Immunoregulatory interactions between lymphoid and non-lymphoid cells (Homo sapiens)
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Description
<p>Molecules such as KIRs and LILRs form part of a crucial surveillance system that looks out for any derangement, usually caused by cancer or viral infection, in MHC Class I presentation. Somatic cells are also able to report internal functional impairment by displaying surface stress markers such as MICA. The presence of these molecules on somatic cells is picked up by C-lectin NK immune receptors.<p><p>Lymphoid cells are able to regulate their location and movement in accordance to their state of activation, and home in on tissues expressing the appropriate complementary ligands. For example, lymphoid cells may fine tune the presence and concentration of adhesion molecules belonging to the IgSF, Selectin and Integrin class that interact with a number of vascular markers of inflammation.<p><p>Furthermore, there are a number of avenues through which lymphoid cells may interact with antigen. This may be presented directly to a specific T-cell receptor in the context of an MHC molecule. Antigen-antibody complexes may anchor to the cell via a small number of lymphoid-specific Fc receptors that may, in turn, influence cell function further. Activated complement factor C3d binds to both antigen and to cell surface receptor CD21. In such cases, the far-reaching influence of CD19 on B-lymphocyte function is tempered by its interaction with CD21. Original Pathway at Reactome: http://www.reactome.org/PathwayBrowser/#DB=gk_current&FOCUS_SPECIES_ID=48887&FOCUS_PATHWAY_ID=198933</div>
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History
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External references
DataNodes
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Name | Type | Database reference | Comment |
---|---|---|---|
AMICA1 | Protein | Q86YT9 (Uniprot-TrEMBL) | |
AMICA1 | Protein | Q86YT9 (Uniprot-TrEMBL) | |
Antigen peptide bound class I MHC | Complex | REACT_11766 (Reactome) | |
Antigen-bound Ig G Antibody | Complex | REACT_11894 (Reactome) | In view of the highly variable nature of antibody proteins, this biological object is an approximate and fragmented representation of an IgM/IgD antibody, given the limitations of Ig chain enumeration in UniProt. A single mRNA transcript is alternatively spliced to give either IgM or IgD. Thus unactivated B cells contain both classes of antibody. |
Antigen-bound antibody bound to lymphoid Fc gamma receptors | Complex | REACT_11822 (Reactome) | |
B2M | Protein | P61769 (Uniprot-TrEMBL) | |
C3d complexed with antigen | Complex | REACT_11562 (Reactome) | |
C3d fragment | Protein | P01024 (Uniprot-TrEMBL) | |
CD160 | Protein | O95971 (Uniprot-TrEMBL) | |
CD160 | Protein | O95971 (Uniprot-TrEMBL) | |
CD19 | Protein | P15391 (Uniprot-TrEMBL) | |
CD200 | Protein | P41217 (Uniprot-TrEMBL) | |
CD200 bound to CD200R | Complex | REACT_11641 (Reactome) | |
CD200 | Protein | P41217 (Uniprot-TrEMBL) | |
CD200R1 | Protein | Q8TD46 (Uniprot-TrEMBL) | |
CD200R1 | Protein | Q8TD46 (Uniprot-TrEMBL) | |
CD226 PVR | Complex | REACT_11602 (Reactome) | |
CD226 | Protein | Q15762 (Uniprot-TrEMBL) | |
CD226 bound to Nectin 2 | Complex | REACT_11703 (Reactome) | |
CD226 | Protein | Q15762 (Uniprot-TrEMBL) | |
CD247-1 | Protein | P20963-1 (Uniprot-TrEMBL) | |
CD34-1 | Protein | P28906-1 (Uniprot-TrEMBL) | |
CD3D | Protein | P04234 (Uniprot-TrEMBL) | |
CD3E | Protein | P07766 (Uniprot-TrEMBL) | |
CD3G | Protein | P09693 (Uniprot-TrEMBL) | |
CD40 complexed with CD40L | Complex | REACT_11386 (Reactome) | |
CD40-1 | Protein | P25942-1 (Uniprot-TrEMBL) | |
CD40-1 | Protein | P25942-1 (Uniprot-TrEMBL) | |
CD40LG | Protein | P29965 (Uniprot-TrEMBL) | |
CD81 | Protein | P60033 (Uniprot-TrEMBL) | |
CD8A | Protein | P01732 (Uniprot-TrEMBL) | |
CD8B | Protein | P10966 (Uniprot-TrEMBL) | |
CD96 PVR | Complex | REACT_11952 (Reactome) | |
CD96 | Protein | P40200 (Uniprot-TrEMBL) | |
CDH1 | Protein | P12830 (Uniprot-TrEMBL) | |
CRTAM bound to NECL2 | Complex | REACT_11356 (Reactome) | |
CRTAM | Protein | O95727 (Uniprot-TrEMBL) | |
CXADR | Protein | P78310 (Uniprot-TrEMBL) | |
CXADR bound to JAML | Complex | REACT_11619 (Reactome) | |
CXADR | Protein | P78310 (Uniprot-TrEMBL) | |
Complex of CD19, CD81, CD225 and CD21 with C3d-bound Antigen | Complex | REACT_11584 (Reactome) | |
Complex of CD19, CD81, CD225 and CD21 | Complex | REACT_11777 (Reactome) | |
E-cadherin bound to KLRG1 | Complex | REACT_11260 (Reactome) | |
FCGR2B | Protein | P31994 (Uniprot-TrEMBL) | |
FCGR3A | Protein | P08637 (Uniprot-TrEMBL) | |
GLYCAM1 | Protein | Q8IVK1 (Uniprot-TrEMBL) | |
HCST | Protein | Q9UBK5 (Uniprot-TrEMBL) | |
HLA Bw4 interacting with KIR3DL1 | Complex | REACT_11950 (Reactome) | |
