HCSGD entry for PSMB5
1. General information
Official gene symbol | PSMB5 |
---|---|
Entrez ID | 5693 |
Gene full name | proteasome (prosome, macropain) subunit, beta type, 5 |
Other gene symbols | LMPX MB1 X |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
This gene isn't in PPI subnetwork.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000082 | G1/S transition of mitotic cell cycle | TAS | biological_process |
GO:0000209 | Protein polyubiquitination | TAS | biological_process |
GO:0000278 | Mitotic cell cycle | TAS | biological_process |
GO:0000502 | Proteasome complex | TAS | cellular_component |
GO:0002474 | Antigen processing and presentation of peptide antigen via MHC class I | TAS | biological_process |
GO:0002479 | Antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent | TAS | biological_process |
GO:0004298 | Threonine-type endopeptidase activity | IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005634 | Nucleus | IEA | cellular_component |
GO:0005654 | Nucleoplasm | TAS | cellular_component |
GO:0005737 | Cytoplasm | IEA | cellular_component |
GO:0005829 | Cytosol | TAS | cellular_component |
GO:0005839 | Proteasome core complex | IEA ISS | cellular_component |
GO:0006521 | Regulation of cellular amino acid metabolic process | TAS | biological_process |
GO:0006915 | Apoptotic process | TAS | biological_process |
GO:0006977 | DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest | TAS | biological_process |
GO:0006979 | Response to oxidative stress | IEA | biological_process |
GO:0010467 | Gene expression | TAS | biological_process |
GO:0016032 | Viral process | TAS | biological_process |
GO:0016070 | RNA metabolic process | TAS | biological_process |
GO:0016071 | MRNA metabolic process | TAS | biological_process |
GO:0031145 | Anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process | TAS | biological_process |
GO:0034641 | Cellular nitrogen compound metabolic process | TAS | biological_process |
GO:0042590 | Antigen processing and presentation of exogenous peptide antigen via MHC class I | TAS | biological_process |
GO:0042981 | Regulation of apoptotic process | TAS | biological_process |
GO:0043066 | Negative regulation of apoptotic process | TAS | biological_process |
GO:0044281 | Small molecule metabolic process | TAS | biological_process |
GO:0051436 | Negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle | TAS | biological_process |
GO:0051437 | Positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle | TAS | biological_process |
GO:0051439 | Regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle | TAS | biological_process |
GO:0051603 | Proteolysis involved in cellular protein catabolic process | IEA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.0606817142 | 0.8642229968 | 0.5335298064 | 1.0000000000 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.7483077015 |
GSE13712_SHEAR | Down | -0.2193148157 |
GSE13712_STATIC | Up | 0.0160169891 |
GSE19018 | Up | 0.5265832261 |
GSE19899_A1 | Up | 0.2985841287 |
GSE19899_A2 | Up | 0.4576893906 |
PubMed_21979375_A1 | Up | 0.3425879423 |
PubMed_21979375_A2 | Up | 0.1850528078 |
GSE35957 | Down | -0.3593218879 |
GSE36640 | Up | 0.3214533004 |
GSE54402 | Up | 0.5164264088 |
GSE9593 | Up | 0.0478671175 |
GSE43922 | Up | 0.1495050488 |
GSE24585 | Down | -0.4150701997 |
GSE37065 | Down | -0.1695595236 |
GSE28863_A1 | Up | 0.0680854635 |
GSE28863_A2 | Up | 0.0120286473 |
GSE28863_A3 | Down | -0.3762337579 |
GSE28863_A4 | Up | 0.2177727381 |
GSE48662 | Down | -0.1253503769 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
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- Drugs
Name | Drug | Accession number |
---|---|---|
(3AR,6R,6AS)-6-((S)-((S)-CYCLOHEX-2-ENYL)(HYDROXY)METHYL)-6A-METHYL-4-OXO-HEXAHYDRO-2H-FURO[3,2-C]PYRROLE-6-CARBALDEHYDE | DB08515 | - |
Carfilzomib | DB08889 | - |
- MicroRNAs
- mirTarBase
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-142-3p | MIMAT0000434 | MIRT021543 | Microarray | Functional MTI (Weak) | 17612493 |
hsa-miR-18a-5p | MIMAT0000072 | MIRT031323 | Sequencing | Functional MTI (Weak) | 20371350 |
hsa-miR-423-3p | MIMAT0001340 | MIRT042548 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-30e-5p | MIMAT0000692 | MIRT044149 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-221-3p | MIMAT0000278 | MIRT046973 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
No target information from mirRecord
- mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
24393841 | Ameliorating replicative senescence of human bone marrow stromal cells by PSMB5 overexpression |
24393841 | In the present study, we confirmed that proteasomal activity directly contributes to senescence of hBMSCs, which could be reversed by overexpression of the beta5-subunit (PSMB5) |
24393841 | Knocking down PSMB5 led to decreased proteasomal activity concurrent with reduced cell proliferation in early-stage hBMSCs, which is similar to the senescent phenotype observed in late-stage cells |
24393841 | In contrast, overexpressing PSMB5 in late-stage cells efficiently restored the normal activity of 20S proteasomes and promoted cell growth, possibly via upregulating the Cyclin D1/CDK4 complex |
24393841 | Additionally, PSMB5 could enhance cell resistance to oxidative stress, as evidenced by the increased cell survival upon exposing senescent hBMSCs to hydrogen peroxide |
24393841 | Furthermore, PSMB5 overexpression retained the pluripotency of late-stage hBMSCs by facilitating their neural differentiation both in vitro and in vivo |
24393841 | Collectively, our work reveals a critical role of PSMB5 in 20S proteasome-mediated protection against replicative senescence, pointing to a possible strategy for maintaining the integrity of culture-expanded hBMSCs by manipulating the expression of PSMB5 |
15381105 | Loss of proteasome function was not associated with decreased proteasome content but with partial replacement of the proteolytic subunit PSMB5 with the inducible subunit LMP7 |
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