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P34910 (EVI2B_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 100. 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·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Protein EVI2B
Alternative name(s):
Ecotropic viral integration site 2B protein homolog
Short name=EVI-2B
CD_antigen=CD361
Gene names
Name:EVI2B
Synonyms:EVDB
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length448 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level

General annotation (Comments)

Subcellular location

Membrane; Single-pass type I membrane protein.

Tissue specificity

Bone marrow, peripheral blood mononuclear cells, fibroblasts and Epstein-Barr virus-transformed lymphoblastoid cell lines.

Ontologies

Keywords
   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   DiseaseProto-oncogene
   DomainSignal
Transmembrane
Transmembrane helix
   PTMGlycoprotein
Phosphoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular_componentcytoplasm

Inferred from direct assay. Source: HPA

integral to plasma membrane

Traceable author statement Ref.1. Source: ProtInc

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 2121 Potential
Chain22 – 448427Protein EVI2B
PRO_0000021213

Regions

Topological domain22 – 202181Extracellular Potential
Transmembrane203 – 22624Helical; Potential
Topological domain227 – 448222Cytoplasmic Potential

Amino acid modifications

Modified residue2681Phosphoserine By similarity
Modified residue2711Phosphoserine By similarity
Modified residue2781Phosphoserine By similarity
Modified residue2941Phosphoserine By similarity
Glycosylation161N-linked (GlcNAc...) Potential
Glycosylation501N-linked (GlcNAc...) Potential
Glycosylation1141N-linked (GlcNAc...) Potential

Natural variations

Natural variant531G → R.
Corresponds to variant rs9903564 [ dbSNP | Ensembl ].
VAR_056871

Experimental info

Sequence conflict371F → Y in AAA35816. Ref.1

Sequences

Sequence LengthMass (Da)Tools
P34910 [UniParc].

Last modified December 15, 2009. Version 2.
Checksum: 5BF2DC46798577E3

FASTA44848,666
        10         20         30         40         50         60 
MDPKYFILIL FCGHLNNTFF SKTETITTEK QSQPTLFTSS MSQVLANSQN TTGNPLGQPT 

        70         80         90        100        110        120 
QFSDTFSGQS ISPAKVTAGQ PTPAVYTSSE KPEAHTSAGQ PLAYNTKQPT PIANTSSQQA 

       130        140        150        160        170        180 
VFTSARQLPS ARTSTTQPPK SFVYTFTQQS SSVQIPSRKQ ITVHNPSTQP TSTVKNSPRS 

       190        200        210        220        230        240 
TPGFILDTTS NKQTPQKNNY NSIAAILIGV LLTSMLVAII IIVLWKCLRK PVLNDQNWAG 

       250        260        270        280        290        300 
RSPFADGETP DICMDNIREN EISTKRTSII SLTPWKPSKS TLLADDLEIK LFESSENIED 

       310        320        330        340        350        360 
SNNPKTEKIK DQVNGTSEDS ADGSTVGTAV SSSDDADLPP PPPLLDLEGQ ESNQSDKPTM 

       370        380        390        400        410        420 
TIVSPLPNDS TSLPPSLDCL NQDCGDHKSE IIQSFPPLDS LNLPLPPVDF MKNQEDSNLE 

       430        440 
IQCQEFSIPP NSDQDLNESL PPPPAELL 

« Hide

References

« Hide 'large scale' references
[1]"cDNA sequence and genomic structure of EVI2B, a gene lying within an intron of the neurofibromatosis type 1 gene."
Cawthon R.M., Andersen L.B., Buchberg A.M., Xu G., O'Connell P., Viskochil D., Weiss R.B., Wallace M.R., Marchuk D.A., Culver M., Stevens J., Jenkins N.A., Copeland N.G., Collins F.S., White R.
Genomics 9:446-460(1991) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA].
Tissue: Bone marrow.
[2]"DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage."
Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., Nicholson C., Searle S.M., Wilming L., Young S.K., Abouelleil A., Allen N.R., Bi W., Bloom T., Borowsky M.L., Bugalter B.E., Butler J., Chang J.L. expand/collapse author list , Chen C.-K., Cook A., Corum B., Cuomo C.A., de Jong P.J., DeCaprio D., Dewar K., FitzGerald M., Gilbert J., Gibson R., Gnerre S., Goldstein S., Grafham D.V., Grocock R., Hafez N., Hagopian D.S., Hart E., Norman C.H., Humphray S., Jaffe D.B., Jones M., Kamal M., Khodiyar V.K., LaButti K., Laird G., Lehoczky J., Liu X., Lokyitsang T., Loveland J., Lui A., Macdonald P., Major J.E., Matthews L., Mauceli E., McCarroll S.A., Mihalev A.H., Mudge J., Nguyen C., Nicol R., O'Leary S.B., Osoegawa K., Schwartz D.C., Shaw-Smith C., Stankiewicz P., Steward C., Swarbreck D., Venkataraman V., Whittaker C.A., Yang X., Zimmer A.R., Bradley A., Hubbard T., Birren B.W., Rogers J., Lander E.S., Nusbaum C.
Nature 440:1045-1049(2006) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"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] [Europe PMC] [Abstract]
Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
Tissue: Leukemic T-cell.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
M60830 Genomic DNA. Translation: AAA35816.1.
AC134669 Genomic DNA. No translation available.
IPIIPI01014207.
PIRA38445.
RefSeqNP_006486.3. NM_006495.3.
UniGeneHs.5509.

3D structure databases

ProteinModelPortalP34910.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000333779.

PTM databases

PhosphoSiteP34910.

Polymorphism databases

DMDM281185464.

Proteomic databases

PaxDbP34910.
PRIDEP34910.

Protocols and materials databases

DNASU2124.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000330927; ENSP00000333779; ENSG00000185862.
ENST00000577894; ENSP00000462682; ENSG00000185862.
GeneID2124.
KEGGhsa:2124.
UCSCuc002hgk.2. human.

Organism-specific databases

CTD2124.
GeneCardsGC17M029630.
H-InvDBHIX0013696.
HGNCHGNC:3500. EVI2B.
HPAHPA007436.
MIM158381. gene.
neXtProtNX_P34910.
PharmGKBPA27914.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG44114.
HOVERGENHBG051514.
InParanoidP34910.
KOK16854.
OrthoDBEOG48PMK6.
PhylomeDBP34910.

Gene expression databases

ArrayExpressP34910.
BgeeP34910.
CleanExHS_EVI2B.
GenevestigatorP34910.
GermOnlineENSG00000185862. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

GenomeRNAi2124.
NextBio8593.
SOURCESearch...

Entry information

Entry nameEVI2B_HUMAN
AccessionPrimary (citable) accession number: P34910
Entry history
Integrated into UniProtKB/Swiss-Prot: February 1, 1994
Last sequence update: December 15, 2009
Last modified: May 1, 2013
This is version 100 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 cell differentiation molecules

CD nomenclature of surface proteins of human leucocytes and list of entries

Human chromosome 17

Human chromosome 17: 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