HLA class I histocompatibility antigen, A-1 alpha chain precursor | Protein | P30443 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-11 alpha chain | Protein | P13746 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-2 alpha chain | Protein | P01892 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-23 alpha chain | Protein | P30447 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-24 alpha chain | Protein | P05534 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-25 alpha chain | Protein | P18462 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-26 alpha chain | Protein | P30450 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-29 alpha chain | Protein | P30512 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-3 alpha chain precursor | Protein | P04439 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-30 alpha chain | Protein | P16188 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-31 alpha chain | Protein | P16189 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-32 alpha chain | Protein | P10314 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-33 alpha chain | Protein | P16190 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-34 alpha chain | Protein | P30453 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-36 alpha chain | Protein | P30455 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-43 alpha chain | Protein | P30456 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-66 alpha chain | Protein | P30457 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-68 alpha chain | Protein | P01891 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-69 alpha chain | Protein | P10316 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-74 alpha chain | Protein | P30459 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, A-80 alpha chain | Protein | Q09160 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-1 alpha chain | Protein | P30499 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-12 alpha chain | Protein | P30508 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-14 alpha chain | Protein | P30510 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-15 alpha chain | Protein | Q07000 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-16 alpha chain | Protein | Q29960 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-17 alpha chain | Protein | Q95604 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-18 alpha chain | Protein | Q29865 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-2 alpha chain | Protein | P30501 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-3 alpha chain precursor | Protein | P04222 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-4 alpha chain precursor | Protein | P30504 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-5 alpha chain precursor | Protein | Q9TNN7 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-6 alpha chain precursor | Protein | Q29963 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-7 alpha chain precursor | Protein | P10321 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, Cw-8 alpha chain | Protein | P30505 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, E alpha chain precursor | Protein | P13747 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, alpha chain F precursor | Protein | P30511 (Uniprot-TrEMBL) | |
HLA class I histocompatibility antigen, alpha chain G precursor | Protein | P17693 (Uniprot-TrEMBL) | |
HLA-A3 interacting with KIR3DL2 | Complex | REACT_11887 (Reactome) | |
HLA-A3 | Complex | REACT_11726 (Reactome) | |
HLA-Bw4 | Complex | REACT_11642 (Reactome) | |
HLA-C Cw3 | Complex | REACT_11404 (Reactome) | |
HLA-C Cw4 | Complex | REACT_11388 (Reactome) | |
HLA-C group 1 interacting with KIR2DL2/3 | Complex | REACT_11577 (Reactome) | |
HLA-C group 1 interacting with KIR2DS2 | Complex | REACT_11521 (Reactome) | |
HLA-C group 2 interacting with KIR2DL1 | Complex | REACT_11338 (Reactome) | |
HLA-C group 2 interacting with KIR2DS1 | Complex | REACT_11864 (Reactome) | |
HLA-C group-I-interacting KIRs | Protein | REACT_11748 (Reactome) | |
HLA-E interacting with KLRC1 KLRD1 | Complex | REACT_11770 (Reactome) | |
HLA-E | Complex | REACT_11603 (Reactome) | |
HLA-G interacting with KIR2DL4 | Complex | REACT_11741 (Reactome) | |
HLA-G | Complex | REACT_11699 (Reactome) | |
ICAM 1-4 | Protein | REACT_11859 (Reactome) | |
ICAM1 | Protein | P05362 (Uniprot-TrEMBL) | |
ICAM2 | Protein | P13598 (Uniprot-TrEMBL) | |
ICAM3 | Protein | P32942 (Uniprot-TrEMBL) | |
ICAM4 | Protein | Q14773 (Uniprot-TrEMBL) | |
IFITM1 | Protein | P13164 (Uniprot-TrEMBL) | |
IGHV7-81 | Protein | Q6PIL0 (Uniprot-TrEMBL) | |
IGHV | Protein | A2KUC3 (Uniprot-TrEMBL) | |
IGKC | Protein | P01834 (Uniprot-TrEMBL) | |
IGKV1-5 | Protein | P01602 (Uniprot-TrEMBL) | |
IGKV4-1 | Protein | P06312 (Uniprot-TrEMBL) | |
IGKVA18 | Protein | A2NJV5 (Uniprot-TrEMBL) | |
IGLC1 | Protein | P0CG04 (Uniprot-TrEMBL) | |
IGLC2 | Protein | P0CG05 (Uniprot-TrEMBL) | |
IGLC3 | Protein | P0CG06 (Uniprot-TrEMBL) | |
IGLC6 | Protein | P0CF74 (Uniprot-TrEMBL) | |
IGLC7 | Protein | A0M8Q6 (Uniprot-TrEMBL) | |
IGLV1-36 | Protein | Q5NV67 (Uniprot-TrEMBL) | |
IGLV1-40 | Protein | Q5NV69 (Uniprot-TrEMBL) | |
IGLV1-44 | Protein | Q5NV81 (Uniprot-TrEMBL) | |
IGLV10-54 | Protein | Q5NV86 (Uniprot-TrEMBL) | |
IGLV11-55 | Protein | Q5NV87 (Uniprot-TrEMBL) | |
IGLV2-11 | Protein | Q5NV84 (Uniprot-TrEMBL) | |
IGLV2-18 | Protein | Q5NV65 (Uniprot-TrEMBL) | |
IGLV2-23 | Protein | Q5NV89 (Uniprot-TrEMBL) | |
IGLV2-33 | Protein | Q5NV66 (Uniprot-TrEMBL) | |
IGLV3-12 | Protein | Q5NV85 (Uniprot-TrEMBL) | |
IGLV3-16 | Protein | Q5NV64 (Uniprot-TrEMBL) | |
IGLV3-22 | Protein | Q5NV75 (Uniprot-TrEMBL) | |
IGLV3-25 | Protein | Q5NV90 (Uniprot-TrEMBL) | |
IGLV3-27 | Protein | Q5NV91 (Uniprot-TrEMBL) | |
IGLV4-3 | Protein | Q5NV61 (Uniprot-TrEMBL) | |
IGLV4-60 | Protein | Q5NV79 (Uniprot-TrEMBL) | |
IGLV4-69 | Protein | Q5NV92 (Uniprot-TrEMBL) | |
IGLV5-37 | Protein | Q5NV68 (Uniprot-TrEMBL) | |
IGLV5-45 | Protein | Q5NV82 (Uniprot-TrEMBL) | |
IGLV7-43 | Protein | Q5NV80 (Uniprot-TrEMBL) | |
IGLV7-46 | Protein | Q5NV83 (Uniprot-TrEMBL) | |
