IndraLab
Statements
reach
"USP33 promotes the generation of excessive centriolar foci due to elevated levels of CP110 because (1) over-expression of human or murine USP33 led to CP110 up-regulation in multiple cell lines (XREF_SUPPLEMENTARY) and (2) depletion of CP110 overrode USP33 mediated generation of centriolar foci (XREF_SUPPLEMENTARY)."
sparser
"The proteasome has both ubiquitin ligases and DUBs that associate with it (Crosas et al., 2006) , and several DUB-ligase pairs interact directly, including BRCC36-BRCA1, BAP1-BRCA1, USP4-Ro52, USP7-MDM2, USP8-GRAIL, USP20-pVHL, USP33-pVHL and USP44-APC (Kee and Huibregtse, 2007; Marfany and Denuc, 2008; Ventii and Wilkinson, 2008) ."
"In our previous studies, we have shown that VDU1 (pVHL-interacting deubiquitinating enzyme-1) can be ubiquitinated for rapid degradation in a pVHL-dependent manner"
"Finally, we demonstrate that VDU1 is able to be ubiquitinated via a pVHL-dependent pathway for proteasomal degradation, and VHL mutations that disrupt the interaction between VDU1 and pVHL abrogate the ubiquitination of VDU1"
USP33 affects cell population proliferation
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21
USP33 inhibits cell population proliferation.
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11
USP33 activates cell population proliferation.
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10
USP33 activates cell population proliferation. 10 / 10
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10
reach
"On the other hand, USP33 knock-down promoted cell proliferation and invasion under SDF-1 stimulation; whereas dynasore (an internalization inhibitor) pretreatment in USP33 silencing cells showed a distinct antipromoting effect, revealing the participation of CXCR4 internalization in regulating tumor progress."
sparser
"The proteasome has both ubiquitin ligases and DUBs that associate with it (Crosas et al., 2006) , and several DUB-ligase pairs interact directly, including BRCC36-BRCA1, BAP1-BRCA1, USP4-Ro52, USP7-MDM2, USP8-GRAIL, USP20-pVHL, USP33-pVHL and USP44-APC (Kee and Huibregtse, 2007; Marfany and Denuc, 2008; Ventii and Wilkinson, 2008) ."
USP33 affects Neoplasm Invasiveness
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1
16
USP33 inhibits Neoplasm Invasiveness.
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9
USP33 activates Neoplasm Invasiveness.
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1
7
USP33 activates Neoplasm Invasiveness. 8 / 8
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1
7
reach
"On the other hand, USP33 knock-down promoted cell proliferation and invasion under SDF-1 stimulation; whereas dynasore (an internalization inhibitor) pretreatment in USP33 silencing cells showed a distinct antipromoting effect, revealing the participation of CXCR4 internalization in regulating tumor progress."
MiR-365a-3p affects USP33
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10
MiR-365a-3p activates USP33.
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7
reach
"To further verify that miR-365a-3p directly targets and downregulates USP33, the wild-type 3 ' UTR of USP33 (WT USP33 3 ' UTR) or a mutated USP33 3 ' UTR (Mut USP33 3 ' UTR) was cloned into a dual-luciferase UTR vector and then co-transfected with agomiR-365 or a negative control (agomiR-NC) into A549 and SPC-A-1 cells."
MiR-365a-3p inhibits USP33.
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2
MiR-365a-3p binds USP33.
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1
USP33 affects Neoplasm Metastasis
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1
7
USP33 activates Neoplasm Metastasis.
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1
4
USP33 inhibits Neoplasm Metastasis.
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3
USP33 affects E7
5
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1
2
reach
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45] ."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45]."
USP33 is modified
2
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6
E7 affects USP33
5
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1
2
reach
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45] ."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45]."
reach
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL) - interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of beta-mercaptoethanol, which dissociates selenium, suggesting a selenium dependent interaction of SELENBP1 and VDU1."
sparser
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL)- interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of β-mercaptoethanol, which dissociates selenium (Jeong et al., xref ), suggesting a selenium dependent interaction of SELENBP1 and VDU1."
reach
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL) - interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of beta-mercaptoethanol, which dissociates selenium, suggesting a selenium dependent interaction of SELENBP1 and VDU1."
sparser
"SELENBP1 has also been implicated in ubiquitination from a study demonstrating the binding of SELENBP1 to von Hippel- Lindau protein (pVHL)- interacting deubiquitinating enzyme 1 (VDU1) that was abolished with the incubation of β-mercaptoethanol, which dissociates selenium (Jeong et al., xref ), suggesting a selenium dependent interaction of SELENBP1 and VDU1."
reach
"DIO2 works as a dimer that associates with Hedgehog inducible ubiquitin ligase WD repeat and SOCS box containing 1 (WSB-1) [XREF_BIBR], ubiquitin conjugases UBC6 and UBC-7 [XREF_BIBR], and DIO2 specific deubiquitinating enzymes ubiquitin specific peptidase 20 (USP20), and ubiquitin specific peptidase 33 (USP33) [XREF_BIBR]."
