of-function genetic approach, a bipartite nuclear localization signal (NLS) derived from

195 vity by releasing importin alpha/beta from a bipartite nuclear localization signal (NLS) located in t

196 SAP11 contains a bipartite nuclear localization signal (NLS) that targets

197 this study, we report that Nurr1 contains a bipartite nuclear localization signal (NLS) within its D

198 Both proteins contain a consensus bipartite nuclear localization signal and were found in

199 We demonstrate that the putative bipartite nuclear localization signal is not required, b

200 protein, referred to as pUL31, containing a bipartite nuclear localization signal, an intrinsically

201 the MK2 Ile-366-Ala-390, which includes the bipartite nuclear localization signal, binds to the p38a

202 Nuclear entry of dreCmas1 was mediated by a bipartite nuclear localization signal, which seemed irre

203 clear localization of RBM45 is mediated by a bipartite nuclear-localization sequence (NLS) located at

204 ignificantly bends its DNA substrate using a bipartite, nucleolytic center formed at an N-terminal di

205 terize this entanglement by treating it as a bipartite one between a single mode of phonons and a sin

206 ral way with Rubidium and Caesium atoms in a bipartite optical lattice involving laser-dressed Rydber

207 This bipartite or two-signal mechanism has likely evolved to

208 Limited proteolysis reveals a bipartite organization consisting of an N-terminal ATPas

209 The discovery of a novel bipartite organization in the parasite centrosome that s

210 Oomycete genomes display a strongly bipartite organization in which conserved housekeeping g

211 c chromatin contacts, we discover a specific bipartite organization of the mouse inactive X chromosom

212 e p130(cas) carboxyl terminus, adjacent to a bipartite p130(cas) Src-binding domain (SBD) and induces

213 These studies identify a unique bipartite pathway for activation of beta-cell proliferat

214 space during cocultivation with seedlings in bipartite Petri dishes, and (35)S was assimilated from t

215 Finally, pulldown assays reveal a bipartite physical interaction between hpol eta and WRN

216 omoter consisted of the core sequence of the bipartite PLAG1 consensus site, but lacked the G-cluster

217 Instead, bipartite PML I binding domains located in the N-termina

218 These substrates share a bipartite polybasic recognition determinant (BPR) flanki

219 ntains a site of palmitoylation as well as a bipartite polybasic region.

220 Daz interacting protein 1 (Dzip1) has bipartite positive and negative functions in the Hh path

221 of the nodavirus Flock House virus (FHV), a bipartite positive-strand RNA genome consisting of RNA1

222 Bean pod mottle virus (BPMV) is a bipartite, positive-sense (+) RNA plant virus in the Sec

223 aenorhabditis elegans or any nematode, has a bipartite, positive-sense RNA genome.

224 ega virus is a T=4, icosahedral virus with a bipartite, positive-sense RNA genome.

225 TRV is a bipartite, positive-strand RNA virus with the TRV1 and T

226 ey lack the two major IMS-targeting signals, bipartite presequences and cysteine motifs.

227 it emerged from the DNA-A component of a NW bipartite progenitor via convergent evolution and recomb

228 suggests that apicomplexan parasites possess bipartite promoters with basal and regulated cis-element

229 A bipartite protein complex of LptD and LptE assembles LPS

230 Cut12 harbors a bipartite protein phosphatase 1 (PP1) docking domain.

231 The zona pellucida (ZP) domain is a bipartite protein structural element comprised of ZP-N a

232 s a superconducting two-level system and the bipartite quantum channel is a microwave photonic entang

233 For a bipartite quantum state, the classical correlation is th

234 xperimental approach, we have identified the bipartite RCD1-binding SLiM as (DE)X(1,2)(YF)X(1,4)(DE)L

235 Our study reveals a bipartite regulation of presynaptic activity by endolyso

236 everal known NLRP3 activators, demonstrating bipartite regulatory potential of pH on the activity of

237 We infer that the vertebrate Hox bipartite regulatory system is an evolutionary novelty g

238 partitioning system to equal segregation is bipartite- replication-independent and replication-depen

239 We find that bipartite resource competition networks are better predi

240 Quantum discord is the minimal bipartite resource which is needed for a secure quantum

241 LARP6 has a distinctive bipartite RNA binding domain not found in other members

242 gy) domains of ZBP1 specifically recognize a bipartite RNA element comprised of a 5' element (CGGAC)

243 gy) domains of ZBP1 specifically recognize a bipartite RNA element located within the first 28 nucleo

244 STAR proteins function as dimers and bind to bipartite RNA sequences; however, the structural and fun

245 Flock house virus (FHV), a bipartite RNA virus of insects and a member of the Nodav

246 The structure reveals a bipartite RNA-binding motif on the distal face that is c

247 In this study, we have identified the bipartite role of Hsp90 in chaperoning CRAF kinase.

248 tetramer by BldD is selective and requires a bipartite RXD-X8-RXXD signature.

