COPS5 - COP9 signalosome subunit 5 Gene

Also Known as CSN5; JAB1; SGN5; MOV-34

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 10987

About COPS5

Cytogenetic location: 8q13.1 Genomic coordinates (GRCh38): 8:67,043,079-67,062,133 (from NCBI)

This gene has 13 transcripts (splice variants), 224 orthologues and 3 paralogues. Ubiquitous expression in testis (RPKM 37.3), heart (RPKM 32.6) and 25 other tissues.

Summary

The protein encoded by this gene is one of the eight subunits of COP9 signalosome, a highly conserved protein complex that functions as an important regulator in multiple signaling pathways. The structure and function of COP9 signalosome is similar to that of the 19S regulatory particle of 26S Proteasome. COP9 signalosome has been shown to interact with SCF-type E3 ubiquitin ligases and act as a positive regulator of E3 ubiquitin ligases. This protein is reported to be involved in the degradation of cyclin-dependent kinase inhibitor CDKN1B/p27Kip1. It is also known to be an coactivator that increases the specificity of JUN/AP1 transcription factors. [provided by RefSeq, Jul 2008]

COPS5 Products (1)

mRNA Protein Name
NM_006837.3 NP_006828.2 COP9 signalosome complex subunit 5
Molecular Function GO Annotation Evidence 参考文献 由来
enables metal-dependent deubiquitinase activity IDA
IDA: Inferred from direct assay
19246649 GOA
enables metallopeptidase activity IMP
IMP: Inferred from mutant phenotype
19214193 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12082530 GOA
Biological Process GO Annotation Evidence 参考文献 由来
involved in exosomal secretion IDA
IDA: Inferred from direct assay
19246649 GOA
involved in negative regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
20978819 GOA
involved in positive regulation of DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
20978819 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
16410250 GOA
involved in protein deneddylation IDA
IDA: Inferred from direct assay
19141280 GOA
involved in protein deneddylation IMP
IMP: Inferred from mutant phenotype
19214193 GOA
involved in regulation of IRE1-mediated unfolded protein response IMP
IMP: Inferred from mutant phenotype
15234121 GOA
involved in regulation of JNK cascade IDA
IDA: Inferred from direct assay
16410250 GOA
Cellular Component GO Annotation Evidence 参考文献 由来
part of COP9 signalosome IDA
IDA: Inferred from direct assay
18850735 GOA
part of COP9 signalosome IPI
IPI: Inferred from physical interaction
25043011 GOA
located in chromatin IDA
IDA: Inferred from direct assay
20978819 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
16300740 GOA
located in cytosol IDA
IDA: Inferred from direct assay
20978819 GOA
located in nucleus IDA
IDA: Inferred from direct assay
16300740 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
16300740 GOA
located in synaptic vesicle IDA
IDA: Inferred from direct assay
21102408 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

COPS5 Protein Structure

JAB

JAB: JAB1/Mov34/MPN/PAD-1 ubiquitin protease (54 - 163)

