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NKG2A_MACMU
ID   NKG2A_MACMU             Reviewed;         233 AA.
AC   Q9MZJ3; Q9MZI8; Q9MZJ0; Q9MZJ1;
DT   15-MAY-2002, integrated into UniProtKB/Swiss-Prot.
DT   01-OCT-2000, sequence version 1.
DT   25-MAY-2022, entry version 99.
DE   RecName: Full=NKG2-A/NKG2-B type II integral membrane protein;
DE   AltName: Full=CD159 antigen-like family member A;
DE   AltName: Full=NK cell receptor A;
DE   AltName: Full=NKG2-A/B-activating NK receptor;
DE   AltName: CD_antigen=CD159a;
GN   Name=NKG2A;
OS   Macaca mulatta (Rhesus macaque).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini;
OC   Cercopithecidae; Cercopithecinae; Macaca.
OX   NCBI_TaxID=9544;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS NKG2-A; NKG2-ADTM; NKG2-B AND
RP   NKG2-BDTM).
RX   PubMed=10866118; DOI=10.1007/s002510050650;
RA   LaBonte M.L., Levy D.B., Letvin N.L.;
RT   "Characterization of rhesus monkey CD94/NKG2 family members and
RT   identification of novel transmembrane-deleted forms of NKG2-A, B, C, and
RT   D.";
RL   Immunogenetics 51:496-499(2000).
CC   -!- FUNCTION: Immune inhibitory receptor involved in self-nonself
CC       discrimination. In complex with KLRD1 on cytotoxic and regulatory
CC       lymphocyte subsets, recognizes non-classical major histocompatibility
CC       (MHC) class Ib molecule MHC-E loaded with self-peptides derived from
CC       the signal sequence of classical MHC class Ia molecules. Enables
CC       cytotoxic cells to monitor the expression of MHC class I molecules in
CC       healthy cells and to tolerate self. Upon MHC-E-peptide binding,
CC       transmits intracellular signals through two immunoreceptor tyrosine-
CC       based inhibition motifs (ITIMs) by recruiting INPP5D/SHP-1 and
CC       INPPL1/SHP-2 tyrosine phosphatases to ITIMs, and ultimately opposing
CC       signals transmitted by activating receptors through dephosphorylation
CC       of proximal signaling molecules. Key inhibitory receptor on natural
CC       killer (NK) cells that regulates their activation and effector
CC       functions. Dominantly counteracts T cell receptor signaling on a subset
CC       of memory/effector CD8-positive T cells as part of an antigen-driven
CC       response to avoid autoimmunity. On intraepithelial CD8-positive gamma-
CC       delta regulatory T cells triggers TGFB1 secretion, which in turn limits
CC       the cytotoxic programming of intraepithelial CD8-positive alpha-beta T
CC       cells, distinguishing harmless from pathogenic antigens. In MHC-E-rich
CC       tumor microenvironment, acts as an immune inhibitory checkpoint and may
CC       contribute to progressive loss of effector functions of NK cells and
CC       tumor-specific T cells, a state known as cell exhaustion.
CC       {ECO:0000250|UniProtKB:P26715}.
CC   -!- SUBUNIT: Heterodimer with KLRD1; disulfide-linked. KLRD1-KLRC1
CC       heterodimer interacts with peptide-bound MHC-E-B2M heterotrimeric
CC       complex. Competes with KLRC2 for its interaction with MHC-E. Interacts
CC       (via ITIM) with INPP5D/SHIP-1 and INPPL1/SHIP-2 (via SH2 domain).
CC       {ECO:0000250|UniProtKB:P26715}.
CC   -!- SUBCELLULAR LOCATION: Cell membrane {ECO:0000250|UniProtKB:P26715};
CC       Single-pass type II membrane protein {ECO:0000255}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=4;
CC       Name=NKG2-A;
CC         IsoId=Q9MZJ3-1; Sequence=Displayed;
CC       Name=NKG2-B;
CC         IsoId=Q9MZJ3-2; Sequence=VSP_003064;
CC       Name=NKG2-Adtm;
CC         IsoId=Q9MZJ3-3; Sequence=VSP_003063;
CC       Name=NKG2-Bdtm;
CC         IsoId=Q9MZJ3-4; Sequence=VSP_003065;
CC   -!- TISSUE SPECIFICITY: Natural killer cells.
CC   -!- DOMAIN: The cytosolic N-terminus contains two immunoreceptor tyrosine-
CC       based inhibitory motifs (ITIMs), which are essential for the
CC       association with INPP5D/SHIP-1 and INPPL1/SHIP-2 phosphatases and
CC       functional inhibition. {ECO:0000250|UniProtKB:P26715}.
CC   -!- PTM: Phosphorylated. {ECO:0000250|UniProtKB:P26715}.
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DR   EMBL; AF190979; AAF73835.1; -; mRNA.
DR   EMBL; AF190981; AAF73837.1; -; mRNA.
DR   EMBL; AF190982; AAF73838.1; -; mRNA.
DR   EMBL; AF190984; AAF73840.1; -; mRNA.
DR   AlphaFoldDB; Q9MZJ3; -.
DR   SMR; Q9MZJ3; -.
