ライフサイエンスコーパス: cysteine-rich

1 ritically dependent on palmitoylation of its cysteine-rich (173)CCPCC(177) motif and are also highly

2 ShK toxin is a cysteine-rich 35-residue protein ion-channel ligand isol

3 Cysteine rich 61 (CCN1) is an extracellular matrix (ECM)

4 Resistin, a cysteine-rich adipocytokine, proposed as a link between

5 IGFBPs are composed of cysteine-rich amino- (N-) and carboxyl- (C-) terminal do

6 een ORF31 and ORF24, (ii) the amino-terminal cysteine-rich and carboxyl-terminal basic domains of ORF

7 pe lectin-like domains, where the N-terminal cysteine-rich and fibronectin domains reside at the cent

8 double-ring "head," in which the N-terminal cysteine-rich and fibronectin II domains were folded bac

9 CCN1 is a secreted cysteine-rich and integrin-binding matricellular protein

10 Secreted Wnt lipoproteins are cysteine-rich and lipid-modified morphogens that bind to

11 analyses that, in binding VWF, the ADAMTS13 cysteine-rich and spacer domain exosites bring enzyme an

12 mutagenesis of ADAMTS-4 identified that the cysteine-rich and spacer domains are responsible for bin

13 structs showed that membrane-proximal stalk, cysteine-rich, and disintegrin domains of ADAM10 mediate

14 TspanC8 binding requirements for the stalk, cysteine-rich, and disintegrin domains.

15 terminal disintegrin-like, thrombospondin-1, cysteine-rich, and spacer domains to bind substrates and

16 looxygenase 2, and the matricellular protein cysteine-rich angiogenic inducer 61 (CCN1).

17 RNA-Seq analysis showed that both ID2 and Cysteine-rich angiogenic inducer 61 (CYR61) expression l

18 s to up-regulate the target genes, including cysteine-rich angiogenic inducer 61 (CYR61), connective

19 connective tissue growth factor (CTGF), and cysteine-rich angiogenic inducer 61 (CYR61).

20 ent pro-angiogenic secreted molecule, CYR61 (cysteine-rich angiogenic inducer 61).

21 Among those is hepcidin, a small cysteine-rich antimicrobial peptide that is also the key

22 xins delta-SVIE and MrVIA), nodule-specific, cysteine-rich antimicrobial peptides (NCR), and a malari

23 Cysteine-rich antimicrobial peptides isolated from plant

24 Cysteine-rich Asp-His-His-Cys (DHHC) domain-containing e

25 zinc probe monitoring, for identification of cysteine-rich binding sites with nanomolar and picomolar

26 In contrast, the accumulation of the cysteine-rich Bowman-Birk protease inhibitor was several

27 Here, we characterized a novel cysteine-rich C-terminal domain (CRD), which is present

28 and both auxiliary clusters are housed in a cysteine-rich C-terminal domain, termed SPASM domain, th

29 r plasma membrane localization, and that the cysteine-rich C-terminus is extracellular.

30 Defensins are cysteine-rich cationic antimicrobial peptides contributi

31 Here, we show that the carboxyl-terminal cysteine-rich (CCR) domain of this protein functions as

32 Fab1 kinase region and an upstream conserved cysteine-rich (CCR) domain.

33 receptors (FRalpha, FRbeta and FRgamma) are cysteine-rich cell-surface glycoproteins that bind folat

34 In Arabidopsis, pollen tubes are guided by cysteine-rich chemoattractants to target the female game

35 The RUN domain Beclin-1-interacting cysteine-rich-containing Rubicon protein associates cons

36 embrane binding of dystrophin depends on its cysteine-rich (CR) domain.

37 allothionein genes (CMT1 and CMT2), encoding cysteine-rich Cu binding and detoxifying proteins, whose

38 ehensive functional analysis of the ADAMTS13 cysteine-rich (Cys-rich) domain using engineered glycans

39 We identified reactive epitopes in the cysteine-rich (CysR), C-type lectin domain 1 (CTLD1), an

40 cognized a protein complex consisting of the cysteine-rich (CysR), fibronectin-like type II (FnII), a

41 Def1 and MtDef4 from Medicago spp. are small cysteine-rich defensins with potent antifungal activity

42 2.3 A crystal structure of the extracellular cysteine rich domain (CRD) of vertebrate Smo and show th

43 y, homozygous deletion of src homology 3 and cysteine rich domain 3 (Stac3) in mice results in comple

44 rane receptor with a conserved extracellular cysteine rich domain for ligand binding.

