ライフサイエンスコーパス: homologous protein

1 n directly attributed to this protein or any homologous protein.

2 aspase-12 and the transcription factor C/EBP homologous protein.

3 by enhanced transcription of ATF4 and C/EBP homologous protein.

4 rylation, and a binding site for calcineurin homologous protein.

5 wnstream proapoptotic effector nuclear C/EBP homologous protein.

6 expression of CCAAT/enhancer binding protein homologous protein.

7 e proteins, especially for distantly related homologous proteins.

8 Key mutations differentiate the functions of homologous proteins.

9 lytic function, and sequence conservation in homologous proteins.

10 erform analogous functions despite not being homologous proteins.

11 we identified and characterized a number of homologous proteins.

12 forces that shape sequence divergence among homologous proteins.

13 us the promiscuity of peptide binding in the homologous proteins.

14 functional role may also exist for other FRP homologous proteins.

15 generated by recombining gene fragments from homologous proteins.

16 rences in the binding site between Grp78 and homologous proteins.

17 l structure of a disulfide-linked complex of homologous proteins.

18 in all reported structures of L7Ae and other homologous proteins.

19 r computational annotation of some groups of homologous proteins.

20 rs by inspecting protein complexes formed by homologous proteins.

21 (ASL19)/LBD30 and ASL20/LBD18, which encode homologous proteins.

22 hod to a cognate-ligand bound dataset of non-homologous proteins.

23 ch represent multiple sequence alignments of homologous proteins.

24 umb domain and 8-KD domain) conserved in the homologous proteins.

25 movements observed for the active states of homologous proteins.

26 conserved patterns of O-glycans on distinct homologous proteins.

27 GCPs 2-6 constitute a family of homologous proteins.

28 data and conformational similarities across homologous proteins.

29 ing threading tools perform poorly on remote homologous proteins.

30 ors share no more sequence identity than non-homologous proteins.

31 re highly selective for POP over a number of homologous proteins.

32 ased lipidomics, we identified calcineurin B homologous protein 1 (CHP1) as a major regulator of ER g

33 Calcineurin homologous protein 1 (CHP1) is a widely expressed, 22-kD

34 ich syndrome protein (WASP)-family verprolin homologous protein 1 (WAVE1 or WASF1) as part of a negat

35 ich syndrome protein (WASP)-family verprolin homologous protein 1 (WAVE1) controls depolarization-ind

36 ich syndrome protein (WASP) family verprolin homologous protein 1 (WAVE1) regulates actin-related pro

37 found that overexpression of the calcineurin homologous protein-1 (CHP1) in opossum kidney cells incr

38 NHE3, when complexed with the calcineurin homologous protein-1 (CHP1), had a shift in pHi sensitiv

39 We found that C/EBP homologous protein 10 (CHOP), a mediator of the endoplas

40 ses ER stress-induced up-regulation of C/EBP homologous protein 10 (CHOP)-the transcription factor ce

41 dj4, BiP, and CCAAT/enhancer binding protein homologous protein 10 (CHOP).

42 C/EBP homologous protein-10 (CHOP-10) is a novel developmental

43 e include WASp and the WASp family verprolin-homologous protein-2 (WAVE2).

44 Here we show that the cap-binding eIF4E-homologous protein 4EHP is an integral component of the

45 complex, including Reticulocyte binding-like Homologous protein 5 (PfRH5) and the RH5-interacting pro

46 smodium falciparum reticulocyte binding-like homologous protein 5 (PfRH5) is an indispensable parasit

47 ation and nuclear translocation of the C/EBP homologous protein, a proapoptotic transcription factor

48 C/EPB homologous protein, a transcription factor that can modu

49 The homologous proteins Aap and SasG mediate biofilm formati

50 edge-alignment paradigm: they first identify homologous proteins across networks and then consider in

51 In cyanobacteria, a homologous protein (activase-like cyanobacterial protein

52 In F-plasmid and related systems, the homologous protein acts in pilus production, mating pair

53 Is this function conserved for the homologous protein ADNP2?

54 Mutations in homologous proteins affect changes in the backbone confo

55 , expression of stress response genes (C/EBP homologous protein and activating transcription factor 4

56 D+GBA and PD brains, whereas increased C/EBP homologous protein and binding immunoglobulin protein le

57 regulation of CCAAT/enhancer-binding protein homologous protein and immunoglobulin heavy chain bindin

58 oftware suite is widely used for analysis of homologous protein and nucleotide sequences with high se

59 c/EBP homologous protein and X box binding protein 1 have been

60 rotocol was tested on a large set of 285 non-homologous proteins and generated structural models with

61 in our study on insertions and deletions in homologous proteins and how they enable or disable compl

62 ult to compute and rely on a large number of homologous proteins and interaction marks of protein par

63 cleocapsid is formed by a heterodimer of two homologous proteins and is membrane enveloped, while SSR

64 zinc triggers a switch between these paired homologous proteins and therefore chose one of these pai

65 tivating transcription factor-4, CHOP (C/EBP homologous protein), and apoptosis.

