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stub1  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc stub1
    A) Predominant subcellular localization of the QC E3 ligases and reporters used in this study. Dark and light blue represent strong or circumstantial localization evidence in the indicated compartment, respectively, while white indicates no evidence. Data for subcellular localization of E3 ligases was determined through Human Protein Atlas, Uniprot annotations, and existing literature. <t>STUB1,</t> UBE2O, and UBR4 have been reported to localize to both the cytosol and nucleus, whereas UBR5 and HUWE1 are primarily nuclear (Go et al., 2021; Kim et al., 2018; Mashtalir et al., 2014; Tasaki et al., 2013). Subcellular localization of the reporters was determined by microscopy in a previous study (Baker et al., 2025). B) Western blots of indicated E3 ligase KO cells along with the parental HEK293T cells (HEK). * = indicates unspecific band. HUWE1 KO clones were a gift from Yihong Ye’s lab (Xu et al., 2016). C) Schematic of bicistronic fluorescent reporter construct used in D). D) Log 2 (EGFP/DsRed) levels of the missense mutant reporters and corresponding WT in STUB1 KO cells. Three independent KO clones of STUB1 were used. Results from a one-way ANOVA test are shown with the mean and standard deviation (n=3-9, p > 0.05 = ns). E) Schematic of bicistronic fluorescent reporter used in F-J. F) Log 2 (mClover2/RFP) of the mutant reporter and corresponding WT in HEK293T cells. Results from an unpaired t-test are shown with the mean and standard deviation (n=3; **** p < 0.0001). G-I) Log 2 (mClover2/RFP) of the missense mutant reporters CBS L456P, GNMT H177N, and TPMT A80P expressed in (G) UBR4, (H) UBR5 and (I) HUWE1 WT and KO clone(s). Results from an unpaired t-test are shown with the mean and standard deviation (n=3; p > 0.05 = ns, * p < 0.05, ** p <0.01, *** p < 0.001). J) Density plot of the Log 2 (mClover2/RFP) signal of CBS L456P, GNMT H177N, and TPMT A80P in UBE2O WT and KO clones (n=1).
    Stub1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/stub1/pmc13069449-98-3-4?v=Cell+Signaling+Technology+Inc
    Average 86 stars, based on 1 article reviews
    stub1 - by Bioz Stars, 2026-07
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    Images

    1) Product Images from "Turnover of missense mutant cytosolic proteins proceeds in the absence of major quality control E3 ligases"

    Article Title: Turnover of missense mutant cytosolic proteins proceeds in the absence of major quality control E3 ligases

