1. Gene
  2. PSMB10 - proteasome 20S subunit beta 10 Gene

PSMB10 - proteasome 20S subunit beta 10 Gene

Homo sapiens

Also known as LMP10; MECL1; PRAAS5; beta2i

Gene ID: 5699 | Gene type: protein coding

About PSMB10

Cytogenetic location: 16q22.1 Genomic coordinates (GRCh38): 16:67,934,506-67,936,850 (from NCBI)

This gene has 5 transcripts (splice variants), 172 orthologues, 18 paralogues and is associated with 1 phenotype. Ubiquitous expression in spleen (RPKM 53.2), lymph node (RPKM 48.6) 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. Proteolytic processing is required to generate a mature subunit. Expression of this gene is induced by gamma interferon, and this gene product replaces catalytic subunit 2 (Proteasome beta 7 subunit) in the immunoproteasome. [provided by RefSeq, Jul 2008]

PSMB10 Products(1)

mRNA Protein Name
NM_002801.4 NP_002792.1 proteasome subunit beta type-10
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
14733938 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

PSMB10 Protein Structure

Proteasome

Proteasome: Proteasome subunit (37 - 217)

Pr_beta_C

Pr_beta_C: Proteasome beta subunits C terminal (231 - 269)

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

proteasome subunit beta type-10

low molecular mass protein 10

PSMB10 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
PSMB10 P40306 DMWD Homo sapiens G5E9A7
Validated Y2H
32814053
Intra
PSMB10 P40306 DMWD Homo sapiens G5E9A7
Y2H Array
32814053
Intra
PSMB10 P40306 DMWD Homo sapiens G5E9A7
Y2H Pooling
32814053
Intra
PSMB10 P40306 PRKN Homo sapiens O60260-5
Validated Y2H
32814053
Intra
PSMB10 P40306 PRKN Homo sapiens O60260-5
Y2H Pooling
32814053
Intra
PSMB10 P40306 PRKN Homo sapiens O60260-5
Y2H Array
32814053
Intra
PSMB10 P40306 RNF11 Homo sapiens Q9Y3C5
Y2H Pooling
32814053
Intra
PSMB10 P40306 RNF11 Homo sapiens Q9Y3C5
Validated Y2H
32814053
Intra
PSMB10 P40306 RNF11 Homo sapiens Q9Y3C5
Y2H Array
32814053
Intra
PSMB10 P40306 SPRED1 Homo sapiens Q7Z699
Validated Y2H
32814053
Intra
PSMB10 P40306 SPRED1 Homo sapiens Q7Z699
Y2H Pooling
32814053
Intra
PSMB10 P40306 SPRED1 Homo sapiens Q7Z699
Y2H Array
32814053
Intra
PSMB10 P40306 PSMB3 Homo sapiens P49720
Y2H
14733938
Intra
PSMB10 P40306 CRX Homo sapiens O43186
Validated Y2H
25416956
Intra
PSMB10 P40306 CRX Homo sapiens O43186
Y2H Prey Pooling
25416956
Intra
PSMB10 P40306 MEOX2 Homo sapiens P50222
Y2H Prey Pooling
25416956
Intra
PSMB10 P40306 MEOX2 Homo sapiens P50222
Y2H Array
25416956
Intra
PSMB10 P40306 CCNDBP1 Homo sapiens O95273
Y2H
21516116
Intra
PSMB10 P40306 CCNDBP1 Homo sapiens O95273
Y2H Array
31515488
Intra
PSMB10 P40306 CCNDBP1 Homo sapiens O95273
Y2H Prey Pooling
25416956
Intra
PSMB10 P40306 CCNDBP1 Homo sapiens O95273
Validated Y2H
25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Proteasome-Associated Autoinflammatory Syndrome 5

PRAAS5

Proteasome-Associated Autoinflammatory Syndrome

Aldd Syndrome

Autoinflammation-Lipodystrophy-Dermatosis Syndrome

Praas

Proteasome Disability Syndrome

Immunodeficiency 12

Combined Immunodeficiency Due To Malt1 Deficiency

IMD12

Immunodeficiency, Type 12

Hypertensive Retinopathy
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
Felis catus PSMB10 VGNC VGNC:97570
Canis familiaris PSMB10 VGNC VGNC:57370
Mus musculus PSMB10 MGD MGI:1096380
Rattus norvegicus PSMB10 RGD RGD:1307428
Bos taurus PSMB10 VGNC VGNC:97305