IL16
Pro-interleukin-16
Also known as: FLJ16806, FLJ42735, HsT19289, IL-16, IL16_HUMAN, LCF, prIL-16
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14005
- Gene
- IL16
- Ensembl
- ENSG00000172349
- Chromosome
- 15
- Canonical length
- 1332 aa
- Protein class
- Cancer-related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Nuclear speckles,Plasma membrane,Cytosol
- Secretome location
- Secreted to blood
- Quaternary structure
- Homotetramer
OverviewNCBI Gene
The protein encoded by this gene is a pleiotropic cytokine that functions as a chemoattractant, a modulator of T cell activation, and an inhibitor of HIV replication. The signaling process of this cytokine is mediated by CD4. The product of this gene undergoes proteolytic processing, which is found to yield two functional proteins. The cytokine function is exclusively attributed to the secreted C-terminal peptide, while the N-terminal product may play a role in cell cycle control. Caspase 3 is reported to be involved in the proteolytic processing of this protein. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
Canonical amino-acid sequenceUniProt
1332 residues, UniProt reviewed canonical sequence.
>Q14005|IL16
1 MESHSRAGKS RKSAKFRSIS RSLMLCNAKT SDDGSSPDEK YPDPFEISLA QGKEGIFHSS
61 VQLADTSEAG PSSVPDLALA SEAAQLQAAG NDRGKTCRRI FFMKESSTAS SREKPGKLEA
121 QSSNFLFPKA CHQRARSNST SVNPYCTREI DFPMTKKSAA PTDRQPYSLC SNRKSLSQQL
181 DCPAGKAAGT SRPTRSLSTA QLVQPSGGLQ ASVISNIVLM KGQAKGLGFS IVGGKDSIYG
241 PIGIYVKTIF AGGAAAADGR LQEGDEILEL NGESMAGLTH QDALQKFKQA KKGLLTLTVR
301 TRLTAPPSLC SHLSPPLCRS LSSSTCITKD SSSFALESPS APISTAKPNY RIMVEVSLQK
361 EAGVGLGIGL CSVPYFQCIS GIFVHTLSPG SVAHLDGRLR CGDEIVEISD SPVHCLTLNE
421 VYTILSHCDP GPVPIIVSRH PDPQVSEQQL KEAVAQAVEN TKFGKERHQW SLEGVKRLES
481 SWHGRPTLEK EREKNSAPPH RRAQKVMIRS SSDSSYMSGS PGGSPGSGSA EKPSSDVDIS
541 THSPSLPLAR EPVVLSIASS RLPQESPPLP ESRDSHPPLR LKKSFEILVR KPMSSKPKPP
601 PRKYFKSDSD PQKSLEEREN SSCSSGHTPP TCGQEARELL PLLLPQEDTA GRSPSASAGC
661 PGPGIGPQTK SSTEGEPGWR RASPVTQTSP IKHPLLKRQA RMDYSFDTTA EDPWVRISDC
721 IKNLFSPIMS ENHGHMPLQP NASLNEEEGT QGHPDGTPPK LDTANGTPKV YKSADSSTVK
781 KGPPVAPKPA WFRQSLKGLR NRASDPRGLP DPALSTQPAP ASREHLGSHI RASSSSSSIR
841 QRISSFETFG SSQLPDKGAQ RLSLQPSSGE AAKPLGKHEE GRFSGLLGRG AAPTLVPQQP
901 EQVLSSGSPA ASEARDPGVS ESPPPGRQPN QKTLPPGPDP LLRLLSTQAE ESQGPVLKMP
961 SQRARSFPLT RSQSCETKLL DEKTSKLYSI SSQVSSAVMK SLLCLPSSIS CAQTPCIPKE
1021 GASPTSSSNE DSAANGSAET SALDTGFSLN LSELREYTEG LTEAKEDDDG DHSSLQSGQS
1081 VISLLSSEEL KKLIEEVKVL DEATLKQLDG IHVTILHKEE GAGLGFSLAG GADLENKVIT
1141 VHRVFPNGLA SQEGTIQKGN EVLSINGKSL KGTTHHDALA ILRQAREPRQ AVIVTRKLTP
1201 EAMPDLNSST DSAASASAAS DVSVESTAEA TVCTVTLEKM SAGLGFSLEG GKGSLHGDKP
1261 LTINRIFKGA ASEQSETVQP GDEILQLGGT AMQGLTRFEA WNIIKALPDG PVTIVIRRKS
1321 LQSKETTAAG DSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IL16 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.56
- Highest tissue expression
- 127 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 127 nTPM
- lymph node: 124 nTPM
- thymus: 122 nTPM
- spleen: 81 nTPM
- appendix: 60 nTPM
- bone marrow: 59 nTPM
Single-cell type
- choroid plexus epithelial cells: 242 nCPM
- ependymal cells: 233 nCPM
- mesothelial cells: 192 nCPM
- fibro-adipogenic progenitors: 142 nCPM
- respiratory ciliated cells: 132 nCPM
- epicardial cells: 116 nCPM
Immune cell
- total PBMC: 338 nTPM
- eosinophil: 322 nTPM
- neutrophil: 283 nTPM
- basophil: 253 nTPM
- naive CD4 T-cell: 226 nTPM
- NK-cell: 214 nTPM
Brain region
- cerebellum: 117 nTPM
- choroid plexus: 29 nTPM
- pons: 22 nTPM
- white matter: 16 nTPM
- medulla oblongata: 13 nTPM
- hypothalamus: 12 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.69
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.7
- DepMap mean gene effect
- 0.16
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cytokine-mediated signaling pathway
- immune response
- induction of positive chemotaxis
- leukocyte chemotaxis
- positive regulation of inflammatory response
- positive regulation of interleukin-1 alpha production
- positive regulation of interleukin-12 production
- positive regulation of interleukin-6 production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- PDZ domain
- PDZ superfamily
- PDZ domain
- Interleukin-16
- Interleukin-16-like
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IL16 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IL16 as an antibody target. Whether an autoantibody or antibody against IL16 could matter depends on whether native IL16 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IL16 is annotated as secreted, so native IL16 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label IL16 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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