P61201
Gene name |
COPS2 (CSN2, TRIP15) |
Protein name |
COP9 signalosome complex subunit 2 |
Names |
SGN2, Signalosome subunit 2, Alien homolog, JAB1-containing signalosome subunit 2, Thyroid receptor-interacting protein 15, TR-interacting protein 15, TRIP-15 |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:9318 |
EC number |
|
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
13 structures for P61201
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 4D10 | X-ray | 380 A | B/J | 1-443 | PDB |
| 4D18 | X-ray | 408 A | B/J | 1-443 | PDB |
| 4WSN | X-ray | 550 A | B/J/R/Z/h/p | 1-443 | PDB |
| 6A73 | X-ray | 245 A | A/B | 29-162 | PDB |
| 6R6H | EM | 840 A | B | 1-443 | PDB |
| 6R7F | EM | 820 A | B | 1-443 | PDB |
| 6R7H | EM | 880 A | B | 30-443 | PDB |
| 6R7I | EM | 590 A | B | 1-443 | PDB |
| 6R7N | EM | 650 A | B | 1-443 | PDB |
| 8H38 | EM | 425 A | B | 1-443 | PDB |
| 8H3A | EM | 751 A | B | 1-443 | PDB |
| 8H3F | EM | 673 A | B | 1-443 | PDB |
| AF-P61201-F1 | Predicted | AlphaFoldDB |
126 variants for P61201
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
|
rs755145333 CA392454274 |
4 | M>L | No |
ClinGen ExAC gnomAD |
|
|
rs536586238 CA7551069 |
4 | M>T | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
CA7551070 rs755145333 |
4 | M>V | No |
ClinGen ExAC gnomAD |
|
|
rs757080604 CA7551067 |
9 | M>L | No |
ClinGen ExAC gnomAD |
|
|
CA392454158 rs1268578320 |
12 | D>E | No |
ClinGen TOPMed |
|
| rs1566888918 | 14 | E>missing | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs763856167 CA7551065 |
15 | D>E | No |
ClinGen ExAC |
|
|
rs1243867053 CA392454118 |
15 | D>V | No |
ClinGen gnomAD |
|
| TCGA novel | 16 | Y>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA7551064 rs755900606 |
17 | D>N | No |
ClinGen ExAC gnomAD |
|
|
rs1208008862 CA392453019 |
28 | P>A | No |
ClinGen TOPMed |
|
|
CA392453015 rs1340643217 |
28 | P>R | No |
ClinGen gnomAD |
|
|
rs751093881 CA7551041 |
31 | D>N | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 36 | Y>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs765862293 CA7551040 |
41 | A>T | No |
ClinGen ExAC gnomAD |
|
|
rs1488295405 CA392452801 |
45 | D>E | No |
ClinGen TOPMed |
|
|
CA392452781 rs1225323673 |
47 | P>A | No |
ClinGen gnomAD |
|
| TCGA novel | 49 | A>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA7551038 rs368659951 |
49 | A>V | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
| TCGA novel | 50 | A>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1442543054 CA392452711 |
52 | S>N | No |
ClinGen gnomAD |
|
|
CA392452684 rs1322055026 |
53 | S>N | No |
ClinGen gnomAD |
|
|
CA270190808 rs868430080 |
68 | G>* | No |
ClinGen Ensembl |
|
|
CA7551014 rs754387847 |
75 | M>I | No |
ClinGen ExAC gnomAD |
|
|
rs1241730917 CA392452480 |
79 | N>T | No |
ClinGen gnomAD |
|
|
rs111854025 CA270190790 |
80 | F>L | No |
ClinGen Ensembl |
|
|
CA392451689 rs1292541283 |
83 | T>A | No |
ClinGen TOPMed gnomAD |
|
|
rs1012786288 CA270187170 |
83 | T>K | No |
ClinGen TOPMed |
|
|
CA392451599 rs1271315556 |
90 | N>S | No |
ClinGen gnomAD |
|
|
COSM555294 rs1433446000 CA392451589 |
91 | R>T | lung Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] | No |
ClinGen cosmic curated NCI-TCGA gnomAD |
|
rs1391201034 CA392451474 |
100 | R>Q | No |
ClinGen TOPMed |
|
|
CA7550998 rs745372669 |
100 | R>W | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
|
rs1428898469 CA392451462 |
101 | S>T | No |
ClinGen TOPMed |
|
|
CA392451455 rs1168726113 |
102 | A>S | No |
ClinGen gnomAD |
|
| TCGA novel | 108 | S>Y | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 110 | K>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs961534479 CA270187067 |
112 | I>V | No |
ClinGen Ensembl |
|