  • 0
  • 100
  • 200
  • 300
  • 334 a.a.
Protein Preferred Names Protein Names

COP9 signalosome complex subunit 5

  • 38 kDa Mov34 homolog

COPS5 Protein-protein interaction Information

Type
タンパク質名 Protein ID Interactor Interactor Species Interactor ID Detection Method 参考文献
Intra
COPS5 Q92905 RNF20 Homo sapiens Q5VTR2 19214193
Intra
COPS5 Q92905 OPRM1 Homo sapiens P35372
Y2H
23840749
Intra
COPS5 Q92905 OPRM1 Homo sapiens P35372 23840749
Intra
COPS5 Q92905 OPRM1 Homo sapiens P35372 23840749
Intra
COPS5 Q92905 BRSK2 Homo sapiens Q8IWQ3 22609399
Intra
COPS5 Q92905 BRSK2 Homo sapiens Q8IWQ3 22609399
Intra
COPS5 Q92905 BRSK2 Homo sapiens Q8IWQ3 22609399
Intra
COPS5 Q92905 BRSK2 Homo sapiens Q8IWQ3
Y2H
22609399
Intra
COPS5 Q92905 BRSK2 Homo sapiens Q8IWQ3 22609399
Intra
COPS5 Q92905 COPS3 Homo sapiens Q9UNS2
TAP
18850735
Intra
COPS5 Q92905 COPS3 Homo sapiens Q9UNS2 19615732
Intra
COPS5 Q92905 COPS3 Homo sapiens Q9UNS2 20399188
Intra
COPS5 Q92905 COPS3 Homo sapiens Q9UNS2
TAP
21145461
Intra
COPS5 Q92905 COPS3 Homo sapiens Q9UNS2 33961781
Intra
COPS5 Q92905 COPS3 Homo sapiens Q9UNS2 28514442
Intra
COPS5 Q92905 SMAD7 Homo sapiens O15105 14993265
Intra
COPS5 Q92905 SMAD7 Homo sapiens O15105 14993265
Intra
COPS5 Q92905 SMAD7 Homo sapiens O15105 14993265
Intra
COPS5 Q92905 SMAD7 Homo sapiens O15105
Y2H
14993265
Intra
COPS5 Q92905 F2RL1 Homo sapiens P55085
Y2H
16410250
Intra
COPS5 Q92905 F2RL1 Homo sapiens P55085 16410250
Intra
COPS5 Q92905 F2RL1 Homo sapiens P55085 16410250
Intra
COPS5 Q92905 CUL3 Homo sapiens Q13618 33961781
Intra
COPS5 Q92905 CUL3 Homo sapiens Q13618
TAP
21145461
Intra
COPS5 Q92905 CUL3 Homo sapiens Q13618
TAP
18850735
Intra
COPS5 Q92905 CUL3 Homo sapiens Q13618 19615732
Intra
COPS5 Q92905 COPS6 Homo sapiens Q7L5N1 20399188
Intra
COPS5 Q92905 COPS6 Homo sapiens Q7L5N1 25043011
Intra
COPS5 Q92905 COPS6 Homo sapiens Q7L5N1
TAP
18850735
Intra
COPS5 Q92905 COPS6 Homo sapiens Q7L5N1 19615732
Intra
COPS5 Q92905 COPS6 Homo sapiens Q7L5N1
TAP
21145461
Intra
COPS5 Q92905 CDKN1B Homo sapiens P46527 15480426
Intra
COPS5 Q92905 TXN Homo sapiens P10599 15480426
Intra
COPS5 Q92905 TXN Homo sapiens P10599
TAP
21145461
Intra
COPS5 Q92905 TXN Homo sapiens P10599 15480426
Intra
COPS5 Q92905 TXN Homo sapiens P10599 15480426
Intra
COPS5 Q92905 UCHL1 Homo sapiens P09936
Y2H
12082530
Intra
COPS5 Q92905 UCHL1 Homo sapiens P09936
IF
12082530
Intra
COPS5 Q92905 UCHL1 Homo sapiens P09936 12082530
Intra
COPS5 Q92905 MINDY3 Homo sapiens Q9H8M7 21499297
Intra
COPS5 Q92905 MINDY3 Homo sapiens Q9H8M7
Y2H
21499297
Intra
COPS5 Q92905 GPS1 Homo sapiens Q13098 19615732
Intra
COPS5 Q92905 GPS1 Homo sapiens Q13098 20399188
Intra
COPS5 Q92905 GPS1 Homo sapiens Q13098
TAP
21145461
Intra
COPS5 Q92905 GPS1 Homo sapiens Q13098
TAP
18850735
Intra
COPS5 Q92905 GPS1 Homo sapiens Q13098 33961781
Intra
COPS5 Q92905 GTPBP3 Homo sapiens Q969Y2 32296183
Intra
COPS5 Q92905 CCNDBP1 Homo sapiens O95273 15887118
Cross: Cross-species interaction Intra: Intraspecies interaction

COPS5 抗体

製品番号 製品名 アプリケーション 反応性
HY-P83414 JAB1 Antibody (YA3159) WB, IHC-P, ICC/IF, IP Human, Mouse, Rat

関連疾患

Diseases Alias
Maxillary Sinus Adenocarcinoma
  • Adenocarcinoma Of Maxillary Sinus

