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1 ain (which mediates interactions with the E3 ubiquitin ligase complex).
2  with Skp2, a key component of the SCF(skp2) ubiquitin ligase complex.
3 teins function as adaptors of the Cullin3 E3 ubiquitin ligase complex.
4 in a Cul5-independent manner by RhoBTB3-Cul3 ubiquitin ligase complex.
5 hromatin structure independently of the CRL4 ubiquitin ligase complex.
6 for the SCF (Skip1-Cullin1-F-box protein) E3 ubiquitin ligase complex.
7 2 mutant that does not participate in the E3 ubiquitin ligase complex.
8  the transcription cofactor CBF-beta to this ubiquitin ligase complex.
9 function as adaptors for the Cullin-3 (Cul3) ubiquitin ligase complex.
10 hich is the substrate-binding component of a ubiquitin ligase complex.
11  and SLX8, encoding the sumoylation-targeted ubiquitin ligase complex.
12  factor and a ligand-dependent adaptor in an ubiquitin ligase complex.
13 mplex/cyclosome and its coactivator Cdh1) E3 ubiquitin ligase complex.
14 e adaptor for an SCF (Skp-Cullin 1-F box) E3 ubiquitin ligase complex.
15  are members of the Skp, Cullin, F box (SCF) ubiquitin ligase complex.
16 mponents of the Skp1-Cullin-F-box (SCF) type ubiquitin ligase complex.
17 equired for assembly of a functional Cul5-E3 ubiquitin ligase complex.
18  functions independent of the VHL/elongin E3 ubiquitin ligase complex.
19 TAT1 for proteasomal degradation via the VDC ubiquitin ligase complex.
20 proteins, by recruitment of the SCF(Skp2) E3 ubiquitin ligase complex.
21 p is a recently discovered member of the HRD ubiquitin ligase complex.
22 DB2), which is part of a multiprotein UV-DDB ubiquitin ligase complex.
23 reased activity of a CUL-6/cullin-containing ubiquitin ligase complex.
24 initiation factor Cdt1 via the CRL4(Cdt2) E3 ubiquitin ligase complex.
25  can recruit key components of the SCF(Skp2) ubiquitin ligase complex.
26 BD1 and R-domain and are sensed by the RMA-1 ubiquitin ligase complex.
27 iting factor for p21 to the rest of the CRL4 ubiquitin ligase complex.
28  substrate recognition subunit of a Cullin-2 ubiquitin ligase complex.
29 biquitinated and degraded via the SCF(Fbxl3) ubiquitin ligase complex.
30 tion, which induces binding to the SCF(Fbw7) ubiquitin ligase complex.
31 ith HSP90 and recruitment of the Elongin-C/B ubiquitin ligase complex.
32 nent of the SKP1-CUL1-F-box-protein (SCF) E3 ubiquitin ligase complex.
33 d F box protein, suggesting a role in an SCF ubiquitin ligase complex.
34 viously shown that CSA is a subunit of an E3 ubiquitin ligase complex.
35 1 regulator of the Cul1-Rbx1-Skp1-Fbox(Skp2) ubiquitin ligase complex.
36  specificity-determinant of the SCF(Grr1) E3 ubiquitin ligase complex.
37 nding of the SCF(Skp2) (Skp1-Cul1-Rbx1-Skp2) ubiquitin ligase complex.
38 rate adaptor protein for a Cul3-dependent E3 ubiquitin ligase complex.
39 rate adaptor protein for a Cul3-dependent E3 ubiquitin ligase complex.
40 dge the BRD9 bromodomain and the cereblon E3 ubiquitin ligase complex.
41 at CLC-1 degradation is mediated by cullin 4 ubiquitin ligase complex.
42 e role of Ddb1, a component of the CUL4-DDB1 ubiquitin ligase complex.
43 phthalimide moiety to hijack the cereblon E3 ubiquitin ligase complex.
44 ate adaptor for the SKP1-CUL1-F-box (SCF) E3 ubiquitin ligase complex.
45 , thereby blocking formation of a functional ubiquitin ligase complex.