66 ase-related PKR-like ER kinase), CHOP (C/EBP homologous protein), and MyD88 (myeloid differentiation

67 vation of the CCAAT-enhancer-binding protein homologous protein, and activation of the cyclic adenosi

68 ponent YscD appeared elongated compared to a homologous protein, and molecular dynamics simulations d

69 First, we transfer the GO terms of the homologous protein, and then assign the bit-score as wei

70 the type of amino acid, its conservation in homologous proteins, and its tendency of being exposed t

71 We show that cofactors Brain Tumor and eIF4E Homologous Protein are not obligatory for Pumilio and Na

72 The structures of homologous proteins are generally better conserved than

73 nstructions of TCPM mutants in which the non-homologous proteins are individually deleted, we propose

74 metric based on 'evolutionary preservation': homologous proteins are used to reconstruct the likely s

75 erve that the assembly properties of the two homologous proteins are very different.

76 Sv0189 and homologous proteins are widely distributed among Strepto

77 ressor of cAMP receptor/WASP-family verpolin homologous protein-ARP2/3 pathway, must have been coopte

78 ption factor CCAAT/-enhancer-binding protein homologous protein as well as phosphorylation of eukaryo

79 by the sequential assembly of C5b with four homologous proteins as follows: one copy each of C6, C7,

80 he conserved structural scaffold observed in homologous proteins, as well as distinctive features, pr

81 clustering method that ensures there are no homologous proteins between sets yet maintains the maxim

82 s indicated by decreased expression of C/EBP homologous protein, binding immunoglobulin protein, and

83 m of the XBP1 protein as well as CHOP (C/EBP homologous protein), both transcriptional activators of

84 RVA and RVB are predicted to encode mostly homologous proteins but differ significantly in the prot

85 H-NS can interact with itself or with homologous proteins, but protein family diversity and re

86 formation via the sequential recruitment of homologous proteins: C7, C8, and 12-18 copies of C9, eac

87 CS via BLAST, adding hits to their cart, and homologous proteins can be aligned using MUSCLE and view

88 mic reticulum (ER); gammaKA-PE induced C/EBP homologous protein CHOP and BiP expression and p38 MAPK

89 f ER stress reduced gammaKA-PE-induced C/EBP homologous protein CHOP and BiP expression as well as EC

90 excessive levels of the ER regulatory C/EBP homologous protein CHOP.

91 tase and CCAAT/enhancer-binding protein beta homologous protein (CHOP) and decreased mammalian target

92 Both C/EBP homologous protein (CHOP) and Elk1 are required for cele

93 Based on roles for C/EPB homologous protein (CHOP) and ER calcium release in apop

94 asurements of CCAAT/enhancer-binding protein homologous protein (chop) and immunoglobulin heavy chain

95 iption factor CCAAT enhancer-binding protein homologous protein (CHOP) as silencing of these signalin

96 ines that the CCAAT/enhancer binding protein homologous protein (CHOP) binding site is responsible fo

97 actor CCAAT/enhancer-binding protein (C/EBP) homologous protein (CHOP) but did not lead to apoptotic

98 changes correlated with an increase in C/EBP homologous protein (CHOP) expression and the activation

99 regulation of CCAAT enhancer binding protein homologous protein (CHOP) in hepatocytes.

100 y associated with the ER stress marker C/EBP homologous protein (CHOP) in insulin target tissues of d

101 le of the pro-apoptotic stress protein C/EBP homologous protein (CHOP) in MCD-mediated liver injury w

102 es in ATF4 and CAAT/enhancer binding protein homologous protein (CHOP) in multiple cell lines.

103 cal role of the cellular stress sensor C/EBP-homologous protein (Chop) in the accumulation and immune

104 iption factor CCAAT enhancer-binding protein homologous protein (CHOP) in vertebrates.

