ライフサイエンスコーパス: paralogous

1 Here, we report the identification of four paralogous 2-oxoglutarate/Fe(II)-dependent oxygenases in

2 This analysis identified two highly paralogous 24.5 kb blocks within the FCGR2C/FCGR3B/FCGR2

3 In the paralogous 4.1B gene, we identified approximately 120 kb

4 vertebrate haemoglobin, a heterotetramer of paralogous alpha- and beta-subunits that mediates respir

5 Two paralogous alpha/beta hydrolases, KAI2 and D14, are resp

6 The paralogous and functionally redundant GATA transcription

7 lternative splicing, among a large number of paralogous and orthologous genes.

8 observed, and it tends to occur in pairs of paralogous and redundant proteins.

9 M. truncatula, providing a multidimensional paralogous-antagonistic regulatory paradigm for fine-tun

10 Using the paralogous Arabidopsis thaliana inositol transporters IN

11 Based on the paralogous aspartate-beta-semialdehyde dehydrogenase str

12 te that Archaeal AMP-Acs and ADP-Acs contain paralogous ATPase motifs previously identified in Ack, w

13 stigator data indicated that AtXTH31 and the paralogous AtXTH32 were abundantly expressed in expandin

14 matodes and planaria, however, have a set of paralogous beta-catenins; for example, C. elegans HMP-2

15 ing of haplotype blocks between these highly paralogous blocks that most likely arose from sequential

16 Interestingly, the paralogous BoxR and BzdR regulators act synergistically

17 to concerted action of MICU1 and MICU2, two paralogous, but functionally distinct, EF-hand Ca(2+)-bi

18 The recurrent evolution of paralogous, catalytically dead enzyme-based activating m

19 perties of CaV1.3 in a manner similar to the paralogous CaV1.2.

20 p300, but not the paralogous CBP, induces a dynamic hyper-acetylated chrom

21 n a disaggregation mechanism whereby the two paralogous chaperones alternatively activate the release

22 xpression domain and functional role for the paralogous CINCINNATA-like TCP proteins.

23 Mutation in three paralogous class III homeodomain leucine zipper (HD-ZIPI

24 locus was identified on chromosome 1, and a paralogous ClpP5 gene was isolated and confirmed as the

25 All vertebrates retained the paralogous CLTC gene encoding CHC17 clathrin, which medi

26 However, these genes are located in distinct paralogous clusters in the genome apart from the classic

27 e genomic arrangement of Hox genes into four paralogous clusters is a primitive feature of jawed vert

28 Future, functional tests of homologous and paralogous CMTs will uncover novel roles and consequence

29 By comparing crystal structures of paralogous complexes, we provide a rationale for our obs

30 odular peptidases regularly found in several paralogous copies in animals and plants, where they have

31 tified a 171-bp DNA sequence within multiple paralogous copies of msp2 within the genome of A. phagoc

32 loral-biased expression patterns compared to paralogous copies on autosomes.

33 C-B1 is a NAC transcription factor and has a paralogous copy on chromosome 2B in wheat, GPC-B2.

34 h sublocalization is key to the retention of paralogous cpAPX genes in angiosperms.

35 systems are orthologous and the origin of a paralogous CRZ-type signalling system can be traced to t

36 02-1717) show that Cezanne and Cezanne2, two paralogous deubiquitinating enzymes that are recruited t

37 nown activator of disA encoding one of three paralogous diadenylate cyclases (DAC).

38 e that restricts HO activation to one of two paralogous DNA-binding factors.

39 Truncation of the paralogous domain from the Nedd8 activating enzyme has n

40 ered both alternatively spliced and putative paralogous dsx transcripts from several orders of hexapo

41 cation and has a relatively larger supply of paralogous duplicates, shows SNP enrichment in paralogou

42 me-wide duplications in the vertebrate stem, paralogous Edn pathways functionally diverged, resulting

43 originating in the luminal layer exploit the paralogous EMT-TFs Slug and Snail, respectively, which i

44 ical function of VKORC1-like 1 (VKORC1L1), a paralogous enzyme sharing about 50% protein identity wit

45 ion, while the physiological function of its paralogous enzyme VKOR-like (VKORL) is yet unknown.