    Journal: microPublication Biology

    doi: 10.17912/micropub.biology.001990

    A) Predominant subcellular localization of the QC E3 ligases and reporters used in this study. Dark and light blue represent strong or circumstantial localization evidence in the indicated compartment, respectively, while white indicates no evidence. Data for subcellular localization of E3 ligases was determined through Human Protein Atlas, Uniprot annotations, and existing literature. STUB1, UBE2O, and UBR4 have been reported to localize to both the cytosol and nucleus, whereas UBR5 and HUWE1 are primarily nuclear (Go et al., 2021; Kim et al., 2018; Mashtalir et al., 2014; Tasaki et al., 2013). Subcellular localization of the reporters was determined by microscopy in a previous study (Baker et al., 2025). B) Western blots of indicated E3 ligase KO cells along with the parental HEK293T cells (HEK). * = indicates unspecific band. HUWE1 KO clones were a gift from Yihong Ye’s lab (Xu et al., 2016). C) Schematic of bicistronic fluorescent reporter construct used in D). D) Log 2 (EGFP/DsRed) levels of the missense mutant reporters and corresponding WT in STUB1 KO cells. Three independent KO clones of STUB1 were used. Results from a one-way ANOVA test are shown with the mean and standard deviation (n=3-9, p > 0.05 = ns). E) Schematic of bicistronic fluorescent reporter used in F-J. F) Log 2 (mClover2/RFP) of the mutant reporter and corresponding WT in HEK293T cells. Results from an unpaired t-test are shown with the mean and standard deviation (n=3; **** p < 0.0001). G-I) Log 2 (mClover2/RFP) of the missense mutant reporters CBS L456P, GNMT H177N, and TPMT A80P expressed in (G) UBR4, (H) UBR5 and (I) HUWE1 WT and KO clone(s). Results from an unpaired t-test are shown with the mean and standard deviation (n=3; p > 0.05 = ns, * p < 0.05, ** p <0.01, *** p < 0.001). J) Density plot of the Log 2 (mClover2/RFP) signal of CBS L456P, GNMT H177N, and TPMT A80P in UBE2O WT and KO clones (n=1).
    Figure Legend Snippet: A) Predominant subcellular localization of the QC E3 ligases and reporters used in this study. Dark and light blue represent strong or circumstantial localization evidence in the indicated compartment, respectively, while white indicates no evidence. Data for subcellular localization of E3 ligases was determined through Human Protein Atlas, Uniprot annotations, and existing literature. STUB1, UBE2O, and UBR4 have been reported to localize to both the cytosol and nucleus, whereas UBR5 and HUWE1 are primarily nuclear (Go et al., 2021; Kim et al., 2018; Mashtalir et al., 2014; Tasaki et al., 2013). Subcellular localization of the reporters was determined by microscopy in a previous study (Baker et al., 2025). B) Western blots of indicated E3 ligase KO cells along with the parental HEK293T cells (HEK). * = indicates unspecific band. HUWE1 KO clones were a gift from Yihong Ye’s lab (Xu et al., 2016). C) Schematic of bicistronic fluorescent reporter construct used in D). D) Log 2 (EGFP/DsRed) levels of the missense mutant reporters and corresponding WT in STUB1 KO cells. Three independent KO clones of STUB1 were used. Results from a one-way ANOVA test are shown with the mean and standard deviation (n=3-9, p > 0.05 = ns). E) Schematic of bicistronic fluorescent reporter used in F-J. F) Log 2 (mClover2/RFP) of the mutant reporter and corresponding WT in HEK293T cells. Results from an unpaired t-test are shown with the mean and standard deviation (n=3; **** p < 0.0001). G-I) Log 2 (mClover2/RFP) of the missense mutant reporters CBS L456P, GNMT H177N, and TPMT A80P expressed in (G) UBR4, (H) UBR5 and (I) HUWE1 WT and KO clone(s). Results from an unpaired t-test are shown with the mean and standard deviation (n=3; p > 0.05 = ns, * p < 0.05, ** p <0.01, *** p < 0.001). J) Density plot of the Log 2 (mClover2/RFP) signal of CBS L456P, GNMT H177N, and TPMT A80P in UBE2O WT and KO clones (n=1).

    Techniques Used: Mutagenesis, Microscopy, Western Blot, Clone Assay, Construct, Standard Deviation



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    Image Search Results


    A) Predominant subcellular localization of the QC E3 ligases and reporters used in this study. Dark and light blue represent strong or circumstantial localization evidence in the indicated compartment, respectively, while white indicates no evidence. Data for subcellular localization of E3 ligases was determined through Human Protein Atlas, Uniprot annotations, and existing literature. STUB1, UBE2O, and UBR4 have been reported to localize to both the cytosol and nucleus, whereas UBR5 and HUWE1 are primarily nuclear (Go et al., 2021; Kim et al., 2018; Mashtalir et al., 2014; Tasaki et al., 2013). Subcellular localization of the reporters was determined by microscopy in a previous study (Baker et al., 2025). B) Western blots of indicated E3 ligase KO cells along with the parental HEK293T cells (HEK). * = indicates unspecific band. HUWE1 KO clones were a gift from Yihong Ye’s lab (Xu et al., 2016). C) Schematic of bicistronic fluorescent reporter construct used in D). D) Log 2 (EGFP/DsRed) levels of the missense mutant reporters and corresponding WT in STUB1 KO cells. Three independent KO clones of STUB1 were used. Results from a one-way ANOVA test are shown with the mean and standard deviation (n=3-9, p > 0.05 = ns). E) Schematic of bicistronic fluorescent reporter used in F-J. F) Log 2 (mClover2/RFP) of the mutant reporter and corresponding WT in HEK293T cells. Results from an unpaired t-test are shown with the mean and standard deviation (n=3; **** p < 0.0001). G-I) Log 2 (mClover2/RFP) of the missense mutant reporters CBS L456P, GNMT H177N, and TPMT A80P expressed in (G) UBR4, (H) UBR5 and (I) HUWE1 WT and KO clone(s). Results from an unpaired t-test are shown with the mean and standard deviation (n=3; p > 0.05 = ns, * p < 0.05, ** p <0.01, *** p < 0.001). J) Density plot of the Log 2 (mClover2/RFP) signal of CBS L456P, GNMT H177N, and TPMT A80P in UBE2O WT and KO clones (n=1).