45 17)), which is downstream of its S-acylated, cysteine-rich domain ((85)CGLCVCPC(92)).

46 todomain where loss of an aromatic moiety in cysteine-rich domain (CRD) 2 results in TRAPS disease-as

47 The Frizzled cysteine-rich domain (CRD) and invariant second intracel

48 We identify the conserved extracellular cysteine-rich domain (CRD) as the site of action for oxy

49 y LGR5 and RNF43, with its rod module of the cysteine-rich domain (CRD) contacting LGR5 and a hairpin

50 n binding interface to the RAS G domain, its cysteine-rich domain (CRD) is responsible for associatio

51 involves the binding of a Wnt protein to the cysteine-rich domain (CRD) of a Frizzled receptor.

52 ular protease-associated (PA) domain and the cysteine-rich domain (CRD) of frizzled and the intracell

53 Wnt cis-unsaturated fatty acyl groups by the cysteine-rich domain (CRD) of FZD receptors remains elus

54 The RAS-binding domain (RBD) and cysteine-rich domain (CRD) of RAF engage KRAS and the pl

55 we observed binding of carbamazepine to the cysteine-rich domain (CRD) of the Wnt receptor FZD8 usin

56 Wnt8) in complex with mouse Frizzled-8 (Fz8) cysteine-rich domain (CRD) reveals an unusual two-domain

57 Smo has an extracellular cysteine-rich domain (CRD), indispensable for its functi

58 the conserved Wnt-binding site known as the cysteine-rich domain (CRD), with the highest affinity to

59 curred between the NCAM Ig2 domain and EphA3 cysteine-rich domain (CRD).

60 ted by cholesterol through its extracellular cysteine-rich domain (CRD).

61 nsmembrane domain (TMD) and an extracellular cysteine-rich domain (CRD).

62 tain a conserved catalytic domain called the cysteine-rich domain (CRD).

63 inge domain (HD) and an intact extracellular cysteine-rich domain (CRD).

64 ein Smoothened by binding its extracellular, cysteine-rich domain (CRD).

65 ins that possess a catalytic Asp-His-His-Cys cysteine-rich domain (DHHC-CRD).

66 ering analyses of Norrin in complex with Fz4 cysteine-rich domain (Fz4CRD), of this complex bound wit

67 The cysteine-rich domain 1 (CRD1) of CD40 participated to di

68 UL144 utilizes residues from its N-terminal cysteine-rich domain 1 (CRD1) to interact uniquely with

69 single ligand subunit with contributions of cysteine-rich domain 1 (CRD1), CRD2, and CRD3.

70 and fish null for the protein Stac3 (SH3 and cysteine-rich domain 3) but did not establish the functi

71 Stac3 protein (SH3 and cysteine-rich domain 3) is an essential component of the

72 orphogens, through its Frizzled-like domain (cysteine-rich domain [CRD]).

73 ibition by sequestering the membrane-binding cysteine-rich domain and blocking dimerization of the BR

74 ges formed at C349/C356 and C465/C468 of the cysteine-rich domain are necessary for the enhancement o

75 Akt prevents binding of Rubicon (RUN domain cysteine-rich domain containing beclin1-interacting prot

76 a catalytically inactive PARP6 mutant, or a cysteine-rich domain deletion mutant that has significan

77 Co-deletion of the ADAMTS-5 cysteine-rich domain further reduced versicanase activit

78 ring mutation in the evolutionally conserved cysteine-rich domain had more severe defects in ER exit

79 es localized to the N-terminal extracellular cysteine-rich domain has been described, a functional ro

80 Antibodies to the cysteine-rich domain II of Plasmodium vivax Duffy bindin

81 ary, we present extensive mapping of WNT-FZD cysteine-rich domain interactions complemented by analys