46 xylase (AAAD) family has yielded an array of paralogous enzymes exhibiting divergent substrate prefer

47 e for ethanolamine over choline, whereas two paralogous enzymes from Loxosceles arizonica either pref

48 In particular, they suggest how paralogous enzymes with similar catalytic properties cou

49 There are two paralogous Escherichia coli phosphotransferase systems,

50 es (tissue-specific, alternative splicing of paralogous exons of a single gene) and vertebrates (tiss

51 -specific, alternative splicing of a pair of paralogous exons.

52 derive from the segment corresponding to the paralogous exons.

53 A significant paralogous expansion of key gene families--families enco

54 important membrane-CR scaffolds include the paralogous F-BAR proteins Cdc15 and Imp2.

55 her with Hfq, inhibits the expression of two paralogous fadE mRNAs.

56 ains of life, have genomes that encode large paralogous families of proteins.

57 We found that within paralogous families the expression pattern of individual

58 among the present-day receptors, allowing a paralogous family of transcription factors to control di

59 B transcription factors (TFs), MYB88 and the paralogous FLP (MYB124), in cold stress in apple and Ara

60 ultiple paralogs of Spx, suggesting that two paralogous forms of Spx could simultaneously contact RNA

61 le that gene duplication events discriminate paralogous from orthologous genes, QuartetS has been sho

62 ectable AdoMetDC activity; however, when two paralogous fusion proteins are mixed, AdoMetDC activity

63 Re-expression of the paralogous gamma-globin genes (HBG1/2) could be a univer

64 Here, we show that the two paralogous GATA transcription factors GATA, NITRATE-INDU

65 the Bmal1-knockout mice by expression of the paralogous gene Bmal2, insulin action and activity patte

66 r than tandem gene duplication can result in paralogous gene clustering during genome evolution.

67 ost ontogenesis but might also shed light on paralogous gene evolution.

68 the developmental origin, oncogenic drivers, paralogous gene expression pattern, and chromosomal stru

69 Borrelia burgdorferi genome harbors several paralogous gene families (pgf) that can encode immunogen

70 tified four pathways/gene networks and eight paralogous gene families affected by Microcystis .

71 enes, of which six are fragmented, and seven paralogous gene families are present.

72 regulation of the ribosome, including three paralogous gene families encoding 40S, 60S, and mitochon

73 ray to identify pathways, gene networks, and paralogous gene families responsive to Microcystis stres

74 ion (49.1%) of these CDSs are organized into paralogous gene families, which can now be further explo

75 oxidoreductase gene family) and the trypsin paralogous gene family (a major component of the digesti

76 Members of a paralogous gene family in which variation in one gene is

77 thirteen novel genes that belong to the L1L paralogous gene family of Solanum lycopersicum.

78 d BB0405, members of a common B. burgdorferi paralogous gene family, share 59% similarity.

79 and are grouped into the same B. burgdorferi paralogous gene family.

80 Loss of Hox11 paralogous gene function results in dramatic malformatio

81 Knowledge obtained by untangling specific paralogous gene functions during development might not o

82 In addition, we elucidated the paralogous gene history for the mammalian Hippo pathway

83 A paralogous gene in humans, SMN2, produces low, insuffici

84 Orthologs of bm4 include at least one paralogous gene in maize and various homologs in other g

85 ot only assemble presumed orthologs but also paralogous gene loci in distinct contigs.

86 hat developmental mutations in the zebrafish paralogous gene otpa but not otpb affect both stress res

87 Direct comparison of paralogous gene pairs all duplicated simultaneously reve

88 stitutions per synonymous site (Ks ) between paralogous gene pairs and reconciliation of 578 gene tre

89 n studies of duplicated dps genes shows that paralogous gene pairs are expressed differentially and t

90 through sub- and neo-functionalization among paralogous gene pairs.

91 ted to the dominant expression of individual paralogous gene pairs.

92 t modify the alternative splicing of SMN2, a paralogous gene to SMN1, restoring the survival motor ne

93 SMN2, a paralogous gene to SMN1, undergoes alternative splicing

94 This paralogous gene was previously identified only in the el

95 ethod of differentiating between allelic and paralogous (gene copy) sequence variants, allowing ident

96 Three paralogous genes (BST1, BST2, and BST3) belonging to the

97 nids have seven primary subunits (encoded by paralogous genes a-g), which combine to form a 24-mer (4

98 In Arabidopsis (Arabidopsis thaliana), these paralogous genes are positioned in tandem within a clust

99 (CLC) subunits in vertebrates are encoded by paralogous genes CLTA and CLTB, and both gene products a

100 yanobacterial strains, there are one to four paralogous genes coding for homologs to the NTD of the O

101 olution of genes(3) and the proliferation of paralogous genes during genome-wide duplication events(4

102 r expression patterns diverged from those of paralogous genes elsewhere in the genome.

