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

15 structures for Q92905

Entry ID Method Resolution Chain Position Source
4D10 X-ray 380 A E/M 1-334 PDB
4D18 X-ray 408 A E/M 12-334 PDB
4F7O X-ray 260 A A/B 1-257 PDB
4WSN X-ray 550 A E/M/U/c/k/s 14-334 PDB
5JOG X-ray 246 A A 2-257 PDB
5JOH X-ray 199 A A 2-257 PDB
5M5Q X-ray 220 A A 2-257 PDB
6R6H EM 840 A E 1-334 PDB
6R7F EM 820 A E 24-334 PDB
6R7H EM 880 A E 24-334 PDB
6R7I EM 590 A E 1-334 PDB
8H38 EM 425 A E 1-334 PDB
8H3A EM 751 A E 1-334 PDB
8H3F EM 673 A E 1-334 PDB
AF-Q92905-F1 Predicted AlphaFoldDB

117 variants for Q92905

Variant ID(s) Position Change Description Diseaes Association Provenance
CA371207249
rs1585721644
4 S>A No ClinGen
Ensembl
CA4769966
rs772964914
6 S>R No ClinGen
ExAC
gnomAD
CA371207184
rs1384038745
7 G>R No ClinGen
gnomAD
rs1443256217
CA371207148
8 M>I No ClinGen
TOPMed
gnomAD
rs1804694
CA178225754
9 A>S No ClinGen
Ensembl
CA371207055
rs1585721541
12 T>I No ClinGen
Ensembl
CA178225685
rs866725884
16 A>T No ClinGen
TOPMed
rs780531661
CA4769960
16 A>V No ClinGen
ExAC
gnomAD
CA4769959
rs148576713
17 N>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1490543063
CA371206875
19 M>I No ClinGen
gnomAD
rs1232078431
CA371206859
20 Q>R No ClinGen
TOPMed
rs779252592
CA4769957
22 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs779252592
CA4769958
22 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA4769956
rs757811563
22 A>V No ClinGen
ExAC
TOPMed
gnomAD
rs764258200
CA4769954
24 S>N No ClinGen
ExAC
gnomAD
rs1333739034
CA371206675
28 I>L No ClinGen
gnomAD
rs1482708464
CA371206628
31 Y>H No ClinGen
Ensembl
CA371206563
rs1490507809
33 K>M No ClinGen
TOPMed
CA4769952
rs576133944
36 Q>R No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 41 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs145855785
COSM107766
CA178225628
45 W>* skin [Cosmic] No ClinGen
cosmic curated
Ensembl
rs200023878
CA178225619
48 D>N No ClinGen
1000Genomes
gnomAD
CA4769917
rs778376302
53 K>E No ClinGen
ExAC
gnomAD
rs866280415
CA178223794
55 C>Y No ClinGen
Ensembl
CA371205596
rs1424094783
56 K>R No ClinGen
gnomAD
rs1010003084
CA178223783
57 I>M No ClinGen
TOPMed
gnomAD
TCGA novel 60 L>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs748216094
CA4769915
63 L>P No ClinGen
ExAC
gnomAD
CA918281325
rs1563448122
65 M>Q No ClinGen
Ensembl
CA4769914
rs781307881
67 M>I No ClinGen
ExAC
gnomAD
CA178223767
rs144850801
67 M>K No ClinGen
ESP
TOPMed
gnomAD
rs755211980
CA4769913
68 H>Y No ClinGen
ExAC
gnomAD
rs112353634
CA178223749
69 A>T No ClinGen
Ensembl
rs113434892
CA178223709
74 N>S No ClinGen
Ensembl
CA178223697
rs11557198
80 L>M No ClinGen
Ensembl
TCGA novel 81 M>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 81 M>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA178223688
rs547886299
86 D>N No ClinGen
TOPMed
rs547886299
CA178223682
86 D>Y No ClinGen
TOPMed
TCGA novel 88 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs756985013
CA4769910
91 I>V No ClinGen
ExAC
rs1001853949
CA178223671
93 M>L No ClinGen
TOPMed
CA371204927
rs1269145339
93 M>T No ClinGen
gnomAD
TCGA novel 94 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 99 P>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 101 E>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA178223655
rs11557196
109 A>S No ClinGen
Ensembl
rs760643887
CA4769907
111 A>S No ClinGen
ExAC
gnomAD
CA371204749
rs1306668062
114 Y>F No ClinGen
gnomAD
rs1444548992
CA371204719
118 A>S No ClinGen
TOPMed
rs1347693682
CA371204715
119 A>T No ClinGen
gnomAD
rs1284147503
CA371204697
121 I>T No ClinGen
gnomAD
TCGA novel 124 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs759117469
CA4769904
126 Q>H No ClinGen
ExAC
gnomAD
rs758313448
CA178222790
127 V>F No ClinGen
Ensembl
CA371203416
rs1254987524
129 R>C No ClinGen
TOPMed
CA178222788
rs889246427
129 R>H No ClinGen
TOPMed
CA178222765
rs1051932630
134 I>V No ClinGen
gnomAD
CA371203350
rs1380557410
137 Y>F No ClinGen
TOPMed
gnomAD
CA4769889
rs756075307
145 C>W No ClinGen
ExAC
gnomAD
CA371203160
rs1585716180