IGLV8-61 | Protein | Q5NV62 (Uniprot-TrEMBL) | |
IGLV | Protein | A2NXD2 (Uniprot-TrEMBL) | |
ITGA4 | Protein | P13612 (Uniprot-TrEMBL) | |
ITGAL | Protein | P20701 (Uniprot-TrEMBL) | |
ITGB1 | Protein | P05556 (Uniprot-TrEMBL) | |
ITGB2 | Protein | P05107 (Uniprot-TrEMBL) | |
ITGB7 | Protein | P26010 (Uniprot-TrEMBL) | |
Ig heavy chain V-I region EU | Protein | P01742 (Uniprot-TrEMBL) | |
Ig heavy chain V-I region HG3 | Protein | P01743 (Uniprot-TrEMBL) | |
Ig heavy chain V-I region Mot | Protein | P06326 (Uniprot-TrEMBL) | |
Ig heavy chain V-I region ND | Protein | P01744 (Uniprot-TrEMBL) | |
Ig heavy chain V-I region SIE | Protein | P01761 (Uniprot-TrEMBL) | |
Ig heavy chain V-I region WOL | Protein | P01760 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region ARH-77 | Protein | P06331 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region COR | Protein | P01815 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region DAW | Protein | P01816 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region HE | Protein | P01818 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region MCE | Protein | P01817 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region NEWM | Protein | P01825 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region OU | Protein | P01814 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region SESS | Protein | P04438 (Uniprot-TrEMBL) | |
Ig heavy chain V-II region WAH | Protein | P01824 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region BRO | Protein | P01766 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region BUR | Protein | P01773 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region BUT | Protein | P01767 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region CAM | Protein | P01768 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region DOB | Protein | P01782 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region GA | Protein | P01769 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region GAL | Protein | P01781 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region HIL | Protein | P01771 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region JON | Protein | P01780 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region KOL | Protein | P01772 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region LAY | Protein | P01775 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region NIE | Protein | P01770 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region POM | Protein | P01774 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region TEI | Protein | P01777 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region TIL | Protein | P01765 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region TRO | Protein | P01762 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region TUR | Protein | P01779 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region WAS | Protein | P01776 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region WEA | Protein | P01763 (Uniprot-TrEMBL) | |
Ig heavy chain V-III region ZAP | Protein | P01778 (Uniprot-TrEMBL) | |
Ig kappa chain V region EV15 | Protein | P06315 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region AG | Protein | P01593 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region AU | Protein | P01594 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region BAN | Protein | P04430 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Bi | Protein | P01595 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region CAR | Protein | P01596 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region DEE | Protein | P01597 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Daudi | Protein | P04432 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region EU | Protein | P01598 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Gal | Protein | P01599 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region HK101 | Protein | P01601 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Hau | Protein | P01600 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Ka | Protein | P01603 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Kue | Protein | P01604 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Lay | Protein | P01605 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Mev | Protein | P01612 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Ni | Protein | P01613 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region OU | Protein | P01606 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Rei | Protein | P01607 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Roy | Protein | P01608 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Scw | Protein | P01609 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region WAT | Protein | P80362 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region WEA | Protein | P01610 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Walker | Protein | P04431 (Uniprot-TrEMBL) | |
Ig kappa chain V-I region Wes | Protein | P01611 (Uniprot-TrEMBL) | |
Ig kappa chain V-II region Cum | Protein | P01614 (Uniprot-TrEMBL) | |
Ig kappa chain V-II region FR | Protein | P01615 (Uniprot-TrEMBL) | |
Ig kappa chain V-II region GM607 | Protein | P06309 (Uniprot-TrEMBL) | |
Ig kappa chain V-II region MIL | Protein | P01616 (Uniprot-TrEMBL) | |
Ig kappa chain V-II region RPMI 6410 | Protein | P06310 (Uniprot-TrEMBL) | |