103 We hypothesized that variants in paralogous genes encoding members of the DExD/H-box RNA

104 s (Arabidopsis thaliana) genome contains two paralogous genes encoding stomatin-like proteins (SLPs;

105 ces of P. aeruginosa reveal it to have three paralogous genes for this protease, designated as ampD,

106 all RNA targeting, relating to the multicopy paralogous genes generated from whole genome triplicatio

107 single crossover chimeras between duplicated paralogous genes is a known process for increasing diver

108 hat functional redundancy between duplicated paralogous genes is the molecular mechanism for the inte

109 The local regulators are the products of two paralogous genes mapping at positions adjacent to the co

110 epeat (OPR) proteins encoded in a cluster of paralogous genes on chromosome 15.

111 which predicted functional divergence in the paralogous genes per clade.

112 The seven families of paralogous genes recognized in EEHV1 are also represente

113 licates accumulate relatively more SNPs than paralogous genes retained from genome duplication.

114 Analyses of paralogous genes suggest a whole-genome duplication shar

115 tromeres, TET/JBP transposons, and multicopy paralogous genes that are not expressed, but rarely mark

116 nomes allowed the tracing of orthologous and paralogous genes to understand the co-evolution of polyp

117 ying this metric, the authors concluded that paralogous genes within the mouse genome or the human ge

118 cleotide diversity, copy number variation of paralogous genes, and long repetitive sequences.

119 Two highly similar paralogous genes, clag 3.1 and clag 3.2, are mutually ex

120 ly as fetal gamma-globin expression from two paralogous genes, hemoglobin subunit gamma 1 (HBG1) and

121 y of target genes to the loss of one or both paralogous genes, including preferential effects on spec

122 The present study investigated paralogous genes, involved in three-spined stickleback (

123 The paralogous genes, jamb2 and jamc2, were not detected in

124 d CyHV3 have five, six, and five families of paralogous genes, respectively.

125 (SMN), a protein expressed in humans by two paralogous genes, SMN1 and SMN2.

126 Paralogous genes, such as sex comb on midleg homolog 1/s

127 ssociated with such mutations are functional paralogous genes, suggesting that epistatic interactions

128 Two paralogous genes, tomosyn-1 and -2, occur in mammals and

129 Humans have two paralogous genes, TWIST1 and TWIST2, and mutations in ea

130 Here we show that Hox11 paralogous genes, which developmentally pattern the zeug

131 tions in homologous positions across sets of paralogous genes.

132 tribution of TEs between flanking regions of paralogous genes.

133 s more to the higher expressing gene copy of paralogous genes.

134 h convergent subgenome parallel selection of paralogous genes.

135 , a high coding density, and a low number of paralogous genes.

136 ous genes are functionally more similar than paralogous genes.

137 s, as they evolve functions more slowly than paralogous genes.

138 for differential expression of known and new paralogous genes.

139 ralogous duplicates, shows SNP enrichment in paralogous genes.

140 2/FCGR3 genes are arranged across two highly paralogous genomic segments on chromosome 1q23.

141 r heterozygous missense substitutions in the paralogous glutamic acid residue in TWIST2 (p.Glu75Ala,

142 Several invertebrate deuterostomes have two paralogous glycine carrier genes, with one gene in the p

143 also described the identification of a novel paralogous glycoprotein hormone thyrostimulin and design

144 ny fishes, one leading to a newly identified paralogous group (we have termed CHIO).

145 We then identified a paralogous group of secreted chaperone proteins in the H

146 ing the high level of redundancy in this Hox paralogous group.

147 owever, to what extent members of individual paralogous groups can undergo functional changes during

148 diverse cyanobacteria, occurring as multiple paralogous groups, with two representatives exhibiting s

149 IsdG and IsdI are paralogous heme degrading enzymes from the bacterium Sta

150 Most species encode numerous paralogous histidine kinases that exhibit significant st

151 nundrum, it is necessary to directly compare paralogous (horizontal) evolution of repeats within prot

152 The paralogous iron-responsive transcription factors Aft1 an

153 etabolic vulnerability upon targeting of its paralogous isoform ME3.

154 e auxotrophy in a leuB(-) strain lacking the paralogous isopropylmalate dehydrogenase enzyme.