150 I>V No ClinGen
Ensembl
CA371203109
rs1343218790
153 S>N No ClinGen
gnomAD
rs775341801
CA4769887
158 N>S No ClinGen
ExAC
gnomAD
CA4769886
rs759037579
166 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs866340690
CA178222234
171 D>Y No ClinGen
Ensembl
CA4769864
rs201634747
174 R>G No ClinGen
1000Genomes
ExAC
gnomAD
CA178222199
rs199708915
175 T>A No ClinGen
1000Genomes
rs765529888
CA4769860
176 I>T No ClinGen
ExAC
gnomAD
CA4769861
rs369630651
176 I>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA4769859
rs762186633
177 S>A No ClinGen
ExAC
TOPMed
gnomAD
CA4769857
rs764699097
178 A>S No ClinGen
ExAC
gnomAD
TCGA novel 178 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs951219755
CA178222117
185 A>G No ClinGen
Ensembl
CA4769853
rs372916530
185 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1289111343
CA371202707
186 F>L No ClinGen
gnomAD
CA178221246
rs1038600714
192 G>C No ClinGen
Ensembl
CA371201944
rs1332197567
192 G>D No ClinGen
TOPMed
CA178221213
rs201539863
193 Y>C No ClinGen
1000Genomes
rs746955448
CA4769792
195 P>T No ClinGen
ExAC
gnomAD
CA371201799
rs1340467886
199 G>E No ClinGen
TOPMed
TCGA novel 204 Q>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 206 I>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA4769788
rs778260803
219 K>R No ClinGen
ExAC
gnomAD
CA4769789
rs778260803
219 K>T No ClinGen
ExAC
gnomAD
CA371200197
rs1229286706
223 A>D No ClinGen
gnomAD
TCGA novel 234 D>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1378846658
COSM1700166
CA371200005
235 R>C Variant assessed as Somatic; 0.0 impact. skin [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs138638780
CA4769758
235 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 236 K>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1307575325
CA371199815
249 T>A No ClinGen
gnomAD
TCGA novel 249 T>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1367430036
CA371199775
252 S>T No ClinGen
TOPMed
gnomAD
rs766493793
CA4769755
253 S>C No ClinGen
ExAC
gnomAD
TCGA novel 256 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1158572768
CA371197212
259 A>V No ClinGen
TOPMed
rs759216042
CA4769726
263 T>I No ClinGen
ExAC
gnomAD
CA4769724
rs766276256
266 V>F No ClinGen
ExAC
TOPMed
gnomAD
CA178212534
rs766276256
266 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs762937165
CA4769723
267 F>S No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 271 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1444521716
CA371196934
279 Q>H No ClinGen
TOPMed
CA178212500
rs866920136
281 G>* No ClinGen
Ensembl
TCGA novel 282 R>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs760694418
CA178212457
282 R>Q No ClinGen
Ensembl
CA4769718
rs769096210
286 M>T No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 291 T>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA4769717
rs143525514
COSM289061
291 T>M Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs201128315
CA178212408
299 K>R No ClinGen
1000Genomes
CA4769712
rs757365559
304 T>A No ClinGen
ExAC
TOPMed
gnomAD
CA371196166
rs1585707100
304 T>I No ClinGen
Ensembl
CA371195561
rs1459788146
308 C>F No ClinGen
gnomAD
rs1332891390
CA371195350
315 I>V No ClinGen
TOPMed
gnomAD
CA4769700
rs776171390
325 D>N No ClinGen
ExAC
gnomAD
CA371195042
rs776171390
325 D>Y No ClinGen
ExAC
gnomAD
CA178210511
rs541187848
333 I>M No ClinGen
1000Genomes
CA371194814
rs1224571316
333 I>V No ClinGen
gnomAD
rs75381739
CA178210509
334 S>Y No ClinGen
Ensembl

No associated diseases with Q92905

3 regional properties for Q92905

Type Name Position InterPro Accession
domain JAB1/MPN/MOV34 metalloenzyme domain 53 - 191 IPR000555
domain MPN domain 55 - 192 IPR037518
domain Cop9 signalosome subunit 5 C-terminal domain 251 - 329 IPR040961

Functions

Description
EC Number
Subcellular Localization
  • Cytoplasm, cytosol
  • Nucleus
  • Cytoplasm, perinuclear region
  • Cytoplasmic vesicle, secretory vesicle, synaptic vesicle
  • Nuclear localization is diminished in the presence of IFIT3
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