Ig kappa chain V-II region TEW | Protein | P01617 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region B6 | Protein | P01619 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region CLL | Protein | P04207 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region GOL | Protein | P04206 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region HAH | Protein | P18135 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region HIC | Protein | P18136 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region IARC/BL41 | Protein | P06311 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region NG9 | Protein | P01621 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region POM | Protein | P01624 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region SIE | Protein | P01620 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region Ti | Protein | P01622 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region VG | Protein | P04433 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region VH | Protein | P04434 (Uniprot-TrEMBL) | |
Ig kappa chain V-III region WOL | Protein | P01623 (Uniprot-TrEMBL) | |
Ig kappa chain V-IV region B17 | Protein | P06314 (Uniprot-TrEMBL) | |
Ig kappa chain V-IV region JI | Protein | P06313 (Uniprot-TrEMBL) | |
Ig kappa chain V-IV region Len | Protein | P01625 (Uniprot-TrEMBL) | |
Ig kappa chain V-IV region STH | Protein | P83593 (Uniprot-TrEMBL) | |
Ig lambda chain V region 4A | Protein | P04211 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region BL2 | Protein | P06316 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region EPS | Protein | P06888 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region HA | Protein | P01700 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region MEM | Protein | P06887 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region NEW | Protein | P01701 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region NEWM | Protein | P01703 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region NIG-64 | Protein | P01702 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region VOR | Protein | P01699 (Uniprot-TrEMBL) | |
Ig lambda chain V-I region WAH | Protein | P04208 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region BO | Protein | P01710 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region BOH | Protein | P01706 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region BUR | Protein | P01708 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region MGC | Protein | P01709 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region NEI | Protein | P01705 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region NIG-58 | Protein | P01713 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region NIG-84 | Protein | P04209 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region TOG | Protein | P01704 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region TRO | Protein | P01707 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region VIL | Protein | P01711 (Uniprot-TrEMBL) | |
Ig lambda chain V-II region WIN | Protein | P01712 (Uniprot-TrEMBL) | |
Ig lambda chain V-III region LOI | Protein | P80748 (Uniprot-TrEMBL) | |
Ig lambda chain V-III region SH | Protein | P01714 (Uniprot-TrEMBL) | |
Ig lambda chain V-IV region Bau | Protein | P01715 (Uniprot-TrEMBL) | |
Ig lambda chain V-IV region Hil | Protein | P01717 (Uniprot-TrEMBL) | |
Ig lambda chain V-IV region Kern | Protein | P01718 (Uniprot-TrEMBL) | |
Ig lambda chain V-IV region MOL | Protein | P06889 (Uniprot-TrEMBL) | |
Ig lambda chain V-IV region X | Protein | P01716 (Uniprot-TrEMBL) | |
Ig lambda chain V-V region DEL | Protein | P01719 (Uniprot-TrEMBL) | |
Ig lambda chain V-VI region AR | Protein | P01721 (Uniprot-TrEMBL) | |
Ig lambda chain V-VI region EB4 | Protein | P06319 (Uniprot-TrEMBL) | |
Ig lambda chain V-VI region NIG-48 | Protein | P01722 (Uniprot-TrEMBL) | |
Ig lambda chain V-VI region SUT | Protein | P06317 (Uniprot-TrEMBL) | |
Ig lambda chain V-VI region WLT | Protein | P06318 (Uniprot-TrEMBL) | |
Ig lambda chain V-VII region MOT | Protein | P01720 (Uniprot-TrEMBL) | |
IgH heavy chain V-III region VH26 precursor | Protein | P01764 (Uniprot-TrEMBL) | |
Integrin alpha4beta7 MADCAM1 | Complex | REACT_11447 (Reactome) | |
Integrin alpha4beta7 | Complex | REACT_11974 (Reactome) | |
Integrin alphaLbeta2 | Complex | REACT_11837 (Reactome) | |
KIR2DL1 | Protein | P43626 (Uniprot-TrEMBL) | |
KIR2DL1 | Protein | P43626 (Uniprot-TrEMBL) | |
KIR2DL2 | Protein | P43627 (Uniprot-TrEMBL) | |
KIR2DL3 | Protein | P43628 (Uniprot-TrEMBL) | |
KIR2DL4 | Protein | Q99706 (Uniprot-TrEMBL) | |
KIR2DL4 | Protein | Q99706 (Uniprot-TrEMBL) | |
KIR2DS1 | Protein | Q14954 (Uniprot-TrEMBL) | |
KIR2DS1 complexed with DAP12 | Complex | REACT_11752 (Reactome) | |
KIR2DS2 | Protein | P43631 (Uniprot-TrEMBL) | |
KIR2DS2 complexed with DAP12 | Complex | REACT_11717 (Reactome) | |
KIR3DL1 | Protein | P43629 (Uniprot-TrEMBL) | |
KIR3DL1 | Protein | P43629 (Uniprot-TrEMBL) | |
KIR3DL2 | Protein | P43630 (Uniprot-TrEMBL) | |
KIR3DL2 | Protein | P43630 (Uniprot-TrEMBL) | |
KLRC1 | Protein | P26715 (Uniprot-TrEMBL) | |
KLRC1 | Protein | P26715 (Uniprot-TrEMBL) | |
KLRD1 | Protein | Q13241 (Uniprot-TrEMBL) | |
KLRD1 | Protein | Q13241 (Uniprot-TrEMBL) | |
KLRG1 | Protein | Q96E93 (Uniprot-TrEMBL) | |
KLRG1 | Protein | Q96E93 (Uniprot-TrEMBL) | |
KLRK1 | Protein | P26718 (Uniprot-TrEMBL) | |
L-selectin interacting with known ligands | Complex | REACT_11760 (Reactome) | |