82 Binding of a modulatory antibody to the cysteine-rich domain liberates the catalytic domain from

83 The BRAF cysteine-rich domain occupies a central position that st

84 Here we show that this cysteine-rich domain of DPP6 is required for its export

85 Our findings show that the cysteine-rich domain of DPP6 plays an important role in

86 d on structural studies of the TWEAK-binding cysteine-rich domain of Fn14, several homology models of

87 Wnt's fatty acyl moiety by the extracellular cysteine-rich domain of FZD has become clear only very r

88 s are mediated by an HS-binding motif in the cysteine-rich domain of HHIP1 that is required for its l

89 Fine mapping revealed that the cysteine-rich domain of MRC binds to the chondroitin sul

90 in the acetylation of lysine residues in the cysteine-rich domain of NPC1.

91 The cysteine-rich domain of sFRP2 is sufficient for Ror2 act

92 on through direct interaction with the first cysteine-rich domain of the extracellular region.

93 for ROR1/ROR2 heterooligomerization and the cysteine-rich domain or intracellular proline-rich domai

94 cipated architecture in which the C-terminal cysteine-rich domain partially occludes the enzyme activ

95 axis by KCP, and by extension possibly other cysteine-rich domain proteins, can attenuate both acute

96 A unique 6-cysteine-rich domain structure within Pfs230 have thwart

97 structure of this newly characterized small cysteine-rich domain suggests potential involvement of J

98 ansferase domain, ankyrin repeat domain, and cysteine-rich domain) were unnecessary for G9a coactivat

99 removal of a membrane-tethering domain, the cysteine-rich domain, and a disintegrin domain, respecti

100 is coupled to the transmembrane domain via a cysteine-rich domain, and LBD closure seems to be the fi

101 tinct from the 7-transmembrane domain or the cysteine-rich domain.

102 transforming growth factor-beta1 through its cysteine-rich domain.

103 Wnts bind FZD cysteine-rich domains (CRDs) with high affinity through

104 e closed-open (co) active conformation], the cysteine-rich domains (CRDs), and the transmembrane doma

105 at similar to other TNFRSFs, m4-1BB has four cysteine-rich domains (CRDs).

106 We highlight LMCD1 (LIM and cysteine-rich domains 1), which encodes a transcription

107 t interaction of the two receptors via their cysteine-rich domains also promotes Ror2-mediated papc e

108 2 encodes four N-terminal scavenger receptor cysteine-rich domains and the highly conserved C-termina

109 Interactions between the cysteine-rich domains and the second extracellular loops

110 O-fucose is added to cysteine-rich domains called thrombospondin type 1 repea

111 Whereas both the TSP-N domain and cysteine-rich domains can bind to retinal axons in vivo,

112 present a method for the isolation of small, cysteine-rich domains from bovine antibody ultralong com

113 e in cultured retinal axons, suggesting that cysteine-rich domains interact with and activate an inhi

114 ubunit dimer interface, thereby bringing the cysteine-rich domains into close proximity.

115 ng purified WNTs, we show that different FZD cysteine-rich domains prefer to bind to distinct WNTs wi

116 g Venus flytrap domains, which are linked by cysteine-rich domains to their 7-transmembrane domains.

117 rminal thrombospondin-1 (TSP-N) domain, five cysteine-rich domains, and six EGF-like domains.

118 Using ligand binding assays with cysteine-rich domains-fused p75 neurotrophin receptor, w

119 eracts with these 2 receptors with different cysteine-rich domains.

120 as more enriched with the scavenger receptor cysteine-rich domains.

121 at (LRR) domains, each of which is capped by cysteine-rich domains.

122 orm lacking the first two scavenger receptor cysteine-rich domains.

123 It lacks the auxiliary cysteine-rich, EGF, and transmembrane domains, as well a

124 ly that contains a characteristic N-terminal cysteine-rich EMI domain.

125 growth, thereby linking the redox status of cysteine-rich envelope proteins with progression of the

126 These tetrameric, cysteine-rich enzymes require activation by reductive cl

127 a predicted transmembrane domain and a large cysteine-rich extracellular C-terminus.

128 modified through the removal or addition of cysteine-rich extracellular domains to produce a panel o

129 Gp340 is a member of the scavenger receptor cysteine-rich family of innate immune molecules and also

130 L1 belongs to the group B scavenger receptor cysteine-rich family of proteins, where the CD163-L1 gen

131 members, are part of the scavenger receptor cysteine-rich family.