46  recognition component of the SCF(beta-TrCP) ubiquitin ligase complex.
47 logous to the cellular Skp1-Cul1-F-box (SCF) ubiquitin ligase complex.
48  component of the Skp1/Cullin1/F-box protein ubiquitin ligase complex.
49 uired for targeting TDG to the CRL4(Cdt2) E3 ubiquitin ligase complex.
50 ts YAP1 for degradation via the betaTrCP-SCF ubiquitin ligase complex.
51 L4A to cause ubiquitination through the CRL4 ubiquitin ligase complex.
52 bstrate receptor for the Skp1-Cul1-Rbx1/Roc1 ubiquitin ligase complex.
53 x component of the Skp-Cullin-F-box (SCF) E3 ubiquitin ligase complex.
54  disrupting its interaction with TRAF2.cIAP2 ubiquitin ligase complex.
55 's ability to bind the cellular beta-TrCP-E3-ubiquitin ligase complex.
56 nical pathways by disrupting the TRAF2-cIAP2 ubiquitin ligase complex.
57 such as SEL-10, are components of the SCF E3 ubiquitin-ligase complex.
58  Cullin 3 (Cul3) and linking GluR6 to the E3 ubiquitin-ligase complex.
59 mammalian orthologs of the yeast Hrd1p/Hrd3p ubiquitin-ligase complex.
60  MUF1 as the first substrate for RhoBTB-Cul3 ubiquitin ligase complexes.
61 ng subunits of SCF (Skp1-Cul1-F-box protein) ubiquitin ligase complexes.
62 n the formation of cullin 3 (Cul3)-dependent ubiquitin ligase complexes.
63 r HIF-1alpha, which are substrates for other ubiquitin ligase complexes.
64 tiple steps of this process are regulated by ubiquitin ligase complexes.
65 strate ubiquitination by cullin-dependent E3 ubiquitin ligase complexes.
66 ion in Skp1-Cdc53/Cullin-F-box protein (SCF) ubiquitin ligase complexes.
67  for defining new modes of regulation of SCF ubiquitin ligase complexes.
68 s, which function as scaffold proteins of E3 ubiquitin ligase complexes.
69 e molecule is control of the activity of SCF ubiquitin ligase complexes.
70 en) using the RAD6-RAD18 and UBC13-MMS2-RAD5 ubiquitin ligase complexes.
71 e is reminiscent of multisubunit cullin-RING ubiquitin ligase complexes.
72 evelopment by modulating the activity of SCF ubiquitin ligase complexes.
73 -ubiquitination and proteolysis by Cullin-E3 ubiquitin-ligase complexes.
74 ors for SCF (Skp1, cullin, F-box protein) E3 ubiquitin-ligase complexes.
75 s mediated by the activity of the CRL4(Cdt2) ubiquitin ligase complex [5, 13, 14].
76 nt of the SCF (Skp1/Cullin/F-box protein) E3 ubiquitin ligase complex acts as a tumor suppressor in s
77 echanism for assembly of the BIV Vif-APOBEC3 ubiquitin ligase complex advances our understanding of v
78 more, knockdown of other members of the Cul3 ubiquitin ligase complex also led to increased cytokine
79 se agents bind to cereblon, a component of a ubiquitin ligase complex, altering the specificity of th
80 ubunit 1 (Cks1), a cofactor of the SCF(Skp2) ubiquitin ligase complex and a downstream target of MYC,
81    We reconstituted the functional human H2A ubiquitin ligase complex and a panel of subcomplexes of
82 f these photoreceptors, such as SPA1/COP1 E3 ubiquitin ligase complex and bHLH transcription factors
83 s paper, we characterize the gp78-containing ubiquitin ligase complex and define its functional inter
84 ROTEIN1 (SKP1)/Cullin/F-box protein (SCF) E3 ubiquitin ligase complex and directly interact with type
85  HINT1 directly interacts with the SCF(SKP2) ubiquitin ligase complex and inhibits the ubiquitylation
86 usly ubiquitylated by the KEAP1-CUL3-RBX1 E3 ubiquitin ligase complex and is targeted to the proteaso
87 bstrate recognition adaptor of CRL4(Cdt2) E3 ubiquitin ligase complex and plays a pivotal role in the
88 Vpr involved in binding to the DCAF1/DDB1/E3 ubiquitin ligase complex and prevention of cell cycle pr
89  SPA1 act in concert to form a functional E3 ubiquitin ligase complex and provide a molecular basis f