105 the absence of ARC increased levels of C/EBP homologous protein (CHOP) in wild type isolated islets s

106 rther amplify CCAAT/enhancer binding protein homologous protein (CHOP) induction through activation o

107 -requiring protein 1alpha, to suppress C/EBP homologous protein (CHOP) induction.

108 Transcription factor C/ebp homologous protein (Chop) is thought to be an important

109 In particular, C/EBP homologous protein (CHOP) is undetectable under normal c

110 lated CCAAT/enhancer-binding protein (C/EBP) homologous protein (CHOP) participates in the transcript

111 The STAT3-binding region of the C/EBP-homologous protein (CHOP) promoter was found to be local

112 ion initiation factor alpha (eIF2alpha)-CEBP homologous protein (CHOP) signaling and CHOP-mediated ce

113 provokes a sustained CCAAT/enhancer binding homologous protein (CHOP) upregulation, and deletion of

114 the C/EBP family members C/EBPbeta and C/EBP homologous protein (CHOP) were largely dispensable for i

115 CCAAT/enhancer-binding protein homologous protein (CHOP)(-/-) mice made diabetic with s

116 Here, we report that C/EBP homologous protein (Chop), a downstream sensor of severe

117 ting ubiquitination and degradation of C/EBP homologous protein (CHOP), a key mediator of ER stress-i

118 dent manner, induced the expression of C/EBP homologous protein (CHOP), a molecule involved in endopl

119 C/EBP-homologous protein (CHOP), a transcription factor induce

120 ting transcription factor 3 (ATF3) and C/EBP homologous protein (CHOP), and reveal that BAP1 binds to

121 ctivation and changes in expression of C/EBP homologous protein (CHOP), Bcl-2 family members, and dea

122 n of the ER-initiated apoptotic signal C/EBP homologous protein (CHOP), ER distention, and podocyte i

123 ein (BiP) and CCAAT/enhancer-binding protein homologous protein (Chop), in seven additional models of

124 e induction of CAAT/enhancer-binding protein homologous protein (CHOP), inasmuch as gene silencing of

125 ting transcription factor 4 (ATF4) and C/EBP-homologous protein (CHOP), that serve to implement UPR t

126 Ablation of CCAAT-enhancer-binding protein homologous protein (CHOP), the major ER stress-associate

127 orrelated with increased expression of C/EBP homologous protein (CHOP), TRAIL, and DR5, while express

128 and hepatic steatosis in mice lacking C/EBP homologous protein (CHOP), whereas direct activation of

129 ER stress-induced transcription factor C/EBP homologous protein (CHOP), which exhibited enhanced bind

130 c kidneys resulted in up-regulation of C/EBP homologous protein (CHOP), which may play a role in incr

131 expression of CCAAT/enhancer-binding protein homologous protein (CHOP), which mediates endoplasmic re

132 induction of CCAAT-enhancer-binding protein homologous protein (CHOP), which triggers apoptosis.

133 d protein levels of the stress-induced C/EBP homologous protein (CHOP), whose dominant negative funct

134 C/EBP homologous protein (CHOP), X2-Box-binding protein 1 (XBP

135 This cell death is C/EBP homologous protein (CHOP)-dependent, connecting these ev

136 mic reticulum-CCAAT enhancer-binding protein homologous protein (CHOP)-mediated stress status.

137 cancer cell apoptosis mediated through C/EBP homologous protein (CHOP).

138 iption factor CCAAT/enhancer-binding protein-homologous protein (CHOP).

139 drives expression of the proapoptotic C/EBP homologous protein (CHOP).

140 proapoptotic CCAAT/enhancer binding protein homologous protein (CHOP).

141 ivated by the CCAAT/Enhancer-Binding Protein Homologous Protein (CHOP).

142 levated level of phospho-eIF2alpha and C/EBP homologous protein (CHOP).

143 iption factor CCAAT/enhancer binding protein homologous protein (CHOP).

144 rred loss of the pro-apoptotic protein C/EBP homologous protein (CHOP).

145 e-thymidine (CCAAT)/enhancer-binding protein homologous protein (CHOP).

146 es, which was reversed by silencing of C/EBP homologous protein (CHOP).

147 ddition, both caspase-3 activation and C/EBP homologous protein (CHOP, also known as GADD153) inducti

148 H chain binding protein (BiP; GRP78), C/Ebp homologous protein (CHOP; GADD153), endoplasmic reticulu

149 e downstream transcriptional regulator C/EBP homologous protein (CHOP; GADD153/DDIT3).

150 um (ER) stress (binding protein [BiP], C/EBP homologous protein [CHOP]).

