ライフサイエンスコーパス: superfamily

1 on factor and member of the nuclear receptor superfamily.

2 ncluded that DddY should belong to the cupin superfamily.

3 ependent enzymes of the alpha/beta-hydrolase superfamily.

4 t cut-and-paste transposons are from the hAT superfamily.

5 the RAD2/XPG structure-specific 5'-nuclease superfamily.

6 exists within this diverse and heterogenous superfamily.

7 , a member of the ATP-binding cassette (ABC) superfamily.

8 lysophosphospholipid acyltransferase (LPLAT) superfamily.

9 sugar transporters of the major facilitator superfamily.

10 to the expansion of the grape homeobox gene superfamily.

11 member of the acyl-CoA oxidase/dehydrogenase superfamily.

12 s a member of the complement control protein superfamily.

13 functions remain to be uncovered within the superfamily.

14 -inflammatory cytokine belonging to the IL-1 superfamily.

15 ation, including the oncoproteins of the RAS superfamily.

16 of reactions catalyzed by the amidohydrolase superfamily.

17 the transforming growth factor-beta receptor superfamily.

18 tial future highlights of research on the NR superfamily.

19 ceptors, a subset of the TNF receptor (TNFR) superfamily.

20 mbers of the transforming growth factor beta superfamily.

21 nificantly differs from other members of the superfamily.

22 e protease inhibitor belonging to the serpin superfamily.

23 l model for the eukaryotic Cys-loop receptor superfamily.

24 ubstrate binding and recognition in the P450 superfamily.

25 esterase enzymes of the alpha/beta-hydrolase superfamily.

26 drug efflux protein of the major facilitator superfamily.

27 is homologous to, but distinct from the PAS superfamily.

28 are infamously oncogenic members of the PTP superfamily.

29 binding that is unparalleled within the FKBP superfamily.

30 onal analysis of proteins comprising the Prx superfamily.

31 espite absence of such enzymes within the AP superfamily.

32 ks the characteristic disulfide bonds of the superfamily.

33 o other nonpolymerizing members of the actin superfamily.

34 ylsugar acyltransferases (ASATs) of the BAHD superfamily.

35 and 2-oxoglutarate (2OG)-dependent oxygenase superfamily.

36 rs that are members of the major facilitator superfamily.

37 is shared by multiple cytokines in the IL-10 superfamily.

38 s of the pentameric ligand-gated ion channel superfamily.

39 o the identification of the nuclear receptor superfamily.

40 n the pancreatic-type ribonuclease (ptRNase) superfamily.

41 based drug discovery for this important gene superfamily.

42 ructure/function transitions in other enzyme superfamilies.

43 ovides a means to analyse trends across many superfamilies.

44 nistic data, for structurally defined domain superfamilies.

45 location along ssDNA that sheds light on how superfamily 1 and 2 helicases turn ATP hydrolysis into m

46 IGSF1 (Immunoglobulin Superfamily 1) gene defects cause central hypothyroidism

47 Unlike other superfamily 2 (SF2) helicases, JFH-1 NS3 does not requir

48 substates of the ATP hydrolysis cycle of the superfamily 2 helicase Hel308 during translocation on si

49 eral viruses of the NCLDV clade, which use a superfamily 3 helicase for replication, as do poxviruses

50 4-1BB (CD137, tumor necrosis factor receptor superfamily 9) is an inducible costimulatory receptor ex

51 es high-quality manual classification of new superfamilies, a key feature of SCOP.

52 We speculate that the superfamily active-site architecture involved in nucleop

53 Immunoglobulin superfamily adhesion molecules are among the most abunda

54 tem-cell pluripotency, including the TGFbeta superfamily, all of which are aberrantly elevated in DND

55 ogenin (ANG), a member of the Ribonuclease A superfamily (also known as RNase 5) are known to be asso

56 ividual members of the glycyl radical enzyme superfamily among the microbiomes of healthy humans.

57 s into 15 functional classes, 689 structural superfamilies and 1404 families; (ii) 446 complexes of b

58 ridomorph clades, including the monophyly of superfamilies and families, except for Ascaridiidae, whi

59 and SsoMCM, these enzymes are from different superfamilies and unwind DNA with opposite polarities.

