Deubiquitinase

Deubiquitinase

The proper regulation of apoptosis is essential for the survival of multicellular organisms. It has become clear that the post-translational modification of apoptotic proteins by ubiquitination regulates key components in cell death signaling cascades. Ubiquitination, which describes the covalent modification of target proteins with ubiquitin, has a profound bearing on the fate and function of its substrates and requires the enzymic activity of an E1, an E2 and an E3 protein (of which many subtypes are known to date). While ubiquitination, similarly to phosphorylation, is a reversible modification, in mammals, approximately 100 DUBs (EC 3.4.19.12) function to depolymerize and remove ubiquitin adducts as well. Human ubiquitin-specific protease 1 (USP1), which is associated with UAF1, has been identified as the deubiquitinase (DUB) responsible for deubiquitinating PCNA, FANCD2 and FANCI in the DNA damage response. USP1 is also required for the FANCD2 foci formation in both mouse and human cells. A high level of genomic instability has been linked to deficiency in human ATAD5 (the human ortholog of yeast Elg1), which mediates PCNA deubiquitination by USP1-UAF1. Together, these observations suggest that the DUB activity of USP1-UAF1 is important for the normal cellular response to DNA damage. USP7 and USP47 are two other examples of deubiquitination enzymes that assist in the highly complex processes that regulate apoptosis. USP7 (or HAUSP) is most popularly known as a direct antagonist of Mdm2, the E3 ubiquitin ligase for the p53 tumor suppressor protein. Similarly, USP47 was recently identified as a novel interactor of the E3 ubiquitin ligase SCFβ-Trcp. However, in contrast with the effects of USP7, USP47 depletion seems not to depend on p53 status.USP2 is a deubiquitinating enzyme (DUB) that removes ubiquitin thereby stabilizing a range of substrates, including MDM2 (a regulator of p53), fatty-acid synthase, cyclin D1, and proteins important for the circadian rhythm, such as CRY1. Moreover, USP2 is up-regulated in various cancers.

Read More
sort-descending
  • WP 1130
    1779
    WP 1130
    The price depends on the options chosen on the product page

    From $104.50

  • Eeyarestatin I
    1798
    Eeyarestatin I
    The price depends on the options chosen on the product page

    From $88.00

  • P 22077
    1906
    P 22077
    The price depends on the options chosen on the product page

    From $104.50

  • P 005091
    2011
    P 005091
    The price depends on the options chosen on the product page

    From $104.50

  • NSC 687852
    2228
    NSC 687852
    The price depends on the options chosen on the product page

    From $99.00

  • ML 323
    2309
    ML 323
    The price depends on the options chosen on the product page

    From $104.50

  • TCID
    2333
    TCID
    The price depends on the options chosen on the product page

    From $88.00

  • LDN 57444
    2449
    LDN 57444
    The price depends on the options chosen on the product page

    From $108.90

  • Spautin 1
    2512
    Spautin 1
    The price depends on the options chosen on the product page

    From $104.50

  • ML364
    2678
    ML364
    The price depends on the options chosen on the product page

    From $137.50

  • USP7-USP47 inhibitor
    2991
    USP7-USP47 inhibitor
    The price depends on the options chosen on the product page

    From $99.00

  • ML 367
    2995
    ML 367
    The price depends on the options chosen on the product page

    From $137.50

  • IU1-47
    3426
    IU1-47
    The price depends on the options chosen on the product page

    From $88.00

  • STD1T
    3608
    STD1T
    The price depends on the options chosen on the product page

    From $176.00

  • HBX 41,108
    3732
    HBX 41,108
    The price depends on the options chosen on the product page

    From $99.00

Items 1-15 of 21

More About Deubiquitinase

The proper regulation of apoptosis is essential for the survival of multicellular organisms. It has become clear that the post-translational modification of apoptotic proteins by ubiquitination regulates key components in cell death signaling cascades. Ubiquitination, which describes the covalent modification of target proteins with ubiquitin, has a profound bearing on the fate and function of its substrates and requires the enzymic activity of an E1, an E2 and an E3 protein (of which many subtypes are known to date). While ubiquitination, similarly to phosphorylation, is a reversible modification, in mammals, approximately 100 DUBs (EC 3.4.19.12) function to depolymerize and remove ubiquitin adducts as well.
Human ubiquitin-specific protease 1 (USP1), which is associated with UAF1, has been identified as the deubiquitinase (DUB) responsible for deubiquitinating PCNA, FANCD2 and FANCI in the DNA damage response. USP1 is also required for the FANCD2 foci formation in both mouse and human cells. A high level of genomic instability has been linked to deficiency in human ATAD5 (the human ortholog of yeast Elg1), which mediates PCNA deubiquitination by USP1-UAF1. Together, these observations suggest that the DUB activity of USP1-UAF1 is important for the normal cellular response to DNA damage[1]. USP7 and USP47 are two other examples of deubiquitination enzymes that assist in the highly complex processes that regulate apoptosis[2]. USP7 (or HAUSP) is most popularly known as a direct antagonist of Mdm2, the E3 ubiquitin ligase for the p53 tumor suppressor protein[3]. Similarly, USP47 was recently identified as a novel interactor of the E3 ubiquitin ligase SCFβ-Trcp. However, in contrast with the effects of USP7, USP47 depletion seems not to depend on p53 status[4].
USP2 is a deubiquitinating enzyme (DUB) that removes ubiquitin thereby stabilizing a range of substrates, including MDM2 (a regulator of p53), fatty-acid synthase, cyclin D1, and proteins important for the circadian rhythm, such as CRY1. Moreover, USP2 is up-regulated in various cancers.[5]

[1] Q. Liang et al.A selective USP1-UAF1 inhibitor links deubiquitination toDNA damage responses. Nat Chem. Biol. 2014, 10, 298-304.
[2] Ubiquitylation in apoptosis: a post-translational modification at the edge of life and death. D. Vucic, V.M. Dixit, I.E. Wertz. Nat. Rev. Mol. Cell Biol. 2011, 12, 439-452.
[3] M. Li, D. Chen, A. Shiloh, J. Luo, A.Y. Nikolaev, J. Qin, W. Gu. Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilization. Nature 2002, 416, 648-653.
[4] The ubiquitin-specific protease USP47 is a novel β-TRCP interactor regulating cell survival. A. Peschiaroli, J.R. Skaar, M. Pagano, G. Melino. Oncogene 2010, 29, 1384-1393.
[5] M.I. Davis et al. Small Molecule Inhibition of the Ubiquitin-specific Protease USP2 Accelerates cyclin D1 Degradation and Leads to Cell Cycle Arrest in Colorectal Cancer and Mantle Cell Lymphoma Models. J. Biol. Chem. 2016, 291(47), 24628-24640.

Loading...