COPS2

Last updated
COPS2
Available structures
PDB Human UniProt search: PDBe RCSB
Identifiers
Aliases COPS2 , ALIEN, CSN2, SGN2, TRIP15, COP9 signalosome subunit 2
External IDs OMIM: 604508 HomoloGene: 134283 GeneCards: COPS2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004236
NM_001143887

n/a

RefSeq (protein)

NP_001137359
NP_004227

n/a

Location (UCSC) Chr 15: 49.11 – 49.16 Mb n/a
PubMed search [2] n/a
Wikidata
View/Edit Human

COP9 signalosome complex subunit 2 is a protein that in humans is encoded by the COPS2 gene. [3] [4] [5] It encodes a subunit of the COP9 signalosome.

Contents

Interactions

COPS2 has been shown to interact with:

Related Research Articles

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<span class="mw-page-title-main">DAX1</span> Protein-coding gene in humans

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<span class="mw-page-title-main">Methyl-CpG-binding domain protein 2</span> Protein-coding gene in the species Homo sapiens

Methyl-CpG-binding domain protein 2 is a protein that in humans is encoded by the MBD2 gene.

<span class="mw-page-title-main">COPS6</span> Protein-coding gene in humans

COP9 signalosome complex subunit 6 is a protein that in humans is encoded by the COPS6 gene.

<span class="mw-page-title-main">EIF3S6</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">COUP-TFI</span> Protein found in humans

COUP-TF1 also known as NR2F1 is a protein that in humans is encoded by the NR2F1 gene. This protein is a member of nuclear hormone receptor family of steroid hormone receptors.

<span class="mw-page-title-main">Thyroid hormone receptor alpha</span> Protein-coding gene in the species Homo sapiens

Thyroid hormone receptor alpha (TR-alpha) also known as nuclear receptor subfamily 1, group A, member 1 (NR1A1), is a nuclear receptor protein that in humans is encoded by the THRA gene.

<span class="mw-page-title-main">COP9 constitutive photomorphogenic homolog subunit 5</span> Protein-coding gene in the species Homo sapiens

COP9 constitutive photomorphogenic homolog subunit 5 (Arabidopsis), also known as COPS5 or Csn5, is a gene conserved from humans to Saccharomyces cerevisiae.

<span class="mw-page-title-main">PSME2</span> Protein found in humans

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<span class="mw-page-title-main">CUL2</span> Protein-coding gene in humans

Cullin-2 is a protein that in humans is encoded by the CUL2 gene.

<span class="mw-page-title-main">RBBP8</span> Protein-coding gene in the species Homo sapiens

Retinoblastoma-binding protein 8 is a protein that in humans is encoded by the RBBP8 gene.

<span class="mw-page-title-main">COP9 signalosome complex subunit 3</span> Protein-coding gene in the species Homo sapiens

COP9 signalosome complex subunit 3 is a protein that in humans is encoded by the COPS3 gene. It encodes a subunit of the COP9 signalosome.

<span class="mw-page-title-main">COPS4</span> Protein-coding gene in humans

COP9 signalosome complex subunit 4 is a protein that in humans is encoded by the COPS4 gene.

<span class="mw-page-title-main">COPS8</span> Protein-coding gene in humans

COP9 signalosome complex subunit 8 is a protein that in humans is encoded by the COPS8 gene.

<span class="mw-page-title-main">IRF8</span> Protein-coding gene in the species Homo sapiens

Interferon regulatory factor 8 (IRF8) also known as interferon consensus sequence-binding protein (ICSBP), is a protein that in humans is encoded by the IRF8 gene. IRF8 is a transcription factor that plays critical roles in the regulation of lineage commitment and in myeloid cell maturation including the decision for a common myeloid progenitor (CMP) to differentiate into a monocyte precursor cell.

<span class="mw-page-title-main">GPS1</span> Protein-coding gene in the species Homo sapiens

COP9 signalosome complex subunit 1 is a protein that in humans is encoded by the GPS1 gene.

