ライフサイエンスコーパス: cysteine-rich

1 d mutations in the gene Grxcr1 (glutaredoxin cysteine-rich 1) in five independent allelic strains of

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

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

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

5 d levels of connective tissue growth factor, cysteine-rich 61, collagen I (COL1A2), and collagen III

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

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

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

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

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

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

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 of a rigid module formed by the disintegrin, cysteine-rich, and epidermal growth factor-like domains.

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

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

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

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

20 increasing expression of protein CYR61 (the cysteine-rich angiogenic inducer 61, or CCN1) in colonic

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 inding regions of LRP consist of clusters of cysteine-rich approximately 40-residue complement-like r

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

26 Protegrin-1 (PG-1) is an 18 residues long, cysteine-rich beta-sheet antimicrobial peptide (AMP).

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 ectivity brought about by alterations in the cysteine-rich carboxy-terminal domains of the ligands.

31 Defensins are cysteine-rich cationic antimicrobial peptides contributi

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

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

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

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 M superfamily and contain the characteristic cysteine-rich CX(3)CX(2)C motif.

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

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

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

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

43 2.3 A crystal structure of the extracellular cysteine rich domain (CRD) of vertebrate Smo and show th

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

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

46 r domain (ECD) of Fz, in particular its CRD (cysteine rich domain), as critical for nonautonomous Fz-

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

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

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

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

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

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

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

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

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

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 ises three immunoglobulin-like domains and a cysteine-rich domain (Fz-CRD) related to those in Frizzl

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

64 entarity between the C-domain (IGF1) and the cysteine-rich domain (IGF1R).

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

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

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

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

69 ession and purification of soluble mouse Fz8 cysteine-rich domain and human LRP6 extracellular domain

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

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

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

73 AB0023 was mapped to the scavenger receptor cysteine-rich domain four of human LOXL2.

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

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

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

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

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

79 ncatalytic spacer domain of ADAMTS-4 and the cysteine-rich domain of ADAMTS-5, blocking activity agai

80 The cysteine-rich domain of ADAMTS-7 is required for its int

81 een the cysteine-rich domain of ASIP and the cysteine-rich domain of AgRP.

82 developed by interchanging loops between the cysteine-rich domain of ASIP and the cysteine-rich domai

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

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

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

86 ed by immunizing Fzd4 knockout mice with the cysteine-rich domain of FZD4.

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

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

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

90 ngly, a truncated form of Smo that lacks the cysteine-rich domain of the ECD localizes to the cilium

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

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

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

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

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

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

97 Here, we characterize a novel cysteine-rich domain which is crucial for sensing excess

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

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

100 Chordin is the prototype of a group of cysteine-rich domain-containing proteins that bind and m

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

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

103 rate groove, and the steric hindrance by the cysteine-rich domain.

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

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

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

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

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

109 2 encodes four N-terminal scavenger receptor cysteine-rich domains and the highly conserved C-termina

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 ar, both containing three scavenger receptor cysteine-rich domains in their extracellular regions.

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

114 myocilin to the surface of cells expressing cysteine-rich domains of different Frizzled and sFRPs.

115 Recognition by scavenger receptor cysteine-rich domains on membrane proteins regulates inn

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

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

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

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

122 mm-1 function, as did mutations in conserved cysteine-rich domains.

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

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

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

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

127 idity is achieved by disulfide bonding among cysteine-rich envelope-associated proteins.

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

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

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

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

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

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

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

135 one of these families, the nodule-specific, cysteine-rich gene family, is specific to the galegoid l

136 ction of the intestinal mucin MUC2, a large, cysteine-rich glycoprotein that forms the protective muc

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

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

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

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

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

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

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

144 d and disulfide linked form) is a 32-residue cysteine-rich host-defense peptide, expressed and releas

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

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

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

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

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

150 ofibril-associated glycoproteins (MAGPs) are cysteine-rich low molecular weight components of the fib

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

152 PL - an amino-terminal acidic domain and the cysteine-rich Ly6 domain.

153 CCN6 is a secreted cysteine-rich matricellular protein (36.9 kDa) that exer

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

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

156 ssociation is because of palmitoylation of a cysteine-rich motif, CCPCC, located within the catalytic

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

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

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

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

161 A cysteine-rich N-terminal domain, which clearly distingui

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 Additionally, cysteine-rich peptides that potentially represent novel

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

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

193 SMYD2 domains including the MYND domain, the cysteine-rich post-SET domain, and the C-terminal domain

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

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

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

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

198 The cysteine-rich protein (CRP) family is a subgroup of LIM

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

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

201 B silencing leads to increased expression of cysteine-rich protein 61 (CCN1/CYR61) known to mediate a

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

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

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

205 ke molecule alpha (Relm-alpha) is a secreted cysteine-rich protein belonging to a newly defined famil

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

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

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

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

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

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

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

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

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

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

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

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

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

219 Here, we report that a cysteine-rich protein, E-selectin ligand-1 (ESL-1), acts

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

221 is mediated in part by a CCN-family member, cysteine-rich protein-61 (CYR61/CCN1).

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

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

224 cluding the major outer membrane protein and cysteine-rich proteins (OmcA and OmcB), constitute the o

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

226 Cysteine-rich proteins cover many important families in

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

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

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

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

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

232 Most fungal effectors are secreted, cysteine-rich proteins, and a role in virulence has been

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

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

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

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

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

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

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

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

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

242 ADAM17 revealed that within its disintegrin/cysteine-rich region are two highly conserved, vicinal c

243 of similarity to glutaredoxin proteins and a cysteine-rich region at its C terminus.

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

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

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

247 contains a proline-to-serine transition in a cysteine-rich region that precedes the SET domain.

248 pidermal growth factor (EGF)-like domains, a cysteine-rich region which includes a domain of eight cy

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

250 lves domains in the N terminus of anosmin-1 (cysteine-rich region, whey acidic protein-like domain an

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

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

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

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

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

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

257 -locus receptor kinase (SRK) and its S-locus cysteine rich (SCR) ligand.

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

259 e (SRK) [1] by pollen coat-localized S-locus cysteine-rich (SCR) ligand [2-5] and the resulting rejec

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

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

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

263 Connective tissue growth factor (CTGF) is a cysteine-rich secreted matricellular protein involved in

264 ike molecule (RELM)-beta, belongs to a novel cysteine-rich secreted protein family named FIZZ/RELM.

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

266 molecule alpha, belongs to a novel class of cysteine-rich secreted proteins.

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

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

269 tein classes (two lectins, a protease, and a cysteine-rich secretory protein).

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

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

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

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

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

275 efensin-related Defcr-rs genes that code for cysteine-rich sequence 4C (CRS4C) peptides that have a u

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

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

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

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

280 ns is present, containing scavenger receptor cysteine-rich (SRCR) and C-type lectin domains, which fu

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

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

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

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

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

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

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

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

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

290 LMO1 encodes a cysteine-rich transcriptional regulator, and its paralog

291 protein with sequence homology to vertebrate Cysteine-rich transmembrane BMP regulator 1 (Crim1).

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

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

294 ysis, we identify a hitherto uncharacterized cysteine-rich, transmembrane (TM) module, CYSTM, found i

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

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

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

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

299 variants of T-cell PTP (TCPTP) that possess cysteine-rich WPD loops.

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