132 Importantly, six novel cysteine-rich frameworks were revealed which may have no

133 Norrin is a cysteine-rich growth factor that is required for angioge

134 sitively charged residues at the base of the cysteine-rich head and two variant residues in the dorsa

135 fluorometry to investigate movements in the cysteine-rich head domain of the rat P2X1R (A118-I125) t

136 and desensitization involve movements of the cysteine-rich head domain.

137 lobes coordinated by positive charge on the cysteine-rich head region and residues in the adjacent d

138 oximately 135-fold in chimeras replacing the cysteine-rich head, and the dorsal fin region below it i

139 etric beta-barrel-like covalent dimer of the cysteine-rich host-defense peptide human defensin 5 (HD5

140 bodies requires an evolutionarily conserved cysteine-rich hydrophobic motif harbored within a unique

141 These include cysteine-rich, hydrophobic peptides (conotoxins delta-SV

142 eractions are mediated by different types of cysteine-rich interdomain region (CIDR) domains found in

143 fEMP1 types can be classified based on their cysteine-rich interdomain region (CIDR) domains.

144 cassette bound to brain endothelium and the cysteine-rich interdomain region 1 inhibited binding of

145 Plasmodium falciparum virulence factors: two cysteine-rich interdomain regions (CIDR) alpha1 (IT4var1

146 ge extracellular ectodomains made from CIDR (cysteine-rich interdomain regions) and DBL (Duffy-bindin

147 ual cysteine residues within the non-amyloid cysteine-rich Kringle-like domain stabilizes the disulfi

148 This change is in the cysteine-rich luminal loop of the NPC1 protein and is hi

149 Metallothioneins, a group of cysteine-rich metal-ion binding proteins, are known to b

150 a large nuclear protein that shares a novel cysteine rich motif with known transcription factors.

151 critically depends on palmitoylation of its cysteine-rich motif (-CCPCC-) and is modulated by the me

152 Included in this domain is a cysteine-rich motif, the function of which is unknown.

153 ch is dependent upon a set of four conserved cysteine-rich motifs in the C-terminal domain of ORF66.

154 inal domain, which contains highly conserved cysteine-rich motifs reminiscent of zinc finger motifs.

155 Cysteine-rich motor neuron 1 (Crim1), a type I transmemb

156 mouse retina as a model system, we show that cysteine-rich motor neuron 1 (Crim1), a type I transmemb

157 domains that are protease-resistant and has cysteine-rich N and C termini responsible for polymeriza

158 es including the activation of more than 600 cysteine-rich NCR genes expressed only in nodules.

159 vent that is induced by host nodule-specific cysteine rich (NCR) antimicrobial peptides and requires

160 The nodule cysteine-rich (NCR) groups of defensin-like (DEFL) genes

161 onstrate that NFS2 encodes a nodule-specific cysteine-rich (NCR) peptide that acts to promote bacteri

162 We show that NFS1 encodes a nodule-specific cysteine-rich (NCR) peptide.

163 able of degrading a range of nodule-specific cysteine-rich (NCR) peptides encoded by M. truncatula.

164 pproximately 600 of them are nodule-specific cysteine-rich (NCR) peptides produced in the rhizobium-i

165 rentiation is driven by host nodule-specific cysteine-rich (NCR) peptides that orchestrate the adapta

166 me Medicago truncatula, ~700 nodule-specific cysteine-rich (NCR) peptides with conserved cysteine sig

167 ber of antimicrobial peptides, called nodule cysteine-rich (NCR) peptides, to control the outcome of

168 der control by an arsenal of nodule-specific cysteine-rich (NCR) peptides, which induce the bacteria

169 atula produce >300 different nodule-specific cysteine-rich (NCR) peptides.

170 fensin-like peptides called "nodule-specific cysteine-rich" (NCR) peptides.

171 expression of the secreted protein, acidic, cysteine-rich (osteonectin) (SPARC) gene, which encodes

172 predicting small plant peptides such as the cysteine-rich peptide families.

