IL12A_SIGHI
ID IL12A_SIGHI Reviewed; 215 AA.
AC Q91ZK6;
DT 26-APR-2004, integrated into UniProtKB/Swiss-Prot.
DT 01-DEC-2001, sequence version 1.
DT 03-AUG-2022, entry version 70.
DE RecName: Full=Interleukin-12 subunit alpha;
DE Short=IL-12A;
DE AltName: Full=Cytotoxic lymphocyte maturation factor 35 kDa subunit;
DE Short=CLMF p35;
DE AltName: Full=IL-12 subunit p35;
DE Flags: Precursor;
GN Name=IL12A;
OS Sigmodon hispidus (Hispid cotton rat).
OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea;
OC Cricetidae; Sigmodontinae; Sigmodon.
OX NCBI_TaxID=42415;
RN [1]
RP NUCLEOTIDE SEQUENCE [MRNA].
RA Blanco J.C., Pletneva L.M., Prince G.A.;
RT "Sigmodon hispidus cytokines, chemokines and interferons.";
RL Submitted (SEP-2001) to the EMBL/GenBank/DDBJ databases.
CC -!- FUNCTION: Heterodimerizes with IL12B to form the IL-12 cytokine or with
CC EBI3/IL27B to form the IL-35 cytokine. IL-12 is primarily produced by
CC professional antigen-presenting cells (APCs) such as B-cells and
CC dendritic cells (DCs) as well as macrophages and granulocytes and
CC regulates T-cell and natural killer-cell responses, induces the
CC production of interferon-gamma (IFN-gamma), favors the differentiation
CC of T-helper 1 (Th1) cells and is an important link between innate
CC resistance and adaptive immunity. Mechanistically, exerts its
CC biological effects through a receptor composed of IL12R1 and IL12R2
CC subunits. Binding to the receptor results in the rapid tyrosine
CC phosphorylation of a number of cellular substrates including the JAK
CC family kinases TYK2 and JAK2. In turn, recruited STAT4 gets
CC phosphorylated and translocates to the nucleus where it regulates
CC cytokine/growth factor responsive genes (By similarity). As part of IL-
CC 35, plays essential roles in maintaining the immune homeostasis of the
CC liver microenvironment and functions also as an immune-suppressive
CC cytokine (By similarity). Mediates biological events through
CC unconventional receptors composed of IL12RB2 and gp130/IL6ST
CC heterodimers or homodimers. Signaling requires the transcription
CC factors STAT1 and STAT4, which form a unique heterodimer that binds to
CC distinct DNA sites (By similarity). {ECO:0000250|UniProtKB:P29459,
CC ECO:0000250|UniProtKB:P43431}.
CC -!- SUBUNIT: Heterodimer with IL12B; disulfide-linked. This heterodimer is
CC known as interleukin IL-12. Heterodimer with EBI3/IL27B; not disulfide-
CC linked. This heterodimer is known as interleukin IL-35.
CC {ECO:0000250|UniProtKB:P29459}.
CC -!- SUBCELLULAR LOCATION: Secreted {ECO:0000250|UniProtKB:P29459}.
CC -!- SIMILARITY: Belongs to the IL-6 superfamily. {ECO:0000305}.
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DR EMBL; AF421396; AAL16937.1; -; mRNA.
DR AlphaFoldDB; Q91ZK6; -.
DR SMR; Q91ZK6; -.
DR GO; GO:0005615; C:extracellular space; IEA:UniProtKB-KW.
DR GO; GO:0005125; F:cytokine activity; IEA:UniProtKB-KW.
DR GO; GO:0008083; F:growth factor activity; IEA:UniProtKB-KW.
DR GO; GO:0005143; F:interleukin-12 receptor binding; IEA:InterPro.
DR GO; GO:0006955; P:immune response; IEA:InterPro.
DR Gene3D; 1.20.1250.10; -; 1.
DR InterPro; IPR009079; 4_helix_cytokine-like_core.
DR InterPro; IPR004281; IL-12_alpha.
DR Pfam; PF03039; IL12; 1.
DR SUPFAM; SSF47266; SSF47266; 1.
PE 2: Evidence at transcript level;
KW Cytokine; Disulfide bond; Glycoprotein; Growth factor; Secreted; Signal.
FT SIGNAL 1..22
FT /evidence="ECO:0000250"
FT CHAIN 23..215
FT /note="Interleukin-12 subunit alpha"
FT /id="PRO_0000015613"
FT CARBOHYD 89
FT /note="N-linked (GlcNAc...) asparagine"
FT /evidence="ECO:0000255"
FT DISULFID 60..192
FT /evidence="ECO:0000250"
FT DISULFID 81..119
FT /evidence="ECO:0000250"
FT DISULFID 92
FT /note="Interchain (with C-200 in IL12B)"
FT /evidence="ECO:0000250"
SQ SEQUENCE 215 AA; 24042 MW; 435DF86A7D72A244 CRC64;
MCSSRCLLFL ATLAFLIHLS LARATPVSTP AQCLAHSQNL LRTTNHMLEK AIQTLKHYPC
TAEDIDHEDI TEDKTSTLNA CLPPELAKNE SCWASGKTSS VTRGSCLPPQ KTSSMMTLCL
SSIYEDLKMY QTEFKAINAE LLDHNRKQII LDENMLTAID ELMQALNLNG ETRPQKPSLE
EADPYKVKIK LCILLHAFSI RAITINRVMS YLNSA