| TCGA novel | 116 | L>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 117 | D>G | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA392451280 rs1268138380 |
118 | Y>C | No |
ClinGen TOPMed |
|
|
CA392451253 rs1361040987 |
120 | S>C | No |
ClinGen TOPMed |
|
|
CA392451233 rs1418483204 |
122 | S>F | No |
ClinGen gnomAD |
|
|
rs1162777362 CA392450918 |
125 | M>K | No |
ClinGen gnomAD |
|
|
CA392450846 rs1566883521 |
135 | T>S | No |
ClinGen Ensembl |
|
|
CA392450780 rs1480090014 |
144 | N>S | No |
ClinGen gnomAD |
|
|
CA392450719 rs1207048242 |
152 | N>K | No |
ClinGen gnomAD |
|
|
CA270185010 rs907944247 |
159 | Y>C | No |
ClinGen TOPMed gnomAD |
|
|
CA392450663 rs1317524775 |
159 | Y>H | No |
ClinGen gnomAD |
|
|
CA392450649 rs1302271098 |
161 | E>Q | No |
ClinGen gnomAD |
|
|
rs376675090 CA7550954 |
162 | R>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA270184996 rs376675090 |
162 | R>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
| TCGA novel | 171 | I>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1345232593 CA392450578 |
171 | I>V | No |
ClinGen gnomAD |
|
|
CA7550952 rs769174765 |
173 | R>C | No |
ClinGen ExAC gnomAD |
|
|
CA392450541 rs1429106377 |
176 | H>R | No |
ClinGen TOPMed gnomAD |
|
| TCGA novel | 176 | H>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1360968547 CA392450531 |
177 | Q>H | No |
ClinGen TOPMed |
|
| TCGA novel | 179 | C>W | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA7550930 rs762726219 |
189 | K>R | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 191 | G>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 191 | G>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 192 | T>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 207 | A>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA270182301 rs996466507 |
209 | K>R | No |
ClinGen TOPMed |
|
| TCGA novel | 211 | N>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 211 | N>missing | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA392449889 rs1167693947 |
216 | A>G | No |
ClinGen gnomAD |
|
|
rs1566882707 CA392449884 |
217 | L>V | No |
ClinGen Ensembl |
|
|
rs1291943803 CA392449496 |
250 | E>Q | No |
ClinGen gnomAD |
|
| TCGA novel | 254 | A>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 259 | F>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 260 | E>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1278623390 CA392449395 |
263 | K>R | No |
ClinGen gnomAD |
|
| TCGA novel | 265 | Y>H | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs749399929 CA7550899 |
274 | T>S | No |
ClinGen ExAC gnomAD |
|
|
CA392449315 rs1384326741 |
275 | T>A | No |
ClinGen TOPMed |
|
| TCGA novel | 279 | Y>H | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 286 | L>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs78807047 CA270181866 |
290 | G>E | No |
ClinGen Ensembl |
|
| TCGA novel | 297 | Q>G | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs758646732 CA270181700 |
300 | K>R | No |
ClinGen Ensembl |
|
|
CA392449087 rs1307746794 |
305 | D>N | No |
ClinGen TOPMed |
|
|
rs758202372 CA7550874 COSM701132 |
307 | E>Q | lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] | No |
ClinGen cosmic curated ExAC NCI-TCGA gnomAD |
|
rs750242581 CA7550873 |
311 | M>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs757068018 CA7550871 |
315 | V>I | No |
ClinGen ExAC gnomAD |
|
|
rs1357436726 CA392448804 |
318 | Y>H | No |
ClinGen gnomAD |
|
|
rs1314432566 CA392448786 |
319 | Q>P | No |
ClinGen gnomAD |
|
|
rs748242784 CA7550858 |
320 | N>S | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 325 | E>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 328 | K>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1439764650 CA392448695 |
329 | I>F | No |
ClinGen gnomAD |
|
|
rs1263479924 CA392448643 |
336 | N>S | No |
ClinGen TOPMed gnomAD |
|
