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salivary exosomal PSMA7 was present at high levels in salivary exosomes from subjects with Inflammatory bowel disease. It can be a very promising biomarker
Data indicate that proteasome subunit alpha 6 (PSMA6 (show PSMA6 Proteins)) direct contacts with proteasome subunit alpha 7 (PSMA7) tetradecamer.
Studies have found significant associations of the treatment response with the 26S proteasome non-ATPase subunit (show PSMD14 Proteins) 9 (show ATP5G1 Proteins) (PSMD9 (show PSMD9 Proteins)), proteasome alpha type 7 subunit (PSMA7) and PSMD13 (show PSMD13 Proteins) genes.
c-Abl (show ABL1 Proteins) regulates proteasome abundance by controlling the ubiquitin-proteasomal degradation of PSMA7 subunit
PSMA7 functions partially through downregulation NOD1 (show NOD1 Proteins).
PSMA7 inhibits the proliferation, tumorigenicity and invasion of A549 cells in vitro
CNB (show PPP3R1 Proteins) binds to proteasome subunit alpha type 7 (PSMA7) and inhibits the transactivation activity of hypoxia-inducible factor-1alpha (HIF-1alpha (show HIF1A Proteins)) via the proteasome pathway.
High expression of PSMA7 was significantly correlated with liver metastasis.
The present study demonstrates that c-Abl (show ABL1 Proteins) and Arg (abl (show ABL1 Proteins)-related gene) tyrosine kinases associate with and phosphorylate the proteasome PSMA7 (alpha4) subunit at Tyr (show TYR Proteins)-153.
PSMA7 may play an important role in colorectal cancer progression.
Expression of proteasomal subunit PSMA7 results in potent inhibition of retinoic acid induced gene-1 (RIG)-1 (show ROBO3 Proteins) and MAVS (show MAVS Proteins)-mediated interferon-beta (show IFNB1 Proteins) promoter activity.
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. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. This gene encodes a member of the peptidase T1A family that functions as a 20S core alpha subunit. The encoded protein interacts with the hepatitis B virus X protein and plays a role in regulating hepatitis C virus internal ribosome entry site (IRES) activity, an activity essential for viral replication. The encoded protein also plays a role in the cellular stress response by regulating hypoxia-inducible factor-1alpha. A pseudogene of this gene is located on the long arm of chromosome 9.
proteasome subunit RC6-1
, proteasome subunit XAPC7
, proteasome subunit alpha 4
, proteasome subunit alpha type-7
, proteasome subunit alpha type 7
, proteasome alpha 7 subunit
, proteasome 28 kDa subunit homolog
, proteasome alpha subunit type 7
, 20S proteasome alpha 4 subunit
, proteasome subunit alpha 4-B
, proteasome subunit alpha type-7-B