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Reviewed, UniProtKB/Swiss-Prot P12841 (FOS_RAT)

Last modified December 16, 2008. Version 73. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (1) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Proto-oncogene protein c-fos
Alternative name(s):
    Cellular oncogene fos
Gene names
Name: Fos
OrganismRattus norvegicus (Rat)
Taxonomic identifier10116 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresGliresRodentiaSciurognathiMuroideaMuridaeMurinaeRattus

Protein attributes

Sequence length380 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at protein level.

General annotation (Comments)

Function

Nuclear phosphoprotein which forms a tight but non-covalently linked complex with the JUN/AP-1 transcription factor. Has a critical function in regulating the development of cells destined to form and maintain the skeleton. It is thought to have an important role in signal transduction, cell proliferation and differentiation.

Subunit structure

Heterodimer. Interacts with DSIPI; this interaction inhibits the binding of active AP1 to its target DNA By similarity. Interacts with MAFB.

Subcellular location

Nucleus.

Post-translational modification

Phosphorylated in the C-terminal upon stimulation by nerve growth factor (NGF) and epidermal growth factor (EGF). Phosphorylated, in vitro, by MAPK and RSK1. Phosphorylation on both Ser-362 and Ser-374 by MAPK1/2 and RSK1/2 leads to protein stabilization with phosphorylation on Ser-374 being the major site for protein stabilization on NGF stimulation. Phosphorylation on Ser-362 and Ser-374 primes further phosphorylations on Thr-325 and Thr-331 through promoting docking of MAPK to the DEF domain. Phosphorylation on Thr-232, induced by HA-RAS, activates the transcriptional activity and antagonizes sumoylation. Phosphorylation on Ser-362 by RSK2 in osteoblasts contributes to osteoblast transformation By similarity.

Constitutively sumoylated by SUMO1, SUMO2 and SUMO3. Desumoylated by SENP2. Sumoylation requires heterodimerization with JUN and is enhanced by mitogen stimulation. Sumoylation inhibits the AP-1 transcriptional activity and is, itself, inhibited by Ras-activated phosphorylation on Thr-232 By similarity.

Sequence similarities

Belongs to the bZIP family. Fos subfamily.

Contains 1 bZIP domain.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 380380Proto-oncogene protein c-fos
PRO_0000076469

Regions

Domain165 – 19329Leucine-zipper
DNA binding139 – 16022Basic motif Ref.3

Amino acid modifications

Modified residue2321Phosphothreonine
Modified residue3251Phosphothreonine
Modified residue3311Phosphothreonine
Modified residue3621Phosphoserine; by MAPK and RPS6KA3
Modified residue3741Phosphoserine; by MAPK
Cross-link113Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin) By similarity
Cross-link265Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO) By similarity

Experimental info

Mutagenesis2321T → A: Abolishes HA-RAS-mediated activation. Loss of in vitro ERK2-mediated phosphorylation. No change in sumoylation levels
Mutagenesis3251T → A: Loss of NGF-mediated phosphorylation; when associated with A-331
Mutagenesis3311T → A: Loss of NGF-mediated phosphorylation; when associated with A-325
Mutagenesis343 – 3453FTY → ATA: Decreased phosphorylation levels. Reduced NGF-mediated enhanced transactivation
Mutagenesis3621S → A: Some loss of protein stabilization on NGF-treatment; when associated with D-374
Mutagenesis3621S → D: Increased protein stabilization on NGF-treatment, but no increase when treated with MAPK-inhibitor; when associated with D-374
Mutagenesis3741S → A: Greatly reduced protein stabilization on NGF stimulation
Mutagenesis3741S → D: Increased protein stabilization on NGF-treatment, but no increase when treated with MAPK-inhibitor; when associated with D-362. Some loss of protein stablization on NGF-treatment; wnen associated with A-362

Sequences

Sequence LengthMass (Da)Tools
P12841-1 [UniParc].