90 -L1 disrupts a complex between the DDB1-CUL4 ubiquitin ligase complex and raptor and counteracts DDB1
91 netic screen, we found the Ddb1-Cul4(Cdt)(2) ubiquitin ligase complex and ribonucleotide reductase (R
92     BOK is ubiquitylated by the AMFR/gp78 E3 ubiquitin ligase complex and targeted for proteasomal de
93 , Nrf2 is ubiquitinated by the Keap1-Cul3-E3 ubiquitin ligase complex and targeted to the 26S proteas
94 factor for the Skp1-Cul1-F-box protein (SCF) ubiquitin ligase complex and targets several proteins re
95 s targeted for degradation by the SCF(Slimb) ubiquitin ligase complex and that disruption of this pro
96 ciated with an enzymatically active cullin 2 ubiquitin ligase complex and that the HPV16 E7/pRB compl
97 ent mechanism that requires the Golgi Dsc E3 ubiquitin ligase complex and the proteasome.
98 he interaction of Vpr with the DCAF1/DDB1 E3 ubiquitin ligase complex and the yet-to-be-identified ho
99 horylation of Ci/Gli triggers binding to SCF ubiquitin ligase complexes and consequent proteolysis.
100 h core kinetochore and SCF (Skp1-Cul1-F-box) ubiquitin ligase complexes and is also implicated in pla
101  insights into the operation of cullin-based ubiquitin ligase complexes and potential means by which
102 ial for their recognition by pVHL containing ubiquitin ligase complexes and subsequent degradation in
103 synthesized membrane proteins are queried by ubiquitin ligase complexes and triaged between degradati
104 he von Hippel-Lindau protein (VHL)-Elongin C ubiquitin-ligase complex and degradation by the 26 S pro
105 ts ubiquitylation by targeting the SCF(SKP2) ubiquitin ligase complex, and 2) it inhibits the phospho
106 tein COP1 has been shown to operate as an E3 ubiquitin ligase complex, and a number of putative subst
107 in of the Skp1-Cullin-F-box protein (SCF) E3 ubiquitin ligase complex, and promotes the stability of
108 ctly with the Skp1 component of the host SCF ubiquitin ligase complex, and that the binding of M-T5 t
109 n Hippel-Lindau (VHL)/Elongin-C/Elongin-B E3 ubiquitin ligase complex, and the proteasome.
110 n1/Cullin1/F-box protein COI1 (SCF(COI1)) E3 ubiquitin ligase complex, and their degradation by the 2
111 ullin3 (Cul3), a scaffolding component of E3 ubiquitin ligase complexes, and the previously uncharact
112                   During S and G2 phases the ubiquitin ligase complex APC/C is inhibited by Emi1 prot
113  protein (Fzr), which as an activator of the ubiquitin ligase complex; APC/C (anaphase promoting comp
114 Strikingly, selected E2 and E3 components of ubiquitin ligase complexes are enriched by this mechanis
115  is subject to degradation by the CRL4(Cdt2) ubiquitin ligase complex as a function of the cell cycle
116 Our studies identify the Cul4-DDB1[VprBP] E3 ubiquitin ligase complex as the downstream effector of l
117 cle protein to control local activation of a ubiquitin ligase complex at the mitochondrial outer memb
118  of 69 human SCF (SKP1, CUL1, F-box protein) ubiquitin ligase complexes) binds IP3R3 and targets it f
119 a, a member of the Skp1/Cullin/Rbx1/F-box E3 ubiquitin ligase complex, binds directly to p300 and co-
120 requires ubiquitination of Gap1p by an Rsp5p ubiquitin ligase complex, but amino acid abundance does
121 red Skp2, a substrate-binding subunit of SCF ubiquitin ligase complexes, but also relied on CHIP, a c
122 AMHD1 is recruited to the CRL4(DCAF1-Vpx) E3 ubiquitin ligase complex by interacting with the DCAF1 s
123 protein) is part of a large multi-protein E3 ubiquitin ligase complex called LUBAC (linear ubiquitin
124 t includes upregulation of several predicted ubiquitin ligase complex components such as the cullin c