60 ors belong to the G protein-coupled receptor superfamily and are composed of eight members encoded by

61 mbers of the transforming growth factor beta superfamily and are often perceived to serve similar or

62 l analysis of similarities across the entire superfamily and computed a sequence similarity network t

63 e transforming growth factor-beta (TGF-beta) superfamily and has been implicated in various biologica

64 which belongs to the metallo-beta-lactamase superfamily and is a paralog of CPSF-73, the endonucleas

65 in (TRPML) channel family belongs to the TRP superfamily and is composed of three members: TRPML1-TRP

66 3 (INSL3) is a member of the relaxin/insulin superfamily and is expressed in testicular Leydig cells.

67 lls is predicted to serve the large cadherin superfamily and other proteins.

68 s have evolved within a structurally defined superfamily and provides a means to analyse trends acros

69 e and mechanism of an entire ABC transporter superfamily and the many diverse functions it supports.

70 DddY has not been classified into a protein superfamily, and its structure and catalytic mechanism a

71 s into the mechanistic design of the ptRNase superfamily, and presents a structural basis for evoluti

72 of the PdxA, class II aldolase, and RuBisCO superfamilies are phosphorylated, we postulated that the

73 Enzymes in Uracil DNA glycosylase (UDG) superfamily are essential for the removal of uracil.

74 ing data indicate that activation of the RAS superfamily are poor biomarkers of statin sensitivity, a

75 Representative members of this superfamily are the Campylobacter PglCs, which initiate

76 olecular basis of charge selectivity for the superfamily as a whole, we performed extensive mutagenes

77 eiodinase is a member of the same structural superfamily as many nitroreductases but does not directl

78 tructures of two members of the glucose EIIC superfamily, bcChbC in the inward-facing conformation an

79 a member of the tumor necrosis factor (TNF) superfamily, binds to CD40, leading to many effects depe

80 They belong to the voltage-gated ion channel superfamily but their activities are controlled by intra

81 We recently discovered that the cadherin superfamily carries O-linked mannose (O-Man) glycans at

82 the dimethylallyltryptophan synthase (DMATS) superfamily catalyze the attachment of prenyl or prenyl-

83 ick (Sdk) 1 and 2 are related immunoglobulin superfamily cell adhesion proteins required for appropri

84 00348), a subgroup of the terpenoid synthase superfamily (CL0613) whose members have a characteristic

85 o the well-studied alkaline phosphatase (AP) superfamily, comparing three of its members, two evoluti

86 al calcium sensor subclass of the calmodulin superfamily, confers Ca(2+)-sensitive activation of reti

87 ever, DUI is not found in all three Unionida superfamilies (confirmed in Hyrioidea and Unionoidea but

88 s expressed by venomous marine snails in the superfamily Conoidea.

89 led of the G protein-coupled receptor (GPCR) superfamily, constituting a key component of the Hedgeho

90 show that Fas, a member of the TNF receptor superfamily, contributes to mitochondrial dysfunction, s

91 he complement receptor of the immunoglobulin superfamily, CRIg.

92 Members of the CAP superfamily (cysteine-rich secretory proteins, antigen 5

93 c expression of different members of the RAS superfamily did not uniformly sensitize cells to fluvast

94 and together with a preceding immunoglobulin-superfamily domain (IgSF).

95 form is transported by the major facilitator superfamily domain containing 2A (MFSD2A) through the en

96 CPV resolvase is dimer of RNase H superfamily domains related to Escherichia coli RuvC, wi

97 tein domains classified into 2737 homologous superfamilies, doubling the number of predicted protein

98 n chromosomal region 20p12 belongs to a gene superfamily encoding TGF-beta-signaling proteins involve

99 rRNA methylation mechanism by a radical SAM superfamily enzyme, indicating that two resistance mecha

100 are highly conserved members of the tubulin superfamily essential for microtubule nucleation.

101 tructure of the olfactory receptor (OR) gene superfamily: expansion or contraction of OR subfamilies

102 tebrate protein found to possess the RNase A superfamily fold, and homologs of this toxin are associa

103 ily of carotenoproteins within the NTF2-like superfamily found across all kingdoms of life.

104 We name this superfamily Fusexins: fusion proteins essential for sexu

105 ononucleotide-dependent nitroreductase (NTR) superfamily (>24,000 sequences from all domains of life,

106 (a pan-inhibitor of the Jumonji demethylase superfamily) had the opposite effect and was ~8-fold mor

107 gests that the carotenoid cleavage oxygenase superfamily has evolved in the "extremely high turnover"

108 eptor of the transforming growth factor-beta superfamily, has been reported to identify functional lo

109 f the tumour necrosis factor receptor (TNFR) superfamily, has the capacity to cause extensive apoptos

110 ycle for which divergent members of the YcaO superfamily have been biosynthetically implicated.

111 ins of the PR-1 (pathogenesis-related 1)/CAP superfamily have been implicated in fungal virulence and

112 model in which contemporary subgroups of the superfamily have diverged in a radial manner from a mini

113 ically inactive members of the rhomboid-like superfamily, have been shown to control the ER-to-Golgi

114 , the only known tumor necrosis factor (TNF) superfamily homolog in Drosophila, Coxiella-infected fli

115 Here we present an updated atlas of the Prx superfamily identified using a novel method called MISST

116 secreted proteins containing immunoglobulin superfamily (IgSF) domains discovered a network formed b

117 ine (SVM) to automatically assign domains to superfamilies; improved search facilities to return alig

118 transporters form one of the largest protein superfamilies in all domains of life, catalyzing the mov

119 (AIPL1) is a distinctive member of the FKBP superfamily in terms of its biochemical properties, and

120 e first genome-wide analysis of the expansin superfamily in the Arachis genus identified 40 members i

121 of FunTree that has expanded to include 2340 superfamilies including both enzymes and proteins with n

122 with several members of the nuclear receptor superfamily, including the human vitamin D receptor (hVD

123 s transforming growth factor beta (TGF beta) superfamily inhibitors of erythropoiesis, giving rise to

124 n-binding domain of LAIR1, an immunoglobulin superfamily inhibitory receptor encoded on chromosome 19

125 Specificity versus other TNF-superfamily interactions (TNF-R1-TNF-alpha) and lack of

126 r and iron, in the heme-copper oxidase (HCO) superfamily is critical to the enzymatic activity of red

127 In mice, the TGF-beta superfamily is implicated in the regulation of white and

128 slation of the fundamental mechanisms of TNF superfamily is leading to the design of therapeutics tha

129 The Phospholipase D (PLD) superfamily is linked to neurological disease, cancer, a

130 belief in the evolutionary stability of this superfamily is misconceived.

131 show that CD40, a member of the TNF receptor superfamily, is a major regulator of dendrite growth and

132 CD27, a member of the TNFR superfamily, is constitutively expressed in most T cells

133 inine is conserved with the HerA/FtsK ATPase superfamily; (iv) a molecular docking model of the penta

134 P) shares no homology with the two other HPP superfamilies known previously in prokaryotes and resemb

135 the ubiquitous major facilitator transporter superfamily, lactose permease.

136 a LTR-retrotransposons, members of the gypsy superfamily, led to genome expansion in C. baccatum.

137 es and domain structures defined at the fold superfamily level of SCOP classification.

138 pteran phylogeny since 1975, emphasizing the superfamily level, and discuss some resulting advances i

139 imerization upon binding to its trimeric TNF superfamily ligand (4-1BBL) to stimulate immune response

140 In this study, we demonstrate that the TNF superfamily ligand-receptor pair CD70/CD27 is expressed

141 ceptors for a distinct class of the TGF-beta superfamily ligands.

142 yeast cells, indicating that members of this superfamily may generally bind sterols or related small

143 increased osteoblastic tumor necrosis factor superfamily member 11 (Tnfsf11) expression.

144 ed to upregulated expression of TNF receptor superfamily member 12a, also known as fibroblast growth

145 ron gamma (IFN-gamma), tumor necrosis factor superfamily member 14 (TNFSF14, also known as LIGHT), mo

146 AIMS: Variants in the tumor necrosis factor superfamily member 15 gene (TNFSF15, also called TL1A) h

147 Thioesterase superfamily member 2 (Them2) is a mitochondria-associate

148 The human transmembrane 6 superfamily member 2 (TM6SF2) gene has been implicated i

149 The transmembrane 6 superfamily member 2 (TM6SF2) loss-of-function variant r

150 ining protein 3 rs738409 nor transmembrane 6 superfamily member 2 rs58542926 polymorphisms influenced

151 and proteomics, we identified immunoglobulin superfamily member 21 (IgSF21) as a neurexin2alpha-inter

152 ifferentiation factor 8 (GDF8) is a TGF-beta superfamily member, and negative regulator of skeletal m

153 ame UL144 is an ortholog of the TNF receptor superfamily member, herpesvirus entry mediator (HVEM; TN

154 g depends on signaling from Nodal, a TGFbeta superfamily member.

155 IL-33 is an IL-1 cytokine superfamily member.

156 functions of the two most prominent TGF-beta superfamily members activin and TGF-beta in advanced col

157 Various TGF-beta superfamily members are important in colorectal cancer m

158 Prx superfamily members are widespread across phylogeny and

159 ese dimeric voltage-gated ion channel (VGIC) superfamily members have a unique topology comprising tw

160 Superfamily members need not be identified initially-MIS

161 , provide clues for functional inference for superfamily members of unknown function, and facilitate

162 d and delineate new differences between GLTP superfamily members that are specific for C1P versus gly

163 Seven death domain superfamily members were tested for crystallization with

164 hyde dehydrogenase 2 (ALDH2), one of 19 ALDH superfamily members, catalyzes the NAD(+)-dependent oxid

165 rmore conserved among additional coronavirus superfamily members, including lineage A betacoronavirus

166 Here we report that additional coronavirus superfamily members, including lineage A betacoronavirus

167 ology with other known low-Pi-responsive HAD superfamily members.

168 m of biological signals mediated by TGF-beta superfamily members.

169 t comparative mitogenome analysis across the superfamily Membracoidea.

170 t encodes a protein with a major facilitator superfamily (MFS) domain.

171 ulted in downregulation of Major Facilitator Superfamily (MFS) genes, while DEGs of the DEM treatment

172 Pho84, a major facilitator superfamily (MFS) protein, is the main high-affinity Pi

173 ath one homolog (PD-1H) is an immunoglobulin superfamily molecule and primarily acts as a coinhibitor

174 levels of the tumor necrosis factor receptor superfamily molecule GITR, whose stimulation is closely

175 Here we show that a deficiency of the TNF superfamily molecule TWEAK (TNFSF12) in mice results in

176 Homophilic binding of immunoglobulin superfamily molecules such as the Aplysia cell adhesion

177 inct differences from the three metal ion AP superfamily monoesterase, from Escherichia coli AP (EcAP

178 igand-gated nicotinic acetylcholine receptor superfamily (namely alpha-amino-3-hydroxy-5-methyl-4-iso

179 Several theories describe multiple superfamilies of proteins to be involved in the process.

180 discuss six publications that describe three superfamilies of T6SS proteins, each dedicated to mediat

181 The superfamily of 3'-5' polymerases synthesize RNA in the o

182 A; a pollen-specific member of the NETWORKED superfamily of actin-binding proteins.

183 The cadherin (cdh) superfamily of adhesion molecules carry O-linked mannose

184 redoxins (Prxs or Prdxs) are a large protein superfamily of antioxidant enzymes that rapidly detoxify

185 K(+) channels, a superfamily of approximately 80 members, control cell ex

186 of initiator proteins belonging to the AAA+ superfamily of ATPases.

187 ionine (SAM) enzymes are emerging as a major superfamily of biological catalysts involved in the bios

188 oorly characterized protein belonging to the superfamily of C-type lectins.

189 n export is centrin, a member of the EF-hand superfamily of Ca(2+)-binding proteins.

190 Cadherins are a superfamily of calcium-dependent cell adhesion molecules

191 afish Gdf3 (Dvr1) is a member of the TGFbeta superfamily of cell signaling ligands that includes Xeno

192 A superfamily of cell wall proteins, the hydroxyproline-ri

193 G protein-coupled receptors (GPCRs), a superfamily of cell-surface receptors involved in virtua

194 tory response, when self-limited, produces a superfamily of chemical mediators that stimulate resolut

195 The IL-1 superfamily of cytokines and receptors has been studied

196 Aminoacyl-tRNA synthetases (AARSs) are a superfamily of enzymes responsible for the faithful tran

197 er of the radical S-adenosylmethionine (SAM) superfamily of enzymes, but it does not catalyze the for

198 e growing radical S-adenosylmethionine (SAM) superfamily of enzymes, which use a reduced [4Fe-4S] clu

199 The superfamily of G protein-coupled receptors (GPCRs) media

200 IA PI3Ks are activated downstream of the Ras superfamily of GTPases, and Ras-PI3K interaction plays a

201 zed by bioinformatics as a member of the FRD superfamily of heme-containing membrane proteins, which

202 Over evolutionary time, members of a superfamily of homologous proteins sharing a common stru

203 mposed of arabinogalactan proteins (AGPs), a superfamily of hydroxyproline-rich glycoproteins present