Last modified October 1, 1989. Version 1.
Checksum: E62D16A88CB2BEE9

FASTA38040,927
        10         20         30         40         50         60 
MMFSGFNADY EASSSRCSSA SPAGDSLSYY HSPADSFSSM GSPVNTQDFC ADLSVSSANF 

        70         80         90        100        110        120 
IPTVTAISTS PDLQWLVQPT LVSSVAPSQT RAPHPYGLPT PSTGAYARAG VVKTMSGGRA 

       130        140        150        160        170        180 
QSIGRRGKVE QLSPEEEEKR RIRRERNKMA AAKCRNRRRE LTDTLQAETD QLEDEKSALQ 

       190        200        210        220        230        240 
TEIANLLKEK EKLEFILAAH RPACKIPNDL GFPEEMSVTS LDLTGGLPEA TTPESEEAFT 

       250        260        270        280        290        300 
LPLLNDPEPK PSLEPVKNIS NMELKAEPFD DFLFPASSRP SGSETARSVP DVDLSGSFYA 

       310        320        330        340        350        360 
ADWEPLHSSS LGMGPMVTEL EPLCTPVVTC TPSCTTYTSS FVFTYPEADS FPSCAAAHRK 

       370        380 
GSSSNEPSSD SLSSPTLLAL 

« Hide

References

[1]"Isolation and characterization of the c-fos(rat) cDNA and analysis of post-translational modification in vitro."
Curran T., Gordon M.B., Rubino K.L., Sambucetti L.C.
Oncogene 2:79-84(1987) [PubMed: 3325886] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[2]"cFOS expression in rat."
Weiler E.
Submitted (JUN-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
Strain: Sprague-Dawley.
Tissue: Liver.
[3]"Expression and purification of the leucine zipper and DNA-binding domains of Fos and Jun: both Fos and Jun contact DNA directly."
Abate C., Luk D., Gentz R., Rauscher F.J. III, Curran T.
Proc. Natl. Acad. Sci. U.S.A. 87:1032-1036(1990) [PubMed: 2105492] [Abstract]
Cited for: DNA-BINDING.
[4]"Rat maf-related factors: the specificities of DNA binding and heterodimer formation."
Matsushima-Hibiya Y., Nishi S., Sakai M.
Biochem. Biophys. Res. Commun. 245:412-418(1998) [PubMed: 9571165] [Abstract]
Cited for: INTERACTION WITH MAFB.
[5]"Phosphorylation of the c-Fos and c-Jun HOB1 motif stimulates its activation capacity."
Bannister A.J., Brown H.J., Sutherland J.A., Kouzarides T.
Nucleic Acids Res. 22:5173-5176(1994) [PubMed: 7816602] [Abstract]
Cited for: PHOSPHORYLATION AT THR-232, FUNCTION, MUTAGENESIS OF THR-232.
[6]"Sustained activation of extracellular signal-regulated kinase by nerve growth factor regulates c-fos protein stabilization and transactivation in PC12 cells."
Pellegrino M.J., Stork P.J.
J. Neurochem. 99:1480-1493(2006) [PubMed: 17223854] [Abstract]
Cited for: PHOSPHORYLATION AT THR-325; THR-331; SER-362 AND SER-374, FUNCTION, MUTAGENESIS OF THR-325; THR-331; 343-PHE--TYR-345; SER-362 AND SER-374.

Cross-references

Sequence databases

X06769 mRNA. Translation: CAA29937.1.
DQ089699 Genomic DNA. Translation: AAZ13764.1.
PIRTVRTFS. A28263.
RefSeqNP_071533.1.
UniGeneRn.103750

3D structure databases

HSSPHSSP built from PDB template 1FOS based on UniProtKB P01100.
SMRP12841. Positions 139-198.
ModBaseSearch...

Protein-protein interaction databases

DIPDIP:6001N.

PTM databases

PhosphoSiteP12841.

Genome annotation databases

EnsemblENSRNOG00000008015. Rattus norvegicus. [Contig view]
GeneID314322.
KEGGrno:314322.

Organism-specific databases

RGD2626. Fos.

Phylogenomic databases

HOVERGENP12841.

Gene expression databases

ArrayExpressP12841.
GermOnlineENSRNOG00000008015. Rattus norvegicus.

Family and domain databases

InterProIPR011700. bZIP_2.
IPR000837. Leuzip_Fos.
IPR004827. TF_bZIP.
[Graphical view]
PfamPF07716. bZIP_2. 1 hit.
[Graphical view]
PRINTSPR00042. LEUZIPPRFOS.
SMARTSM00338. BRLZ. 1 hit.
[Graphical view]
PROSITEPS50217. BZIP. 1 hit.
PS00036. BZIP_BASIC. 1 hit.
[Graphical view]
ProtoNetSearch...

Other Resources

NextBio667476.

Entry information

Entry nameFOS_RAT
AccessionPrimary (citable) accession number: P12841
Secondary accession number(s): Q4FDN1
Entry history
Integrated into UniProtKB/Swiss-Prot: October 1, 1989
Last sequence update: October 1, 1989
Last modified: December 16, 2008
This is version 73 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

Relevant documents

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents