ライフサイエンスコーパス: homologous protein

1 CHOP (C/EBP [CCAAT/enhancer binding protein] homologous protein).

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

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

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

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

6 wnstream proapoptotic effector nuclear C/EBP homologous protein.

7 expression of CCAAT/enhancer binding protein homologous protein.

8 erform analogous functions despite not being homologous proteins.

9 we identified and characterized a number of homologous proteins.

10 movements observed for the active states of homologous proteins.

11 forces that shape sequence divergence among homologous proteins.

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

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

14 generated by recombining gene fragments from homologous proteins.

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

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

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

18 conserved patterns of O-glycans on distinct 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 GCPs 2-6 constitute a family of homologous proteins.

24 data and conformational similarities across homologous proteins.

25 ing threading tools perform poorly on remote homologous proteins.

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

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

28 e proteins, especially for distantly related homologous proteins.

29 alyze publications associated with groups of homologous proteins.

30 Key mutations differentiate the functions of homologous proteins.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

47 The homologous proteins Aap and SasG mediate biofilm formati

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

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

50 Is this function conserved for the homologous protein ADNP2?

51 Mutations in homologous proteins affect changes in the backbone confo

52 teins such as CCAAT/enhancer-binding protein-homologous protein and activated caspase-12, suggesting

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

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

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

56 xpression of the transcription factors C/EBP homologous protein and spliced X box-binding protein 1.

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

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

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

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

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

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

63 vation of CHAC1 by the ATF4-ATF3-CHOP (C/EBP homologous protein), and not parallel XBP1 (X box-bindin

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

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

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

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

68 The structures of homologous proteins are generally better conserved than

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

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

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

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

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

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

75 domains were constructed using structurally homologous proteins as templates, and disease-causing mu

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

77 This function is not shared by the highly homologous protein Bassoon, which indicates that Piccolo

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

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

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

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

82 so follows that allostery is common and that homologous proteins can have different allosteric mechan

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

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

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

86 the levels of CAAT/enhancer binding protein homologous protein (CHOP) and activated a DR5 promoter r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 tion factor 4 (ATF4) mRNA and protein, C/EBP homologous protein (CHOP), and growth arrest, DNA damage

115 iculum stress signaling via eIF2alpha, C/EBP-homologous protein (CHOP), and p21, leading to immediate

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

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

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

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

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

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

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

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

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

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

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

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

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

129 SHetA2 exerted CAAT/enhancer-binding protein homologous protein (CHOP)-dependent transactivation of t

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

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

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

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

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

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

136 h the UPR-induced transcription factor C/EBP homologous protein (CHOP).

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

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

139 regulation of CCAAT/enhancer-binding protein-homologous protein (CHOP)/growth arrest and DNA damage-i

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

141 efective eIF2alpha phosphorylation and C/EBP homologous protein (CHOP, also known as GADD153) inducti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 mino acid and coding nucleotide sequences of homologous protein domains from seven organisms; (iv) co

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

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

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

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

164 m of Trichoderma atroviride) secretes an Sm1-homologous protein, Epl1, with high levels of dimerizati

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

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

167 eticulum stress response, specifically C/EBP homologous protein expression, may contribute to the inh

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

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

170 Homologous protein families share highly conserved seque

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

172 Within a homologous protein family, proteins may be grouped into

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

174 In humans, GGTase-I and the homologous protein farnesyltransferase (FTase) are targe

175 ed to obtain sets of functionally equivalent homologous proteins (FEPs) from different species.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

193 zation of Xenopus tropicalis (Xt) allurin, a homologous protein in X. tropicalis.

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

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

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

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

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

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

200 35 of Ebola virus and to known structures of homologous proteins in the measles, mumps, and Nipah vir

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

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

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

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

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

206 4 and p58(IPK) expression and elevated C/EBP homologous protein induction at late time points.

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

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

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

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

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

212 2alpha, CHOP (CCAAT/enhancer-binding protein homologous protein)), (iv) proteasome impairment with in

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

214 3B and FIS1A (BIGYIN)/FIS1B are two pairs of homologous proteins known to function in both peroxisoma

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

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

217 exposure to Abeta, it is also possible that homologous proteins may induce antibody synthesis.

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

219 Whereas the eukaryotic complex consists of 6 homologous proteins (MCM2-7), the archaeon Sulfolobus so

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

221 y and requires either Cbf1 or one of the two homologous proteins Met31 and Met32 for promoter associa

222 Comparison of homologous protein models identified highly conserved re

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

224 This is because analysis of weakly homologous protein models reveals that about half have a

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

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

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

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

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

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

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

232 The homologous proteins p68 and p72 are members of the DEAD

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

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

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

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

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

238 zing information present in the sequences of homologous proteins, profile-based methods are often abl

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

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

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

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

243 P/rds interacts with the homologous protein rom-1, previously proposed to regulat

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

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

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

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

248 on, and many approaches exist for clustering homologous protein sequences.

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

250 FAR-RED-IMPAIRED RESPONSE1 (FAR1), a pair of homologous proteins sharing significant sequence homolog

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

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

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

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

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

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

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

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

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

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

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

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

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

264 ) and LEUNIG_HOMOLOG (LUH) encode two highly homologous proteins that are similar to the animal and f

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 The H. influenzae HMW1 and HMW2 adhesins are homologous proteins that promote bacterial adherence to

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

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

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

273 ible to discriminate within a dataset of non-homologous proteins those that bind similar ligands base

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

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

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

277 Homologous proteins unique to the order of Kinetoplastid

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

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

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

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

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

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

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

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

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

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

288 GE/cancer testes antigens, a group of highly homologous proteins whose expression is suppressed in al

289 r-interacting protein-associated ICH-1/CED-3 homologous protein with a death domain (RAIDD), and proc

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

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

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

293 Drosophila VAP33, and C. elegans VPR-1) are homologous proteins with an amino-terminal major sperm p

294 The study of homologous proteins with differing thermostabilities off

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

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

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

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

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