Detail Information for IndEnz0002015324
IED ID IndEnz0002015324
Enzyme Type ID protease015324
Protein Name Interleukin-6 receptor subunit alpha
IL-6 receptor subunit alpha
IL-6R subunit alpha
IL-6R-alpha
IL-6RA
IL-6R 1
CD antigen CD126

Cleaved into: Soluble interleukin-6 receptor subunit alpha
sIL6R
Gene Name Il6ra Il6r
Organism Mus musculus (Mouse)
Taxonomic Lineage cellular organisms Eukaryota Opisthokonta Metazoa Eumetazoa Bilateria Deuterostomia Chordata Craniata Vertebrata Gnathostomata (jawed vertebrates) Teleostomi Euteleostomi Sarcopterygii Dipnotetrapodomorpha Tetrapoda Amniota Mammalia Theria Eutheria Boreoeutheria Euarchontoglires Glires (Rodents and rabbits) Rodentia Myomorpha (mice and others) Muroidea Muridae Murinae Mus Mus Mus musculus (Mouse)
Enzyme Sequence MLTVGCTLLVALLAAPAVALVLGSCRALEVANGTVTSLPGATVTLICPGKEAAGNVTIHWVYSGSQNREWTTTGNTLVLRDVQLSDTGDYLCSLNDHLVGTVPLLVDVPPEEPKLSCFRKNPLVNAICEWRPSSTPSPTTKAVLFAKKINTTNGKSDFQVPCQYSQQLKSFSCQVEILEGDKVYHIVSLCVANSVGSKSSHNEAFHSLKMVQPDPPANLVVSAIPGRPRWLKVSWQHPETWDPSYYLLQFQLRYRPVWSKEFTVLLLPVAQYQCVIHDALRGVKHVVQVRGKEELDLGQWSEWSPEVTGTPWIAEPRTTPAGILWNPTQVSVEDSANHEDQYESSTEATSVLAPVQESSSMSLPTFLVAGGSLAFGLLLCVFIILRLKQKWKSEAEKESKTTSPPPPPYSLGPLKPTFLLVPLLTPHSSGSDNTVNHSCLGVRDAQSPYDNSNRDYLFPR
Enzyme Length 460
Uniprot Accession Number P22272
Absorption
Active Site
Activity Regulation ACTIVITY REGULATION: Classic and trans-signaling are both inhibited by tocilizumab, a humanized monoclonal antibody that blocks interleukin IL6R signaling. {ECO:0000250|UniProtKB:P08887}.
Binding Site
Calcium Binding
catalytic Activity
DNA Binding
EC Number
Enzyme Function FUNCTION: Part of the receptor for interleukin 6. Binds to IL6 with low affinity, but does not transduce a signal. Signal activation necessitate an association with IL6ST. Activation leads to the regulation of the immune response, acute-phase reactions and hematopoiesis. The interaction with membrane-bound IL6R and IL6ST stimulates 'classic signaling', the restricted expression of the IL6R limits classic IL6 signaling to only a few tissues such as the liver and some cells of the immune system. Whereas the binding of IL6 and soluble IL6R to IL6ST stimulates 'trans-signaling'. Alternatively, 'cluster signaling' occurs when membrane-bound IL6:IL6R complexes on transmitter cells activate IL6ST receptors on neighboring receiver cells. {ECO:0000305|PubMed:30995492}.; FUNCTION: [Interleukin-6 receptor subunit alpha]: Signaling via the membrane-bound IL6R is mostly regenerative and anti-inflammatory (Probable). Drives naive CD4(+) T cells to the Th17 lineage, through 'cluster signaling' by dendritic cells (PubMed:27893700). {ECO:0000269|PubMed:27893700, ECO:0000305|PubMed:30995492}.; FUNCTION: [Soluble interleukin-6 receptor subunit alpha]: Soluble form of IL6 receptor (sIL6R) that acts as an agonist of IL6 activity (PubMed:11113088). The IL6:sIL6R complex (hyper-IL6) binds to IL6ST/gp130 on cell surfaces and induces signaling also on cells that do not express membrane-bound IL6R in a process called IL6 'trans-signaling'. sIL6R is causative for the proinflammatory properties of IL6 and an important player in the development of chronic inflammatory diseases (By similarity). In complex with IL6, is required for induction of VEGF production (By similarity). Plays a protective role during liver injury, being required for maintenance of tissue regeneration (PubMed:11113088). 'Trans-signaling' in central nervous system regulates energy and glucose homeostasis (PubMed:28402851). {ECO:0000250|UniProtKB:P08887, ECO:0000269|PubMed:11113088, ECO:0000269|PubMed:28402851}.