173 Here, we show that a small cysteine-rich peptide family is required for formation o

174 male S-determinant, PrpS PrsS belongs to the cysteine-rich peptide family, whose members activate div

175 fied roseltide rT1, a hyperstable 27-residue cysteine-rich peptide from Hibiscus sabdariffa, as a kno

176 Hepcidin, a cysteine-rich peptide hormone, secreted mainly by the li

177 Inhibition of the enzyme by this 66-mer cysteine-rich peptide is mediated by its C-terminal sequ

178 clinical relevance of this hepatic ~2.8 kDa cysteine-rich peptide is rapidly increasing, since alter

179 Snakin-1 (SN1) is an antimicrobial cysteine-rich peptide isolated from potato (Solanum tube

180 determined to be an unprecedented 42-residue cysteine-rich peptide named recifin A.

181 Human alpha-defensin 6 (HD6) is a 32-aa cysteine-rich peptide of the innate immune system.

182 eptor kinase family and their ligands, 5-kDa cysteine-rich peptide rapid alkalinization factors (RALF

183 that synthesize a remarkably diverse set of cysteine-rich peptide toxins (conotoxins).

184 is a first-in-class mitochondria-targeting, cysteine-rich peptide with potentials to be developed in

185 a cystine-knotted, six-cysteine hevein-like cysteine-rich peptide.

186 s process is orchestrated by nodule-specific cysteine-rich peptides (NCRs) delivered into developing

187 ant and involves hundreds of nodule specific cysteine-rich peptides (NCRs).

188 ibes chemistry that is broadly applicable to cysteine-rich peptides and the influence of a fourth dis

189 Disulfide bonds within cysteine-rich peptides are important for their stability

190 es a new element of structural diversity for cysteine-rich peptides as well as increased protease res

191 by extrapolation, our findings suggest that cysteine-rich peptides diversified for a variety of spec

192 rminus for the capture reaction, which makes cysteine-rich peptides ideal candidates for the entropy-

193 as likely due to the coordination of Zn with cysteine-rich peptides in the root endodermis, suggestin

194 defense-related proteins, including the two cysteine-rich peptides PDF2.2 and PDF2.3.

195 Defensins are short cationic, amphiphilic, cysteine-rich peptides that constitute the front-line im

196 Additionally, cysteine-rich peptides that potentially represent novel

197 Most spider venoms are dominated by cysteine-rich peptides with a diverse range of pharmacol

198 most abundant transcripts encode families of cysteine-rich peptides, implying roles in cell-cell reco

199 -regulation of 127 genes for nodule-specific cysteine-rich peptides.

200 The binding domain of PvDBP lies in a cysteine-rich portion of the molecule called region II (

201 Cystine knot alpha-amylase inhibitors are cysteine-rich, proline-rich peptides found in the Amaran

202 This has led to the identification of the cysteine-rich protective Ag (CyRPA).

203 ied a conserved GPI-linked parasite protein, Cysteine-rich protective antigen (CyRPA) as an interacti

204 log 5 (RH5), RH5 interacting protein (RIPR), cysteine-rich protective antigen (CyRPA), apical membran

205 Among them, the Plasmodium falciparum Cysteine-Rich Protective Antigen (PfCyRPA) is a crucial

206 Metallothionein (MT), a cysteine rich protein is involved as a radical scavenger

207 ts ligand, the pollen coat-localized S-locus cysteine-rich protein (SCR).

208 ot vasodilator-stimulated phosphoprotein and cysteine-rich protein 1.

209 The CCN1 protein also known as cysteine-rich protein 61 (Cyr61) is a dynamically expres

210 bronectin 1 (FN1), interleukin-1beta (IL1B), cysteine-rich protein 61 (CYR61), and jagged-1 (JAG1), t

211 At a molecular level, we show that cysteine-rich protein 61 (CYR61)/CYR61 connective tissue

212 n , NOTCH1, and nephroblastoma overexpressed/cysteine-rich protein 61/connective tissue growth factor

213 ns in the gene coding for reversion-inducing cysteine-rich protein containing Kazal motifs (Reck).

214 efficient modification of acceptor sites in cysteine-rich protein domains before disulfide bond form

215 flanking sequences and sites located within cysteine-rich protein domains.