L-selectin ligands | Protein | REACT_11759 (Reactome) | |
LFA-1 ICAM 1-4 | Complex | REACT_11942 (Reactome) | |
LILR set | Protein | REACT_11576 (Reactome) | |
LILR-interacting MHC Class I molecules | Complex | REACT_11528 (Reactome) | |
Ligand interacting with NKG2D | Complex | REACT_11751 (Reactome) | |
Lymphoid-expressed Fc-gamma receptors | Protein | REACT_11814 (Reactome) | |
MADCAM1-1 | Protein | Q13477-1 (Uniprot-TrEMBL) | |
MADCAM1-1 | Protein | Q13477-1 (Uniprot-TrEMBL) | |
MHC Class I interacting with CD160 | Complex | REACT_11275 (Reactome) | |
MHC Class I interacting with LILRs | Complex | REACT_11656 (Reactome) | |
MHC Class I molecules interacting with CD160 | Complex | REACT_11830 (Reactome) | |
MICA | Protein | Q5SS58 (Uniprot-TrEMBL) | |
MICB | Protein | Q29980 (Uniprot-TrEMBL) | |
NKG2D complexed with DAP10 | Complex | REACT_11468 (Reactome) | |
NKG2D ligand | Protein | REACT_11351 (Reactome) | |
PVR | Protein | P15151 (Uniprot-TrEMBL) | |
PVRL2 | Protein | Q92692 (Uniprot-TrEMBL) | |
PVRL2 | Protein | Q92692 (Uniprot-TrEMBL) | |
PVR | Protein | P15151 (Uniprot-TrEMBL) | |
RAET1E | Protein | Q8TD07 (Uniprot-TrEMBL) | |
SELL | Protein | P14151 (Uniprot-TrEMBL) | |
SELL | Protein | P14151 (Uniprot-TrEMBL) | |
T-cell receptor alpha chain V region HPB-MLT precursor | Protein | P04436 (Uniprot-TrEMBL) | |
T-cell receptor alpha chain V region PY14 precursor | Protein | P01737 (Uniprot-TrEMBL) | |
T-cell receptor complex with CD8 | Complex | REACT_11534 (Reactome) | |
TCR interacting with antigen-bearing MHC Class I | Complex | REACT_11723 (Reactome) | |
TCRA | Protein | P04437 (Uniprot-TrEMBL) | |
TCRB | Protein | P04435 (Uniprot-TrEMBL) | |
TRAC | Protein | P01848 (Uniprot-TrEMBL) | |
TRBC1 | Protein | P01850 (Uniprot-TrEMBL) | |
TRBV12-3 | Protein | P01733 (Uniprot-TrEMBL) | |
TYROBP | Protein | O43914 (Uniprot-TrEMBL) | |
ULBP1 | Protein | Q9BZM6 (Uniprot-TrEMBL) | |
ULBP3 | Protein | Q9BZM4 (Uniprot-TrEMBL) | |
VCAM1 | Protein | P19320 (Uniprot-TrEMBL) | |
VCAM1 | Protein | P19320 (Uniprot-TrEMBL) | |
VLA-4 VCAM-1 | Complex | REACT_11750 (Reactome) | |
VLA-4 | Complex | REACT_11798 (Reactome) | |
cd21 | Protein | O15181 (Uniprot-TrEMBL) | |
class I MHC B13 | Protein | P30461 (Uniprot-TrEMBL) | |
class I MHC B14 | Protein | P30462 (Uniprot-TrEMBL) | |
class I MHC B15 | Protein | P30464 (Uniprot-TrEMBL) | |
class I MHC B18 | Protein | P30466 (Uniprot-TrEMBL) | |
class I MHC B27 | Protein | P03989 (Uniprot-TrEMBL) | |
class I MHC B35 | Protein | P30685 (Uniprot-TrEMBL) | |
class I MHC B37 | Protein | P18463 (Uniprot-TrEMBL) | |
class I MHC B38 | Protein | Q95365 (Uniprot-TrEMBL) | |
class I MHC B39 | Protein | P30475 (Uniprot-TrEMBL) | |
class I MHC B40 | Protein | Q04826 (Uniprot-TrEMBL) | |
class I MHC B41 | Protein | P30479 (Uniprot-TrEMBL) | |
class I MHC B42 | Protein | P30480 (Uniprot-TrEMBL) | |
class I MHC B44 | Protein | P30481 (Uniprot-TrEMBL) | |
class I MHC B45 | Protein | P30483 (Uniprot-TrEMBL) | |
class I MHC B46 | Protein | P30484 (Uniprot-TrEMBL) | |
class I MHC B47 | Protein | P30485 (Uniprot-TrEMBL) | |
class I MHC B49 | Protein | P30487 (Uniprot-TrEMBL) | |
class I MHC B50 | Protein | P30488 (Uniprot-TrEMBL) | |
class I MHC B51 | Protein | P18464 (Uniprot-TrEMBL) | |
class I MHC B52 | Protein | P30490 (Uniprot-TrEMBL) | |
class I MHC B53 | Protein | P30491 (Uniprot-TrEMBL) | |
class I MHC B54 | Protein | P30492 (Uniprot-TrEMBL) | |
class I MHC B55 | Protein | P30493 (Uniprot-TrEMBL) | |
class I MHC B56 | Protein | P30495 (Uniprot-TrEMBL) | |
class I MHC B57 | Protein | P18465 (Uniprot-TrEMBL) | |
class I MHC B58 | Protein | P10319 (Uniprot-TrEMBL) | |
class I MHC B59 | Protein | Q29940 (Uniprot-TrEMBL) | |
class I MHC B67 | Protein | Q29836 (Uniprot-TrEMBL) | |
class I MHC B7 | Protein | P01889 (Uniprot-TrEMBL) | |
class I MHC B73 | Protein | Q31612 (Uniprot-TrEMBL) | |
class I MHC B78 | Protein | P30498 (Uniprot-TrEMBL) | |
class I MHC B8 | Protein | P30460 (Uniprot-TrEMBL) | |
class I MHC B81 | Protein | Q31610 (Uniprot-TrEMBL) | |
class I MHC B82 | Protein | Q29718 (Uniprot-TrEMBL) |
Annotated Interactions
View all... |
Source | Target | Type | Database reference | Comment |
---|---|---|---|---|
AMICA1 | REACT_11154 (Reactome) | |||
Antigen peptide bound class I MHC | REACT_11080 (Reactome) | |||
Antigen-bound Ig G Antibody | REACT_11087 (Reactome) | |||
C3d complexed with antigen | REACT_11121 (Reactome) | |||
CD160 | REACT_11106 (Reactome) | |||
CD200R1 | REACT_11188 (Reactome) | |||
CD200 | REACT_11188 (Reactome) | |||
CD226 | REACT_11094 (Reactome) | |||
CD226 | REACT_11239 (Reactome) | |||
CD40-1 | REACT_11241 (Reactome) | |||
CD40LG | REACT_11241 (Reactome) | |||
CD96 | REACT_11207 (Reactome) | |||
CDH1 | REACT_11212 (Reactome) | |||
CRTAM | REACT_11097 (Reactome) | |||
CXADR | REACT_11154 (Reactome) | |||
Complex of CD19, CD81, CD225 and CD21 | REACT_11121 (Reactome) | |||
HLA-A3 | REACT_11124 (Reactome) | |||
HLA-Bw4 | REACT_11223 (Reactome) | |||
HLA-C Cw3 | REACT_11140 (Reactome) | |||
HLA-C Cw3 | REACT_11176 (Reactome) | |||
HLA-C Cw4 | REACT_11077 (Reactome) | |||
HLA-C Cw4 | REACT_11210 (Reactome) | |||
HLA-C group-I-interacting KIRs | REACT_11210 (Reactome) | |||
HLA-E | REACT_11119 (Reactome) | |||
HLA-G | REACT_11141 (Reactome) | |||
ICAM 1-4 | REACT_11173 (Reactome) | |||
Integrin alpha4beta7 | REACT_11199 (Reactome) | |||
Integrin alphaLbeta2 | REACT_11173 (Reactome) | |||
KIR2DL1 | REACT_11140 (Reactome) | |||