155 Mice and humans possess three paralogous KDEL receptors, but little is known about the

156 Two paralogous kinases phosphorylate subsets of thylakoid me

157 ubiquitination pathway, here we show that 2 paralogous Legionella effectors, Lpg2154 (DupA; deubiqui

158 cis-abienol synthase (AbCAS), along with the paralogous levopimaradiene/abietadiene synthase and isop

159 The paralogous loci encode maize CRABS CLAW co-orthologs in

160 errors in locus reconstruction, distinguish paralogous loci, rarify raw reads originating from the s

161 elic homologous recombination (NAHR) between paralogous long interspersed nuclear element (LINE) or h

162 We delineated and analyzed directly oriented paralogous low-copy repeats (DP-LCRs) in the most recent

163 Streptomyces species encode paralogous Lsr2 proteins (Lsr2 and Lsr2-like, or LsrL),

164 r site-specific positive selection acting on paralogous main olfactory receptor genes.

165 The paralogous maize (Zea mays) LBD (Lateral Organ Boundarie

166 CTCF and BORIS (CTCFL), two paralogous mammalian proteins sharing nearly identical D

167 RNase II and RNase R are paralogous members of the RNR superfamily of nonspecific

168 showed that Mrr1 regulates expression of two paralogous MG reductases, MGD1 and MGD2, and that both p

169 Expression of clustered paralogous miR-182, miR-96, and miR-183 (collectively, 1

170 The miR-183 cluster, which is comprised of paralogous miRs-183, -96 and -182, is overexpressed in m

171 In vertebrates, the paralogous MLL2 and MLL3 contain multiple domains requir

172 f H4K16ac is conserved in the PHD7 finger of paralogous MLL3.

173 sh, prps1a and prps1b and characterized each paralogous mutant individually as well as the double mut

174 a new candidate Aft1 target-gene (LSO1) and paralogous non-target (LSO2), plus nine putative Cth2 ta

175 In eukaryotic C/D RNP, the paralogous Nop58 and Nop56 proteins specifically associa

176 pected properties and sequence identities of paralogous nuclear encoded mitochondrial sequences, but

177 logenomic analysis, we have revealed two new paralogous OCP families, each distributed among taxonomi

178 A paralogous operon involves a putative nuclease (CinB) ra

179 ity-coverage metrics, tailored solutions for paralogous or low-complexity areas of the genome, and th

180 ifferent fungal lineages and formed distinct paralogous/orthologous clades.

181 me of Mycobacterium tuberculosis encodes two paralogous P1 B 4 -ATPases, CtpD (Rv1469) and CtpJ (Rv37

182 X-linked mouse gene Atp11c, which encodes a paralogous P4-type ATPase, precludes B-cell development

183 differential drought response among retained paralogous pairs suggests further functional diversifica

184 the underlying evolutionary forces of these paralogous pairs through conducting neutrality tests wit

185 Similar paralogous pairs were detected throughout terrestrial pl

186 he circadian expression phase among retained paralogous pairs.

187 nctional complex with its catalytically dead paralogous partner, prozyme.

188 ive, enabling PhoR to avoid crosstalk with a paralogous pathway that arose specifically in alpha-prot

189 psdA that ensure the insulation of these two paralogous pathways at the RR-promoter interface.

190 of these new pairs are orthogonal to all 27 paralogous pathways in E. coli.

191 s depends on the density and distribution of paralogous pathways in the sequence space that is define

192 e original method by extending the theory to paralogous phenotypes.

193 tly, we detected weak encounters between two paralogous phosphotransferase pathways of Escherichia co

194 uld be restored by ectopic expression of the paralogous pilA gene.

195 cosylation on pilus assembly and function of paralogous pilins.

196 Six distinct but paralogous proteasome ATPase proteins, Rpt1 to -6, form

197 ication of toxin-antitoxin systems and other paralogous protein families during evolution.

198 ay help explain the apparent ease with which paralogous protein families expanded in all organisms.

199 Recently, a paralogous protein, geminin coiled-coil domain containin

200 tion in Escherichia coli is regulated by two paralogous proteins (GlnB and GlnK), which orchestrate i

201 NA encoding YapV or each of three individual paralogous proteins (YapK, YapJ, and YapX) was present a

202 iation between the gene profile for the four paralogous proteins and the geographic location of the c

203 ne duplication influence the extent to which paralogous proteins are functionally repurposed.

