SCUBA

PSMC4 — Proteasome 26S subunit, ATPase 4

PSMC4 belongs to a gene co-expression module in 5 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

PSMC4's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsER protein processing
Protein processing & ER
EIF6, KDELR2, PDIA6, PSMC3, SDF2L1, SPCS2, UBE2L3View in SCUBA
CD8⁺ T cellsER Protein Quality Control
Protein processing & ER
ARPC3, CALR, DYNLL1, MRPL47, PDIA3, PPIB, PSMA5, PSMB1 +3 moreView in SCUBA
FibroblastsER Protein Processing
Vesicular traficking
ARPC2, ENO1, GTF3C6, KDELR2, LMAN1, OSTC, P4HB, PRDX4 +5 moreView in SCUBA
Gamma-delta T cellsProteasome Complex
Protein processing & ER
APH1A, EIF3I, JTB, MRPL27, PSMB6, PSMB7, PSMC1, PSMC3 +4 more
Innate lymphoid cellsProteasome ER Proteostasis
Protein processing & ER
ATP5MC1, ATP5PF, DBI, GNG5, GTF3C6, HNRNPK, IL4I1, MANF +19 moreView in SCUBA

About the gene

SynonymsMGC13687, MGC23214, MGC8570, MIP224, RPT3, S6, TBP-7, TBP7
Chromosome19: 39971165-39981764
Predicted locationIntracellular
Essential geneYes
Protein classEssential proteins, Plasma proteins, Predicted intracellular proteins

Function

Component of the 26S proteasome, a multiprotein complex involved in the ATP-dependent degradation of ubiquitinated proteins. This complex plays a key role in the maintenance of protein homeostasis by removing misfolded or damaged proteins, which could impair cellular functions, and by removing proteins whose functions are no longer required. Therefore, the proteasome participates in numerous cellular processes, including cell cycle progression, apoptosis, or DNA damage repair. PSMC4 belongs to the heterohexameric ring of AAA (ATPases associated with diverse cellular activities) proteins that unfolds ubiquitinated target proteins that are concurrently translocated into a proteolytic chamber and degraded into peptides

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.