216 CyRPA is a cysteine-rich protein harboring a predicted signal seque

217 Upon exposure to electrophiles, the cysteine-rich protein Keap1 is covalently modified, and

218 wth factor-like (EGF) repeats are also small cysteine-rich protein motifs that can be O-glycosylated

219 Here, we report that a small cysteine-rich protein PstSCR1 from the wheat rust pathog

220 ilitates the import and oxidative folding of cysteine-rich protein substrates into the mitochondrial

221 Prosaposin, a cysteine-rich protein that contains STT3A-dependent glyc

222 Rubicon is a RUN domain containing cysteine-rich protein that functions as part of a Beclin

223 the tumor suppressor gene reversion-inducing cysteine-rich protein with kazal motifs (RECK) by two ke

224 nd Western blot analysis, reversion-inducing cysteine-rich protein with kazal motifs (Reck) was ident

225 an inactivating lesion in reversion-inducing cysteine-rich protein with Kazal motifs [reck; also know

226 the Notch activator RECK (reversion-inducing cysteine-rich protein with kazal motifs) by releasing it

227 he membrane protein RECK (Reversion-inducing cysteine-rich protein with kazal motifs) controls breast

228 molecule alpha (RELMalpha), a small secreted cysteine-rich protein, is expressed by epidermal keratin

229 press such a large, highly glycosylated, and cysteine-rich protein, limiting structural studies to LR

230 Metallothioneins are a family of small, cysteine rich proteins that have been implicated in a ra

231 Highly diverse small cysteine-rich proteins (CRPs) have been found to play mu

232 llothioneins (MTs) are low-molecular-weight, cysteine-rich proteins believed to play a role in cytoso

233 Cysteine-rich proteins cover many important families in

234 ners with the oxidoreductase Mia40 to import cysteine-rich proteins in the mitochondrial intermembran

235 ing of Mia40 and Erv1 mediates the import of cysteine-rich proteins into the mitochondrial intermembr

236 s the hair and nails by binding and altering cysteine-rich proteins of hair and nails or by means of

237 reallocation in the body of copper bound to cysteine-rich proteins such as metallothioneins.

238 bz linker can be applied to the synthesis of cysteine-rich proteins such the cyclotides Kalata B1 and

239 etallothioneins (MTs) constitute a family of cysteine-rich proteins that play key biological roles fo

240 When applied to 158 non-redundant cysteine-rich proteins, Cyscon predictions helped increa

241 ordin-like (KCP) protein, one of a family of cysteine-rich proteins, suppresses TGF-beta signaling by

242 improve the ab initio structure modeling for cysteine-rich proteins.

243 ase of the inner membrane (Tim) proteins and cysteine-rich proteins.

244 alysis revealed the activation of members of cysteine-rich receptor-like kinase (CRK) genes in the ba

245 Deleting the cysteine-rich region (aa 95-141) that separates the two

246 ions in either the core region (K41A) or the cysteine-rich region (C30G) of Tat abrogated its ability

247 in having an intracellular carboxyl-terminal cysteine-rich region (Ccys).

248 roximity to the glutamate binding domain and cysteine-rich region (R375G and G396V) show both decreas

249 This cysteine-rich region contains two vicinal cysteine pairs

250 ocation across the outer membrane and that a cysteine-rich region directs TraA to the T2SS.

251 Conserved hydrophobic amino acids within the cysteine-rich region of Erv46 were also required for ret

252 rgo binding to a hydrophobic site within the cysteine-rich region of Erv46.

253 A cysteine-rich region of hitherto unknown function is loc

254 we find that a few basic amino acids in the cysteine-rich region of SNAP25 and SNAP23 are essential

255 well known that RET mutations affecting the cysteine-rich region of the protein (MEN2A-like mutation

256 ts suggesting that disulfide linkages in the cysteine-rich region perform a role in releasing bound c

257 bunit and define an approximately 60 residue cysteine-rich region that is unique to the Erv46 family

258 replication initiation factor, followed by a cysteine-rich region, predicted to fold as a Zn knuckle.

259 nsus as TTYRAA and determine that two tandem cysteine rich regions are required for high-affinity DNA

260 s of both the human and Xenopus laevis RecQ4 cysteine-rich regions, and showed by NMR spectroscopy th

261 nt in all Dictyostelia and consist mainly of cysteine-rich repeats.