Temperature Dependency
PH Dependency
Pathway
nucleotide Binding
Features Chain (2); Disulfide bond (4); Domain (3); Glycosylation (4); Motif (1); Sequence conflict (1); Signal peptide (1); Site (1); Topological domain (2); Transmembrane (1)
Keywords Cell membrane;Disulfide bond;Glycoprotein;Immunoglobulin domain;Membrane;Receptor;Reference proteome;Repeat;Secreted;Signal;Transmembrane;Transmembrane helix
Interact With
Induction INDUCTION: [Soluble interleukin-6 receptor subunit alpha]: Levels in the cerebrospinal fluid are increased in obese mice. {ECO:0000269|PubMed:28402851}.
Subcellular Location SUBCELLULAR LOCATION: [Interleukin-6 receptor subunit alpha]: Cell membrane {ECO:0000269|PubMed:27893700}; Single-pass type I membrane protein {ECO:0000255}.; SUBCELLULAR LOCATION: [Soluble interleukin-6 receptor subunit alpha]: Secreted {ECO:0000269|PubMed:28402851}.
Modified Residue
Post Translational Modification PTM: A short soluble form is also released from the membrane by proteolysis (PubMed:26876177). The sIL6R is formed by limited proteolysis of membrane-bound receptors, a process referred to as ectodomain shedding (PubMed:26876177). mIL6R is cleaved by the proteases ADAM10 and ADAM17 (PubMed:26876177). {ECO:0000269|PubMed:26876177}.; PTM: Glycosylated. Glycosylation is dispensable for transport, signaling, and cell-surface turnover. Glycosylation at Asn-55 is a protease-regulatory exosite. Glycosylation is required for ADAM17-mediated proteolysis. {ECO:0000250|UniProtKB:P08887}.
Signal Peptide SIGNAL 1..19
Structure 3D
Cross Reference PDB -
Mapped Pubmed ID 10521784; 11073809; 11197687; 11217851; 11275690; 11937300; 12058253; 12370259; 12413742; 12429018; 12466851; 12643284; 1312474; 14610273; 14960573; 15073037; 15191552; 15457342; 16034137; 16141072; 16435023; 16602821; 17202339; 17567983; 18156493; 18555695; 19420002; 19714627; 19933857; 20026129; 20042582; 20083667; 20351184; 20483735; 2051018; 20691261; 20816090; 20817879; 20861861; 21057510; 21267068; 21454673; 21464300; 21511185; 21960530; 21990364; 22295972; 22467660; 22758208; 23085146; 23209286; 23297399; 23378927; 23564454; 23696660; 23935104; 23954788; 24021059; 24047696; 24194600; 24209760; 24412616; 24681566; 24842874; 24993179; 25127137; 25234944; 25326801; 25429137; 25491772; 25607885; 26010074; 26026268; 26201536; 26253200; 26273529; 26329582; 26359498; 26431949; 26601142; 26705936; 26739431; 26764350; 26839965; 26999594; 27086282; 27096320; 27097661; 27479084; 27563728; 27626380; 27662015; 27694478; 27869785; 27936014; 28087239; 28188245; 28235765; 28456715; 28466852; 28502470; 28683285; 29024103; 29123149; 29398651; 29453398; 29628394; 29629897; 29695802; 29770132; 29784660; 29987839; 30169526; 30315140; 30374128; 30890796; 31165501; 31259624; 31311828; 31413107; 31515941; 31776260; 31924653; 32027619; 32142677; 32242005; 32471947; 32610084; 33414408; 33476547; 33691135; 34301846; 34570961; 7621883; 8392875; 8477802; 8499630; 8676083; 8770556; 8797792; 8836549; 9034153; 9324354; 9659221; 9708822; 9743535; 9874564;
Motif MOTIF 300..304; /note=WSXWS motif
Gene Encoded By
Mass 50,455
Kinetics
Metal Binding
Rhea ID
Cross Reference Brenda