KIR2DL4 | REACT_11141 (Reactome) | |||
KIR2DS1 complexed with DAP12 | REACT_11077 (Reactome) | |||
KIR2DS2 complexed with DAP12 | REACT_11176 (Reactome) | |||
KIR3DL1 | REACT_11223 (Reactome) | |||
KIR3DL2 | REACT_11124 (Reactome) | |||
KLRC1 | REACT_11119 (Reactome) | |||
KLRD1 | REACT_11119 (Reactome) | |||
KLRG1 | REACT_11212 (Reactome) | |||
L-selectin ligands | REACT_11230 (Reactome) | |||
LILR set | REACT_11127 (Reactome) | |||
LILR-interacting MHC Class I molecules | REACT_11127 (Reactome) | |||
Lymphoid-expressed Fc-gamma receptors | REACT_11087 (Reactome) | |||
MADCAM1-1 | REACT_11199 (Reactome) | |||
MHC Class I molecules interacting with CD160 | REACT_11106 (Reactome) | |||
NKG2D complexed with DAP10 | REACT_11178 (Reactome) | |||
NKG2D ligand | REACT_11178 (Reactome) | |||
PVRL2 | REACT_11094 (Reactome) | |||
PVRL2 | REACT_11097 (Reactome) | |||
PVR | REACT_11207 (Reactome) | |||
PVR | REACT_11239 (Reactome) | |||
REACT_11077 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11080 (Reactome) | T cells distinguish foreign material from self through presentation of fragments of the antigen by the MHC cell surface receptors. Only if an MHC molecule presents an appropriate antigenic peptide will a cellular immune response be triggered. The orchestration of recognition and signaling events, from the initial recognition of antigenic peptides to the lysis of the target cell, is performed in a localized environment on the T cell, called the immunological synapse, and requires the coordinated activities of several T-Cell Receptor (TCR)-associated molecules. This particular reaction depicts the interaction of the TCR with MHC Class I molecules on somatic cell, requiring the support of CD3 and CD8 proteins. | |||
REACT_11087 (Reactome) | Most cells of the immune system express receptors for the Fc region of IgG. This heterogeneous family of molecules plays a critical role in immunity, by linking the humoral to the cellular responses. NK cells and B cells have been shown to express exclusively Fc-gamma RIIIa and RIIb respectively. | |||
REACT_11094 (Reactome) | NK cells express adhesion molecules that allow interaction with their tumour targets, promoting their lysis. For instance, the activating receptor CD226 is known to be involved in cytotoxic lymphocyte formation, as well as platelet adhesion to the endothelium. The cytoplasmic domain of CD226 contains binding motifs for members of the band 4.1 family of proteins, and for members of the membrane-associated guanylate kinase homolog (MAGUK) family. These proteins connect the CD226 receptor to the cytoskeleton and may promote clustering with LFA-1 integrin (also discussed in this pathway), which is known to participate in CD226's signaling cascade. CD226 plays a role in transendothelial migration, where it facilitates adherence to endothelial cells and migration between cell junctions. Nectin-2 binds CD226. It is ubiquitously expressed in cells of various tissues, especially in epithelial cells, neurons and fibroblasts. Like many other nectin and Necl proteins, nectin-2 serves as a viral entry receptor for alpha-herpesviruses including herpes simplex virus (HSV-1 and HSV-2). The other CD226 ligand, Necl-5, was initially identified as a receptor for poliovirus. CD96, another ligand for Necl-5, is strongly upregulated in activated NK cells. CRTAM is similarly up-regulated, and has been shown to to bind Necl-2, promoting NK cell cytotoxicity towards otherwise poorly immunogenic targets. | |||
REACT_11097 (Reactome) | NK cells express adhesion molecules that allow interaction with their tumour targets, promoting their lysis. For instance, the activating receptor CD226 is known to be involved in cytotoxic lymphocyte formation, as well as platelet adhesion to the endothelium. The cytoplasmic domain of CD226 contains binding motifs for members of the band 4.1 family of proteins, and for members of the membrane-associated guanylate kinase homolog (MAGUK) family. These proteins connect the CD226 receptor to the cytoskeleton and may promote clustering with LFA-1 integrin (also discussed in this pathway), which is known to participate in CD226's signaling cascade. CD226 plays a role in transendothelial migration, where it facilitates adherence to endothelial cells and migration between cell junctions. Nectin-2 binds CD226. It is ubiquitously expressed in cells of various tissues, especially in epithelial cells, neurons and fibroblasts. Like many other nectin and Necl proteins, nectin-2 serves as a viral entry receptor for alpha-herpesviruses including herpes simplex virus (HSV-1 and HSV-2). The other CD226 ligand, Necl-5, was initially identified as a receptor for poliovirus. CD96, another ligand for Necl-5, is strongly upregulated in activated NK cells. CRTAM is similarly up-regulated, and has been shown to to bind Necl-2, promoting NK cell cytotoxicity towards otherwise poorly immunogenic targets. | |||
REACT_11106 (Reactome) | CD160 is a GPI-anchored lymphocyte surface receptor in which expression is mostly restricted to the highly cytotoxic NK cells. MHC class I molecules bind to CD160 receptors on circulating NK lymphocytes and this triggers their cytotoxic activity and cytokine production. NK cells stimulated by IL-15 secrete soluble CD160 protein that binds to MHC-I molecules, resulting in the inhibition of the cytotoxic CD8+ T lymphocyte activity and of the CD160-mediated NK cell cytotoxicity. | |||