204 Members of the nuclear receptor (NR) superfamily of ligand-regulated transcription factors pl

205 -coupled receptors (GPCRs) belong to a large superfamily of membrane receptors mediating a variety of

206 (Trm10) is a member of the SpoU-TrmD (SPOUT) superfamily of methyltransferases, and Trm10 homologs ar

207 The smallest member of the SPOUT superfamily of methyltransferases, RlmH lacks the RNA re

208 he DHH (Asp-His-His) phosphoesterase protein superfamily of molecules important for cell motility, an

209 Kinesins-13s are members of the kinesin superfamily of motor proteins that depolymerize microtub

210 ane X receptor (PXR, NR1I2), a member of the superfamily of nuclear receptors, is a transcription fac

211 Polynucleotide ligases comprise a ubiquitous superfamily of nucleic acid repair enzymes that join 3'-

212 can be uncoupled from prenylation of the RAS superfamily of oncoproteins.

213 er pump-like subunit (KdpB) belonging to the superfamily of P-type ATPases.

214 sight into the allosteric mechanisms for the superfamily of pentameric ligand-gated channels.

215 ong neurotransmitter-gated ion channels, the superfamily of pentameric ligand-gated ion channels (pLG

216 ast, less is known about a second, extensive superfamily of PGTs that reveals a core structure with d

217 We focus on protein kinases, a superfamily of phosphotransferases that share homologous

218 WRKY proteins are a superfamily of plant transcription factors with importan

219 channel-like subunit (KdpA) belonging to the superfamily of potassium transporters and another pump-l

220 new and distinct subfamily within the broad superfamily of previously studied PII regulatory protein

221 The YcaO superfamily of proteins catalyzes the phosphorylation of

222 g peptide 1-like (NLP) proteins constitute a superfamily of proteins produced by plant pathogenic bac

223 led receptors (GPCRs) constitute the largest superfamily of proteins that compose approximately 4% of

224 PhnH belongs to a superfamily of proteins with a domain of unknown functio

225 Several members of the Kelch superfamily of proteins, which modulate protein stabilit

226 , with each containing a member of the Omp85 superfamily of proteins: BamA in the BAM complex, TamA i

227 Although they belong to the superfamily of short chain dehydrogenase-reductases, the

228 ppreciated that actin is a member of a large superfamily of structurally related protein families fou

229 usly, we found that DXPS is unique among the superfamily of thiamin diphosphate (ThDP)-dependent enzy

230 ure (IR/DR) in a subgroup of the Tc1/mariner superfamily of transposons has been enigmatic.

231 (Oryza sativa) histone chaperone of the NAP superfamily: OsNAPL6.

232 KCP) is a secreted regulator of the TGF-beta superfamily pathways that can inhibit both TGF-beta and

233 tion platform for expressing relaxin/insulin superfamily peptides.

234 meningosepticum, indicate similarities to a superfamily phosphate diesterase [Xanthomonas citri nucl

235 Growth factors of the TGFbeta superfamily play key roles in regulating neuronal and mu

236 members of the luciferase-like monooxygenase superfamily points toward an important role of these pro

237 al diversity displayed by the protein kinase superfamily poses unique challenges in fully defining th

238 ehydrogenase (GAPDH) and a major facilitator superfamily protein (ArsJ).

239 sion molecule C (JAM-C) is an immunoglobulin superfamily protein expressed in epithelial cells, endot

240 a transforming growth factor-beta (TGF-beta) superfamily protein that has a role in cancer, obesity a

241 gCAM) BT-IgSF (brain- and testis-specific Ig superfamily protein) plays a major role in male fertilit

242 gative co-receptor PD-1 and the TNF receptor superfamily proteins GITR and OX40.

243 As observed with other IL-1 superfamily proteins, the IL-36 members require N-termin

244 of other members of the pentameric receptor superfamily provide touchstones for an emerging alloster

245 emergence of functional diversity in enzyme superfamilies, provide clues for functional inference fo

246 VEM; TNFRSF14), a member of the TNF receptor superfamily, provides key signals for MPEC persistence.

247 functional evolution across a wide range of superfamilies, providing insights that will be useful in

248 Three proteins of the CAP superfamily, Pry1, -2, and -3 (pathogen related in yeast

249 kers of the transforming growth factor (TGF) superfamily, purinergic signaling in response to DL was

250 e demonstrate that cross-talk between the Ig-superfamily receptor CD300f and IL-5 is a key checkpoint

251 DCs and identified Acvrl1, a type I TGF-beta superfamily receptor, as a gene strongly induced by Irf8

252 d potent agonists against two different TNFR superfamily receptors and mouse tumor model studies demo

253 ere, we focus attention on the subset of TNF superfamily receptors encoded in the immune response loc

254 ently, generating effective agonists of TNFR superfamily receptors is challenging.