125  These screens uncovered genes that encode a ubiquitin ligase complex, components of the PtdIns 3-kin
126 s part of a Cullin3 (CUL3)-dependent RING-E3 ubiquitin ligase complex comprised of RhoBTB3, CUL3, and
127 E7 interacts with the SCF (Skp-Cullin-F box) ubiquitin ligase complex containing Cullin 1 (Cul1) and
128                                        An E3 ubiquitin ligase complex containing FBXL5 targets IRP2 f
129                                          The ubiquitin ligase complex containing Pam-Fbxo45 likely ta
130 iated with Dishevelled, including a Cullin-3 ubiquitin ligase complex containing the Broad Complex, T
131        This modification, in turn, enables a ubiquitin ligase complex containing the cullin Rtt101 to
132      We identified an ER membrane-associated ubiquitin ligase complex containing the E3 RMA1, the E2
133 IM-domain (JAZ) repressor proteins and an E3 ubiquitin ligase complex containing the F-box CORONATINE
134 latory role played by the Cullin 7 (CUL7) E3 ubiquitin ligase complex containing the Fbw8-substrate-t
135                          We found that an E3 ubiquitin ligase complex containing the FBXL5 protein ta
136 ducible factor-alpha for ubiquitination by a ubiquitin ligase complex containing the von Hippel-Linda
137 hydroxylation generates a binding site for a ubiquitin ligase complex containing the von Hippel-Linda
138 fication that signals for recognition by the ubiquitin ligase complex containing the von Hippel-Linda
139  the host's antiviral defence by hijacking a ubiquitin ligase complex, containing CUL5, ELOC, ELOB an
140 ropose that the HPV16 E7-associated cullin 2 ubiquitin ligase complex contributes to aberrant degrada
141 port that a previously unstudied SCF(FBXO22) ubiquitin ligase complex controls the activity of KDM4A
142                               The SCF(FBXL3) ubiquitin ligase complex controls this negative feedback
143 or MLN4924, which inhibits the cullin1-based ubiquitin ligase complex coopted by Vpu to degrade cellu
144  substrate-specific adaptor for Cullin3-RING ubiquitin ligase complex (CRL3(GCL)).
145 and Vpx engage the cullin4 (CUL4)-containing ubiquitin ligase complex (CRL4) to cause polyubiquitinat
146 onal characterization of a histone H3 and H4 ubiquitin ligase complex, CUL4-DDB-ROC1.
147 xcision repair (NER), associates with the E3 ubiquitin ligase complex Cul4A-DDB1.
148 ation of the FA pathway requires the FA core ubiquitin ligase complex-dependent monoubiquitination of
149                         ID2 binds to the VHL ubiquitin ligase complex, displaces VHL-associated Culli
150  and structural characterization of an E2-E3 ubiquitin ligase complex for LDLR degradation.
151 o a cullin 5 (Cul5) and elongin (Elo) B/C E3 ubiquitin ligase complex for proteasomal degradation.
152 protein is a substrate of the CUL4-DDB1-DET1 ubiquitin ligase complex for the proteasome degradation.
153 p1 recruits Nrf2 into the Cul3-containing E3 ubiquitin ligase complex for ubiquitin conjugation and s
154 nus, encodes a V protein that can assemble a ubiquitin ligase complex from cellular components, leadi
155 tein, the V protein, assembles STAT-specific ubiquitin ligase complexes from cellular components.
156 matin-remodeling gene, and 35% had a mutated ubiquitin ligase complex gene, implicating frequent muta
157 in3 (CUL3), a core protein for the CUL3-RING ubiquitin ligase complex, has been reported to be a tumo
158        However, no substrates of RhoBTB-Cul3 ubiquitin ligase complexes have been identified.
159                             Cullin-dependent ubiquitin ligase complexes have been proposed to undergo
160 creen to find new targets of the E6/E6-AP E3 ubiquitin ligase complex identified NFX1.