REACT_11119 (Reactome) | After interaction with its ligand HLA-E, which is expressed on normal cells, the C-type lectin inhibitory receptor CD94/NKG2A suppresses activation signaling processes. CD94/NKG2A receptors continuously recycle from the cell surface through endosomal compartments and back again in a process that requires energy and the cytoskeleton. This steady state process appears to be largely unaffected by exposure to ligand. | |||
REACT_11121 (Reactome) | CD19 is a lymphocyte cell surface molecule that functions as a general response regulator or rheostat, which defnes signalling thresholds. These responses are infuenced by signals transduced through a CD19-CD21 cell surface receptor complex, where the binding of complement C3d to CD21 links humoral immune responses with the innate immune system. The CD19-CD21 complex is composed of at least four non-covalently associated proteins: CD19, CD21(complement receptor 2),CD81 and CD225. | |||
REACT_11124 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11127 (Reactome) | Leukocyte immunoglobulin (Ig)-like receptors [LILRs, also known as Ig-like transcripts (ILTs)] are a family of inhibitory and stimulatory receptors encoded within the leukocyte receptor complex and are expressed by immune cell types of both myeloid and lymphoid lineage. Several members of the LILR family recognize major histocompatibility complex class I. The immunomodulatory role of LILR receptors indicates that they may exert an influence on signaling pathways of both innate and adaptive immune systems. Signaling mechanisms are employed that are similar to the ones adopted by the closely related killer cell inhibitory receptors (KIRs). ITIMs recruit inhibitory phosphatases that dephosphorylate ITIM and ITAM domains in order to influence intracellular signaling cascades. In contrast, activating LILRs, which lack any signaling domains of their own, rely on association with an adaptor protein such as FceRI-gamma to transmit their signal through its intracellular ITAMs. | |||
REACT_11140 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11141 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11154 (Reactome) | JAM members, such as JAML, bind coxsackie and adenovirus receptor (CXADR) on epithelial and endothelial cells. | |||
REACT_11161 (Reactome) | Integrins play a central role in mediating lymphocyte
adhesion to a number of surfaces. LFA-1 interacts with ICAMs 1-3 that are typically expressed on other immune system cells. ICAM-4 also interacts with LFA-1, and is known to be expressed on telencepahlic neurons.VCAM-1 regulates lymphocyte adhesion to activated endothelial cells via Very Late Antigen-4 (VLA-4). To function in a circulating mode, leukocytes express LFA-1 and VLA-4 in a low ligand binding capacity. When leukocytes reach sites of imflammation, these integrins are switched to a higher binding state to guide the complex process of transmigration, tethering, rolling, arrest, adhesion and shape change. Signal cascades between LFA-1 and VLA-4 may cross-talk affecting binding affinities in a reciprocal fashion. | |||
REACT_11173 (Reactome) | Integrins play a central role in mediating lymphocyte
adhesion to a number of surfaces. LFA-1 interacts with ICAMs 1-3 that are typically expressed on other immune system cells. ICAM-4 also interacts with LFA-1, and is known to be expressed on telencepahlic neurons.VCAM-1 regulates lymphocyte adhesion to activated endothelial cells via Very Late Antigen-4 (VLA-4). To function in a circulating mode, leukocytes express LFA-1 and VLA-4 in a low ligand binding capacity. When leukocytes reach sites of imflammation, these integrins are switched to a higher binding state to guide the complex process of transmigration, tethering, rolling, arrest, adhesion and shape change. Signal cascades between LFA-1 and VLA-4 may cross-talk affecting binding affinities in a reciprocal fashion. | |||
REACT_11176 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11178 (Reactome) | NKG2D is an activating immunoreceptor. By engaging NKG2D, HlA Class I-like molecules such as MICA, MICB, ULBP1-4 and RAE-1 provide powerful costimulation for NK cells and T-cells and can determine the magnitude and outcome of certain effector functions. NKG2D ligands are upregulated on the surfaces of cells under conditions of stress, for example infection or tumorigenesis, and therefore act as molecular flags to the immune system that something is wrong. | |||
REACT_11188 (Reactome) | While not ubiquitously distributed, CD200 is expressed on a wide range of cell types including thymocytes, B-cells, activated T-cells, follicular dendritic cells,
endothelium, CNS neurons in the central nervous system, cells in reproductive organs, keratinocytes and renal glomeruli. CD200R is a myeloid-inhibitory receptor, despite the absence of classical ITIMs in the cytoplasmic portion of the protein. Interestingly, CD200 is also expressed on neurons within the CNS and would be predicted to modulate activation of microglia through CD200R. | |||
REACT_11199 (Reactome) | Mucosal addressin cell adhesion molecule (MADCAM1) is present in the endothelium of mucosa, and binds alpha-4 beta-7 integrin and L-selectin, regulating both the passage and retention of leukocytes in mucosal tissues. MADCAM1 has been shown to be present as a homodimer. | |||