249 to-V2 projections was recently replaced by a bipartite scheme, in which thin stripes receive V1 input

250 ORC (origin recognition complex) binds to a bipartite sequence consisting of an 11 bp ACS element an

251 omputational analysis identified a conserved bipartite sequence element that is found almost exclusiv

252 RNAs in vitro, and we biochemically define a bipartite sequence motif that is necessary and sufficien

253 Type II enzymes, the IIB systems, recognise bipartite sequences, like Type I sites, but cut specifie

254 he 5' and 3' stem-loops forming an essential bipartite signal.

255 al step in HIV-1 assembly, is facilitated by bipartite signals within the matrix (MA) domain: N-termi

256 bsite on PACS-1 and PACS-2 interacted with a bipartite site on Nef formed by the EEEE(65) acidic clus

257 PTF1 binds two canonical bipartite sites within a 0.7-kb transcriptional enhancer

258 e conclude that the pointed-end complex is a bipartite structural domain that stabilizes dynactin and

259 The full-length m-AAA protease has a bipartite structure and is a hexamer in solution.

260 The holocomplex is a hexamer of a bipartite structure composed of a membrane-proximal ATPa

261 east interphase spindle pole body (SPB) is a bipartite structure in which a bulky cytoplasmic domain

262 that SiRTAs on chromosomes V and IX share a bipartite structure in which a core sequence (Core) is d

263 monious model that can reproduce the overall bipartite structure of cooperative partner-partner inter

264 study in Toxoplasma gondii revealed a unique bipartite structure of the centrosome, which coordinates

265 MOC began to strengthen mid-YDS, producing a bipartite structure of the YDS in records from continent

266 at the inactive murine X chromosome adopts a bipartite structure using a novel 3C protocol, termed in

267 he FokI restriction enzyme (which revealed a bipartite structure with a separable DNA-binding domain

268 binds to a DNA-binding motif with an unusual bipartite structure, CTT(N)15-23cagGCC with lower-case b

269 (OMPs) revealed that seven have an Msp-like bipartite structure; phylogenetic analysis revealed that

270 s in the DDI network and makes them complete bipartite sub-networks by adding edges.

271 formation, which identifies partial-complete bipartite sub-networks in the DDI network and makes them

272 n of polyacetylene chains is captured by the bipartite sublattice structure of the SSH model, emblema

273 teractions with the cap and RNA body using a bipartite surface that forms a channel intersecting the

274 ansferrin binding proteins (Tbps) comprise a bipartite system for iron acquisition from human transfe

275 The bipartite system is treated as two black boxes, with no

276 ternal failures the model is equivalent to a bipartite system, which can be useful to model a financi

277 abilities have been demonstrated for diverse bipartite systems, entangled states have not been achiev

278 rate for endogenous RNase P by rendering the bipartite target RNA-EGS complex a precursor tRNA struct

279 C1 mRNA is recruited by means of a conserved bipartite targeting element contained in the 3' untransl

280 al import pathways: whereas preproteins with bipartite targeting sequences are imported within second

281 Here we apply bipartite tetracysteine display to demonstrate that DM a

282 and block coiled coil formation as judged by bipartite tetracysteine display.

283 ters of jawed vertebrates are organized into bipartite three-dimensional chromatin structures that se

284 erred by Ty-1 was also effective against the bipartite tomato severe rugose begomovirus, where a simi

285 prI localize to the outer membrane, adopting bipartite topologies, whereas TprF is periplasmic.

286 interacts with protective antigen to form a bipartite toxin (lethal toxin [LT]) that exerts pleiotro

287 al toxin produced by Bacillus anthracis is a bipartite toxin in which the first protein, protective a

288 Bacillus anthracis secretes two bipartite toxins, edema toxin (ET) and lethal toxin (LT)

289 ty (FC) algorithm to measure centrality in a bipartite trade network, which aims to represent the 'Fi

290 Both cBDNFs consist of a bipartite transcript, with different 5' exons, exon I (2

291 howed that the sorting of AtTic40 requires a bipartite transit peptide, which was first cleaved by th

292 We now show that a bipartite tryptophan-based kinesin-1 binding motif, orig

293 Bioinformatic analysis reveals that related bipartite tryptophan-based motifs are present in over 45

294 shoe-shaped lophophore, supported by a lower bipartite tubular attachment structure with a long pedic

295 nd biochemical analyses that Prp3 contains a bipartite U4/U6 di-snRNA-binding region comprising an ex

296 nsist of a well-defined ubiquitin core and a bipartite UIM helix.

297 forward assignment, reverse assignment, and bipartite weighted-matching algorithms are combined into

298 The p53TAD is bipartite, with two interaction motifs, termed AD1 and A

299 We have explored the evolution of the bipartite World Trade Web (WTW) across the years 1995-20

300 Via its bipartite zona pellucida module (ZP-N/ZP-C), UMOD forms