161  still assemble with Keap1 into a functional ubiquitin ligase complex in vitro.
162 omotes the function of SCF-type cullin-based ubiquitin ligase complexes in vivo.
163 1 also interacts with CUL3, a constituent of ubiquitin ligase complexes in which we propose that ETO1
164 nes with the Gene Ontology term 'cullin-RING ubiquitin ligase complex' in the TQ-r module.
165 ncode several components involved in the SCF ubiquitin ligase complex including a viral Skp1 homolog.
166 tin with Bmi-1, a component of the hPRC1L E3 ubiquitin ligase complex, increases monoubiquityl histon
167 ile this is dependent on the DCAF1/DDB1/CUL4 ubiquitin ligase complex, interaction with human DCAF1 d
168                                      This E3 ubiquitin ligase complex is recruited to Dishevelled in
169                        The Ddb1-Cul4(Cdt)(2) ubiquitin ligase complex is required for degradation of
170 y conserved Highwire (Hiw)/Drosophila Fsn E3 ubiquitin ligase complex is required for normal synaptic
171 ne-bound HMG-CoA reductase degradation (HRD) ubiquitin-ligase complex is a key player of the ER-assoc
172 main (which in mammals, interacts with an E3 ubiquitin ligase complex) is not essential for the inhib
173 ncodes a core component of a cullin-based E3 ubiquitin ligase complex, is overexpressed in breast and
174 a substrate receptor of the Cullin 4 RING E3 ubiquitin ligase complex, is the target of the immunomod
175 ity of the DDB2-DDB1-Cul4A-Roc1 (CRL4(DDB2)) ubiquitin ligase complex, leading to efficient XPC recru
176  von Hippel Lindau protein elongin B/C (VCB) ubiquitin ligase complex, leading to HIF-alpha degradati
177  CP110 is ubiquitylated by the SCF(Cyclin F) ubiquitin ligase complex, leading to its degradation.
178   We identified the CRL2(LRR1) (cullin2 RING ubiquitin ligase complex/leucine-rich repeat protein 1)
179 actions with the cellular DCAF1-DDB1-CUL4 E3 ubiquitin ligase complex limit activation of innate immu
180 hich binds to the Von-Hippel-Lindau (VHL) E3 ubiquitin ligase complex, linked to either dihydroxytest
181      The SCF(FBXO31) (Skp1-Cul1-Rbx1-FBXO31) ubiquitin ligase complex mediates genotoxic stress-induc
182 ow that ASB2, a component of the ECS(ASB) E3 ubiquitin ligase complex, mediates MLL degradation throu
183                     Skp1-Cul1-F-box (SCF) E3 ubiquitin ligase complexes modulate the accumulation of
184                     Thus, the SCF(FBXO17) E3 ubiquitin ligase complex negatively regulates inflammati
185    Here, we demonstrate that NSs requires E3 ubiquitin ligase complexes of the SCF (Skp1, Cul1, F-box
186 le to interact with either the DCAF1/DDB1 E3 ubiquitin ligase complex or a host factor hypothesized t
187 1 and other members of the SCF(beta-TrCP1)E3 ubiquitin ligase complex or overexpression of a dominant
188 l player in the pathway is a multisubunit E3 ubiquitin ligase complex or the FA core complex, which m
189 ate-binding component of the muscle-specific ubiquitin ligase complex Ozz-E3.
190        Here we report that the SCF(Cyclin F) ubiquitin ligase complex prevents DNA re-replication by
191 t-containing protein, a component of the SCF ubiquitin ligase complex, previously shown to be require
192     We found previously that the PALL-SCF E3-ubiquitin ligase complex promotes apoptotic cell clearan
193               We show that the CRL4(Cdt2) E3 ubiquitin ligase complex promotes PCNA monoubiqutination
194                               The DDB1-Cul4A ubiquitin ligase complex promotes protein ubiquitination
195 iments substantiated that the SPOP/CUL3/Rbx1 ubiquitin ligase complex promotes SRC-3 turnover.