  • Adenocarcinoma Of The Maxillary Sinus

Xeroderma Pigmentosum, Complementation Group E
  • Xeroderma Pigmentosum V

  • Xp5

  • Xeroderma Pigmentosum, Group E, Ddb-Negative Subtype

  • Xpe

  • Xp, Group E

  • Xeroderma Pigmentosum, Type 5

  • Xeroderma Pigmentosum Complementation Group E

  • XP-E

  • Xp Group E

Cockayne Syndrome
  • Cockayne'S Syndrome

  • Dwarfism-Retinal Atrophy-Deafness Syndrome

  • Neill-Dingwall Syndrome

  • Progeria-Like Syndrome

  • Progeroid Nanism

  • Cs

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

Pancreatic Cancer
  • Pancreatic Carcinoma

  • Carcinoma Of Pancreas

  • Familial Pancreatic Carcinoma

  • Pancreatic Neoplasm

  • Pancreatic Carcinoma, Familial

  • Malignant Neoplasm Of Pancreas

  • Pancreatic Acinar Carcinoma

  • Pancreatic Tumor

  • Familial Pancreatic Cancer

  • Neoplasm Of The Pancreas

  • Cancer Of The Pancreas

  • Pancreatic Carcinoma, Somatic

  • Pancreatic Cancer, Somatic

  • Ca Body Of Pancreas

  • Ca Head Of Pancreas

  • Ca Tail Of Pancreas

  • Malignant Neoplasm Of Body Of Pancreas

  • Malignant Neoplasm Of Head Of Pancreas

  • Malignant Neoplasm Of Tail Of Pancreas

  • Pancreas Neoplasm

  • Exocrine Cancer

  • Exocrine Pancreas Carcinoma

  • Hereditary Pancreatic Cancer

  • Hereditary Pancreatic Carcinoma

  • PNCA

  • Pancreatic Cancer, Susceptibility To

  • Carcinoma Of Head Of Pancreas

  • Pancreatic Neoplasms

  • Pancreatic Tumors

  • Cancer, Pancreatic

  • Cancer Of Pancreas

  • Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site

Hereditary Ataxia
  • Sca

  • Spinocerebellar Ataxia

  • Ataxias Hereditary

  • Ataxias, Hereditary

Cerebellar Disease
  • Cerebellar Diseases

  • Cerebellar Dysfunction

  • Cerebellar Abnormality

  • Cerebellar Disorders

Machado-Joseph Disease
  • SCA3

  • MJD

  • Spinocerebellar Ataxia 3

  • Azorean Disease

  • Spinocerebellar Ataxia Type 3

  • Spinocerebellar Atrophy

  • Azorean Neurologic Disease

  • Spinopontine Atrophy

  • Nigrospinodentatal Degeneration

  • Spinocerebellar Atrophy Iii

  • Spinocerebellar Atrophy Type 3

  • Azorean Ataxia

  • Azorean Disease Of The Nervous System

  • Machado Disease

  • Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia

  • Disease, Machado-Joseph

  • Ataxia, Spinocerebellar

Hepatocellular Carcinoma
  • Liver Cancer

  • Primary Liver Cancer

  • HCC

  • Hepatoma

  • Malignant Neoplasm Of Liver

  • Liver Neoplasms

  • Cancer, Hepatocellular

  • Liver Cell Carcinoma

  • Lcc

  • Hepatoblastoma, Somatic

  • Hepatic Cancer

  • Primary Malignant Neoplasm Of Liver

  • Rare Tumor Of Liver And Intrahepatic Biliary Tract

  • Hepatocellular Carcinoma, Somatic

  • Hepatocellular Carcinoma, Childhood Type, Somatic

  • Hepatocellular Cancer, Somatic

  • Ca Liver - Primary

  • Hepatic Neoplasm

  • Malignant Hepato-Biliary Neoplasm

  • Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

  • Malignant Neoplasm Of Liver, Primary

  • Malignant Tumor Of Liver

  • Neoplasm Of Liver

  • Non-Resectable Primary Hepatic Malignant Neoplasm

  • Resectable Malignant Neoplasm Of Liver

  • Resectable Malignant Neoplasm Of The Liver

  • Primary Liver Carcinoma

  • Primary Malignant Liver Neoplasm

  • Primary Cancer Of Liver

  • Primary Tumor Of The Liver

  • Rare Tumor Of Liver And Ibt

  • Hepatocellular Cancer

  • Neoplasm Of The Liver

  • Carcinoma, Hepatocellular

  • Hepatomas

  • Liver Neoplasm

  • Liver Carcinoma

  • Liver And Intrahepatic Biliary Tract Carcinoma

  • Malignant Hepatobiliary Neoplasm

  • Adult Primary Hepatocellular Carcinoma

  • Hepatoblastoma

  • Carcinoma Of Liver

  • Malignant Liver Tumour

  • Malignant Hepatic Tumour

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

生物種 Symbol 由来 ID
Felis catus COPS5 VGNC VGNC:61090
Mus musculus COPS5 MGD MGI:1349415
Macaca mulatta COPS5 VGNC VGNC:71317
Bos taurus COPS5 VGNC VGNC:27602
Rattus norvegicus COPS5 RGD RGD:1310301
Canis familiaris COPS5 VGNC VGNC:54110
Others COPS5 NCBI