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Expression of proteasomal subunit PSMA7 results in potent inhibition of retinoic acid induced gene-1 (RIG)-1 (zeige ROBO3 Proteine) and MAVS (zeige MAVS Proteine)-mediated interferon-beta (zeige IFNB1 Proteine) promoter activity.
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 (zeige PSMA6 Proteine)) 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 (zeige PSMD14 Proteine) 9 (zeige ATP5G1 Proteine) (PSMD9 (zeige PSMD9 Proteine)), proteasome alpha type 7 subunit (PSMA7) and PSMD13 (zeige PSMD13 Proteine) genes.
c-Abl (zeige ABL1 Proteine) regulates proteasome abundance by controlling the ubiquitin-proteasomal degradation of PSMA7 subunit
PSMA7 functions partially through downregulation NOD1 (zeige NOD1 Proteine).
PSMA7 inhibits the proliferation, tumorigenicity and invasion of A549 cells in vitro
CNB (zeige PPP3R1 Proteine) binds to proteasome subunit alpha type 7 (PSMA7) and inhibits the transactivation activity of hypoxia-inducible factor-1alpha (HIF-1alpha (zeige HIF1A Proteine)) via the proteasome pathway.
High expression of PSMA7 was significantly correlated with liver metastasis.
The present study demonstrates that c-Abl (zeige ABL1 Proteine) and Arg (abl (zeige ABL1 Proteine)-related gene) tyrosine kinases associate with and phosphorylate the proteasome PSMA7 (alpha4) subunit at Tyr (zeige TYR Proteine)-153.
PSMA7 may play an important role in colorectal cancer progression.
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 alpha type 7
, proteasome alpha 7 subunit
, proteasome alpha subunit type 7
, proteasome subunit alpha type-7-like
, proteasome subunit RC6-1
, proteasome subunit alpha type-7
, proteasome subunit XAPC7
, proteasome subunit alpha 4
, proteasome 28 kDa subunit homolog