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Q6PJ21 (SPSB3_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 72. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (6) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
SPRY domain-containing SOCS box protein 3

Short name=SSB-3
Gene names
Name:SPSB3
Synonyms:C16orf31, SSB3
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length355 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

May be a substrate recognition component of a SCF-like ECS (Elongin BC-CUL2/5-SOCS-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins By similarity.

Pathway

Protein modification; protein ubiquitination.

Subunit structure

Interacts with MET. Ref.5

Domain

The SOCS box domain mediates the interaction with the Elongin BC complex, an adapter module in different E3 ubiquitin ligase complexes By similarity.

Sequence similarities

Belongs to the SPSB family.

Contains 1 B30.2/SPRY domain.

Contains 1 SOCS box domain.

Sequence caution

The sequence AAH41897.1 differs from that shown. Reason: Intron retention.

The sequence AAK61293.1 differs from that shown. Reason: Erroneous gene model prediction.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological_processintracellular signal transduction

Inferred from electronic annotation. Source: InterPro

protein ubiquitination

Inferred from electronic annotation. Source: UniProtKB-UniPathway

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 355355SPRY domain-containing SOCS box protein 3
PRO_0000278778

Regions

Domain85 – 274190B30.2/SPRY
Domain264 – 31552SOCS box

Natural variations

Natural variant1711S → L.
Corresponds to variant rs35816944 [ dbSNP | Ensembl ].
VAR_052034

Experimental info

Sequence conflict2111S → P in AAH47441. Ref.4
Sequence conflict2691R → S in AAH47441. Ref.4
Sequence conflict3391P → H in AAH24244. Ref.4
Sequence conflict3391P → R in AAH47441. Ref.4

Sequences

Sequence LengthMass (Da)Tools
Q6PJ21 [UniParc].

Last modified February 20, 2007. Version 2.
Checksum: 56BFA7A1DA27E254

FASTA35539,376
        10         20         30         40         50         60 
MARRPRNSRA WHFVLSAARR DADARAVALA GSTNWGYDSD GQHSDSDSDP EYSTLPPSIP 

        70         80         90        100        110        120 
SAVPVTGESF CDCAGQSEAS FCSSLHSAHR GRDCRCGEED EYFDWVWDDL NKSSATLLSC 

       130        140        150        160        170        180 
DNRKVSFHME YSCGTAAIRG TKELGEGQHF WEIKMTSPVY GTDMMVGIGT SDVDLDKYRH 

       190        200        210        220        230        240 
TFCSLLGRDE DSWGLSYTGL LHHKGDKTSF SSRFGQGSII GVHLDTWHGT LTFFKNRKCI 

       250        260        270        280        290        300 
GVAATKLQNK RFYPMVCSTA ARSSMKVTRS CASATSLQYL CCHRLRQLRP DSGDTLEGLP 

       310        320        330        340        350 
LPPGLKQVLH NKLGWVLSMS CSRRKAPVSD PQAATSAHPS SREPRPCQRK RCRRT 

« Hide

References

« Hide 'large scale' references
[1]"SOCS box proteins."
Friedel E.J., Nicholson S.E., Nicola N.A., Kile B.T., Hilton D.J.
Submitted (JUL-2001) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[2]"Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16."
Daniels R.J., Peden J.F., Lloyd C., Horsley S.W., Clark K., Tufarelli C., Kearney L., Buckle V.J., Doggett N.A., Flint J., Higgs D.R.
Hum. Mol. Genet. 10:339-352(2001) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. expand/collapse author list , Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., Hunkapiller M.W., Myers E.W., Venter J.C.
Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[4]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Eye, Hypothalamus and Testis.
[5]"The SPRY domain-containing SOCS box protein 1 (SSB-1) interacts with MET and enhances the hepatocyte growth factor-induced Erk-Elk-1-serum response element pathway."
Wang D., Li Z., Messing E.M., Wu G.
J. Biol. Chem. 280:16393-16401(2005) [PubMed] [Europe PMC] [Abstract]
Cited for: INTERACTION WITH MET.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF403028 mRNA. Translation: AAL57347.1.
AE006639 Genomic DNA. Translation: AAK61293.1. Sequence problems.
CH471112 Genomic DNA. Translation: EAW85619.1.
CH471112 Genomic DNA. Translation: EAW85620.1.
BC007588 mRNA. Translation: AAH07588.2.
BC024244 mRNA. Translation: AAH24244.1.
BC041897 mRNA. Translation: AAH41897.1. Sequence problems.
BC047441 mRNA. Translation: AAH47441.2.
IPIIPI00412063.
RefSeqNP_543137.2. NM_080861.3.
UniGeneHs.592080.

3D structure databases

ProteinModelPortalQ6PJ21.
ModBaseSearch...

Protein-protein interaction databases

IntActQ6PJ21. 2 interactions.
STRING9606.ENSP00000301717.

PTM databases

PhosphoSiteQ6PJ21.

Polymorphism databases

DMDM126253805.

Proteomic databases

PaxDbQ6PJ21.
PRIDEQ6PJ21.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000301717; ENSP00000301717; ENSG00000162032.
ENST00000566339; ENSP00000457206; ENSG00000162032.
GeneID90864.
KEGGhsa:90864.
UCSCuc002cmt.3. human.

Organism-specific databases

CTD90864.
GeneCardsGC16M001826.
HGNCHGNC:30629. SPSB3.
HPAHPA046602.
MIM611659. gene.
neXtProtNX_Q6PJ21.
PharmGKBPA142670873.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG151085.
HOVERGENHBG093988.
InParanoidQ6PJ21.
KOK10345.
OMAGWVLSMS.
OrthoDBEOG42NJ0V.

Enzyme and pathway databases

UniPathwayUPA00143.

Gene expression databases

ArrayExpressQ6PJ21.
BgeeQ6PJ21.
CleanExHS_SPSB3.
GenevestigatorQ6PJ21.

Family and domain databases

InterProIPR001870. B30.2/SPRY.
IPR008985. ConA-like_lec_gl_sf.
IPR001496. SOCS_C.
IPR003877. SPRY_rcpt.
[Graphical view]
PfamPF00622. SPRY. 1 hit.
[Graphical view]
SMARTSM00969. SOCS_box. 1 hit.
[Graphical view]
SUPFAMSSF49899. ConA_like_lec_gl. 1 hit.
PROSITEPS50188. B302_SPRY. 1 hit.
PS50225. SOCS. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi90864.
NextBio77012.
SOURCESearch...

Entry information

Entry nameSPSB3_HUMAN
AccessionPrimary (citable) accession number: Q6PJ21
Secondary accession number(s): D3DU78 expand/collapse secondary AC list , Q49A96, Q86X18, Q8WXK5, Q96IE6, Q96RY2
Entry history
Integrated into UniProtKB/Swiss-Prot: February 20, 2007
Last sequence update: February 20, 2007
Last modified: May 1, 2013
This is version 72 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 16

Human chromosome 16: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

PATHWAY comments

Index of metabolic and biosynthesis pathways

SIMILARITY comments

Index of protein domains and families