REACT_11207 (Reactome) | NK cells express adhesion molecules that allow interaction with their tumour targets, promoting their lysis. For instance, the activating receptor CD226 is known to be involved in cytotoxic lymphocyte formation, as well as platelet adhesion to the endothelium. The cytoplasmic domain of CD226 contains binding motifs for members of the band 4.1 family of proteins, and for members of the membrane-associated guanylate kinase homolog (MAGUK) family. These proteins connect the CD226 receptor to the cytoskeleton and may promote clustering with LFA-1 integrin (also discussed in this pathway), which is known to participate in CD226's signaling cascade. CD226 plays a role in transendothelial migration, where it facilitates adherence to endothelial cells and migration between cell junctions. Nectin-2 binds CD226. It is ubiquitously expressed in cells of various tissues, especially in epithelial cells, neurons and fibroblasts. Like many other nectin and Necl proteins, nectin-2 serves as a viral entry receptor for alpha-herpesviruses including herpes simplex virus (HSV-1 and HSV-2). The other CD226 ligand, Necl-5, was initially identified as a receptor for poliovirus. CD96, another ligand for Necl-5, is strongly upregulated in activated NK cells. CRTAM is similarly up-regulated, and has been shown to to bind Necl-2, promoting NK cell cytotoxicity towards otherwise poorly immunogenic targets. | |||
REACT_11210 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11212 (Reactome) | The lectin-like NK cell receptor KLRG1 binds to cadherins on epithelial cells and transmits inhibitory signals to the leukocyte. | |||
REACT_11223 (Reactome) | A hallmark of human NK cells is the expression of HLA class I-specific killer-cell immunoglobulin-like receptors (KIR). KIRs are not only variably expressed on the level of single NK cells but they are also highly polymorphic and polygenic (i.e. the gene content of the KIR cluster varies from individual to individual). There are 15 functional KIR genes known to date, 11 encoding receptors with two immunoglobulin domains (KIR2D genes) and 4 with three domains (KIR3D genes). Inhibitory KIR genes are characterized by long cytoplasmic tails featuring immunoreceptor tyrosine-based inhibitory motifs (ITIM), which upon engagement transmit inhibitory signals leading to the general shutdown of NK cell effector functions. There are six inhibitory KIRs with clearly defined specificities, all of the inhibitory kind and all for HLA class I allotypes: KIR2DL2 and KIR2DL3 for HLA-C group 1, KIR2DL1 for HLA-C group 2, KIR3DL1 for HLA-B (Bw4 epitope), KIR3DL2 with HLA-A3 and KIR2DL4 with HLA-G. In contrast, stimulatory KIR have short cytoplasmic tails lacking ITIM, but have a charged amino acid in the transmembrane region that provides a docking site for the activating adapter molecule DAP12. KIR2DS1 is known to bind HLA-C group 2 and KIR2DS2 binds HLA-C group 1. | |||
REACT_11230 (Reactome) | L-selectin plays a major role in leukocyte traffic through lymph node high endothelial venules. Both MAdCAM and GlyCAM-1 are major L-selectin ligands produced by these venules and mediate leukocyte rolling, particularly in lymphocytes. They are also expressed in mammary tissue and play an important role in the transfer of immune cells into milk secretions. The adhesive properties of CD34 and its potential role in homing lymphocytes to lymphoid tissues mimics the mechanims leukocytes adopt to travel to inflammatory sites. | |||
REACT_11239 (Reactome) | NK cells express adhesion molecules that allow interaction with their tumour targets, promoting their lysis. For instance, the activating receptor CD226 is known to be involved in cytotoxic lymphocyte formation, as well as platelet adhesion to the endothelium. The cytoplasmic domain of CD226 contains binding motifs for members of the band 4.1 family of proteins, and for members of the membrane-associated guanylate kinase homolog (MAGUK) family. These proteins connect the CD226 receptor to the cytoskeleton and may promote clustering with LFA-1 integrin (also discussed in this pathway), which is known to participate in CD226's signaling cascade. CD226 plays a role in transendothelial migration, where it facilitates adherence to endothelial cells and migration between cell junctions. Nectin-2 binds CD226. It is ubiquitously expressed in cells of various tissues, especially in epithelial cells, neurons and fibroblasts. Like many other nectin and Necl proteins, nectin-2 serves as a viral entry receptor for alpha-herpesviruses including herpes simplex virus (HSV-1 and HSV-2). The other CD226 ligand, Necl-5, was initially identified as a receptor for poliovirus. CD96, another ligand for Necl-5, is strongly upregulated in activated NK cells. CRTAM is similarly up-regulated, and has been shown to to bind Necl-2, promoting NK cell cytotoxicity towards otherwise poorly immunogenic targets. | |||
REACT_11241 (Reactome) | CD40 is a member of the Tumour Necrosis Factor receptor family and its ligand CD40L is a type II transmembrane protein of the TNF superfamily. The latter is expressed preferentially on T-cells and platelets. In the immune system, CD40-CD40L interaction affects some key processes such as immune cell activation, differentiation, proliferation, and apoptosis. CD40-CD40L interaction also upregulates costimulatory molecules (ICAM-1, VCAM-1, E-selectin, LFA-3, B7.1, B7.2, class II MHC, and CD40 itself). | |||
SELL | REACT_11230 (Reactome) | |||
T-cell receptor complex with CD8 | REACT_11080 (Reactome) | |||
VCAM1 | REACT_11161 (Reactome) | |||
VLA-4 | REACT_11161 (Reactome) |