PSMB4 - proteasome 20S subunit beta 4 Gene

Also Known as HN3; HsN3; PRAAS3; PROS26; PROS-26

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5692

About PSMB4

Cytogenetic location: 1q21.3 Genomic coordinates (GRCh38): 1:151,399,573-151,401,937 (from NCBI)

This gene has 7 transcripts (splice variants), 212 orthologues, 18 paralogues and is associated with 1 phenotype. Ubiquitous expression in placenta (RPKM 102.8), lymph node (RPKM 94.8) and 25 other tissues.

Summary

The Proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified Proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the Proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. [provided by RefSeq, Jul 2008]

PSMB4 Products (1)

mRNA Protein Name
NM_002796.3 NP_002787.2 proteasome subunit beta type-4
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
15231748 GOA
Cellular Component GO Annotation Evidence References Source
located in ciliary basal body IDA
IDA: Inferred from direct assay
29257953 GOA
is active in cytoplasm IDA
IDA: Inferred from direct assay
34711951 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
34711951 GOA
part of proteasome complex IDA
IDA: Inferred from direct assay
17323924 GOA
part of proteasome core complex IDA
IDA: Inferred from direct assay
34711951 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

PSMB4 Protein Structure

Proteasome

Proteasome: Proteasome subunit (50 - 237)

  • 0
  • 100
  • 200
  • 264 a.a.
Protein Preferred Names Protein Names

proteasome subunit beta type-4

  • 26 kDa prosomal protein

PSMB4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PSMB4 P28070 P4HA3 Homo sapiens Q7Z4N8 32296183
Intra
PSMB4 P28070 TEKT5 Homo sapiens Q96M29 32296183
Intra
PSMB4 P28070 HEMK1 Homo sapiens Q9Y5R4 32296183
Intra
PSMB4 P28070 KRTAP19-5 Homo sapiens Q3LI72 32296183
Intra
PSMB4 P28070 KRTAP19-5 Homo sapiens Q3LI72 32296183
Intra
PSMB4 P28070 KRTAP19-5 Homo sapiens Q3LI72 32296183
Intra
PSMB4 P28070 CCDC57 Homo sapiens Q2TAC2-2 32296183
Intra
PSMB4 P28070 TLE5 Homo sapiens Q08117-2 32296183
Intra
PSMB4 P28070 TFAP2D Homo sapiens Q7Z6R9 32296183
Intra
PSMB4 P28070 SYNPO2L Homo sapiens Q9H987-2 32296183
Intra
PSMB4 P28070 PITX2 Homo sapiens Q99697-2 32296183
Intra
PSMB4 P28070 SOHLH1 Homo sapiens Q5JUK2 32296183
Intra
PSMB4 P28070 SMAD1 Homo sapiens Q15797 32296183
Intra
PSMB4 P28070 KANK2 Homo sapiens Q63ZY3 32296183
Intra
PSMB4 P28070 PSMA3 Homo sapiens P25788 25416956
Intra
PSMB4 P28070 PSMA3 Homo sapiens P25788 33961781
Intra
PSMB4 P28070 PSMA3 Homo sapiens P25788 25416956
Intra
PSMB4 P28070 PFDN5 Homo sapiens Q99471 32296183
Intra
PSMB4 P28070 PFDN5 Homo sapiens Q99471 32296183
Intra
PSMB4 P28070 PSMB5 Homo sapiens P28074 33961781
Intra
PSMB4 P28070 PSMB5 Homo sapiens P28074 28514442
Intra
PSMB4 P28070 PSMB5 Homo sapiens P28074
Y2H
17948026
Intra
PSMB4 P28070 PSMB1 Homo sapiens P20618 35271311
Intra
PSMB4 P28070 TARDBP Homo sapiens Q13148 32814053
Intra
PSMB4 P28070 TARDBP Homo sapiens Q13148 32814053
Intra
PSMB4 P28070 TARDBP Homo sapiens Q13148 32814053
Intra
PSMB4 P28070 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
PSMB4 P28070 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
PSMB4 P28070 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
PSMB4 P28070 MYOZ3 Homo sapiens Q8TDC0 32296183
Intra
PSMB4 P28070 PKN1 Homo sapiens Q16512 32296183
Intra
PSMB4 P28070 PSMB7 Homo sapiens Q99436 33961781
Intra
PSMB4 P28070 PSMB7 Homo sapiens Q99436 28514442
Intra
PSMB4 P28070 PSMB7 Homo sapiens Q99436
Y2H
17948026
Intra
PSMB4 P28070 POMP Homo sapiens Q9Y244 33961781
Intra
PSMB4 P28070 POMP Homo sapiens Q9Y244 28514442
Intra
PSMB4 P28070 DTX2 Homo sapiens Q86UW9 32296183
Intra
PSMB4 P28070 SPG21 Homo sapiens Q9NZD8 32296183
Intra
PSMB4 P28070 CNOT2 Homo sapiens Q9NZN8 32296183
Intra
PSMB4 P28070 GABARAPL1 Homo sapiens Q9H0R8 32296183
Intra
PSMB4 P28070 BCL6 Homo sapiens P41182 32296183
Intra
PSMB4 P28070 AIRIM Homo sapiens Q9NX04 32296183
Intra
PSMB4 P28070 ATXN1 Homo sapiens P54253 32814053
Intra
PSMB4 P28070 ATXN1 Homo sapiens P54253 32814053
Intra
PSMB4 P28070 ATXN1 Homo sapiens P54253 32814053
Intra
PSMB4 P28070 GCA Homo sapiens P28676 32296183
Intra
PSMB4 P28070 GCA Homo sapiens P28676 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Proteasome-Associated Autoinflammatory Syndrome 3
  • Proteasome-Associated Autoinflammatory Syndrome 3, Digenic