DR   STRING; 9544.ENSMMUP00000024076; -.
DR   eggNOG; ENOG502S6IE; Eukaryota.
DR   InParanoid; Q9MZJ3; -.
DR   Proteomes; UP000006718; Unplaced.
DR   GO; GO:0009897; C:external side of plasma membrane; IBA:GO_Central.
DR   GO; GO:0005887; C:integral component of plasma membrane; ISS:UniProtKB.
DR   GO; GO:0030246; F:carbohydrate binding; IEA:UniProtKB-KW.
DR   GO; GO:0062082; F:HLA-E specific inhibitory MHC class Ib receptor activity; ISS:UniProtKB.
DR   GO; GO:0004888; F:transmembrane signaling receptor activity; IBA:GO_Central.
DR   GO; GO:0002250; P:adaptive immune response; IEA:UniProtKB-KW.
DR   GO; GO:0002305; P:CD8-positive, gamma-delta intraepithelial T cell differentiation; ISS:UniProtKB.
DR   GO; GO:0045087; P:innate immune response; IEA:UniProtKB-KW.
DR   GO; GO:0045953; P:negative regulation of natural killer cell mediated cytotoxicity; ISS:UniProtKB.
DR   GO; GO:0001915; P:negative regulation of T cell mediated cytotoxicity; ISS:UniProtKB.
DR   CDD; cd03593; CLECT_NK_receptors_like; 1.
DR   Gene3D; 3.10.100.10; -; 1.
DR   InterPro; IPR001304; C-type_lectin-like.
DR   InterPro; IPR016186; C-type_lectin-like/link_sf.
DR   InterPro; IPR016187; CTDL_fold.
DR   InterPro; IPR033992; NKR-like_CTLD.
DR   Pfam; PF00059; Lectin_C; 1.
DR   SMART; SM00034; CLECT; 1.
DR   SUPFAM; SSF56436; SSF56436; 1.
DR   PROSITE; PS50041; C_TYPE_LECTIN_2; 1.
PE   2: Evidence at transcript level;
KW   Adaptive immunity; Alternative splicing; Cell membrane; Disulfide bond;
KW   Glycoprotein; Immunity; Innate immunity; Lectin; Membrane; Phosphoprotein;
KW   Receptor; Reference proteome; Signal-anchor; Transmembrane;
KW   Transmembrane helix.
FT   CHAIN           1..233
FT                   /note="NKG2-A/NKG2-B type II integral membrane protein"
FT                   /id="PRO_0000046660"
FT   TOPO_DOM        1..70
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        71..93
FT                   /note="Helical; Signal-anchor for type II membrane protein"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        94..233
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   DOMAIN          118..231
FT                   /note="C-type lectin"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00040"
FT   REGION          1..28
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   MOTIF           6..11
FT                   /note="Immunoreceptor tyrosine-based inhibition motif
FT                   (ITIM)"
FT                   /evidence="ECO:0000250|UniProtKB:P26715"
FT   MOTIF           38..43
FT                   /note="Immunoreceptor tyrosine-based inhibition motif
FT                   (ITIM)"
FT                   /evidence="ECO:0000250|UniProtKB:P26715"
FT   MOD_RES         8
FT                   /note="Phosphotyrosine"
FT                   /evidence="ECO:0000250|UniProtKB:P26715"
FT   MOD_RES         40
FT                   /note="Phosphotyrosine"
FT                   /evidence="ECO:0000250|UniProtKB:P26715"
FT   CARBOHYD        102
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        103
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        151
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   DISULFID        116
FT                   /note="Interchain (with C-59 in KLRD1)"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00040"
FT   DISULFID        119..130
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00040"
FT   DISULFID        147..229
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00040"
FT   DISULFID        208..221
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00040"
FT   VAR_SEQ         63..112
FT                   /note="Missing (in isoform NKG2-Bdtm)"
FT                   /evidence="ECO:0000303|PubMed:10866118"
FT                   /id="VSP_003065"
FT   VAR_SEQ         63..95
FT                   /note="DLLSAPEKLIAGILGIICLVLMASVVTIVVIPS -> A (in isoform
FT                   NKG2-Adtm)"
FT                   /evidence="ECO:0000303|PubMed:10866118"
FT                   /id="VSP_003063"
FT   VAR_SEQ         96..113
FT                   /note="Missing (in isoform NKG2-B)"
FT                   /evidence="ECO:0000303|PubMed:10866118"
FT                   /id="VSP_003064"
SQ   SEQUENCE   233 AA;  26286 MW;  237B2BE36E489E76 CRC64;
     MDNQGVIYSD LNLPPNPKRQ QQKPKGNTSS ILVTEQEITY AELNLQKTSQ DFQGNDKTNH
     CKDLLSAPEK LIAGILGIIC LVLMASVVTI VVIPSTLTQK HNNSSLNTRT QKARHCGHCP
     EEWITYSNSC YYIGKEKRTW AESLLACTSK NSSLLSIDNE EEMKFLTAIL TSSWIDVFRD
     SSHHPWVTIN GLTFKHEIKE SDHAEHNCAM LHVRGLFSDE CGSSKIYHCK HKL
 
 
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