USP33 affects Slit-Robo
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6
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
Valproic acid affects USP33
4
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Valproic acid decreases the amount of USP33.
3
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Valproic acid increases the amount of USP33.
1
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USP33 affects cell migration
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3
USP33 activates cell migration.
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2
USP33 inhibits cell migration.
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1
USP33 inhibits cell migration. 1 / 1
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1
E3_Ub_ligase affects USP33
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3
1
E3_Ub_ligase ubiquitinates USP33.
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1
1
E3_Ub_ligase increases the amount of USP33.
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1
E3_Ub_ligase increases the amount of USP33. 1 / 1
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1
E3_Ub_ligase decreases the amount of USP33.
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1
E3_Ub_ligase decreases the amount of USP33. 1 / 1
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1
USP33 affects cell growth
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3
USP33 inhibits cell growth.
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2
USP33 activates cell growth.
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1
USP33 activates cell growth. 1 / 1
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1
USP33 affects Slit
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3
USP33 affects Robo1 receptor
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3
Robo1 receptor affects USP33
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3
Vinclozolin affects USP33
2
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Selenium atom affects USP33
1
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1
Selenium atom decreases the amount of USP33.
1
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Selenium atom binds USP33.
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1
Selenium atom binds USP33. 1 / 1
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1
MiR-206 affects USP33
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2
Dihydroartemisinin affects USP33
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2
Dihydroartemisinin decreases the amount of USP33. 2 / 2
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2
Copper atom affects USP33
2
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Copper atom increases the amount of USP33.
1
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Copper atom decreases the amount of USP33.
1
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Ubiquitin binds USP33.
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1
USP33 affects miR-206
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2
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2
USP33 affects glioma cell migration
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2
USP33 affects beta-arrestins
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2
USP33 affects beta-arrestin
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2
USP33 affects apoptotic process
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2
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45]."
USP33 affects Slit2-Robo1
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2
reach
"Several downstream effectors, including Abl [XREF_BIBR], Dock [XREF_BIBR], Ena (32), ERK1/2 [XREF_BIBR], small Rho GTPases [XREF_BIBR], USP33 [XREF_BIBR] and Vilse [XREF_BIBR], have been reported to mediate the inhibitory effect of Slit2-Robo1 signaling on cell motility, proliferation, apoptosis and angiogenesis in different cell types."
USP33 affects Hemagglutinins
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2
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
USP33 affects Cell Survival
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1
1
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45]."
Hemagglutinins affects USP33
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2
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [ xref ]."
sparser
"The Gaussia princeps luciferase protein complementation assay shows that USP15 interacts with the key oncoprotein human papillomavirus (HPV) E6, while USP29 and USP33 bind to E7 protein, suggesting that cellular DUBs impact HPV tumorigenesis by regulating the stability of the viral proteins [45]."
Vasopressin affects USP33
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1
Vasopressin activates USP33. 1 / 1
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1
Valdecoxib affects USP33
1
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Trichloroethene affects USP33
1
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Thapsigargin affects USP33
1
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Tetrachloromethane affects USP33
1
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Sulforaphane affects USP33
1
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SiUSP33#4 affects USP33
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1
Schizandrin B affects USP33
1
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Response to cold affects USP33
1
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Rapamycin treatment affects USP33
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1
Mono(2-ethylhexyl) phthalate affects USP33
1
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Mitochondrial DNA damage affects USP33
1
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"To better understand the consequences of mtDNA deletions, we microarrayed six cell types containing mtDNA deletions from KSS and CPEO patients. Indicated are transcripts shared and downregulated in cells harboring mtDNA deletions in >3 experiments (Table 4); Differentially expressed genes were identified by comparing GeneChips designated as baseline (muscles, myoblasts, fibroblasts, and lymphoblasts from healthy subjects, fusion control cell lines, and parental 143B cells) with the ones that represent the experimental parameters (muscles, myoblasts, fibroblasts, and lymphoblasts from patients, mutant cybrids, and 143B rho zero cells) using a difference in mean fluorescence ? 30 and a P value < 0.05; 37 downregulated genes; 26 upregulated genes;"
Methyl methanesulfonate affects USP33
1
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Methamphetamine affects USP33
1
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Lipopolysaccharide affects USP33
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1
Lipopolysaccharide activates USP33. 1 / 1
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1
Indometacin affects USP33
1
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Hydroxyurea affects USP33
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1
Hydroxyurea activates USP33. 1 / 1
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1
Hydroperoxide affects USP33
1
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Hydralazine affects USP33
1
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Hsa-miR-877-5p affects USP33
1
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Hsa-miR-148b-3p affects USP33
1
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Hsa-miR-1-3p affects USP33
1
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Gentamycin affects USP33
1
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Dicrotophos affects USP33
1
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Dexamethasone affects USP33
1
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Cyclosporin A affects USP33
1
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Copper(II) sulfate affects USP33
1
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Cobalt dichloride affects USP33
1
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Chlorpyrifos affects USP33
1
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Bisphenol F affects USP33
1
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Bisphenol A affects USP33
1
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Beta-Arr2 affects USP33
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1
Benzo[a]pyrene diol epoxide I affects USP33
1
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Aflatoxin M1 affects USP33
1
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YP_009227196 affects USP33
1
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USP33 affects β -AR recycling
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1
USP33 affects vasopressin receptor
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1
USP33 activates vasopressin receptor. 1 / 1
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1
USP33 affects type 2 deiodinase
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1
USP33 affects stability cellular ATF3 protein
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1
USP33 affects selenium atom
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1
Selenium atom binds USP33. 1 / 1
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1
USP33 affects proteolysis
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1
USP33 inhibits proteolysis. 1 / 1
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1
USP33 affects post-endocytic sorting receptor endosomes autophagosomes
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1
USP33 affects polyubiquitination
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1
USP33 affects pVHL-E3 ligase
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1
USP33 affects neuron migration
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1
USP33 activates neuron migration. 1 / 1
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1
USP33 affects miR-365a-3p
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1
USP33 affects miR-3591-5p
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1
USP33 affects lysosomal trafficking
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1
reach
"A first group is implicated in cell trafficking and endocytosis, such as the golgi protein Galntl4, Rabep1 (or rabaptin), implicated in endocytosis XREF_BIBR, XREF_BIBR, annexin A8 (Anxa 8) which directly regulates organization and function of the late endosome XREF_BIBR, XREF_BIBR, and the deubiquitinase USP33 which inhibits the lysosomal trafficking XREF_BIBR, XREF_BIBR."