151 ighly correlated with the induction of C/EBP homologous protein (CHOP10), an endoplasmic reticulum (E

152 Calcineurin B homologous proteins (CHP) are N-myristoylated, EF-hand C

153 Like a homologous protein cloned from radish (Raphanus sativus)

154 Comparison of data from the two homologous proteins collected at different temperatures

155 The approach was tested on a set of 158 non-homologous proteins collected from the CASP experiments

156 tt-Aldrich syndrome protein-family verprolin-homologous protein complex, which has been implicated in

157 econd phase, the WAVE (WASP-family verprolin homologous protein) complex and the microtubule cytoskel

158 ons in human proteins based on structures of homologous protein complexes, it is still unclear to wha

159 he signal can be perceived and transduced by homologous protein complexes, while their regulation may

160 r signaling pathways often share the same or homologous protein components, yet undesirable crosstalk

161 a structural template, especially for remote homologous proteins, consists of conserved regions inter

162 omparisons of nondisruptive fission sites in homologous proteins could be useful for finding dynamic

163 nd is essential for embryonic development, a homologous protein, Ctr2, has been proposed to function

164 s distinct roles in spermatogenesis from its homologous protein CUL4A.

165 d then boosted the DNA-primed responses with homologous protein delivered subcutaneously (s.c.), intr

166 DsbC, unlike the homologous protein DsbG, reduces the intermolecular disu

167 We found that Far9 and Far10, two homologous proteins each with a tail-anchor domain, loca

168 fibrinogen-binding protein (Efb) and the Efb homologous protein (Ehp) have previously been demonstrat

169 Orai1 has two homologous proteins encoded by separate genes, Orai2 and

170 between 1.65 and 2.5 angstroms, of the four homologous proteins (EutS, EutL, EutK, and EutM) that ar

171 ptotic factor CCAAT/enhancer-binding protein homologous protein expression were observed in the CSMNs

172 -3 cleavage, CCAAT-enhancer-binding proteins homologous protein expression, and B cell lymphoma 2 pho

173 The highly homologous proteins ezrin, radixin, and moesin link prot

174 CORAL provides E-values to aid in detecting homologous protein families and, by respecting block bou

175 Homologous protein families share highly conserved seque

176 c amino-acid substitution frequencies within homologous protein families to calculate a stability sco

177 netic and molecular relationship between two homologous proteins, FAR-RED ELONGATED HYPOCOTYL1 (FHY1)

178 lorescence architecture are modulated by two homologous proteins, FLOWERING LOCUS T (FT) and TERMINAL

179 om such a technique due to the lack of known homologous protein folds or sequences.

180 In this report, we investigate a homologous protein found in strains of the emerging noso

181 alpha and beta-synuclein are homologous proteins found at comparable levels in presyn

182 Together with the apparent absence of a homologous protein from plant mitochondria, our findings

183 hat quantify evolutionary conservation among homologous proteins from different organisms.

184 ved at the NH2-terminal ends of TaGT43-4 and homologous proteins from diverse taxa.

185 om a Gln to Ala mutation unique to EL222 and homologous proteins from marine bacteria.

186 tructural and functional characterization of homologous proteins from other plant species.

187 the transcription factor CHOP (CCAAT-binding homologous protein; GADD 153) is a critical cellular res

188 Additionally, ER stress-induced C/EBP homologous protein, GADD34, and p58(IPK) induction and c

189 At least 46 homologous protein groups from a variety of functional p

190 xpression of the pro-apoptotic protein C/EBP-homologous protein/growth arrest and DNA damage 153.

191 Here, we show that loss of the homologous protein GTPBP1 during tRNA deficiency in the

192 ecially in cases for which no structures for homologous proteins have been experimentally determined(

193 nd analyzing publications related to sets of homologous proteins help in functional annotation of nov

194 sor demonstrated low cross-reactivity with a homologous protein (human Kallikrein 2) and low response

195 nvolve analysis of (i) relationships between homologous proteins, (ii) protein domain architecture an

196 arity in the three-dimensional structures of homologous proteins imposes strong constraints on their

197 or 4, inositol requiring kinase 1, and C/EBP homologous protein in the ipsilateral cortex at 3-21 d a

198 mmunogenic regions of gliadin, as well as in homologous proteins in barley and rye.