262 ocation of a major epitope in the N-terminal cysteine-rich ricin domain of PLA2R that is recognized b

263 either the N-terminal myristoylation nor the cysteine-rich RING H2 domain of rapsyn is required for i

264 wing the identification of the male (S-locus Cysteine Rich/S-locus Protein 11) and female (S Receptor

265 -locus receptor kinase (SRK) and the S-locus cysteine-rich (SCR) genes, as well as unlinked modifier

266 d the other encoding its ligand, the S-locus cysteine-rich (SCR) protein, which is localized in the p

267 ic pollen coat-localized ligand, the S-locus cysteine-rich (SCR) protein.

268 ts pollen coat-localized ligand, the S-locus cysteine-rich (SCR) protein.

269 ry metabolism pathways and of numerous small cysteine-rich secreted proteins.

270 wn that allurin is a truncated member of the Cysteine-Rich Secretory Protein (CRISP) family, whose me

271 ssion of a human CAP superfamily member, the cysteine-rich secretory protein 2 (CRISP2), rescues the

272 unctional characterization of the C-terminal cysteine-rich secretory protein/antigen 5/pathogenesis r

273 of action, the CAP protein superfamily [i.e. cysteine-rich secretory proteins (CRISP), antigen 5, and

274 Members of the CAP superfamily (cysteine-rich secretory proteins, antigen 5, and pathoge

275 ssion of genes encoding highly glycosylated, cysteine-rich secretory proteins, thus preventing ER ove

276 R-1/Sc7 (SCP/TAPS) domain, also known as the cysteine-rich secretory proteins/antigen 5/pathogenesis-

277 protein tablysin-15 is a member of the CAP (cysteine-rich secretory, antigen 5, and pathogenesis-rel

278 monstrate that noncatalytic thrombospondin-1/cysteine-rich/spacer domains are principal modifiers of

279 Replacing the thrombospondin-1/cysteine-rich/spacer domains of ADAMTS5 with those of AD

280 the expression of secreted protein, acidic, cysteine rich (SPARC), myocilin, angiopoietin-like facto

281 Secreted protein, acidic, cysteine-rich (SPARC) is a glycoprotein that binds to co

282 been shown to involve the scavenger receptor cysteine-rich (SRCR) domain 3.

283 the substitution of CD163 scavenger receptor cysteine-rich (SRCR) domain 5 with a homolog of human CD

284 he presence of the fourth scavenger receptor-cysteine-rich (SRCR) domain of LOXL2, which is also the

285 composed of 4 repeats of scavenger receptor cysteine-rich (SRCR) domains in LOX-like (LOXL) 2.

286 to result in between 7-20 scavenger-receptor cysteine-rich (SRCR) domains within each SAG molecule.

287 es involves its conserved Scavenger Receptor Cysteine-Rich (SRCR) domains, localized to a 16-mer cons

288 WC1 coreceptors are scavenger receptor cysteine-rich (SRCR) family members, related to T19 in s

289 isingly, Loxl3 N-terminal scavenger receptor cysteine-rich (SRCR) repeats, rather than the C-terminal

290 o-receptors belong to the scavenger receptor cysteine-rich (SRCR) superfamily and are encoded by a mu

291 T cells and belong to the scavenger receptor cysteine-rich (SRCR) superfamily.

292 ynthesis and delivery of complex mixtures of cysteine-rich toxin peptides.

293 o span 22 kb including exons 14-17 of CRIM1 (cysteine-rich transmembrane bone morphogenetic protein (

294 E2 is a highly conserved, cysteine-rich transmembrane glycoprotein.

295 hrough molecular dynamics simulations on the cysteine-rich trypsin inhibitor MCoTI-II with three disu

296 Four proteins (Scavenger receptor cysteine rich type 1 protein M130, Fatty acid binding pr

297 l of exon 2 of the Sep15 gene coding for the cysteine-rich UDP-glucose:glycoprotein glucosyltransfera

298 UL32 is a cysteine-rich viral protein that contains C-X-X-C motifs

299 ns, adipose differentiation-related protein, cysteine-rich with epidermal growth factor-like domains

300 opsis thaliana) that has similarities to the cysteine-rich zinc-binding domain of DnaJ chaperones.