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Q9Y5U2 (TSSC4_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 71. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Protein TSSC4
Alternative name(s):
Tumor-suppressing STF cDNA 4 protein
Tumor-suppressing subchromosomal transferable fragment candidate gene 4 protein
Gene names
Name:TSSC4
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length329 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Tissue specificity

Expressed in fetal brain, lung, liver and kidney. Widely expressed in adult tissues. Ref.1

Sequence similarities

Belongs to the TSSC4 family.

Ontologies

Keywords
   Coding sequence diversityAlternative splicing
Polymorphism
   PTMAcetylation
Phosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q9Y5U2-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q9Y5U2-2)

The sequence of this isoform differs from the canonical sequence as follows:
     8-71: Missing.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 329329Protein TSSC4
PRO_0000076360

Amino acid modifications

Modified residue1291Phosphoserine Ref.5
Modified residue1321Phosphoserine Ref.6
Modified residue1431Phosphoserine Ref.6
Modified residue1461Phosphoserine Ref.6
Modified residue2171N6-acetyllysine Ref.9
Modified residue3211Phosphoserine Ref.4 Ref.7 Ref.8

Natural variations

Alternative sequence8 – 7164Missing in isoform 2.
VSP_016561
Natural variant171H → P.
Corresponds to variant rs2234278 [ dbSNP | Ensembl ].
VAR_057826
Natural variant1241R → Q.
Corresponds to variant rs1008265 [ dbSNP | Ensembl ].
VAR_060194
Natural variant2301R → S.
Corresponds to variant rs2234280 [ dbSNP | Ensembl ].
VAR_057827
Natural variant2621G → R.
Corresponds to variant rs2234281 [ dbSNP | Ensembl ].
VAR_057828
Natural variant2741H → P. Ref.1 Ref.3
Corresponds to variant rs2234283 [ dbSNP | Ensembl ].
VAR_063128

Experimental info

Sequence conflict721L → F in AAD23579. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified May 18, 2010. Version 3.
Checksum: AFC2D5CBD93844F0

FASTA32934,326
        10         20         30         40         50         60 
MAEAGTGEPS PSVEGEHGTE YDTLPSDTVS LSDSDSDLSL PGGAEVEALS PMGLPGEEDS 

        70         80         90        100        110        120 
GPDEPPSPPS GLLPATVQPF HLRGMSSTFS QRSRDIFDCL EGAARRAPSS VAHTSMSDNG 

       130        140        150        160        170        180 
GFKRPLAPSG RSPVEGLGRA HRSPASPRVP PVPDYVAHPE RWTKYSLEDV TEVSEQSNQA 

       190        200        210        220        230        240 
TALAFLGSQS LAAPTDCVSS FNQDPSSCGE GRVIFTKPVR GVEARHERKR VLGKVGEPGR 

       250        260        270        280        290        300 
GGLGNPATDR GEGPVELAHL AGPGSPEAEE WGSHHGGLQE VEALSGSVHS GSVPGLPPVE 

       310        320 
TVGFHGSRKR SRDHFRNKSS SPEDPGAEV 

« Hide

Isoform 2 [UniParc].

Checksum: 72811C9774FC24C4
Show »