196                 DDB1, a component of a Cul4A ubiquitin ligase complex, promotes nucleotide excision r
197                DDB1, a component of the Cul4 ubiquitin ligase complex, promotes protein ubiquitinatio
198                                        Among ubiquitin ligase complex proteins, Cul1, KPC1, and KPC2
199  of the Skp-Cullin-F-box-containing (SCF) E3 ubiquitin ligase complex, recognizes the NF-kappaB inhib
200 ator of the cullin ring ligase 4-cereblon E3 ubiquitin ligase complex, reduces Aiolos and Ikaros prot
201 d8 modifications from the Cullin subunits of ubiquitin ligase complexes, reducing their activity.
202 f Dishevelled demonstrates that two distinct ubiquitin ligase complexes regulate the Wnt-beta-catenin
203 r, these findings suggest that the SCF(Cdc4) ubiquitin ligase complex regulates Clb6 turnover and tha
204                                      The SCF ubiquitin ligase complex regulates diverse cellular func
205 her, our data indicates that a CUL3-SPOPL E3 ubiquitin ligase complex regulates endocytic trafficking
206 epeat protein2 (FBL2), a component of the E3 ubiquitin ligase complex, regulates amyloid precursor pr
207 e canonical SCF (Skp1, Cullin1, F-box, Rbx1) ubiquitin ligase complex remain unchanged and show littl
208 in (SCF) and Cul4-RING protein ligase (CRL4) ubiquitin ligase complexes, respectively.
209 F3, IRF5, and IRF7) or a component of the E3 ubiquitin ligase complex responsible for activating NF-k
210 ng protein) (SCF(Slimb/beta-TrCP)) as the E3 ubiquitin ligase complex responsible for Ex degradation.
211     We have also purified a novel Cul4A-DDB1 ubiquitin ligase complex responsible for PNKP ubiquityla
212                  Loading of Merlin to the E3 ubiquitin ligase complex resulted in its polyubiquitinat
213 OP, an adaptor protein of the Cullin-RING E3 ubiquitin ligase complex, resulting in rapid ubiquitinat
214 ide evidence to support the idea that the E3 ubiquitin ligase complex RNF8-UBC13 functions independen
215 rolled, partly through ubiquitination by the ubiquitin ligase complex SCF(cyclin F) during G2 and M p
216               CKS1 acts as a cofactor to the ubiquitin ligase complex SCF(SKP2) to promote degradatio
217  by cdk2 and on the Skp1/Cul1/F-box (SCF) E3 ubiquitin ligase complex SCF(Skp2), which targets MEF fo
218 d protein 2 (SKP2), the F-box subunit of the ubiquitin-ligase complex SCF(SKP2) that targets proteins
219 riole overduplication and is mediated by the ubiquitin-ligase complex SCF(Slimb/betaTrCP).
220 A transcriptional repressor proteins and the ubiquitin-ligase complex SCF(TIR1), thus targeting for t
221 ucine (JA-Ile) and as the component of an E3-ubiquitin ligase complex (SCF(COI1) ) that targets JAZ t
222     Here, we show that the Skp1-CUL1-Fbw7 E3 ubiquitin ligase complex (SCF(Fbw7)) targets KLF5 for ub
223 -box domain with members of a Cullin-1-based ubiquitin ligase complex (SCF): Cullin-1 and SkpA.