199 examining interfaces that are shared by many homologous proteins in different CFs, we find that the P

200 (MFN2) is one of two ubiquitously expressed homologous proteins in eukaryote cells, playing a critic

201 tions were evaluated across a total of 9,119 homologous proteins in four mammalian orders (primate, c

202 embles those of the corresponding shells and homologous proteins in other dsRNA viruses: lambda1 in o

203 (CxxMxxMxxC-x(5/6)-C), which occurs also in homologous proteins in other green algae, amoebae, and p

204 Compared with homologous proteins in related mussel species, mcfp-1 fr

205 35 of Ebola virus and to known structures of homologous proteins in the measles, mumps, and Nipah vir

206 as in leptin and discovered 11 structurally homologous proteins in the PDB.

207 Non-homologous proteins in the T4aPM and TCPM are found to f

208 ces cerevisiae has shown that release of the homologous proteins in this complex (Nop7, Erb1, and Ytm

209 Here we explore oligomeric states of homologous proteins in various organisms to better under

210 Because wheat shares homologous proteins (including gluten) with barley and r

211 4 and p58(IPK) expression and elevated C/EBP homologous protein induction at late time points.

212 arian and vertebrate excretory cells express homologous proteins involved in reabsorption and waste m

213 Divergence in function of homologous proteins is based on both sequence and struct

214 sure to disrupt these sequence regions among homologous proteins is inconsistent.

215 One difference between these homologous proteins is the presence of a C-terminal PDZ

216 tners of ISG54 revealed association with two homologous proteins, ISG56/IFIT1 and ISG60/IFIT3.

217 2alpha, CHOP (CCAAT/enhancer-binding protein homologous protein)), (iv) proteasome impairment with in

218 ke transcription factor 1 (Elk1)-CHOP (C-EBP homologous protein) kinase pathways in upregulating tran

219 3B and FIS1A (BIGYIN)/FIS1B are two pairs of homologous proteins known to function in both peroxisoma

220 MDFI) and MDFI domain-containing (MDFIC) are homologous proteins known to regulate myogenic transcrip

221 G9a-like protein (GLP) and G9a are highly homologous protein lysine methyltransferases (PKMTs) sha

222 cose-regulated protein 78 (Grp78), and C/EBP-homologous protein, markers of endoplasmic reticulum str

223 viously determined quaternary structures for homologous proteins may not be sufficient to properly un

224 through activation of CCAAT/enhancer-binding homologous protein-mediated apoptosis, followed by an in

225 Comparison of homologous protein models identified highly conserved re

226 ned pairs of adenine-binding sites in weakly homologous protein models is only 4-9% lower than those

227 IAPP as well as pre-formed fibrils with two homologous proteins, namely cationic lysozyme (Lys) and

228 ucture of the C-type lectin-like domain of a homologous protein, NKR-P1A, using X-ray crystallography

229 Finally, we present several case studies of homologous proteins not recorded in other classification

230 could not detect 2'-O-MTase activity for the homologous protein of a torovirus, equine torovirus, whi

231 acid sequence obtained identified conserved, homologous proteins of unknown function across a wide ra

232 ylene sensitivity1 (rte1) loci, which encode homologous proteins of unknown function, influence ethyl

233 y conserved interactions between families of homologous proteins, over the identification of specific

234 require, however, large joint alignments of homologous protein pairs known to interact.

235 e endoplasmic reticulum kinase via the C/EBP homologous protein pathway.

236 a FIS1/DRP3-independent manner and that the homologous proteins PMD1 and PMD2 perform nonredundant f

237 Synucleins are a family of homologous proteins principally known for their involvem

238 The assemblies of its two homologous proteins produce imprecise various iron oxide

239 block in CHOP (CAAT/enhancer binding protein homologous protein) production despite >30-fold activati

240 tally validated specificity changes to other homologous protein-protein complexes.

241 endence (epistasis) of designed mutations in homologous protein-protein interactions.

242 ns, RGS9.Gbeta5 is instead associated with a homologous protein, R7BP, and regulates reward circuit.

243 Thus, improving fold recognition for remote homologous proteins remains a challenge.

244 Differing crystal and NMR structures of homologous proteins resulted in a controversy regarding

245 have investigated the folding pathway of two homologous proteins, Ros87, which contains a prokaryotic

246 tructure (stressosome) formed by one or more homologous proteins (RsbRA, -B, -C, and -D) onto which t

247 tzmann-learning algorithm to the analysis of homologous protein sequences and develop a coarse-graine

248 ilies that focuses on the rapid discovery of homologous protein sequences.