| TCGA novel | 338 | M>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA270178726 rs941161855 |
339 | D>G | No |
ClinGen Ensembl |
|
|
rs866807621 CA270177686 |
350 | L>I | No |
ClinGen Ensembl |
|
|
CA270177676 rs959577363 |
352 | R>Q | No |
ClinGen gnomAD |
|
|
CA392448226 rs1420030674 |
360 | I>V | No |
ClinGen TOPMed |
|
| TCGA novel | 363 | I>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA270177641 rs1802452 |
367 | T>S | No |
ClinGen Ensembl |
|
| TCGA novel | 369 | I>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs773645165 CA7550842 |
372 | P>L | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 380 | I>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 380 | I>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1431531000 CA392447879 |
381 | D>E | No |
ClinGen TOPMed |
|
|
rs1311699082 CA392447642 |
396 | N>K | No |
ClinGen TOPMed |
|
|
rs747929203 CA7550810 |
397 | T>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs754590801 CA7550808 |
398 | I>V | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 401 | R>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 401 | R>Q | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs746513462 CA7550807 |
405 | V>L | No |
ClinGen ExAC gnomAD |
|
|
CA7550805 rs370391204 |
410 | E>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs1283495283 CA392447461 |
413 | H>D | No |
ClinGen TOPMed |
|
|
rs201832558 CA270176329 |
414 | Q>E | No |
ClinGen Ensembl |
|
|
rs765813477 CA7550803 |
416 | R>G | No |
ClinGen ExAC gnomAD |
|
|
rs1306438790 CA392447398 |
419 | A>E | No |
ClinGen TOPMed gnomAD |
|
|
rs1369277510 CA392447402 |
419 | A>S | No |
ClinGen gnomAD |
|
|
CA270176319 rs377183837 |
420 | R>P | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs377183837 CA7550801 |
420 | R>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs1204426065 CA392447368 |
423 | A>T | No |
ClinGen gnomAD |
|
|
rs1219622231 CA392447296 |
428 | T>A | No |
ClinGen gnomAD |
|
|
rs1271812497 CA392447273 |
430 | Q>E | No |
ClinGen gnomAD |
|
|
CA392447260 rs1284446087 |
431 | L>V | No |
ClinGen gnomAD |
|
|
rs767625268 CA7550797 |
432 | N>S | No |
ClinGen ExAC gnomAD |
|
|
rs143666055 CA7550796 |
434 | L>V | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs773157842 CA7550795 |
435 | N>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA7550794 rs769677428 |
439 | V>D | No |
ClinGen ExAC TOPMed gnomAD |
No associated diseases with P61201
1 regional properties for P61201
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Proteasome component (PCI) domain | 254 - 427 | IPR000717 |
5 GO annotations of cellular component
| Name | Definition |
|---|---|
| COP9 signalosome | A protein complex that catalyzes the deneddylation of proteins, including the cullin component of SCF ubiquitin E3 ligase; deneddylation increases the activity of cullin family ubiquitin ligases. The signalosome is involved in many regulatory process, including some which control development, in many species; also regulates photomorphogenesis in plants; in many species its subunits are highly similar to those of the proteasome. |
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
| nucleoplasm | That part of the nuclear content other than the chromosomes or the nucleolus. |
| nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| transcription corepressor activity | A transcription coregulator activity that represses or decreases the transcription of specific gene sets via binding to a DNA-bound DNA-binding transcription factor, either on its own or as part of a complex. Corepressors often act by altering chromatin structure and modifications. For example, one class of transcription corepressors modifies chromatin structure through covalent modification of histones. A second class remodels the conformation of chromatin in an ATP-dependent fashion. A third class modulates interactions of DNA-bound DNA-binding transcription factors with other transcription coregulators. |
