PSME2 (Gene)

Synonyms:ENTREZ:5721, HGNC:9569, MIM:602161, NM_002818, NP_002809, PA28B, PA28beta, PSME2, REGbeta, XM_006720213, XP_006720276, proteasome activator subunit 2
Id:ENSG00000284889
Description:proteasome activator subunit 2 [Source:HGNC Symbol;Acc:HGNC:9569]
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. The immunoproteasome contains an alternate regulator, referred to as the 11S regulator or PA28, that replaces the 19S regulator. Three subunits (alpha, beta and gamma) of the 11S regulator have been identified. This gene encodes the beta subunit of the 11S regulator, one of the two 11S subunits that is induced by gamma-interferon. Three beta and three alpha subunits combine to form a heterohexameric ring. Six pseudogenes have been identified on chromosomes 4, 5, 8, 10 and 13. [provided by RefSeq, Jul 2008]

Analyze

Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View PSME2's neighborhood in the knowledge graph.

Playbook Workflow Builder
Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with PSME2.

Gene Partnership Appyter
CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using PSME2.

Gene and Drug Landing Page Aggregator
GDLPA Landing Pages Links

The Gene and Drug Landing Page Aggregator (GDLPA) finds links to primary and secondary source information from CFDE and other resources. Discover landing pages for PSME2.

Playbook Workflow Builder
Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with PSME2.

Results found

Linked to

 

Label

Description

 

Phenotype

Accumulation of substantial excess body fat.

Phenotype

The presence of chronic increased pressure in the systemic arterial system.

Phenotype

Intense feelings of nervousness, tension, or panic often arise in response to interpersonal stresses...

Phenotype

Frequently experiencing feelings of being down, miserable, and/or hopeless; struggling to recover fr...

Phenotype

Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usual...

Phenotype

A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.

Phenotype

Autism is a neurodevelopmental disorder characterized by impaired social interaction and communicati...

Phenotype

Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural...

Phenotype

Joint pain.

Phenotype

Sudden impairment of blood flow to a part of the brain due to occlusion or rupture of an artery to t...

  • Phenotype

    Accumulation of substantial excess body fat.


  • Phenotype

    The presence of chronic increased pressure in the systemic arterial system.


  • Phenotype

    Intense feelings of nervousness, tension, or panic often arise in response to interpersonal stresses...


  • Phenotype

    Frequently experiencing feelings of being down, miserable, and/or hopeless; struggling to recover fr...


  • Phenotype

    Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usual...


  • Phenotype

    A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.


  • Phenotype

    Autism is a neurodevelopmental disorder characterized by impaired social interaction and communicati...


  • Phenotype

    Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural...



  • Phenotype

    Sudden impairment of blood flow to a part of the brain due to occlusion or rupture of an artery to t...

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