249 olutionary time, members of a superfamily of homologous proteins sharing a common structural core div

250 trongly suggests that comparative studies of homologous proteins should investigate not only differen

251 The homologous protein, SodCII, is also produced during infe

252 ber of cell wall degrading enzymes and three homologous proteins specific to Phytophthora sojae effec

253 ssion of glucose-regulated protein 78, C/EBP homologous protein, sterol regulatory element-binding pr

254 Two homologous proteins, Sts-1 and Sts-2, have been shown to

255 In contrast to homologous proteins such as Epstein-Barr virus nuclear a

256 In contrast to homologous proteins such as perforin and the cholesterol

257 nt, may be shared in early embryos by weakly homologous proteins, such as BigH1, or even unrelated, n

258 teins, such as BigH1, or even unrelated, non-homologous proteins, such as Elba2.

259 es of CeFIGL-1-AAA distinguish it from other homologous proteins, suggesting that CeFIGL-1 may have a

260 the DNA binding domains in PhnF with that in homologous proteins suggests that its DNA binding activi

261 tress protein CCAAT enhancer-binding protein homologous protein suppressed monocyte adhesion, adhesio

262 rk sets consisting collectively of 1,153 non-homologous protein targets, where CEthreader detected 17

263 t activating transcription factor 4 or C/EBP homologous protein that mediates the eIF2alpha-dependent

264 xpressed cyclin-G-dependent kinase (GAK) are homologous proteins that act as cochaperones to support

265 database to predict binding ligand of 75 non-homologous proteins that bind one of seven different lig

266 MDM2 and MDMX are homologous proteins that bind to p53 and regulate its ac

267 Ups1p, Ups2p, and Ups3p are three homologous proteins that control phospholipid metabolism

268 lial cell loss of KRIT1, CCM2 or PDCD10, non-homologous proteins that form an adaptor complex.

269 racellular C-terminus, including calcineurin homologous protein, the NHERF family and SNX27 (related

270 Without using homologous proteins, the designed sequences can be folde

271 successful and powerful methods to recognize homologous proteins, they can break down when homology b

272 ant is heritable because it attracts soluble homologous protein to join its aggregate, which is then

273 Its mammalian counterparts are two homologous proteins, U1A and U2B''.

274 telomere-associated proteins and reveals how homologous proteins undergo functional evolution.

275 activating transcription factor 4 and C/EBP homologous protein up-regulation, associated with caspas

276 Server automatically collects identifiers of homologous proteins using PSI-Blast, retrieves literatur

277 Furthermore RUNX1/ETO interacts with ETO-homologous proteins via NHR2, thereby multiplying NHR do

278 totic factor, CCAAT/enhancer-binding protein-homologous protein, was up-regulated in the aged transge

279 n 2/3 (Arp2/3) and the WASP-family verprolin homologous protein (WAVE) complex, which assemble branch

280 core component of the WASP-family verprolin homologous protein (WAVE) regulatory complex (WRC), as a

281 tt-Aldrich syndrome protein-family verprolin-homologous protein (WAVE)-regulatory complex, which has

282 functional information often only comes from homologous proteins, we benchmarked the accuracy of pred

283 cally, instead of explicit identification of homologous proteins, we directly infer plausibly alignab

284 Spliced XBP1 and C/EBP homologous protein were quantitated by real-time PCR.

285 Besides plants, homologous proteins were only found in the bacterial pla

286 irect microscopy, demonstrated that the PagK-homologous proteins were secreted through OMV, which wer

287 o-IP(3)R, and CCAAT/enhancer-binding protein homologous protein, were elevated significantly in CNGA3

288 arating training and test mutations from non-homologous proteins, which reflects inherent correlation

289 r interacting protein-associated ICH-1/CED-3 homologous protein with a death domain.

290 teracting protein (RIP)-associated Ich-1/CED homologous protein with death domain) remained susceptib

291 unit, and the availability of structures of homologous proteins with >20% sequence identity.

292 The study of homologous proteins with differing thermostabilities off

293 These two JHM variants encode homologous proteins with few polymorphisms, and little i

294 The Akt family is comprised of three unique homologous proteins with isoform-specific effects, but i

295 ese studies demonstrate how two structurally homologous proteins with seemingly identical in vivo fun

296 pecific scoring matrix, which then finds non-homologous proteins with significant expectation values.

297 s the founding member, we define a family of homologous proteins with similar DNA modification-depend

298 inase substrate (IRAG, Mrvi1, and Jaw1L) are homologous proteins with small ER luminal domains and la

299 ables us to interrogate the conformations of homologous proteins with very similar tertiary structure

300 is possible to design binding activity into homologous proteins without structural information of th