USP33 affects iodothyronine deiodinase
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1
USP33 activates iodothyronine deiodinase. 1 / 1
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1
USP33 affects invasion metastasis cells
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1
USP33 affects hydroxyurea
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1
USP33 inhibits hydroxyurea. 1 / 1
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1
USP33 affects glycolytic process
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1
USP33 activates glycolytic process. 1 / 1
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1
USP33 affects fatty acid
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1
USP33 activates fatty acid. 1 / 1
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1
USP33 affects docetaxel anhydrous
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1
USP33 inhibits docetaxel anhydrous. 1 / 1
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1
USP33 affects colorectal57 breast58 cancer cell migration
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1
USP33 affects cellular component biogenesis
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1
USP33 activates cellular component biogenesis. 1 / 1
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1
USP33 affects cell activation
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1
USP33 activates cell activation. 1 / 1
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1
USP33 affects c-Myc ubiquitination
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1
USP33 affects c-Myc protein
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1
USP33 affects breast cancer cell migration
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1
USP33 affects beta2AR
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1
USP33 affects beta-Arr2
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1
USP33 affects anti-proliferation miR-206
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1
USP33 affects YP_009227196
1
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USP33 affects Ubiquitination
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1
USP33 inhibits Ubiquitination. 1 / 1
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1
USP33 affects Ubiquitin
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1
USP33 affects Slit Robo signaling pathway
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1
USP33 affects SCF cyclin
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1
USP33 affects Robo
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1
USP33 affects ROBO1 receptor
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1
USP33 affects Phosphatase
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1
USP33 deubiquitinates Phosphatase. 1 / 1
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1
USP33 affects Pancreatic Neoplasms
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1
USP33 activates Pancreatic Neoplasms. 1 / 1
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1
USP33 affects KO cells
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1
USP33 affects ISG75
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1
USP33 affects Glioblastoma
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1
USP33 inhibits Glioblastoma. 1 / 1
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1
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
USP33 affects ARs
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1
USP33 affects 7TMR
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1
USP20 affects ARs
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1
Slit2-Robo1 affects USP33
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1
Plant Extracts affects USP33
1
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NudCL2 KO affects USP33
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1
Norepinephrine affects USP33
1
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sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
sparser
"More recently, HERC2 was shown to interact with p53
through the
p53 tetramerization domain, thus affecting p53 oligomerization and
downstream transcriptional activity. xref HERC2
also interacts with the deubiquitinating enzyme USP33 and the SCF
protein FBXL5, regulating their stability through ubiquitin-mediated
proteasomal degradation. xref , xref HERC2 has also been
shown to regulate centrosome morphology and ubiquitin ligase activity
through interactions with NEURL4 and UBE3A (also known as E6AP), respectively."
Class A receptor affects USP33
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1
reach
"The association of USP33 and beta-arrestin 2 itself appears to be dependent on the class of 7TMR as activation of the beta2-adrenergic receptor (beta2AR), a Class A receptor known to have a transient interaction with beta-arrestins, enhances the association of beta-arrestin 2 with USP33 [XREF_BIBR]."
Arrestins affects USP33
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1
Aroclor 1254 affects USP33
1
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ARs affects USP33
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1
ARRB affects 7TMR
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1
AD-VDU1 f affects USP33
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1
7TMR affects USP33
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1
3-isobutyl-1-methyl-7H-xanthine affects USP33
1
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1
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(R)-noradrenaline affects USP33
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1
(R)-noradrenaline activates USP33. 1 / 1
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1
(+)-JQ1 compound affects USP33
1
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1
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