1. Gene
  2. PSMD9 - proteasome 26S subunit, non-ATPase 9 Gene

PSMD9 - proteasome 26S subunit, non-ATPase 9 Gene

Homo sapiens

Also known as p27; Rpn4

Gene ID: 5715 | Gene type: protein coding

About PSMD9

Cytogenetic location: 12q24.31 Genomic coordinates (GRCh38): 12:121,888,790-121,918,297 (from NCBI)

This gene has 11 transcripts (splice variants) and 209 orthologues. Ubiquitous expression in bone marrow (RPKM 16.1), kidney (RPKM 11.1) and 25 other tissues.

Summary

The 26S Proteasome is a multicatalytic proteinase complex with a highly ordered structure composed of 2 complexes, a 20S core and a 19S regulator. The 20S core 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. The 19S regulator is composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase 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 non-ATPase subunit of the 19S regulator. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, May 2012]

PSMD9 Products(2)

mRNA Protein Name
NM_001261400.3 NP_001248329.1 26S proteasome non-ATPase regulatory subunit 9 isoform 2
NM_002813.7 NP_002804.2 26S proteasome non-ATPase regulatory subunit 9 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence Reference Source
involved in proteasome regulatory particle assembly IMP
IMP: Inferred from mutant phenotype
19490896 GOA
Cellular Component GO Annotation Evidence Reference Source
part of proteasome regulatory particle, base subcomplex IDA
IDA: Inferred from direct assay
19490896 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

PSMD9 Protein Structure

PDZ_2

PDZ_2: PDZ domain (137 - 201)

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

26S proteasome non-ATPase regulatory subunit 9

26S proteasome regulatory subunit p27

PSMD9 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
PSMD9 O00233 KLKB1 Homo sapiens P03952 32814053
Intra
PSMD9 O00233 KLKB1 Homo sapiens P03952 32814053
Intra
PSMD9 O00233 KLKB1 Homo sapiens P03952 32814053
Intra
PSMD9 O00233 CCDC136 Homo sapiens Q96JN2-2 25416956
Intra
PSMD9 O00233 CCDC136 Homo sapiens Q96JN2-2 25416956
Intra
PSMD9 O00233 CEP85L Homo sapiens Q5SZL2-5 32296183
Intra
PSMD9 O00233 CEP85L Homo sapiens Q5SZL2-5 32296183
Intra
PSMD9 O00233 CEP85L Homo sapiens Q5SZL2-5 32296183
Intra
PSMD9 O00233 CSH1 Homo sapiens P0DML2 25009770
Intra
PSMD9 O00233 CSH1 Homo sapiens P0DML2 25009770
Intra
PSMD9 O00233 CSH1 Homo sapiens P0DML2 25009770
Intra
PSMD9 O00233 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PSMD9 O00233 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PSMD9 O00233 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PSMD9 O00233 IL6R Homo sapiens P08887-2 25009770
Intra
PSMD9 O00233 IL6R Homo sapiens P08887-2 25009770
Intra
PSMD9 O00233 AHCYL1 Homo sapiens O43865 25416956
Intra
PSMD9 O00233 AHCYL1 Homo sapiens O43865 25416956
Intra
PSMD9 O00233 HNRNPA1 Homo sapiens P09651-2 25009770
Intra
PSMD9 O00233 HNRNPA1 Homo sapiens P09651-2 25009770
Intra
PSMD9 O00233 HNRNPA1 Homo sapiens P09651-2 25009770
Intra
PSMD9 O00233 RPS14 Homo sapiens P62263 25009770
Intra
PSMD9 O00233 RPS14 Homo sapiens P62263 25009770
Intra
PSMD9 O00233 RPS14 Homo sapiens P62263 25009770
Intra
PSMD9 O00233 TRAF2 Homo sapiens Q12933 32296183
Intra
PSMD9 O00233 TRAF2 Homo sapiens Q12933 32296183
Intra
PSMD9 O00233 TRAF2 Homo sapiens Q12933 32296183
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 25416956
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333
Y2H
21516116
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 32296183
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 33961781
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 32296183
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 25416956
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 32296183
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 19490896
Intra
PSMD9 O00233 PSMC6 Homo sapiens P62333 35271311
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 25416956
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 32296183
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 25416956
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 32296183
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 32296183
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 19490896
Intra
PSMD9 O00233 PSMC3 Homo sapiens P17980 33961781
Intra
PSMD9 O00233 TRIM42 Homo sapiens Q8IWZ5 25416956
Intra
PSMD9 O00233 TRIM42 Homo sapiens Q8IWZ5 25416956
Intra
PSMD9 O00233 LPL Homo sapiens P06858 32814053
Intra
PSMD9 O00233 LPL Homo sapiens P06858 32814053
Intra
PSMD9 O00233 LPL Homo sapiens P06858 32814053
Intra
PSMD9 O00233 TRIM39 Homo sapiens Q9HCM9 25416956
Intra
PSMD9 O00233 BANP Homo sapiens Q8N9N5 25416956
Intra
PSMD9 O00233 BANP Homo sapiens Q8N9N5 25416956
Intra
PSMD9 O00233 NCKIPSD Homo sapiens Q9NZQ3 25416956
Intra
PSMD9 O00233 NCKIPSD Homo sapiens Q9NZQ3 25416956
Intra
PSMD9 O00233 TCF3 Homo sapiens P15923-1 25009770
Intra
PSMD9 O00233 TCF3 Homo sapiens P15923-1 25009770
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Carpal Tunnel Syndrome

Cts

Carpal Tunnel Syndrome, Familial

Carpal Tunnel Syndrome 1

CTS1

Amyotrophy, Thenar, Of Carpal Origin

Carpal Tunnel Median Neuropathy

Cts - Carpal Tunnel Syndrome

Median Nerve Entrapment

Carpal Canal

Carpal Tunnel

Compression Neuropathy, Carpal Tunnel

Distal Median Nerve Compression

Distal Median Nerve Entrapment

Entrapment Neuropathy, Carpal Tunnel

Median Neuropathy, Carpal Tunnel

Median Neuropathy Carpal Tunnel

Thenar Amyotrophy Of Crapal Origin

Maturity-Onset Diabetes Of The Young, Type 3

Maturity-Onset Diabetes Of The Young Type 3

MODY3

Mody, Type Iii

Mody Type 3

Mody, Type 3

Maturity-Onset Diabetes Of The Young 3

Mody-3

Diabetes Of The Young, Maturity-Onset, Type 3

Histrionic Personality Disorder
Nerve Compression Syndrome

Entrapment Neuropathies

Compression Neuropathy

Entrapment Neuropathy

Peripheral Nerve Entrapment Syndrome

Nerve Compression Syndromes

Hereditary Liability To Pressure Palsies

Maturity-Onset Diabetes Of The Young

MODY

Maturity Onset Diabetes Mellitus In Young

Mason-Type Diabetes

Mason Type Diabetes

Maturity Onset Diabetes Of The Young

Mody Syndrome

Diabetes Of The Young, Maturity-Onset

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
Canis familiaris PSMD9 VGNC VGNC:52958
Bos taurus PSMD9 VGNC VGNC:53917
Rattus norvegicus PSMD9 RGD RGD:621110
Mus musculus PSMD9 MGD MGI:1914401
Macaca mulatta PSMD9 VGNC VGNC:84901
Felis catus PSMD9 VGNC VGNC:80467