    Journal: microPublication Biology

    Article Title: Turnover of missense mutant cytosolic proteins proceeds in the absence of major quality control E3 ligases

    doi: 10.17912/micropub.biology.001990

    Figure Lengend Snippet: A) Predominant subcellular localization of the QC E3 ligases and reporters used in this study. Dark and light blue represent strong or circumstantial localization evidence in the indicated compartment, respectively, while white indicates no evidence. Data for subcellular localization of E3 ligases was determined through Human Protein Atlas, Uniprot annotations, and existing literature. STUB1, UBE2O, and UBR4 have been reported to localize to both the cytosol and nucleus, whereas UBR5 and HUWE1 are primarily nuclear (Go et al., 2021; Kim et al., 2018; Mashtalir et al., 2014; Tasaki et al., 2013). Subcellular localization of the reporters was determined by microscopy in a previous study (Baker et al., 2025). B) Western blots of indicated E3 ligase KO cells along with the parental HEK293T cells (HEK). * = indicates unspecific band. HUWE1 KO clones were a gift from Yihong Ye’s lab (Xu et al., 2016). C) Schematic of bicistronic fluorescent reporter construct used in D). D) Log 2 (EGFP/DsRed) levels of the missense mutant reporters and corresponding WT in STUB1 KO cells. Three independent KO clones of STUB1 were used. Results from a one-way ANOVA test are shown with the mean and standard deviation (n=3-9, p > 0.05 = ns). E) Schematic of bicistronic fluorescent reporter used in F-J. F) Log 2 (mClover2/RFP) of the mutant reporter and corresponding WT in HEK293T cells. Results from an unpaired t-test are shown with the mean and standard deviation (n=3; **** p < 0.0001). G-I) Log 2 (mClover2/RFP) of the missense mutant reporters CBS L456P, GNMT H177N, and TPMT A80P expressed in (G) UBR4, (H) UBR5 and (I) HUWE1 WT and KO clone(s). Results from an unpaired t-test are shown with the mean and standard deviation (n=3; p > 0.05 = ns, * p < 0.05, ** p <0.01, *** p < 0.001). J) Density plot of the Log 2 (mClover2/RFP) signal of CBS L456P, GNMT H177N, and TPMT A80P in UBE2O WT and KO clones (n=1).

    Article Snippet: Primary antibodies used: STUB1 (Cell Signalling 2080S, 1:1000 dilution), UBE2O (Millipore Sigma HPA023605 1:1000), UBR4 (abcam ab86738, 1:1000), UBR5 (Cell Signalling D608Z, 1:1000), HUWE1 (Bethyl A300-486A, 1:1000), g-Tubulin (Sigma T6557, 1:5000), GAPDH (UBC AbLab Mouse, 1:10,000).

    Techniques: Mutagenesis, Microscopy, Western Blot, Clone Assay, Construct, Standard Deviation

    ALDH1L1 inhibits PEDV replication via the E3 ubiquitin ligase STUB1. ( A ) After HEK 293T cells were cotransfected with plasmids encoding HA-STUB1 and Flag-ALDH1L1, the Co-IP assay was performed using anti-Flag-bound beads. ( B ) After HEK 293T cells were transfected with plasmids coding Flag-ALDH1L1, Co-IP assays were performed using an anti-Flag antibody. ( C ) After inducing GST-STUB1 and ALDH1L1 expression in the BL21(DE3) strain, the interaction between ALDH1L1 and STUB1 was examined via the GST pull-down assay. ( D ) After cotransfecting HeLa cells with Flag-ALDH1L1 and STUB1-HA for 24 h via incubation with an anti-Flag Mab, ALDH1L1 and STUB1 colocalization was confirmed via confocal immunofluorescence microscopy. Scale bars = 100 µm. ( E and F ) After cotransfection with Myc-ALDH1L1, HA-Ub, HA-STUB1, and Flag-N, or Flag-E, HEK 293T cells were treated with CQ and collected. The ubiquitinated N and E proteins were subjected to western blotting after immunoprecipitation with an anti-Flag antibody. ( G and H ) After cotransfecting HEK 293T cells with siRNAs (negative control or STUBA siRNA) and HA-N or HA-E and Flag-ALDH1L1-coding plasmids, western blotting was performed with an anti-HA antibody.