224 yBP/SIP or SIP), a subunit of an SCF-like E3 ubiquitin ligase complex (SCF-TBL1) formed under genotox
225 YAP1 stability through downregulation of the ubiquitin ligase complex substrate recognition factors S
226  system to the substrate-specific arm of SCF ubiquitin ligase complexes, suggesting a role in SCF ass
227 s substrate adaptors in a CUL3(BOP1/BOP2) E3 ubiquitin ligase complex, targeting PIF4 proteins for ub
228 y the Keap1-Cullin3/RING box1 (Cul3-Rbx1) E3 ubiquitin ligase complex targets Nrf2 for proteasomal de
229 the substrate recognition component of an E3 ubiquitin ligase complex, targets DMRT1 for degradation
230  protein (Spop), part of the Cullin-3 (Cul3) ubiquitin ligase complex, targets Gli2 and Gli3 for degr
231 r is coordinated through the SKP1-Cul1-F-box ubiquitin ligase complex that contains cullin 1 and the
232 ted by degradation mediated by a CUL-2-based ubiquitin ligase complex that contains FEM-1 as the subs
233 gradation by a SKP1-CUL1-F-box protein (SCF) ubiquitin ligase complex that contains the orphan F-box
234 closome (APC/C) is a multiprotein subunit E3 ubiquitin ligase complex that controls segregation of ch
235 s, we focused our attention on the SCF(Skp2) ubiquitin ligase complex that controls the rate of degra
236 bstrate adaptor protein for a Cul3-dependent ubiquitin ligase complex that functions as a sensor for
237 in found in the Skp1/Cullin-1/F-box (SCF) E3 ubiquitin ligase complex that functions with the E2 ubiq
238 indau gene (VHL), a key component of the VHL ubiquitin ligase complex that has previously been associ
239   PHR proteins function, in part, through an ubiquitin ligase complex that includes the F-box protein
240                       Mms1 is part of the E3 ubiquitin ligase complex that is linked to replication f
241                    Cul3 and Rbx1 make up the ubiquitin ligase complex that is responsible for the ubi
242 he F-box protein beta-TrCP, a component of a ubiquitin ligase complex that mediates beta-catenin degr
243     We show here that Skp2, a component of a ubiquitin ligase complex that mediates the degradation o
244 teracts with beta-TrCP, a subunit of the SCF ubiquitin ligase complex that mediates the degradation o
245                  FBXL5 is a subunit of an E3 ubiquitin ligase complex that mediates the stability of
246 olecule of an elongin B/elongin C/cullin/Roc ubiquitin ligase complex that mediates the ubiquitinatio
247 L3) and cullin 3 (CUL3)] form a RING-type E3-ubiquitin ligase complex that modulates WNK1 and WNK4 ab
248 -box subunit of a Skp1-cullin-F-box (SCF) E3 ubiquitin ligase complex that positively regulates GA si
249 b55K and E4orf6 gene products assemble an E3 ubiquitin ligase complex that promotes degradation of ce
250 the SCF(Skp2-Cks1) (Skp1/Cul1/F-box protein) ubiquitin ligase complex that regulates entry into S pha
251                    pVHL forms part of the E3 ubiquitin ligase complex that regulates the degradation
252 s the central component of a multiprotein E3 ubiquitin ligase complex that targets beta-catenin for d
253  Hippel Lindau protein, a component of an E3 ubiquitin ligase complex that targets hydroxylated HIF-a
254 ity for the Skp1-Cullin1-F-box protein (SCF) ubiquitin ligase complex that targets multiple oncoprote
255 in-binding protein (CacyBP), a member of the ubiquitin ligase complex that targets nonphosphorylated
256 protein that is part of the SKP-1/Cul1/F-box ubiquitin ligase complex that targets nuclear p27 among
257 ein 2 (Skp2) is the F-box component of an E3 ubiquitin ligase complex that targets p27(Kip1) and cycl
258  mutated in kidney cancer and is part of the ubiquitin ligase complex that targets prolyl hydroxylate
259 FBXO11 is a component of the SKP1-CUL1-F-box ubiquitin ligase complex that targets proteins for ubiqu
260     The VHL gene product, pVHL, is part of a ubiquitin ligase complex that targets the alpha subunits
261 he protein TAZ, an adaptor protein in the E3 ubiquitin ligase complex that targets the ciliary protei
262 ty subunits of the Skp1-Cullin 1-F-box (SCF) ubiquitin ligase complex that targets these CDKI protein
263 ic cardiac hypertrophy by participating in a ubiquitin ligase complex that triggers degradation of ca
264 r an F-box-containing component of an SCF E3 ubiquitin ligase complex that was previously shown to ne
265 s of the SCF (Skp1-Cul1-Rbx1-F- box protein) ubiquitin ligase complexes that control the stability of
266     Mutations and deletions in components of ubiquitin ligase complexes that lead to alterations in p
267 ullin-RING ligases (CRLs) are a family of E3 ubiquitin ligase complexes that rely on either RING-box
268 onent of SCF (for SKP1-Cullin-F box protein) ubiquitin ligase complexes that target proteins for prot
269 We have identified in S. cerevisiae distinct ubiquitin-ligase complexes that define different ERAD pa
270 ons are regulated by a Cullin-3-Diablo/Kelch ubiquitin ligase complex, the activity of which is most
271 n the characterization of the mammalian gp78 ubiquitin ligase complex, the further elucidation of whi
272 ecial challenges to assembling cullin 1-RING ubiquitin ligase complexes through high affinity protein
273  interacts directly with betaTrCP in the SCF ubiquitin-ligase complex through two binding sites, whic
