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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.

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