SCUBA

TAP1 — Transporter 1, ATP binding cassette subfamily B member

TAP1 belongs to a gene co-expression module in 14 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.

TAP1's module in each cell type

Cell typeModuleShares the module with
CD19⁺ B cellsType I Interferon
Anti-viral
GBP2, GBP4, IRF9, ISG15, ISG20, LY6E, MNDA, MX1 +9 moreView in SCUBA
CD4⁺ T cellsInterferon response
Anti-viral
ACTN4, CAPZA1, CHMP4A, CHMP5, EFHD2, IL12RB1, LSP1, PARP14 +7 moreView in SCUBA
CD8⁺ T cellsType I Interferon
Inflammation
BST2, CHMP5, EIF2AK2, LAP3, NAPA, NMI, OASL, PLSCR1 +1 moreView in SCUBA
EndothelialIFN-gamma Response
Inflammation
APOL2, APOL6, BATF2, CARD16, CASP1, CD40, CXCL10, CXCL11 +18 moreView in SCUBA
EnterocytesIFN-gamma STAT1 signaling
Inflammation
C2, ENSG00000283782, GBP4, HLA-E, LAP3, NLRC5, PARP8, STAT1 +1 moreView in SCUBA
FibroblastsType I Interferon
Inflammatory
APOL6, BATF2, CXCL10, GBP1, IFI44L, IFIT2, IFIT3, ISG15 +6 moreView in SCUBA
Gamma-delta T cellsAntiviral ISG Response
Inflammation
ACTR1A, ATRX, CD164, CYTH4, FGD3, GIT2, LASP1, PARP10 +6 more
Glial cellsIFN-gamma Effector Program
Inflammation
APOL1, APOL2, GBP1, IDO1, IFI44L, IL18BP, IL32, LAP3 +5 moreView in SCUBA
Goblet cellsMHC Class I Antigen Presentation
Immune function
APOL1, APOL6, B2M, HLA-A, HLA-B, HLA-C, HLA-E, HLA-F +4 moreView in SCUBA
Innate lymphoid cellsILC1 Effector Activation
activation
ADAM19, ARHGEF3, BATF, CD151, CDK4, FES, FURIN, HLA-F +16 moreView in SCUBA
Lymphatic endothelialApoptosis Immune Regulation
Immune regulation
A4GALT, CFLAR, COX17, GRINA, MPZL1, NINJ1, OPTN, PAWR +2 moreView in SCUBA
MacrophagesIFN-gamma Response
Inflammatory
ANKRD22, APOL2, ATF5, ATP13A1, CD274, CD300LF, CD40, CD48 +21 moreView in SCUBA
MonocytesIFN-gamma Response
Antiviral
APOL2, APOL6, CXCL10, ETV7, GBP1, GBP4, GBP5, IFIH1 +6 moreView in SCUBA
Mucosal-associated invariant T cellMAIT Tissue Residence
Tissue residence
ANAPC16, ARHGDIB, ATP5IF1, CD3E, CD53, CD99, CTSD, CXCR6 +7 more

About the gene

SynonymsABCB2, D6S114E, PSF1, RING4
Chromosome6: 32845209-32853816
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classCancer-related genes, Disease related genes, Enzymes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
Molecular functionTranslocase
Biological processAdaptive immunity, Host-virus interaction, Immunity, Peptide transport, Protein transport, Transport

Function

ABC transporter associated with antigen processing. In complex with TAP2 mediates unidirectional translocation of peptide antigens from cytosol to endoplasmic reticulum (ER) for loading onto MHC class I (MHCI) molecules. Uses the chemical energy of ATP to export peptides against the concentration gradient. During the transport cycle alternates between 'inward-facing' state with peptide binding site facing the cytosol to 'outward-facing' state with peptide binding site facing the ER lumen. Peptide antigen binding to ATP-loaded TAP1-TAP2 induces a switch to hydrolysis-competent 'outward-facing' conformation ready for peptide loading onto nascent MHCI molecules. Subsequently ATP hydrolysis resets the transporter to the 'inward facing' state for a new cycle. Typically transports intracellular peptide antigens of 8 to 13 amino acids that arise from cytosolic proteolysis via IFNG-induced immunoproteasome. Binds peptides with free N- and C-termini, the first three and the C-terminal residues being critical. Preferentially selects peptides having a highly hydrophobic residue at position 3 and hydrophobic or charged residues at the C-terminal anchor. Proline at position 2 has the most destabilizing effect. As a component of the peptide loading complex (PLC), acts as a molecular scaffold essential for peptide-MHCI assembly and antigen presentation.

Human Protein Atlas · Open Targets · UniProt

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