204 Toc75 and OEP80 are paralogous proteins found in the Viridiplantae lineages,

205 in invertebrates are often found as multiple paralogous proteins in vertebrate complexes.

206 e most conserved residues of orthologous and paralogous proteins likely define those most important.

207 he combination of mutations suggest that the paralogous proteins perform redundant functions in motil

208 A targets depends upon its dimerization with paralogous proteins TFAP2C and TFAP2B.

209 FslE (FTT0025) and FupA (FTT0918) are paralogous proteins that are predicted to form beta-barr

210 relies on interactions with Met31 and Met32, paralogous proteins that bind the same cis-regulatory el

211 interfaces) are investigated and compared to paralogous proteins that bind the same protein ligand (f

212 Thus, we identify three distinct but paralogous proteins that donate electrons to NirK.

213 Clustered protocadherins, a large family of paralogous proteins that play important roles in neurona

214 The evolutionary events that cause paralogous proteins to bind different protein ligands (f

215 In this study, we compared these paralogous proteins to identify characteristics correlat

216 he ring of Fungi, which is composed of three paralogous proteins, evolved from a more ancient two-par

217 be (BHD) syndrome, which associates with two paralogous proteins, folliculin-interacting protein (FNI

218 Here we report a group of LRRC26 paralogous proteins, LRRC52, LRRC55, and LRRC38 that pot

219 P. sojae, however, secretes a paralogous PsXEG1-like protein, PsXLP1, that has lost en

220 MiST carefully handles paralogous reads that map ambiguously to the genome and

221 Based on the conserved signaling among paralogous receptors and common knock-out phenotypes of

222 ferentiation-associated protein 5 (MDA5) are paralogous receptors for viral double-stranded RNA (dsRN

223 These paralogous receptors share redundant function during dev

224 ostic panel of odorants and identified three paralogous receptors-Olfr740, Olfr741, and Olfr743-which

225 NPs, while 26% of SNPs might be derived from paralogous regions.

226 cificities toward effectors and DNA sites in paralogous regulators is a fundamental question in biolo

227 thocyanin spot trait depends on two R2R3 MYB paralogous regulators, RED HEART1 (RH1) and RH2.

228 sed in human placenta was found based on the paralogous relationship with a metabolic hormone asprosi

229 tions, and the concept of orthologous versus paralogous relationships at different levels, including

230 regulatory proteins revealed orthologous and paralogous relationships from species divergences and an

231 erminal regions to determine orthologous and paralogous relationships, as well as the influence of se

232 = 26), short inserted sequences (n = 8), or paralogous repeats (n = 3) at the junctions, indicating

233 of molecular function, including hotspots at paralogous residues of Ras-related small GTPases RAC1 an

234 es to phenotypes associated with the loss of paralogous RPs.

235 cts of its own antibiotics by expressing two paralogous rRNA methylase genes pikR1 and pikR2 with see

236 Rcr3 and Pip1 are paralogous secreted papain-like proteases of tomato.

237 e high degree of sequence similarity between paralogous segments has prevented precise definition of

238 Here, we describe a paralogous sensor duo, ScuR and SarF, which circumvents

239 ng existing long-read aligners and leverages paralogous sequence variants (PSVs)-sequence differences

240 sequencing across MAP2K3 identified several paralogous sequence variants indicating that the region

241 r inversion probes designed to target unique paralogous sequence variants.

242 s to establish a detailed map of allelic and paralogous sequence variation across the FCGR2/FCGR3 loc

243 GR2B locus that are devoid of nonpolymorphic paralogous sequence variations and that define the limit

244 ies to allow traversal among orthologous and paralogous sequences across the legumes.

245 ithin high-identity, copy-number polymorphic paralogous sequences that cannot be specifically assayed

246 y nonreciprocal recombination events between paralogous sequences, a phenomenon known as interlocus g

247 ct genotyping include copy-number-variation, paralogous sequences, library preparation, sequencing er

248 variants (PSVs)-sequence differences between paralogous sequences-to distinguish between multiple ali

249 indicated that PnSERK1 and PnSERK2 represent paralogous sequences.

250 For instance, paralogous signaling proteins must acquire mutations tha

251 In addition, the results of analysis of the paralogous small transmembrane protein AppX show that th

252 nts indicated that Arabidopsis possesses two paralogous solanesyl-diphosphate synthases, AtSPS1 (At1g

253 quences of the VapBC toxin family group into paralogous sub-clusters.