12 GO annotations of biological process
| Name | Definition |
|---|---|
| inner cell mass cell proliferation | The proliferation of cells in the inner cell mass. |
| negative regulation of nucleic acid-templated transcription | Any process that stops, prevents or reduces the frequency, rate or extent of nucleic acid-templated transcription. |
| negative regulation of transcription by RNA polymerase II | Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II. |
| neuron differentiation | The process in which a relatively unspecialized cell acquires specialized features of a neuron. |
| protein deneddylation | The removal of a ubiquitin-like protein of the NEDD8 type from a protein. |
| protein neddylation | Covalent attachment of the ubiquitin-like protein NEDD8 (RUB1) to another protein. |
| protein phosphorylation | The process of introducing a phosphate group on to a protein. |
| regulation of protein neddylation | Any process that modulates the frequency, rate or extent of protein neddylation. |
| signal transduction | The cellular process in which a signal is conveyed to trigger a change in the activity or state of a cell. Signal transduction begins with reception of a signal (e.g. a ligand binding to a receptor or receptor activation by a stimulus such as light), or for signal transduction in the absence of ligand, signal-withdrawal or the activity of a constitutively active receptor. Signal transduction ends with regulation of a downstream cellular process, e.g. regulation of transcription or regulation of a metabolic process. Signal transduction covers signaling from receptors located on the surface of the cell and signaling via molecules located within the cell. For signaling between cells, signal transduction is restricted to events at and within the receiving cell. |
| skeletal muscle cell differentiation | The process in which a relatively unspecialized cell acquires specialized features of a skeletal muscle cell, a somatic cell located in skeletal muscle. |
| transcription by RNA polymerase II | The synthesis of RNA from a DNA template by RNA polymerase II (RNAP II), originating at an RNA polymerase II promoter. Includes transcription of messenger RNA (mRNA) and certain small nuclear RNAs (snRNAs). |
| trophectodermal cell proliferation | The proliferation of cells in the trophectoderm. |
4 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| P61202 | Cops2 | COP9 signalosome complex subunit 2 | Mus musculus (Mouse) | PR |
| P61203 | Cops2 | COP9 signalosome complex subunit 2 | Rattus norvegicus (Rat) | PR |
| O01422 | csn-2 | COP9 signalosome complex subunit 2 | Caenorhabditis elegans | PR |
| Q6IQT4 | cops2 | COP9 signalosome complex subunit 2 | Danio rerio (Zebrafish) (Brachydanio rerio) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSDMEDDFMC | DDEEDYDLEY | SEDSNSEPNV | DLENQYYNSK | ALKEDDPKAA | LSSFQKVLEL |
| 70 | 80 | 90 | 100 | 110 | 120 |
| EGEKGEWGFK | ALKQMIKINF | KLTNFPEMMN | RYKQLLTYIR | SAVTRNYSEK | SINSILDYIS |
| 130 | 140 | 150 | 160 | 170 | 180 |
| TSKQMDLLQE | FYETTLEALK | DAKNDRLWFK | TNTKLGKLYL | EREEYGKLQK | ILRQLHQSCQ |
| 190 | 200 | 210 | 220 | 230 | 240 |
| TDDGEDDLKK | GTQLLEIYAL | EIQMYTAQKN | NKKLKALYEQ | SLHIKSAIPH | PLIMGVIREC |
| 250 | 260 | 270 | 280 | 290 | 300 |
| GGKMHLREGE | FEKAHTDFFE | AFKNYDESGS | PRRTTCLKYL | VLANMLMKSG | INPFDSQEAK |
| 310 | 320 | 330 | 340 | 350 | 360 |
| PYKNDPEILA | MTNLVSAYQN | NDITEFEKIL | KTNHSNIMDD | PFIREHIEEL | LRNIRTQVLI |
| 370 | 380 | 390 | 400 | 410 | 420 |
| KLIKPYTRIH | IPFISKELNI | DVADVESLLV | QCILDNTIHG | RIDQVNQLLE | LDHQKRGGAR |
| 430 | 440 | ||||
| YTALDKWTNQ | LNSLNQAVVS | KLA |