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    UBXN6 UBX domain protein 6 [ Homo sapiens (human) ]

    Gene ID: 80700, updated on 3-Apr-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    UBX Domain Protein 6 Positively Regulates JAK-STAT1/2 Signaling.

    UBX Domain Protein 6 Positively Regulates JAK-STAT1/2 Signaling.
    Ketkar H, Harrison AG, Graziano VR, Geng T, Yang L, Vella AT, Wang P., Free PMC Article

    10/2/2021
    Structure of the PUB Domain from Ubiquitin Regulatory X Domain Protein 1 (UBXD1) and Its Interaction with the p97 AAA+ ATPase.

    Structure of the PUB Domain from Ubiquitin Regulatory X Domain Protein 1 (UBXD1) and Its Interaction with the p97 AAA+ ATPase.
    Blueggel M, van den Boom J, Meyer H, Bayer P, Beuck C., Free PMC Article

    09/19/2020
    In HIV-positive long-term non-progressors, a higher prevalence of Ala31Thr in UBXN6 was found within its N-terminal region

    Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals.
    Díez-Fuertes F, De La Torre-Tarazona HE, Calonge E, Pernas M, Bermejo M, García-Pérez J, Álvarez A, Capa L, García-García F, Saumoy M, Riera M, Boland-Auge A, López-Galíndez C, Lathrop M, Dopazo J, Sakuntabhai A, Alcamí J.

    07/4/2020
    UBXD1 as mitochondrial recruitment factor for p97 further connects the ubiquitin-proteasome system to Parkin-dependent mitophagy and underlines the close cooperation between the different mechanisms involved in mitochondrial maintenance.

    UBXD1 is a mitochondrial recruitment factor for p97/VCP and promotes mitophagy.
    Bento AC, Bippes CC, Kohler C, Hemion C, Frank S, Neutzner A., Free PMC Article

    10/26/2019
    These results indicate that the outer membrane protein MCL1 is degraded by the VCP-UBXD1 complex and that the process is promoted by the presence of mutant Huntingtin.

    VCP cooperates with UBXD1 to degrade mitochondrial outer membrane protein MCL1 in model of Huntington's disease.
    Guo X, Qi X., Free PMC Article

    12/22/2018
    Upon damage, p97 translocates to lysosomes and there cooperates with a distinct set of cofactors including UBXD1, PLAA, and the deubiquitinating enzyme YOD1, which we term ELDR components for Endo-Lysosomal Damage Response.

    VCP/p97 cooperates with YOD1, UBXD1 and PLAA to drive clearance of ruptured lysosomes by autophagy.
    Papadopoulos C, Kirchner P, Bug M, Grum D, Koerver L, Schulze N, Poehler R, Dressler A, Fengler S, Arhzaouy K, Lux V, Ehrmann M, Weihl CC, Meyer H., Free PMC Article

    07/15/2017
    UBXD1-N intercalates into the p97-ND1 interface, thereby modulating interdomain communication of p97 domains and its activity with relevance for disease pathogenesis

    The N-terminal Region of the Ubiquitin Regulatory X (UBX) Domain-containing Protein 1 (UBXD1) Modulates Interdomain Communication within the Valosin-containing Protein p97.
    Trusch F, Matena A, Vuk M, Koerver L, Knævelsrud H, Freemont PS, Meyer H, Bayer P., Free PMC Article

    04/23/2016
    Data indicate that endosomal trafficking of CAV1 depends on ubiquitination of the N-terminal region and the subsequent recruitment of VCP-UBXD1.

    Ubiquitination of the N-terminal region of caveolin-1 regulates endosomal sorting by the VCP/p97 AAA-ATPase.
    Kirchner P, Bug M, Meyer H., Free PMC Article

    05/4/2013
    UBXD1 modulates the trafficking of ERGIC-53-containing vesicles by controlling the interaction of transport factors with the cytoplasmic tail of ERGIC-53.

    Protein interaction profiling of the p97 adaptor UBXD1 points to a role for the complex in modulating ERGIC-53 trafficking.
    Haines DS, Lee JE, Beauparlant SL, Kyle DB, den Besten W, Sweredoski MJ, Graham RL, Hess S, Deshaies RJ., Free PMC Article

    10/13/2012
    Data show that expression of VCP mutant proteins, or siRNA-mediated depletion of UBXD1 leads to a block of CAV1 transport at the limiting membrane of enlarged endosomes in cultured cells.

    Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations.
    Ritz D, Vuk M, Kirchner P, Bug M, Schütz S, Hayer A, Bremer S, Lusk C, Baloh RH, Lee H, Glatter T, Gstaiger M, Aebersold R, Weihl CC, Meyer H., Free PMC Article

    12/10/2011
    these findings suggest that UBXD1 is a regulatory component of endoplasmic reticulum-associated degradation that may modulate the adaptor binding to VCP.

    UBXD1 is a VCP-interacting protein that is involved in ER-associated degradation.
    Nagahama M, Ohnishi M, Kawate Y, Matsui T, Miyake H, Yuasa K, Tani K, Tagaya M, Tsuji A.

    01/21/2010
    An additional p97 binding site in UBXD1 that competed with the p47 cofactor for binding to the N domain of p97 was identified.

    UBXD1 binds p97 through two independent binding sites.
    Kern M, Fernandez-Sáiz V, Schäfer Z, Buchberger A.

    01/21/2010
    UBXD1 is a novel co-factor of the human p97 ATPase.

    Ubxd1 is a novel co-factor of the human p97 ATPase.
    Madsen L, Andersen KM, Prag S, Moos T, Semple CA, Seeger M, Hartmann-Petersen R.

    01/21/2010
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