  • PRAAS3

  • Proteasome-Associated Autoinflammatory Syndrome 3 And Digenic Forms

Proteasome-Associated Autoinflammatory Syndrome 1
  • Jmp Syndrome

  • Nakajo-Nishimura Syndrome

  • Nkjo

  • Autoinflammation, Lipodystrophy, And Dermatosis Syndrome

  • Proteasome-Associated Autoinflammatory Syndrome 1 And Digenic Forms

  • Nakajo Syndrome

  • PRAAS1

  • Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy And Elevated Temperature Syndrome

  • Candle

  • Joint Contractures, Muscular Atrophy, Microcytic Anemia, And Panniculitis-Induced Lipodystrophy

  • Aldd

  • Inflammation

  • Joint Contractures - Muscle Atrophy - Microcytic Anemia - Panniculitis-Induced Lipodystrophy

  • Nakajo Nishimura Syndrome

  • Amyotrophy Fat Tissue Anomaly

  • Japanese Autoinflammatory Syndrome With Lipodystrophy

  • Jasl

  • Joint Contractures Muscular Atrophy Microcytic Anemia And Panniculitis-Induced Lipodystrophy

  • Nns

  • Nodular Erythema With Digital Changes

  • Secondary Hypertrophic Osteoperiostosis With Pernio

Nakajo Syndrome
  • Nodular Erythema Digital Changes

Panniculitis
  • Nodular Panniculitis

Proteasome-Associated Autoinflammatory Syndrome
  • Aldd Syndrome

  • Autoinflammation-Lipodystrophy-Dermatosis Syndrome

  • Praas

  • Proteasome Disability Syndrome

Atrophoderma Vermiculata
  • Atrophoderma Vermiculatum

  • Folliculitis Ulerythematosa Reticulata

  • Atrophodermia Vermiculata

  • Honeycomb Atrophy

  • Atrophodermia Reticulata Symmetrica Faciei

  • AVA

  • Atrophodermia Reticulata

  • Folliculitis Ulerythematosa

  • Folliculitis Ulerythematosa Reticulate

  • Burnett Schwartz Berberian Syndrome

Nodular Episcleritis
Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Basal Ganglia Calcification
  • Fahr'S Syndrome

  • Fahr'S Disease

  • Fahr Disease

Basal Ganglia Disease
  • Basal Ganglia Diseases

  • Basal Ganglia Disorders

  • Abnormality Of The Basal Ganglia

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Aicardi-Goutieres Syndrome
  • Aicardi Goutieres Syndrome

  • Cree Encephalitis

  • Aicardi-Goutières Syndrome

  • Encephalopathy With Basal Ganglia Calcification

  • Ags

  • Encephalopathy With Intracranial Calcification And Chronic Lymphocytosis Of Cerebrospinal Fluid

  • Pseudotoxoplasmosis Syndrome

  • Encephalopathy, Familial Infantile, With Calcification Of Basal Ganglia And Chronic Cerebrospinal Fluid Lymphocytosis

  • Familial Infantile Encephalopathy With Intracranial Calcification And Chronic Cerebrospinal Fluid Lymphocytosis

  • Aicardi-Goutieres Syndrome 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

Species Symbol Source ID
Macaca mulatta PSMB4 VGNC VGNC:76444
Rattus norvegicus PSMB4 RGD RGD:61877
Canis familiaris PSMB4 VGNC VGNC:45096
Bos taurus PSMB4 VGNC VGNC:33448
Felis catus PSMB4 VGNC VGNC:69110
Mus musculus PSMB4 MGD MGI:1098257
Others PSMB4 NCBI