    Journal: Journal of Virology

    Article Title: ALDH1L1 suppresses the replication of porcine epidemic diarrhea virus by degrading viral nucleocapsid and envelope proteins

    doi: 10.1128/jvi.01933-25

    Figure Lengend Snippet: ALDH1L1 inhibits PEDV replication via the E3 ubiquitin ligase STUB1. ( A ) After HEK 293T cells were cotransfected with plasmids encoding HA-STUB1 and Flag-ALDH1L1, the Co-IP assay was performed using anti-Flag-bound beads. ( B ) After HEK 293T cells were transfected with plasmids coding Flag-ALDH1L1, Co-IP assays were performed using an anti-Flag antibody. ( C ) After inducing GST-STUB1 and ALDH1L1 expression in the BL21(DE3) strain, the interaction between ALDH1L1 and STUB1 was examined via the GST pull-down assay. ( D ) After cotransfecting HeLa cells with Flag-ALDH1L1 and STUB1-HA for 24 h via incubation with an anti-Flag Mab, ALDH1L1 and STUB1 colocalization was confirmed via confocal immunofluorescence microscopy. Scale bars = 100 µm. ( E and F ) After cotransfection with Myc-ALDH1L1, HA-Ub, HA-STUB1, and Flag-N, or Flag-E, HEK 293T cells were treated with CQ and collected. The ubiquitinated N and E proteins were subjected to western blotting after immunoprecipitation with an anti-Flag antibody. ( G and H ) After cotransfecting HEK 293T cells with siRNAs (negative control or STUBA siRNA) and HA-N or HA-E and Flag-ALDH1L1-coding plasmids, western blotting was performed with an anti-HA antibody.

    Article Snippet: Anti-ACTB/β-actin antibody (66009-1-Ig), anti-GST antibody (HRP-66001), anti-STUB1 antibody (68407-1-Ig), anti-TOLLIP antibody (68170-1-Ig), horseradish peroxidase-labeled anti-rabbit and mouse antibodies, and IgG antibodies (SA00001-1, SA00001-2) were supplied by Proteintech.

    Techniques: Ubiquitin Proteomics, Co-Immunoprecipitation Assay, Transfection, Expressing, Pull Down Assay, Incubation, Immunofluorescence, Microscopy, Cotransfection, Western Blot, Immunoprecipitation, Negative Control

    Antiviral mechanism by which ALDH1L1 inhibits PEDV replication. During infection with PEDV, ALDH1L1 interacts with the E3 ubiquitin ligase STUB1 to ubiquitinate the PEDV N or E protein. Subsequently, it recruits the cargo receptor TOLLIP to recognize and autophagosomally transport ubiquitinated N or E protein for degradation.

    Journal: Journal of Virology

    Article Title: ALDH1L1 suppresses the replication of porcine epidemic diarrhea virus by degrading viral nucleocapsid and envelope proteins

    doi: 10.1128/jvi.01933-25

    Figure Lengend Snippet: Antiviral mechanism by which ALDH1L1 inhibits PEDV replication. During infection with PEDV, ALDH1L1 interacts with the E3 ubiquitin ligase STUB1 to ubiquitinate the PEDV N or E protein. Subsequently, it recruits the cargo receptor TOLLIP to recognize and autophagosomally transport ubiquitinated N or E protein for degradation.

    Article Snippet: Anti-ACTB/β-actin antibody (66009-1-Ig), anti-GST antibody (HRP-66001), anti-STUB1 antibody (68407-1-Ig), anti-TOLLIP antibody (68170-1-Ig), horseradish peroxidase-labeled anti-rabbit and mouse antibodies, and IgG antibodies (SA00001-1, SA00001-2) were supplied by Proteintech.

    Techniques: Infection, Ubiquitin Proteomics