<span class="mw-page-title-main">COPS7A</span> Protein-coding gene in humans

COP9 signalosome complex subunit 7a is a protein that in humans is encoded by the COPS7A gene.

<span class="mw-page-title-main">COPS7B</span> Protein-coding gene in humans

COP9 signalosome complex subunit 7b is a protein that in humans is encoded by the COPS7B gene.

<span class="mw-page-title-main">SAP130</span> Protein-coding gene in the species Homo sapiens

Histone deacetylase complex subunit SAP130 is an enzyme that in humans is encoded by the SAP130 gene.

<span class="mw-page-title-main">COP9 signalosome</span>

COP9 signalosome (CSN) is a protein complex with isopeptidase activity. It catalyses the hydrolysis of NEDD8 protein from the cullin subunit of Cullin-RING ubiquitin ligases (CRL). Therefore, it is responsible for CRL deneddylation – at the same time, it is able to bind denedyllated cullin-RING complex and retain them in deactivated form. COP9 signalosome thus serves as a sole deactivator of CRLs. The complex was originally identified in plants, and subsequently found in all eukaryotic organisms including human. Human COP9 signalosome consists of 8 subunits - CSN1, CSN2, CSN3, CSN4, CSN5, CSN6, CSN7, CSN8. All are essential for full function of the complex and mutation in some of them is lethal in mice.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000166200 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. Lee JW, Choi HS, Gyuris J, Brent R, Moore DD (July 1995). "Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor". Mol Endocrinol. 9 (2): 243–54. doi: 10.1210/mend.9.2.7776974 . PMID   7776974.
  4. Seeger M, Kraft R, Ferrell K, Bech-Otschir D, Dumdey R, Schade R, Gordon C, Naumann M, Dubiel W (April 1998). "A novel protein complex involved in signal transduction possessing similarities to 26S proteasome subunits". FASEB J. 12 (6): 469–78. doi: 10.1096/fasebj.12.6.469 . PMID   9535219. S2CID   25424324.
  5. "Entrez Gene: COPS2 COP9 constitutive photomorphogenic homolog subunit 2 (Arabidopsis)".
  6. Altincicek B, Tenbaum SP, Dressel U, Thormeyer D, Renkawitz R, Baniahmad A (March 2000). "Interaction of the corepressor Alien with DAX-1 is abrogated by mutations of DAX-1 involved in adrenal hypoplasia congenita". J. Biol. Chem. 275 (11): 7662–7. doi: 10.1074/jbc.275.11.7662 . PMID   10713076.
  7. Cohen H, Azriel A, Cohen T, Meraro D, Hashmueli S, Bech-Otschir D, Kraft R, Dubiel W, Levi BZ (December 2000). "Interaction between interferon consensus sequence-binding protein and COP9/signalosome subunit CSN2 (Trip15). A possible link between interferon regulatory factor signaling and the COP9/signalosome". J. Biol. Chem. 275 (50): 39081–9. doi: 10.1074/jbc.M004900200 . PMID   10991940.
  8. Akiyama H, Fujisawa N, Tashiro Y, Takanabe N, Sugiyama A, Tashiro F (March 2003). "The role of transcriptional corepressor Nif3l1 in early stage of neural differentiation via cooperation with Trip15/CSN2". J. Biol. Chem. 278 (12): 10752–62. doi: 10.1074/jbc.M209856200 . PMID   12522100.
  9. Dressel U, Thormeyer D, Altincicek B, Paululat A, Eggert M, Schneider S, Tenbaum SP, Renkawitz R, Baniahmad A (May 1999). "Alien, a highly conserved protein with characteristics of a corepressor for members of the nuclear hormone receptor superfamily". Mol. Cell. Biol. 19 (5): 3383–94. doi:10.1128/mcb.19.5.3383. PMC   84131 . PMID   10207062.

Further reading