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

Functions

Description
EC Number
Subcellular Localization
  • Cytoplasm
  • Nucleus
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

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