255 The polytopic PGT superfamily, represented by MraY and WecA, has been the

256 this novel method is demonstrated by the Prx superfamily results, laying the foundation for potential

257 ent esterase MGS0169 from the amidohydrolase superfamily revealed a novel active site with a bound un

258 Expanding to the immunoglobulin superfamily reveals that a subset of non-antibody domain

259 mbers of the transforming growth factor-beta superfamily sharing 89% protein sequence homology.

260 solution) of a mycetozoan peroxidase of this superfamily shows the presence of a post-translationally

261 and proteomic profiling reveal that TGFbeta superfamily signaling pathways are preferentially activa

262 dings demonstrate that shifting the TGF-beta superfamily signaling with a secreted protein can alter

263 The 10th FASEB meeting 'The TGFbeta Superfamily: Signaling in Development and Disease' took

264 Members of enzyme superfamilies specialize in different reactions but ofte

265 nesis-related 1 proteins), also known as SCP superfamily (sperm-coating proteins), have been implicat

266 -metal-ion branch that contains all known AP superfamily sulfatases.

267 ups representing the other two cicadomorphan superfamilies supported the monophyly of Membracoidea, a

268 There are two PGT superfamilies that differ significantly in overall struc

269 -18 (IL18), a cytokine belonging to the IL-1 superfamily that can induce synthesis of several other c

270 ANO5 is a member of the Anoctamin/TMEM16 superfamily that encodes both ion channels and regulator

271 GDF-15) is a member of the TGF-beta cytokine superfamily that is widely expressed and may be induced

272 sine kinases and small G-proteins of the Ras superfamily that stimulate specific isoforms of phosphat

273 eductase that is a member of the heme-copper superfamily that utilizes ubiquinol-8 (Q8H2) as a substr

274 (MVI) is the only known member of the myosin superfamily that, upon dimerization, walks processively

275 functional information about members of both superfamilies, the mechanism by which uphill potassium t

276 Despite extensive scrutiny of the myosin superfamily, the lack of high-resolution structures of a

277 An enzyme superfamily, the lytic transglycosylases (LTs), occupies

278 Within this protein superfamily, there exists a group that is able to transf

279 Since mutations are pooled across the superfamily, these positions may be important to many pr

280 Members of the TNF receptor superfamily (TNFRSF) are key costimulators of T cells du

281 4-1BB (CD137) is a TNF receptor superfamily (TNFRSF) member that is thought to undergo r

282 TNFR superfamily (TNFRSF) members have important immunoregula

283 This study links the BAR protein superfamily to the ESCRT pathway for MP biogenesis in ma

284 hanism across the entire helix-hairpin-helix superfamily to which MutY belongs.

285 The major facilitator superfamily transporter Fub11 functions in the export of

286 way for quality control of major facilitator superfamily transporters that occurs before the first tr

287 The tautomerase superfamily (TSF) consists of more than 11,000 nonredund

288 shed that LigY belongs to the amidohydrolase superfamily, unlike previously characterized MCP hydrola

289 nts, the transposition mechanism of the MULE superfamily was previously unknown.

290 her factors may influence evolution across a superfamily, we turned to the well-studied alkaline phos

291 However, MmpT5 belongs to the TetR superfamily, whereas MmpR5 is a MarR family protein.

292 member of the PPAR nuclear hormone receptor superfamily, which can be activated by fibrate ligands.

293 ellular PAS-like domains belong to the Cache superfamily, which is homologous to, but distinct from t

294 aromyces cerevisiae belongs to the Ty1/Copia superfamily, which is present in every eukaryotic genome

295 member of the tumor necrosis factor receptor superfamily, whose activity has been linked to membrane

296 This superfamily-wide analysis indicates a decomposition of t

297 ecrosis factor (TNF) and immunoglobulin (Ig) superfamilies with diverse, and often opposing, outcomes

298 s both within and among the approximately 43 superfamilies, with unsolved problems now yielding to mu

299 e human cold shock domain-containing protein superfamily, with known functions in cell proliferation,

300 oup species representing other cicadomorphan superfamilies, yielded the same topology in which Scapho