254 ic, consisting of two stacked rings of eight paralogous subunits each.

255 mapped within 55 bp in approximately 7.8-kb paralogous subunits of 95.3% sequence identity located i

256 ion breakpoints within the directly oriented paralogous subunits of the flanking LCR clusters, demons

257 contain a conserved set of 17 genes encoding paralogous subunits of the three major photosynthetic co

258 family member unveils critical dependence on paralogous subunits.

259 ther tumor suppressor lesions/complexes with paralogous subunits.

260 chromosome I, encodes one of two V-ATPase B paralogous subunits.

261 Comparison of the structure of GALNS to paralogous sulfatases shows a wide variety of active-sit

262 dominant human fungal pathogen, contains two paralogous TAF12 genes, CaTAF12L and CaTAF12, encoding H

263 We have previously shown that 2 paralogous tetraspanins in Caenorhabditis elegans, TSP-1

264 ion models, we show that even in the case of paralogous TF with highly similar position weight matric

265 However, many paralogous TFs (i.e. members of the same TF family) perf

266 for studying the genomic binding profiles of paralogous TFs and identifying their putative co-factors

267 Predicting how 2 paralogous TFs bind in vivo using DNA sequence alone is

268 rate that the genome-wide binding targets of paralogous TFs can be discriminated using sequence infor

269 r determinants of protein-DNA recognition by paralogous TFs is of central importance for understandin

270 s input two sets of genomic regions bound by paralogous TFs, and it identifies a small set of putativ

271 co-factors that might provide specificity to paralogous TFs.

272 ns as a bona fide cleavage factor, while the paralogous TFS4 evolved into a potent RNA polymerase inh

273 stresscopin and stresscopin-related peptide, paralogous to CRH, were also identified based on the con

274 rkably, the E17K mutation in AKT3 is exactly paralogous to E17K mutations in AKT1 and AKT2 recently d

275 SYP-5 and SYP-6 are paralogous to each other and play redundant roles in syn

276 -stranded telomere DNA-binding protein Teb1, paralogous to heterotrimeric replication protein A (RPA)

277 of two partially redundant proteins that are paralogous to IDN2 and that form a stable complex with I

278 F169, an uncharacterized E3 ubiquitin ligase paralogous to RNF168, accumulated in DSB repair foci thr

279 that the zebra finch GRC contains >115 genes paralogous to single-copy genes on 18 autosomes and the

280 poorly polymorphic HLA-DQA2/HLA-DQB2 genes, paralogous to the HLA-DQA1/HLA-DQB1 genes, has never bee

281 Teb1 is paralogous to the large subunit of the general single-st

282 recruitment of the MCM8-9 complex, which is paralogous to the MCM2-7 replicative helicase.

283 d archaea encode varying numbers of proteins paralogous to their main recombinase.

284 Phylogenetic analyses indicate that they are paralogous to, but quite distinct from, classical dynami

285 Stp1 and Stp2 are paralogous transcription factors (TFs) regulated by the

286 To understand how paralogous transcription factors evolve divergent DNA sp

287 The paralogous transcriptional cofactors Yes-associated prot

288 -independent 3a and 3b (Sin3a and Sin3b) are paralogous transcriptional coregulators that direct cell

289 Paralogous transcriptional regulators MarA, Rob, and Sox

290 Here, we show that two paralogous transmembrane Rsp5 adaptors, Rcr1 and Rcr2, a

291 afish, as a model for teleost fish, have two paralogous troponin C (TnC) genes that are expressed in

292 we survey the role of neuronally expressed, paralogous tumor necrosis factor receptor super family (

293 BceRS and PsdRS are paralogous two-component systems in Bacillus subtilis co

294 IFs (QYE motif), we tested the effect of the paralogous Tyr in glial fibrillary acidic protein (GFAP)

295 le PDZ protein harmonin is not involved, its paralogous USH2 proteins, PDZD7 and whirlin, function sy

296 S cells markedly decreases expression of the paralogous UTY gene encoded by Y chromosome, but has no

297 d or removed and core histones exchanged for paralogous variants, in concert with changing demands on

298 The paralogous yeast proteins Lsb1 and Lsb2 bind the actin a

299 g of ZF DNA binding and provide evidence for paralogous ZFs utilizing alternate modes of DNA binding

300 athogen Pseudomonas aeruginosa harbors three paralogous zinc proteases annotated as AmpD, AmpDh2, and