274  Vpr engages a DDB1- and cullin4A-containing ubiquitin-ligase complex through VprBP/DCAF1.
275 small recognition sequences of a specific E3 ubiquitin ligase complex to a known ligand for the recep
276 om A3G-mediated restriction by forming an E3-ubiquitin ligase complex to polyubiquitinate A3G and tri
277  elegans DRE-1/FBXO11 functions in an SCF E3-ubiquitin ligase complex to regulate the transition to a
278 rate adaptor protein for a Cul3-dependent E3 ubiquitin ligase complex to repress steady-state levels
279 ylate p16, priming the BMI1-containing PRC1L ubiquitin ligase complex to silence p16.
280 iral infectivity factor (Vif) form a CRL5 E3 ubiquitin ligase complex to suppress virus restriction b
281 lentivirus HIV-1 and SIV Vif proteins form a ubiquitin ligase complex to target host antiviral APOBEC
282 ates germination by causing the SCF(SLY1) E3 ubiquitin ligase complex to trigger ubiquitination and d
283 scaffold proteins that assemble multisubunit ubiquitin ligase complexes to confer substrate specifici
284 munodeficiency virus (SIV), and BIV all form ubiquitin ligase complexes to target host antiviral APOB
285  ASB2alpha, the specificity subunit of an E3-ubiquitin ligase complex, triggers acute proteasomal deg
286 are controlled by a cullin 1-containing E(3) ubiquitin ligase complex upon dual phosphorylation by ca
287                        A component of the E3 ubiquitin ligase complex, von Hippel-Lindau (VHL) facili
288  chemical inhibitors of proteins in the Hrd1 ubiquitin ligase complex, we demonstrate that the Sel1L,
289                               APC/C is an E3 ubiquitin ligase complex well characterized for its role
290 L3) and Cullin 3 (CUL3), components of an E3 ubiquitin ligase complex, were found to cause PHAII, sug
291                      CDC4/FBXW7 is part of a ubiquitin ligase complex which targets molecules such as
292  3 in the Kelch-like homologue 9-Cullin 3-E3 ubiquitin ligase complex, which is involved in ubiquitin
293 GENIC 1-SUPPRESSOR OF PHYA-105 1 (COP1-SPA1) ubiquitin ligase complex, which promotes turnover of CO.
294 ssociation of NIK with the cIAP1-cIAP2-TRAF2 ubiquitin ligase complex, which resulted in NIK stabiliz
295 ession of Skp2 and Cks1, subunits of the SCF ubiquitin ligase complex, which ubiquitinates p27(Kip1)
296 on subunits of SCF (Skp1-Cul1-F-box protein) ubiquitin ligase complexes, which mediate the timely pro
297         Keap1 assembles into a functional E3 ubiquitin ligase complex with Cul3 and Rbx1 that targets
298  a mechanism whereby Keap1, as part of an E3 ubiquitin ligase complex with Cul3 and Rbx1, facilitates
299 radation by linking the Elongin-BC-dependent ubiquitin ligase complex with the APOBEC3 proteins.
300  Caenorhabditis elegans RPM-1 functions in a ubiquitin ligase complex with the F-box protein FSN-1 an

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