FASTA26527,935

References

« Hide 'large scale' references
[1]"Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting."
Lee M.P., Brandenburg S., Landes G.M., Adams M., Miller G., Feinberg A.P.
Hum. Mol. Genet. 8:683-690(1999) [PubMed: 10072438] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY, VARIANT PRO-274.
[2]"Human chromosome 11 DNA sequence and analysis including novel gene identification."
Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. expand/collapse author list , Jaffe D.B., LaButti K., Nicol R., Park H.-S., Seaman C., Sougnez C., Yang X., Zimmer A.R., Zody M.C., Birren B.W., Nusbaum C., Fujiyama A., Hattori M., Rogers J., Lander E.S., Sakaki Y.
Nature 440:497-500(2006) [PubMed: 16554811] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"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: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2), VARIANT PRO-274.
Tissue: Brain and Lymph.
[4]"Large-scale characterization of HeLa cell nuclear phosphoproteins."
Beausoleil S.A., Jedrychowski M., Schwartz D., Elias J.E., Villen J., Li J., Cohn M.A., Cantley L.C., Gygi S.P.
Proc. Natl. Acad. Sci. U.S.A. 101:12130-12135(2004) [PubMed: 15302935] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-321, MASS SPECTROMETRY.
Tissue: Cervix carcinoma.
[5]"Global, in vivo, and site-specific phosphorylation dynamics in signaling networks."
Olsen J.V., Blagoev B., Gnad F., Macek B., Kumar C., Mortensen P., Mann M.
Cell 127:635-648(2006) [PubMed: 17081983] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-129, MASS SPECTROMETRY.
Tissue: Cervix carcinoma.
[6]"A quantitative atlas of mitotic phosphorylation."
Dephoure N., Zhou C., Villen J., Beausoleil S.A., Bakalarski C.E., Elledge S.J., Gygi S.P.
Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed: 18669648] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-132; SER-143 AND SER-146, MASS SPECTROMETRY.
Tissue: Cervix carcinoma.
[7]"Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach."
Gauci S., Helbig A.O., Slijper M., Krijgsveld J., Heck A.J., Mohammed S.
Anal. Chem. 81:4493-4501(2009) [PubMed: 19413330] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-321, MASS SPECTROMETRY.
Tissue: Embryonic kidney.
[8]"Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions."
Mayya V., Lundgren D.H., Hwang S.-I., Rezaul K., Wu L., Eng J.K., Rodionov V., Han D.K.
Sci. Signal. 2:RA46-RA46(2009) [PubMed: 19690332] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-321, MASS SPECTROMETRY.
Tissue: Leukemic T-cell.
[9]"Lysine acetylation targets protein complexes and co-regulates major cellular functions."
Choudhary C., Kumar C., Gnad F., Nielsen M.L., Rehman M., Walther T., Olsen J.V., Mann M.
Science 325:834-840(2009) [PubMed: 19608861] [Abstract]
Cited for: ACETYLATION [LARGE SCALE ANALYSIS] AT LYS-217, MASS SPECTROMETRY.
[10]"Initial characterization of the human central proteome."
Burkard T.R., Planyavsky M., Kaupe I., Breitwieser F.P., Buerckstuemmer T., Bennett K.L., Superti-Furga G., Colinge J.
BMC Syst. Biol. 5:17-17(2011) [PubMed: 21269460] [Abstract]
Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF125568 mRNA. Translation: AAD23579.1.
AC124057 Genomic DNA. No translation available.
BC006091 mRNA. Translation: AAH06091.1.
BC050616 mRNA. Translation: AAH50616.1.
IPIIPI00305144.
IPI00657787.
RefSeqNP_005697.2. NM_005706.2.
UniGeneHs.523424.

3D structure databases

ProteinModelPortalQ9Y5U2.
ModBaseSearch...

Protein-protein interaction databases

IntActQ9Y5U2. 3 interactions.
MINTMINT-1380986.
STRINGQ9Y5U2.

PTM databases

PhosphoSiteQ9Y5U2.

Polymorphism databases

DMDM296453006.

Proteomic databases

PRIDEQ9Y5U2.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000333256; ENSP00000331087; ENSG00000184281.
GeneID10078.
KEGGhsa:10078.
UCSCuc001lwi.2. human.
uc001lwj.1. human.

Organism-specific databases

CTD10078.
GeneCardsGC11P002421.
H-InvDBHIX0009365.
HGNCHGNC:12386. TSSC4.
HPAHPA041801.
MIM603852. gene.
neXtProtNX_Q9Y5U2.
PharmGKBPA37054.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG19882.
GeneTreeENSGT00390000011846.
HOGENOMHBG283334.
HOVERGENHBG059835.
InParanoidQ9Y5U2.
OMARSRDHFR.
OrthoDBEOG402WSX.
PhylomeDBQ9Y5U2.

Gene expression databases

ArrayExpressQ9Y5U2.
BgeeQ9Y5U2.
CleanExHS_TSSC4.
GenevestigatorQ9Y5U2.
GermOnlineENSG00000184281. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio38103.
SOURCESearch...

Entry information

Entry nameTSSC4_HUMAN
AccessionPrimary (citable) accession number: Q9Y5U2
Secondary accession number(s): C9JS66, Q86VL2, Q9BRS6
Entry history
Integrated into UniProtKB/Swiss-Prot: December 20, 2005
Last sequence update: May 18, 2010
Last modified: January 25, 2012
This is version 71 of the entry and version 3 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 11

Human chromosome 11: 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

SIMILARITY comments

Index of protein domains and families