9 GO annotations of cellular component

Name Definition
anchoring junction A cell junction that mechanically attaches a cell (and its cytoskeleton) to neighboring cells or to the extracellular matrix.
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.
eukaryotic translation initiation factor 3 complex A complex of several polypeptides that plays at least two important roles in protein synthesis: First, eIF3 binds to the 40S ribosome and facilitates loading of the Met-tRNA/eIF2.GTP ternary complex to form the 43S preinitiation complex. Subsequently, eIF3 apparently assists eIF4 in recruiting mRNAs to the 43S complex. The eIF3 complex contains five conserved core subunits, and may contain several additional proteins; the non-core subunits are thought to mediate association of the complex with specific sets of mRNAs.
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.
perinuclear region of cytoplasm Cytoplasm situated near, or occurring around, the nucleus.
synaptic vesicle A secretory organelle, typically 50 nm in diameter, of presynaptic nerve terminals; accumulates in high concentrations of neurotransmitters and secretes these into the synaptic cleft by fusion with the 'active zone' of the presynaptic plasma membrane.

9 GO annotations of molecular function

Name Definition
deNEDDylase activity An isopeptidase activity that cleaves NEDD8 from a target protein to which it is conjugated.
enzyme binding Binding to an enzyme, a protein with catalytic activity.
macrophage migration inhibitory factor binding Binding to the cytokine, macrophage migration inhibitory factor.
metal ion binding Binding to a metal ion.
metal-dependent deubiquitinase activity An metal-dependent isopeptidase activity that cleaves ubiquitin from a target protein to which it is conjugated.
metalloendopeptidase activity Catalysis of the hydrolysis of internal, alpha-peptide bonds in a polypeptide chain by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.
metallopeptidase activity Catalysis of the hydrolysis of peptide bonds by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.
transcription coactivator activity A transcription coregulator activity that activates or increases 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. Coactivators often act by altering chromatin structure and modifications. For example, one class of transcription coactivators 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. A fourth class of coactivator activity is the bridging of a DNA-binding transcription factor to the general (basal) transcription machinery. The Mediator complex, which bridges sequence-specific DNA binding transcription factors and RNA polymerase, is also a transcription coactivator.
translation initiation factor activity Functions in the initiation of ribosome-mediated translation of mRNA into a polypeptide.

13 GO annotations of biological process

Name Definition
exosomal secretion The process whereby a membrane-bounded vesicle is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane.
negative regulation of apoptotic process Any process that stops, prevents, or reduces the frequency, rate or extent of cell death by apoptotic process.
positive regulation of DNA-binding transcription factor activity Any process that activates or increases the frequency, rate or extent of activity of a transcription factor, any factor involved in the initiation or regulation of transcription.
positive regulation of transcription by RNA polymerase II Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter.
post-translational protein modification The process of covalently altering one or more amino acids in a protein after the protein has been completely translated and released from the ribosome.
protein deneddylation The removal of a ubiquitin-like protein of the NEDD8 type from a protein.
protein deubiquitination The removal of one or more ubiquitin groups from a protein.
protein neddylation Covalent attachment of the ubiquitin-like protein NEDD8 (RUB1) to another protein.
regulation of cell cycle Any process that modulates the rate or extent of progression through the cell cycle.
regulation of IRE1-mediated unfolded protein response Any process that modulates the frequency, rate or extent of the IRE1-mediated unfolded protein response.
regulation of JNK cascade Any process that modulates the frequency, rate or extent of signal transduction mediated by the JNK cascade.
regulation of protein neddylation Any process that modulates the frequency, rate or extent of protein neddylation.
translation The cellular metabolic process in which a protein is formed, using the sequence of a mature mRNA or circRNA molecule to specify the sequence of amino acids in a polypeptide chain. Translation is mediated by the ribosome, and begins with the formation of a ternary complex between aminoacylated initiator methionine tRNA, GTP, and initiation factor 2, which subsequently associates with the small subunit of the ribosome and an mRNA or circRNA. Translation ends with the release of a polypeptide chain from the ribosome.

2 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
O35864 Cops5 COP9 signalosome complex subunit 5 Mus musculus (Mouse) PR
Q6PC30 cops5 COP9 signalosome complex subunit 5 Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MAASGSGMAQ KTWELANNMQ EAQSIDEIYK YDKKQQQEIL AAKPWTKDHH YFKYCKISAL
70 80 90 100 110 120
ALLKMVMHAR SGGNLEVMGL MLGKVDGETM IIMDSFALPV EGTETRVNAQ AAAYEYMAAY
130 140 150 160 170 180
IENAKQVGRL ENAIGWYHSH PGYGCWLSGI DVSTQMLNQQ FQEPFVAVVI DPTRTISAGK
190 200 210 220 230 240
VNLGAFRTYP KGYKPPDEGP SEYQTIPLNK IEDFGVHCKQ YYALEVSYFK SSLDRKLLEL
250 260 270 280 290 300
LWNKYWVNTL SSSSLLTNAD YTTGQVFDLS EKLEQSEAQL GRGSFMLGLE THDRKSEDKL
310 320 330
AKATRDSCKT TIEAIHGLMS QVIKDKLFNQ INIS